The idiopathic Coronavirus disease 2019 (COVID-19) pandemic outbreak caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has reached global proportions; the World Health Organization (WHO) declared it as a public health emergency during the month of January 30, 2020. The major causes of the rise of new variants of SARS-CoV-2 are genetic mutations and recombination. Some of the variants with high infection and transmission rates are termed as variants of concern (VOCs) like currently Omicron variants. Pregnant women, aged people, and immunosuppressed and compromised patients constitute the most susceptible human population to the SARS-CoV-2 infection, especially to the new evolving VOCs. To effectively manage the pathological condition of infection, the focus should be directed towards prevention and prophylactic approach. In this narrative review, we aimed to analyze the current scenario of COVID-19 management and discuss the treatment and prevention strategies. We also focused on the complications prevalent during the COVID-19 and post-COVID period and to discuss the novel approaches developed for mitigation of the global pandemic. We have also emphasized on the COVID-19 management approaches for the special population including children, pregnant women, aged groups, and immunocompromised patients. We conclude that the advancements in therapeutic and pharmacological domains have provided opportunities to develop and design novel diagnosis, treatment, and prevention strategies. New advanced techniques such as RT-LAMP, RT-qPCR, High-Resolution Computed Tomography, etc., efficiently diagnose patients with SARS-CoV-2 infection. In the case of treatment options, new drugs like paxlovid, combinations of β-lactum drugs and molnupiravir are found to be effective against even the new emerging variants. In addition, vaccination is an essential approach to prevent the infection or to reduce its severity. Vaccines for against COVID-19 from Comirnaty by Pfizer-BioNTech, SpikeVax by Moderna, and Vaxzevria by Oxford-AstraZeneca are approved and used widely. Similarly, numerous vaccines have been developed with different percentages of effectiveness against VOCs. New developments like nanotechnology and AI can be beneficial in providing an efficient and reliable solution for the suppression of SARS-CoV-2. Public health concerns can be efficiently treated by a unified scientific approach, public engagement, and better diagnosis.
The viruses are intracellular parasites that always emerge suddenly and infect numerous people within a short interval of time. The initial severe acute respiratory syndrome coronavirus (SARS-CoV) epidemic occurred in 2002, followed by the Middle East respiratory syndrome coronavirus (MERS-CoV) outbreak in 2012, and SARS-CoV-2-triggered coronavirus disease 2019 (COVID-19) during the month of December 2019 [1, 2]. According to the World Health Organization's (WHO) updates on COVID-19 cases, there have been over 601 million identified as positive COVID-19 cases and 6.4 million deaths as of 2nd September 2022, with the numbers continuing to rise .
Several factors lead to complications in COVID-19 management. These include social factors (like vaccine hesitancy , effect of social inequities on healthcare , lack of social protection , etc.), economic factors (economic inequalities) , an outbreak of other infectious diseases (like monkeypox, severe acute hepatitis, multi-organ failure, black fungus eye infection, etc.). The monkeypox outbreak is currently complicating the COVID-19 management scenario [7, 8]. In a similar context, another outbreak of severe acute hepatitis of unknown etiology in children is reported in United Kingdom, regions of America, Western Pacific, South East Asia, and Eastern Mediterranean . Additionally, environmental factors are also found to be associated with complications in COVID-19 management like pollution, chemical exposures, climate, and built environment .
The US government has constituted the SARS-CoV-2 Interagency Group (SIG), which categorizes the variants of the virus into three distinct categories—(1) Variant being Monitored (VbM), (2)Variant of Interest (VOI), and (3)Variant of Concern (VOC). There is also a fourth category in this classification, (4) Variant of High Consequence (VOHC). However, no VOHC has been identified in the US, till date . Presently, the prominent VOCs are the different lineages of the Omicron variant [12,13,14]. The WHO has also classified the SARS-CoV-2 variants under same categories like VOI, VOC, and VOHC.
The SARS-CoV-2 virus has five different structural proteins. The spike (S) glycoprotein that makes up the virus's envelope surface is the main structural protein involved in interaction with the host cells' angiotensin-converting enzyme 2 (ACE2) receptors to enable the entrance of infectious virus particles . The reports in this context reveals that the most successful medications are those that target the interaction of S glycoprotein with the ACE2 receptor . However, the Omicron variant of this virus not only exhibits stronger binding with the ACE2 receptor unlike the other variants but also shows an evolved mode of invasion into the host cell in the Transmembrane protease, serine 2 (TMPRSS2) independent approach, through the endosomal route . Furthermore, the BA.1 and BA.2 variants of Omicron favor the TMPRSS2-independent endosomal entry route. This corresponds to specific regions on the spike protein leading to the alteration in antigenicity and could be an important factor in rapid transmission and changes in pathogenicity of the Omicron variants . The altered entry route of Omicron variants facilitate infection into several different animal species such as horseshoe bat, mice, domesticated avian species, etc., increasing the susceptibility to reverse zoonosis . In the latest report of WHO, it was found that the Omicron variant constituted the 99.6% sequences reported for the period of 29th July 2022–29th August 2022 .
A recent study reported that the replication complex of this virus is the fastest RNA-dependent RNA polymerases among all classes of coronavirus . Because of the fast elongation mechanism, it is liable to include mismatch mutations easily producing high variability in genomic sequences giving rise to numerous strains with different features. This further increases the difficulty of designing an efficient drug to target the virus . Although the virus has faster transmission rates, the mutation rates are relatively lower at 1 × 10–6 per cycle than influenza viruses which have a mutation rate of 3 × 10–5. It is due to the linear genome (instead of segmented) and the presence of proofreading (nsp14) that are absent in influenza viruses. The lower mutation rate of SARS-CoV-2 facilitates the development of vaccines with a longer duration of protection than influenza viruses [21, 22].
The generation of new variants of a virus follow two basic mechanisms—random point mutations (Alpha, Beta, Gamma, Mu, Delta, and Omicron have evolved by this approach) and recombination (coronaviruses, influenza virus, HIV, etc.) [14, 23, 24]. The factors responsible for genetic diversity, in the case of coronaviruses, are mutations coupled with recombination, horizontal gene transfer, or gene duplication. Homologous recombination and gene transfer contribute to the larger genome by increasing plasticity for the gain and modification of genes . This results in coronaviruses gaining the ability to explore new hosts via the interaction between their spike protein and various cellular receptors of the host. This attributes to natural selection and the evolution of viruses . The B.1.1.7, B.1.351, P.1, and B.1.1.529 lineages corresponding to alpha, beta, gamma, and omicron variants that are found to have high transmission rates . The B.1.617.2 variant, also known as the Delta variant is a highly infectious variant responsible for the second wave of COVID-19 in India [28, 29] and had become the dominant variant globally in 2021 . The different strains of the virus show different patterns of disease prognosis .
It has now become crucial to study the development of novel hybrid strains of the virus that can potentially magnify the situation of a pandemic by rapidly increasing the number of clinical cases positive. Three recombinant strains of omicron variants have been identified to date, namely, XD, XE, and XF. The recombination between delta and BA.1 lineage of omicron had led to the development of XD, whereas XF is formed by the recombination between BA.1 and UK delta variants . The BA.4 and BA.5 variants of Omicron are important in its evolutionary trajectory. Though these variants possess similarities with BA.2, they contain unique mutations like L452R and F486V in the spike proteins. These variants can infect people who are immune to other variants of the virus, including Omicron, and increase hospitalization . The monthly report of WHO for the month of August 2022 also stated that currently, the BA.5 lineage of Omicron is found to be dominant globally, with an increase in incidence to 78.2% per week .
The emergence of new variants of concern resulting from mutations in the viral genome has become a great problem in the treatment of infection and prevention by vaccination. This is because many of the widely used repurpose drugs and some vaccines are rendered ineffective when used against the new variants. There is a list of monoclonal antibodies (anti-RBD monoclonal antibodies) that are clinically used against various variants of Omicron. For example, VIR-7831 (sotrovimab), COV2-2196 and COV2-2130 (AstraZeneca), etc. However, their efficacy is greatly reduced due to the high mutation rate of S protein of the new variants of the virus in addition to the fact that monoclonal antibodies are specifically designed to target S protein .
To effectively manage the transmission of the SARS-CoV-2 virus in the population it is important to educate and encourage people to adhere to the emerging norms and rules pertain to prevent the infection . Additionally, the public governments need to send clear updates on COVID-19 without any confusion. . The major goal to mitigate and manage COVID-19 is by effective prophylactic measures and prevention, and initiation of recording patients’ immune responses from time to time with the help of healthcare personnel . It also involves the introduction of innovative approaches by creating safe healthcare environment for the healthcare workers who are at risk.
The objective of this narrative study is to comprehensively understand the pharmacological and therapeutic domains of COVID-19 management. We aim to analyze COVID-19 management, pharmacological and therapeutical advancements as well as to provide a holistic picture of vaccination. We also discuss the major complications observed during COVID-19 and in the long COVID scenario as well as containment of the pandemic. Additionally, we have emphasized on the COVID-19 management approaches for the special populations like children, pregnant women, aged groups, and immunocompromised patients.
Current scenario: transition in COVID-19 management
The transition phase of COVID-19 is associated with many changes, it enhances the use of hand sanitizers, aerosols, surface sterilizing agents, cleaning solutions, PPE kits, face masks, and gloves . It sparks the condition of health, age, including acceleration in innovation, collaboration, discovery, catalyzing future health and medicine, thereby reimaging health and medicine. It has opened a broad area of research in the field of medical technology including computational biology, gene sequencing, design, and delivery of antibodies and drugs [14, 36].
The upsurge and spread of SARS-CoV-2 have given rise to severe threat to global public health. Reliable and rapid tests are needed to affirm infections. Currently, diagnostic approaches include clinical chest CT scanning including chest X-rays and laboratory diagnoses (Nucleic acid RT-PCR, RT-LAMP, qRT-PCR), protein testing, point of care testing, and fluorescence-based biosensors tests are used to confirm COVID-19 [36, 37]. X-rays are one of the common techniques for imaging cardiothoracic and pulmonary disorders . It played an important role in diagnosing pneumonia and assessing its severity. It has been discovered that CT scans of COVID-19 patients exhibit peculiar imaging with multilobar and aberrant peripheral distribution [39,40,41]. Nucleic acid testing involves reverse transcriptase-polymerase chain reaction (RT-PCR), which involves the generation of single-strand cDNA from RNA through retroviral DNA polymerase, accompany by PCR amplification of the target cDNA regions . RT-qPCR is a highly specific, rapid, and molecular-based assay to detect infection . It can also detect and measure negligible amount of antibodies from various samples . Moreover, the WHO has approved some of the testing samples for laboratory purposes. In another technique, fluorescence-based biosensors are used for cheap and quick detection of antibodies in the serum .
The efficiency of these techniques can be improved by designing the combination of two or more methodologies. For instance, the integrated RT-LAMP and CRISPR-Cas12 method can prove to be an efficient, simple, and rapid test when designed in the form of a kit that could be used anywhere . The advancement in technologies has resulted in up-gradation and improvement in the currently followed techniques making them more reliable, accurate, easy to perform, and cost-effective (Table 1). This is intending to provide benefits to a large number of people globally, irrespective of their economic status.
During the initial phases of the COVID-19 pandemic, a notable number of diagnostic companies were proactively involved in the design, development, validation, verification, and distribution of diagnostic tests. Hundreds of molecular tests and immunoassays were created quickly, albeit many are still awaiting clinical validation and approval by regulatory authorities. However, greater test refinements, substantial molecular epidemiological confirmation and official FDA certification, are still required. Furthermore, the data on biobanks and the follow-up of actual patients are insufficient. Therefore, AI and machine learning techniques for data interpretation must be created and used. To battle present and future pandemics, there must be a worldwide unity in terms of test availability, control of infectious diseases and diagnostic strategies. The person diagnosing should inform about the therapy selection and follow-up on its success. It is important to highlight that deep learning algorithms combined with imaging modalities provide only limited information regarding sick individuals. The global research scenario supports the fact that deep learning approaches cannot replace the function of physicians or clinicians in clinical diagnosis. Deep learning specialists hoped to collaborate proactively with radiologists and medical professionals in the near future to give adequate support systems for diagnosing COVID-19, particularly in the early stages of the disease, or evaluating the level of severity of the SARS-CoV-2 infection. Recently, it was found that the PCR assay, specifically the AIGS (Automatic Integrated Gene Detection System) RNA detection kit, can be used to test respiratory tract samples from COVID-19 patients for the presence of the Omicron variant. With the aid of this kit, it has been anticipated that 95.1% of all Omicron variant (BA.1 through BA.5) sublineages are prevalent . This diagnosis is beneficial in identifying the individuals infected and history of infection. The specific antibodies against the SARS-CoV-2 nucleocapsid protein can be considered as a relatively early diagnostic biomarker. To quantify the specific SARS-CoV-2 immunoglobulins in SARS-CoV-2 positive and non-infected individuals, powerful, flexible, and sensitive biotools have been developed recently. These tools are based on the surface of magnetic microbeads functionalized with nucleocapsid (N) and internally expressed recombinant spike (S) proteins.
Currently, there are few standard drugs available in the market that are recently approved by FDA in the USA; however, repurposing drugs is a beneficial solution, that provides a better, immediate strategy to tackle the disease. Presently available treatments include drugs of small size molecules that prevent the entry of the virus into host cells or prevent the assembly and block replication of viruses [13, 49,50,51,52,53]. The literature showed that remdesivir reduces the recovery time of hospitalized patients, thus reducing mortality . Beigel et al. in their final report for the treatment of COVID-19 presented data on 1062 patients, where 541 patients were assigned with remdesivir and 521 on placebos. According to existing evidence, patients on treatment have an average hospitalization time of 15 days, whereas patients on remdesivir have an average hospitalization time of 11 days. Chu et al. demonstrated the role of Lopinavir/ Ritonavir in the treatment of COVID-19 in 41 patients for 3 weeks. Clinical data suggested lower adverse effects in the treatment group than in the control. It has been seen that there is a reduction in infection rate and steroid usage where the patients were treated with Lopinavir/ Ritonavir combination. Thus, patients treated with these drugs show a decrease in viral load and a rise in blood cell count, thereby ensuring a positive outcome and better recovery . Arbidol was found to be a more effective drug as compared to lopinavir, meta-analysis studies reveal a conversion rate of SARS-CoV-2 nucleic acid on day 7 (p = 0.03) and day 14 (p = 0.006). Further, it showed a higher improvement rate on day14 (p = 0.02) and a lower rate of mortality (p = 0.007). Mehra et al.analyzed chloroquine with and without macrolide for treatment, total of 96,032 patients with COVID-19 were hospitalized, 14,888 patients were selected, among them 81,144 people were there in the control group and 1868 and 3016 received chloroquine and hydroxychloroquine alone, whereas 3,782 and 6,221 patients received both drugs in combination with a macrolide. Unfortunately, the observed outcome showed a negative result as treatment with these drugs decreases survival and increases the frequency of arrhythmias.
Cathrine et al. in their randomized trials on chloroquine and hydroxychloroquine has found that hydroxychloroquine increases the mortality risk in COVID-19 patients; moreover, there is no benefit of chloroquine in the treatment .
Recent research indicates that favipiravir can reduce inflammatory mediators but not respiratory status fully. SARS-CoV-2 respiratory distress is hypothesized to be caused by both direct viral activity and chemical mediators generated by SARS-CoV-2. In some patients, inflammation and cytokine storms persisted following Favipiravir therapy, although they were manageable with steroids .
Currently, molnupiravir is approved by U.S. Food and Drug Administration (USFDA) for the management of COVID-19 . Molnupiravir is an oral bioavailable ribonucleoside analog of B-D-N4-Hydroxycytidine . It acts as an antiviral agent showing a broad spectrum of activity against various RNA viruses. Molnupiravir inhibits the replication of viruses; it has been found that molnupiravir is highly effective for limiting nasopharyngeal viral load. B-D-N4-Hydroxycytidine-5-Isopropyl ester is a prodrug of molnupiravir (EIDD1931); after entering into the host cell, this active form of drug inhibits the replication of viruses by incorporating itself into the virus instead of uracil or cytosine. These base-pair changes lead to mutation, resulting in a viral replication error. Research demonstrates that molnupiravir has been effective against various influenza and coronavirus variants. Results from Phase I/II/III trials revealed that molnupiravir reduces the risk of death and hospitalization for mild COVID-19 patients. Studies on animals indicate that the administration of molnupiravir in humanized mouse models significantly reduces in vivo replication and symptoms of SARS-CoV-2 in patients. During a pandemic wave dominated by the omicron BA.2 subvariant, the cohort study conducted by Wong et al., sought to assess the virological effects in relation to the consumption of molnupiravir or nirmatrelvir–ritonavir in hospitalized patients with mild-to-moderate COVID-19. Molnupiravir was administered to 1,856 of the 40,776 COVID-19 hospitalized patients. Molnupiravir-treated patients were shown to have a decreased risk of death from all causes. When compared to non-receptors, receiving molnupiravir or nirmatrelvir–ritonavir was linked to considerably lower odds of all-cause death and the overall disease progression outcome, as well as a decreased need for oxygen therapy . The reduction in the mortality rate was greatly visible in patients with higher risk of hospitalization, such as those above 80 years in age . In the same study, 890 patients were administered Paxlovid, the results indicates that this drug was also efficient in lowering the mortality rate . Paxlovid is a combination of the second-generation protease inhibitor nilmatrelvir and the pharmacological enhancer ritonavir for the treatment of SARS-CoV-2 infectious. Paxlovid acts as an active protease inhibitor, exerting antiviral efficacy by inhibiting the virus replication process .
Biological products such as pAbs (polyclonal antibodies), mAbs (monoclonal antibodies), convalescent plasma, and hyperimmune γ-globulin are used as passive immunotherapy for the treatment of COVID-19 . Repurposed mAbs are also used for the treatment, of hospitalized patients 12 years of age or older. Likewise, mAbs such as bamlanivimab–etesevimab, casirivimab–imdevimab, and sotrovimab are administered. It acts by neutralization of the viral proteome and by balancing the number of cytokines. Patients who are hospitalized are not given mAb therapy, and patients with hypoxia are excluded. The drugs utilized for the treatment of COVID-19 are summarized in Table 2. The research community is focusing on developing SARS-CoV-2 specific antivirals and mAbs; many of them are under different stages of clinical trials.
Administration of neutralizing monoclonal antibodies offers a prompt and passive immunization, that can reduce virus load and result in the rearrangement of immune-modulatory molecules. The monoclonal antibodies are capable of eliciting an immune response. Currently, clinical studies are going on ruvalizumab which is a recombinant monoclonal antibody that targets CS. It acts as an anti-inflammatory agent. Other mAbs under ongoing clinical trials include AK119, JMB2002, LY-CoVMab, ADM03820, HLX70 and DXP604. USFDA approved a few mAbs for emergency use in COVID-19 including tocilizumab (TCZ), regdanvimab (CT-P59), sotrivimab (VIR-7831), SCT-401 and levilimab. The mAbs that work against various variants (alpha, beta, gamma, delta and omicron) of coronavirus include sotrovimab, tixagevimab plus and cilgavimab, casirivimab and imdevimab .
Immunization plays an important role in preventing and limiting the spread of disease, to bring down this pandemic, a large proportion of the world needs to be vaccinated. According to recent data, 66.8% of the world population have received at least one dose of a COVID-19 vaccine and 12.15 billion doses have been administered globally . Various vaccines have been discovered worldwide, including mRNA vaccines based on the introduction of mRNA sequences for disease-specific antigens, and DNA-based, attenuated, and vector-based vaccines are used, as they provide a promising, faster, and cheaper alternative to conventional approaches. Different types of vaccines are shown in Fig. 1. Even vaccines for veterinary usage are approved in different parts of the world to seize transmission from household pets .
The inactivated vaccine consists of whole virus particles that have been killed or inactivated by heat or chemicals such as formaldehyde or formalin, thus destroying the pathogen’s ability to replicate, though they retain some epitopes so that the immune system can still recognize it . The attenuated vaccine contains active pathogens particles that have been weakened or modified by attenuation but can replicate inside the body eliciting a long immune response. Subunit vaccines use only part of an antigen that stimulates an immune response. Another class of vaccine includes toxoid vaccines, conjugated vaccines, and Nuclei acid vaccines like RNA, and DNA vaccines which use a piece of mRNA or DNA to produce the same antigenic molecules as a disease-causing pathogen . Table 3 summarizes details of approved vaccines for the prevention of COVID-19.
The US Food and Drug Administration has just fully approved the Pfizer/BioNTech vaccine for human use, while 38 vaccine candidates are undergoing emergency use licensing . Almost 60% of the world population, i.e., around 12 billion vaccine doses have been injected with a single vaccine dose as of May 2022. Since SARS-CoV-2 vaccines follow quick regulatory paths, vaccinovigilance (Phase 4 of the clinical trial) and the development of a comprehensive vaccination program are essential for the protection of public health. Vaccination is the safest method for combating the COVID-19 pandemic. According to a recent press release by US FDA, they have authorized limited use of Johnson and Johnson (J&J) COVID-19 vaccine for the individuals that are 18 years or greater in age but do not have access to the approved vaccines as well as to those who opt for J&J vaccine . Almost 7.7% of the US population has taken primary vaccination with the J&J vaccine. The reports define the safety concern relating to rare events of blood clots reported previously also for the adenovirus-based vaccines . This reaction is triggered by antibodies to aggregates generated between adenovirus and platelet factor 4. This aggregate is bound by antibodies, resulting in platelet activation. The sequence of events leads to the life-threatening step, i.e., thrombosis with thrombocytopenia syndrome. A recent report has been made for other vaccines like AZD122, which indicates that the population vaccinated with these vaccines experience skin rashes, characteristic vesicular plaque formation, muscle weakness, pitting edema on the hands, and foot neuropathic pain . FDA officials concluded the revision based on the detailed investigative reports submitted for such post-vaccination events as well as data on the safety and efficacy of the vaccine. There is currently a boom in mRNA clinical research for infectious diseases, especially as the impact of mRNA-based technologies is becoming apparent as these first-generation vaccines are deployed globally. This prompts industry researchers and experts to see increased interest in other therapeutic areas, especially mRNA platforms in oncology and rare autoimmune diseases and neurodegenerative disorders. In contrast to the initial SARS-CoV-2 virus, the Omicron (B.1.1.529) variant of concern has shown to be more contagious and infectious . Ad26.COV2.S or BNT162b2 vaccine recipients exhibited long-lasting spike-specific CD8 + and CD4 + T cell responses that displayed significant cross-reactivity against both the Delta and the Omicron variants. Multiple doses of vaccine has been proven to be efficient in eliciting immune response against several variants of the virus. In the same context, a booster dose is intended to restore vaccine efficacy from the immune protection point that has been determined to be insufficient. A third booster dose is also being advised currently because, in the words of Agrawal and colleagues, "Omicron symbolises a significant challenge to the existing two-dose vaccination tactic currently adopted by many countries globally (17–22-fold reduction in neutralization titers)". There are various mRNA vaccines available commercially and among them the effectiveness of the BioNTech/Pfizer BNT162b2 messenger RNA (mRNA) vaccine against the Omicron variant was examined by Muik et al. . According to their findings, three doses of BNT162b2 mRNA are inevitably mandated to defend against Omicron-driven COVID-19 .
In December 2020, the alpha variant was confirmed as a variant of concern. It can be also written as B.1.1.7. The variant has a total of seventeen variations in its genome and was found to increase its transmissibility rate [79, 80]. Beta variant (B.1.351) was detected in South Africa (May 2020). It contains three mutations located in RBD. More recently omicron (B.1.1.529) has been detected in multiple countries (Nov 2021), it has more mutations that are located in the receptor-binding domain . WHO approved various vaccines for emergency use. These vaccines can be categorized based on their manufacture and mode of action. Table 3 summarizes details of approved vaccines for the prevention of COVID-19.
Lauring et al. conducted a study to compare the effectiveness of mRNA vaccines and to characterize the clinical severity of covid19 patients with different variants of viruses. A total of 11,690 population participated and the outcome shows that the mRNA vaccine has the effectiveness of 85%, 94% and 65% for alpha, delta and omicron variants, respectively. Finally, the mRNA vaccine was effective over almost every variant of coronaviruses. Therefore, vaccinated people show lower severity against COVID-19 .
On January 2021, drug regulators in India granted emergency approval for the covid vaccine co-developed by AstraZeneca and the university of Oxford. Mahadevaiah et al. in their study of immunogenicity, safety, and efficacy of covishield vaccine, showed seropositivity of 69.67% which is an acceptable level of safety profile. Another study on BNT162b2 mRNA vaccine phase III clinical trial consist of 43,548 individuals, among 17,411 individual 8 cases of COVID-19 positive were identified, and among 17,511 individuals 162 COVID-19-positive cases were confirmed showing 95% of vaccine efficiency . BNT162b2 efficacy in volunteers aged between 16 and 55 years was 95.6% and for individuals above 55 years, above or equal to 65 or 75 years of age, efficacies were found to be 93.7%, 94.7% and 100%. Lindsey conducted a phase III trial in the United States across 99 centers for checking the efficacy and safety of mRNA vaccines. The setup consists of 30,420 individuals who were randomly administrated with vaccines or placebo in a ratio of 1:1. The mRNA vaccines showed a 94.1% efficacy rate at preventing COVID-19 infections .
SARS-CoV-2 impact on children, pregnant women, and aged populations
The COVID-19 caused by the SARS-CoV-2 virus infect people from all age groups; however, there are variations in severity observed. The symptoms of infection observed in children on exposure to the virus is similar to adults and sign and symptoms include fever, cough, sore throat, malaise, nasal discharge, sometimes vomiting, nausea, body pain and diarrhea . The major observation is that in the majority of cases the infected children are asymptomatic. These children are carriers for transmission to other age groups with greater susceptibility . However, the severity is more in children with chronic conditions like cancer, chronic pulmonary or heart disease, neurological diseases, known immunodeficiency, or cardio-vascular diseased condition [87, 88]. The infection caused in children is mild and the severity is lower than that of adults with an exception of infants who on exposure to the virus experiences serious illness [87, 89]. The severe health implication in children during COVID-19 infection is in the form of the multisystem inflammatory disorder  and it is thought that as the virus is transitioning from pandemic to epidemic, a greater proportion of children will be affected by the SARS-CoV-2 infection like in the scenarios of other epidemic coronaviruses .
In the case of pregnant women, it was found that the symptomatic patients are more susceptible to serious disease conditions and can have adverse pregnancy with neonatal outcomes like pre-term delivery or intrapartum fetal distress [91, 92]. On the contrary, expecting mothers with asymptomatic COVID-19 infections faced complications similar to non-infected ones . The novel variants with high transmission rates are a threat to the health of pregnant women and neonates. To protect them from the disease and complications, it is essential to prioritize vaccination and immunization schedule .
It is found that aging is accompanied by immunosenescence which is diminished activity of the immune system. On the other hand, the aged population also shows constant production of inflammatory mediators and cytokines . In patients, who are 65 years and above, SARS-CoV-2 infection shows a high mortality rate in addition to more percentage of hospitalization [95, 96]. Chronic conditions like cardiovascular diseases, diabetes, obesity, etc., are the risk factors that increase the virus infection .
Immunocompromised patients and patients with comorbidities are found to be at greater risk of mortality and complications during hospitalization than the normal population [97, 98]. The infection can alter their primary disease condition which worsens their situation . Such people are more likely to be admitted to intensive care units (ICUs) and have an increased risk of mortality. This category includes people with conditions like cancer, hematopoietic cell transplant, solid organ transplant, diabetes mellitus, hypertension, etc.[97, 99]. The disease pathogenesis in such patients is very rapid and serious, irrespective of the age group of patients (Fig. 2) . Thus, it is a major cause of concern today to save the lives of immunocompromised patients and patients with comorbidities.
Some monoclonal antibody treatment regimes (like bamlanivimab–etesevimab, casirivimab–imdevimab and sotrovimab) have been authorized for emergency use for patients with 2 more risk factors. These factors include age above 65 years, pregnancy, immunocompromised patients, patients with comorbidities or chronic conditions like hypertension, diabetes, obesity, etc. Therefore, monoclonal antibody based treatment is appropriate for the above mentioned special groups in the population . Molnupiravir-based treatment is also applicable for the patients with high risk of hospitalization, older age groups and patients with chronic health conditions. However, it is not recommended for pregnant and breast-feeding women and children . According to the USFDA, The Moderna COVID-19 Vaccine and the Pfizer-BioNTech COVID-19 Vaccine may be used for COVID-19 prevention in children as young as 6 months old under emergency circumstances .
COVID-19 and associated complications
The SARS-CoV-2 virus affects the lower respiratory tract. The pathological symptoms range from asymptomatic (mild infection) to severe complications, which could eventually become life-threatening. Mild symptoms are cured in about a week . Patients from the older age group, having chronic health conditions or compromised immune system are more prone to severe infection which could also lead to death [102, 103]. However, even the younger population without any pre-existing health condition has been found to develop severe infections. The major causes of mortality due to this infection include hypoxemia and cardiovascular complications which could lead to anomalous blood clotting. Cases with strokes, kidney injury, cardiac injury, and ecchymosis are attributed to disseminated intravascular coagulopathy.
The COVID-19 is also linked with the initiation of autoimmune responses. Development of autoimmune thyroid diseases, Guillain–Barre syndrome, autoimmune hemolytic anemia, Kawasaki disease, immune thrombocytopenic purpura, and identification of autoantibodies indicates that SARS-CoV-2 virus is capable of generating autoimmune responses. However, more research is required in this domain for a complete understanding of the potential impacts of this virus on the host body .
SARS-CoV-2 pathogenesis comprises multiple factors that result in severe damage, first in the lungs and then with systemic dissemination. Acute lung failure, acute liver failure, acute kidney damage, and cardiovascular illness, in addition to a wide spectrum of hematological abnormalities and neurological problems are characteristics of multi-organ dysfunction (Table 4) . The most important pathways are linked to SARS-CoV-2 and indirect pathogenic properties. Even though the presence of ACE2, a SARS-CoV-2 receptor, has been confirmed in the lung, heart, kidney, liver, and nervous system, there are some worries about the presence of SARS-CoV-2 RNA in these organs . COVID-19 has the greatest impact on the lungs, heart, brain, kidney, liver, and gastrointestinal tract. As a result, measures should be taken, and patients should be consulted before they are discharged from the hospital to understand other possible anomalies that may emerge during the post-COVID healing phase . One of the numerous variables is an increase in the rates of blood clots reported in COVID-19 patients, which will cause a slew of downstream difficulties. Another major explanation for the rapid development of mucormycosis is the use of steroids as a treatment for seriously and critically sick covid patients [107, 108]. Many COVID-19 patients who have recovered reveal hypercoagulation diseases ranging from disseminated intravascular coagulation to venous thromboembolism, all of which can contribute to cerebrovascular illness. Signs and symptoms of the antiphospholipid syndrome include antiphospholipid antibodies and the lupus anticoagulant, as well as venous and arterial thrombosis . Cardiovascular problems can arise during the post-COVID recovery period, resulting in cardiac arrest and, in extreme circumstances, a heart attack. COVID-19 is an inflammatory illness that also causes blood vessel inflammation. An increase in blood thickness occurs, which leads to clot formation in the lungs and heart arteries, producing symptoms such as shortness of breath, very rapid or slow heart rate, dizziness, and unconsciousness in those recovering from COVID-19 [110, 111]. After recovering from COVID-19, patients with moderate to severe symptoms from SARS-CoV-2 infection have various organ damage and additional consequences. Patients with a history of various health issues or illnesses are more likely to have serious consequences. Mental health issues have emerged as a result of the extended epidemic, which is caused by multiple lockdowns and stay-at-home situations .
Limitations of COVID-19 management
The SAR-CoV-2 virus-caused pandemic has a significant impact on every aspect of life around the world, including society, politics, the economy, health, and professional fields.. This results in numerous challenges in these domains. The major challenge to controlling the pandemic is the mass vaccination of people. Despite the fact that 66.8% of the world's population has received at least one dose of vaccine, the entire course of vaccination is necessary to control the global epidemic.This requires increasing the production of vaccines which can be done by constructing more manufacturing units and obtaining suitable quantities of the required raw materials. The aim should be to provide vaccines to all especially in low-income countries, which are unable to afford them. In addition to infrastructural challenges in the production of vaccines, there are also certain limitations associated with its efficacy against all variants of the virus. To ensure the development, approval, dissemination, administration, and monitoring of efficient vaccines, there are also strict policy matters and challenges that have to be looked upon . The health care centers, procuring necessary oxygen cylinders and quarantine facilities should be well equipped in advance, with all these requirements and necessities to prevent the rise in mortality, specially in cases where mutations in the virus leads to development of variants of concern which could have catastrophic effect on the population. For instance, the situation of delta variant which claimed numerous lives resulted in second or third wave of infection in many countries.The facilities should be designed and constructed focusing on effective operation during the situation of emergency. Some of the important factors for operational design are healthcare networks, patient safety, indoor air quality, etc. The designed facilities should have the capacity and necessities for critical care for terminally ill patients . It is also discovered that front-line employees and healthcare professionals face a variety of difficulties throughout their careers, including increased workload, psychological stress, a lack of high-quality personal protective equipment (PPE), social exclusion and stigmatization, an absence of incentives, a lack of coordination, and improper management. . The improper disposal of contaminated wastes like PPE kits, gloves, etc., also poses an important challenge as these become a cause of environmental pollution and a source for transmission of infection [115, 116]. Thus, it results in a new environmental crisis. This can only be controlled by promoting sustainable plastic waste management and implementing policies to ensure the safe disposal of harmful wastes . Many new challenges arise as a result of the emergence of omicron virus subvariants. Although BA.4/5 is significantly (4.2-fold) more resistant, it is also more likely to cause infections that result in the development of vaccine-resistant strains. The SARS-CoV-2 Omicron lineage is still evolving, producing subvariants that are not only more contagious but also quite resistant to antibodies. There has been a geographical divide observed in the prevalence of different variants of Omicron, dominant over different regions of the world. The high percentage of positive cases in Europe and other continents can be attributed to this high transmissibility rate, for example, the BA.2 variant of Omicron. According to preliminary findings from Denmark's Statens Serum Institut (SSI), BA.2 is 1.5 times more highly infectious than BA.1. The high transmissibility of BA.2 was demonstrated in Denmark, where the number of positive cases doubled in less than a week. . In Gauteng, the omicron variant prevailed over the B.1.617.2 (delta) variant and accounted for 98.4% of all new cases sequenced in South Africa in December 2021. Following the initial Omicron (BA.1) peak in January 2022, the almost total replacement of Omicron BA.1 by BA.2 resulted in a second peak in SARS-CoV-2 infections and previously unheard-of levels of infection in England in March 2022. In lower-income nations, there are still nearly one billion unvaccinated individuals as of May 22, 2022. 70% of the population has been vaccinated in only 57 nations, almost all of which are high-income nations.
Innovative and novel approaches for COVID-19 management
The discovery of new drugs, vaccines, repurposing of drugs, in vitro drug screening, in silico screening platforms, development of new technologies, and novel diagnostic techniques have added new directions to the field of science. Artificial intelligence (AI) is one of the most emerging areas of research, which provides a new direction to research and development leading to the identification and development of new drugs [122, 123]. It involves early detection and diagnosis of the infection via CT scanning, X-ray, lab testing, and genome sequencing. It shows a tremendous capability for contributing toward novel drug discovery and repurposing of available drugs that could be used for treating COVID-19 [124, 125]. It utilizes several datasets to identify potential inhibitory human coronavirus activities . Recently, it has been noticed that due to side effects and reduced efficiency of many drugs there is a decline in the number of new FDA-approved drugs. Earlier the process of drug discovery was very costly and sophisticated, however, it has been seen that AI can accelerate various scenarios including repurposing and drug discovery. AI helps us to determine the protein structure of the virus and, thus, plays an important role to determine its function inside the cell for the development of drugs and vaccines to combat COVID-19 . AI is being used successfully for the identification, diagnosis, and treatment of disease. Further, it helps in contact tracing, finding the risk of mortality, and discovering new drugs and vaccines, moreover reducing the burden on healthcare workers . The list of companies using AI for the development of treatment against COVID-19 by repurposing drugs includes Innoplexus, gero, healx, and deargen. Exscientia lktos and SRI International are some of the companies that developed new drugs by applying AI for the treatment of COVID-19 .
Drug repurposing is also known as repositioning of the drug . It is a procedure that seeks to identify new application and utilities of existing drugs and is considered a cost-effective approach . The outbreak of COVID-19 has challenged health workers, scientists, and pharmacists to select an appropriate drug for treatment; however, discovery of new vaccines and drugs was costly and time-consuming with a success rate of only 2.01% , hence considering the cost and time lag, the repurposing of drugs for the treatment of COVID-19 came into existence. The systematic approach to drug repurposing can be classified into computational and experimental approaches . Several drugs used for the treatment of different stages of COVID-19 include lopinavir, hydroxychloroquine, atazanavir, nintedanib, tocilizumab, and remdesivir [132, 133].
Remdesivir was the first drug to be approved for the treatment of coronavirus disease. It acts as an analog of nucleoside mainly ATP that inhibits RNA polymerase . It is an antiviral drug that inhibits the replication of the virus  and exhibits a wide antiviral spectrum among RNA viruses including ebolavirus, MERS-CoV, and SARS-CoV-2 . Recently available evidence about the antiviral effects of remdesivir against viruses is majorly based on in vitro and in vivo studies . Moreover, effective and positive studies against coronavirus led to the emergence use of the drugs during COVID-19 . Lopinavir/ ritonavir is another class of drug which has been repurposed for the treatment of COVID-19, It acts as protease inhibitor used for treating HIV infection . Currently, studies indicate that both these drugs can be useful in inhibiting SARS-CoV 3C-like protease enzyme .
Recent clinical trials on COVID-19 patients showed that nintedanib leads to a decrease in the expression of IL‐1 and IL‐6, which play a major role in the COVID‐19 cytokine storm leading to fibrogenesis in the lungs . It is given to COVID-19 patients who have Idiopathic Pulmonary Fibrosis, as it may provide a novel approach for managing COVID-19 . Ivermectin is an FDA-approved anti-parasitic drug that is devised as an 80:20 mixture of the equipotent homologous 22,23-dihydro ivermectin, which has shown to inhibit SARS-CoV-2 in vitro with an undisclosed mechanism of action . An extensive computational analysis was done to distinguish the best docking of ivermectins to viral proteins and, later, to analyze potential structural alterations with molecular dynamics. Ivermectins can bind to the protease 3CL-superficial and internal pockets, as well as the HR2-domain, causing unfolding/folding and altering the native conformation of these proteins . Chloroquine (CQ), an aminoquinoline, for many years malaria was traditionally treated with chloroquine phosphate. It is a quinolone with anti-inflammatory properties as well as some amoebic properties. Chloroquine's anti-viral and anti-inflammatory activities may be responsible for CQ's efficacy in treating COVID-19 patients .
In an expanding pharmaceutical market collaboration between medicines, and regulators are essential. The regulatory agency needs to ensure the safety, efficacy, quality, and performance of medical products. National regulatory agencies are responsible for ensuring pharmaceuticals and biological products meet standards of quality and safety. A global training network on vaccine quality is also available to identify gaps and support plans. Other agencies like EMA, CHMP, COVID-ETF, SAWP, FDA, MAHs, and ICMR have been working in collaboration with each other to fight COVID-19 worldwide.
Nanotechnology is one of the emerging areas in the era of COVID-19. The study in this direction helps us to manipulate, organize and assay molecule and atomic level in nanometres. It converges various fields like biotechnology, computational biology, biological sciences, diagnosing and treating COVID-19. It is used for drug discovery and brings out new opportunities for inexpensive detection methods and vaccines against COVID-19. Several nanomaterials can be used for the prevention of COVID-19, such as the integration of nanomaterials into personal protective equipment kits that can protect health workers. Cellular binding of the viral particles can be prevented by targeting nanoparticles against ACE receptors, moreover, nanoparticle-based vaccines, and drug delivery systems can be used to prevent SARS-CoV-2 . Nanosensors and nano-filter face masks can be used to prevent infectious diseases . Recently field effect transistor-based biosensing has been developed to detect infection, Some nanomaterials like carbon black, graphene, gold, and silver particles are used in biosensors for detecting SARS-CoV-2 infectious . However more research is needed to be done to find the application of nanotechnology in the era of this pandemic, safety measures must be encouraged as well as the use of nanoparticles for covid management must be accelerated. Moreover, expansion in the field of nanotechnology can help us to control and eliminate the spread and reoccurrence of COVID-19 .
Viruses invade humans via the nasal portal during inhalation, therefore researchers around the world are focusing on the vaccines that can prevent the aerosols which invade the nose. The intranasal vaccine can intercept the virus and triggers the immunity to combat the viruses at the site of viral entry, thus preventing the multiplication of viruses. Nasal vaccines are easy to administer and produce secretory IgA, which can elicit an immune response at the site of virus entry[151, 152]. A recent study from India, which tested nasal vaccine, comparing it with mRNA and traditional vaccines, found that nasal vaccine can reduce replicating lower the viral load considerably, prevent inflammation and pneumonia more efficiently than other vaccines and can show higher neutralization capacities . Nasal vaccines are sprayed into the nostrils, therefore can also be a solution for people who are reluctant to get vaccinated as it involves syringes. Another study from Hong Kong found that a single dose of nasal vaccine resulted in eliciting immune response in both the upper and lower respiratory tracts of hamsters, thereby preventing viral spreading . Several other studies indicated that nasal vaccines can enhance systemic immunity. Fabispray recently received regulatory approval as part of the accelerated approval process. It is found that this spray can be effective in killing about 94% of viral load in the upper respiratory tract within 24 h of administration and within 48 h it can reduce viral load up to > 98%. According to a study conducted at the Utah state university USA, the nasal spray was found to kill 99.9% of the SARS-CoV-2 virus including all the variants of the coronavirus .
Recent clinical trial data show that a nasal vaccine consisting of nitride oxide is safe and effective to inhibit SARS-CoV-2 infection. King et al. in their studies on mice found that a single dose of intranasal vaccine administration can elicit both mucosal and systemic immune responses .
Frank et al. in their research study found that nasal spray with povidone-iodine exhibits anti-virucidal properties. A nasal spray containing povidone-iodine (1.25%) completely inactivates SARS-CoV-2 within 15 s of contact and this spray also provides a protection layer for up to 4 h, thus reducing viral loads and transmission of disease . Some of the examples of nasal vaccines are ChAdOx1 nCoV-19, Ad5-nCoV vaccine, NasoVAX, DelNS1-nCoV-RBD LAIV, and Mv-014–212, these are currently in phase I and Phase II trials .
The scientific study reveals that a unified, scientific approach, public engagement, and better prophylactic measures are the three key steps to combat against such public health emergencies in the long run. This outbreak has led China and other nations to learn the importance of enhancing readiness to quickly detect and control the dissemination of evolving infectious disease. Ultimately, the biggest lesson learned from COVID-19, in our opinion, is that global pandemic regulation depends on the sustained pandemic response at local, international, and regional levels that is quick, efficient, synchronized, and efficient . The current global pandemic has highlighted the importance of rapid reaction strategies at both the regional and international levels to prevent possible future outbreaks .
SARS-CoV-2 binds to its host receptor, angiotensin-converting enzyme-2, by the receptor-binding domain (RBD) of the spike protein. The RBD glycoprotein is a key target for the development of neutralizing antibodies and vaccines against SARS-CoV-2 . Nanobodies are small size effective molecules which can be produced easily. Several recent studies showed that these nanobodies can bind to RBD thereby inhibiting and neutralizing the viruses . Tingting Li et al. in their study demonstrated the protecting ability of nanobodies in mice from SARS-CoV-2. They constructed a potent antagonistic mechanism to block the RBD-ACE2 interaction. Using crystallography, they have tested the efficacy and analyzed the binding mechanism; furthermore, they developed an effective platform to produce neutralizing sybodies, with a higher neutralizing ability and stability making it suitable for the treatment of COVID-19 . Other studies reported that sybody 23 shows high neutralization activity when binded to the recombinant RBD. An X-ray scattering model and cryo-EM structure of Sb23 indicate that it effectively blocks ACE2 binding .
Notable outbreaks include those caused by SARS-CoV-1, MERS-CoV, Ebola, and H1N1, and also the lessons learned from each: the value of good personal hygienic practices, testing when feasible, isolating those who are exposed to the virus, personal protective materials for healthcare professionals and many others related to the care of the infected persons and the exhaustive search for therapies and immunizations . The COVID-19 pandemic has led the researchers, scientists, and medical practitioners to explore more areas in the field of animal and environmental research on the virus origin, epidemiological studies, clinical characterization and management, research in therapeutics and advancement, development of vaccine research and ethical considerations for the research . The current global pandemic has highlighted the importance of rapid reaction strategies at both the regional and international levels to prevent possible future outbreaks .
Conclusion and future prospects
COVID-19 has posed a great challenge to the healthcare system, but it has also created an opportunity for the creation of new and innovative roles that could have far-reaching implications for the healthcare system. The COVID-19 outbreak has emphasized the significance of public healthcare as well as the need for novel strategies to mitigate global pandemics. The COVID-19 pandemic has emphasized on the significance of quick diagnosis . Diagnostic approaches like Nucleic Acid Amplification Tests (NAAT) like RT-PCR are the most widely used approaches for the detection of SARS-CoV-2 infection, followed by Rapid Antigen Tests. However, they tend to provide false-positive and false-negative result, respectively . Thus, the design and development of more reliable tools for efficient diagnosis of the infection is important. In the case of treatment options, newly developed drug, Molnupiravir is found to be efficient in treating Omicron variants. Some of the currently used drugs are found to be facing a reduction in their efficacies against the emerging novel variants and subvariants of the virus. In a similar context, many of the vaccines are also reducing their effectiveness. However, with the advancement in technology and a wide range of ongoing research in the domain of pharmacology and therapeutics, novel and reliable treatment and vaccination approaches are being developed. For enhanced mitigation and containment of the infection, a new strategy of Genomic surveillance is being applied. It involves sequencing (using next-gen sequencing tools) and phylogenetic analysis of the viral genome to study the evolutionary pattern of the variants and anticipate new variants. Consecutively, we can initiate containment approaches on time, in case of an outbreak of new variants . This approach also helps to identify patients infected with multiple variants and understand the rearrangement of the viral genome to generate a hybrid. For instance, in the case of Deltacron infected patients, this hybrid was produced in host patient’s cells which were simultaneously infected with Delta and Omicron variants.
For efficient containment and management of the infection, it is necessary to conduct a mass vaccination drive on a global scale. With improvement in scientific understanding and research methodologies, novel personalized vaccines could be developed, considering the environment and susceptibility of an individual towards different variants of the virus.
The large-scale global research aims to develop different aspects associated with COVID-19 including diagnostic methods, treatment (development of specific large and small molecules) and vaccines are being considered by the support of different government agencies. Currently, according to the Clinical trial reports by the US government, there are about 4,653 ongoing trials .
It is crucial to raise the level of awareness and readiness among the persons of the targeted society, particularly the less skilled ones, as the COVID-19 vulnerability on a worldwide scale continues to emerge .
Due to the emergence of COVID-19, many digital sensing technologies were designed and developed. This led to the rapid development of new technologies and research concepts during COVID-19. High-performance infrared thermal cameras and smartphone software were developed by many countries and designed due to COVID-19 and it aids in the detection of fever . Also, many IT and AI-based industries have made it easier to monitor people and stop the transmission of infection, which has aided in COVID-19 preparation . AI might speed up the judicial process by analyzing health records, treatments, and lab results, which would enhance the monitoring of patients .
Consequently, AI might be developed to recognize lesions that resemble coronavirus infection, assess the thickness, volume, and structure morphology, and evaluate different lung lesions from the picture. Furthermore, the current growth trajectory of telemedicine is expected to continue in the post-pandemic era, since face-to-face physician appointments are not always possible in the atmosphere of the COVID-19 pandemic, patients have typically been contented with remote medical care service providers. During the pandemic, telemedicine facilities emerged as an effective healthcare delivery approach, and this trend is expected to continue in the future. As a result, telemedicine services can be easily adopted in the post-COVID-19 era. Until we discover efficient and medically verified therapeutics further than vaccines, the world battle against COVID-19 may last a long time . Whenever it is feasible, smart working and remote work should indeed be followed. If this is not feasible, social segregation and safety precautions including protective gear, hygiene practices, and antimicrobials must be made available everywhere. To survive this challenging moment, innovations and development of feasible technologies for safeguarding the human population is necessary to combat emerging idiopathic infections .
- ACE 2:
Angiotensin-converting enzyme 2
Automatic integrated gene detection system
Centers for Disease Control and Prevention
Complementary dioxyribo nucleic acid
Coronavirus disease 2019
Clustered regularly interspaced short palindromic repeats–CRISPR-associated protein 12
Food and Drug Administration
Intensive care unit
Middle East respiratory syndrome coronavirus
Nucleic acid amplification tests
Quantitative reverse transcription-polymerase chain reaction
Reverse transcription loop-mediated isothermal amplification
Reverse transcription-polymerase chain reaction
Severe acute respiratory syndrome coronavirus 2
Transmembrane protease, serine 2
United States Food and Drug Administration
Variants of interest
Variants of concern
Variants of high consequence
Variant being monitored
Veno-arterial extracorporeal membrane oxygenation
World Health Organization
Chavda VP, Patel AB, Vihol D, Vaghasiya DD, Ahmed KMSB, Trivedi KU, et al. Herbal remedies, nutraceuticals, and dietary supplements for COVID-19 management: an update. Clin Complement Med Pharmacol. 2022. https://doi.org/10.1016/j.ccmp.2022.100021.
Chavda VP, Bezbaruah R, Athalye M, Parikh PK, Chhipa AS, Patel S, et al. Replicating viral vector-based vaccines for COVID-19: potential avenue in vaccination arena. Viruses. 2022. https://doi.org/10.3390/v14040759.
Korber B, Fischer WM, Gnanakaran S, Yoon H, Theiler J, Abfalterer W, et al. Tracking changes in SARS-CoV-2 spike: evidence that D614G increases infectivity of the COVID-19 virus. Cell. 2020;182:812-827.e19. https://doi.org/10.1016/J.CELL.2020.06.043.
Chavda VP, Sonak SS, Munshi NK, Dhamade PN. Pseudoscience and fraudulent products for COVID-19 management. Environ Sci Pollut Res Int. 2022. https://doi.org/10.1007/s11356-022-21967-4.
Upshaw TL, Brown C, Smith R, Perri M, Ziegler C, Pinto AD. Social determinants of COVID-19 incidence and outcomes: a rapid review. PLoS One. 2021;16: e0248336. https://doi.org/10.1371/JOURNAL.PONE.0248336.
Paremoer L, Nandi S, Serag H, Baum F. Covid-19 pandemic and the social determinants of health. BMJ. 2021. https://doi.org/10.1136/BMJ.N129.
Chavda VP, Apostolopoulos V. Rare monkeypox: is it really a threat to the elderly? Maturitas. 2022. https://doi.org/10.1016/j.maturitas.2022.05.014.
Chavda VP, Vora LK, Apostolopoulos V. Monkeypox: a new face of outbreak. Expert Rev Vaccines. 2022. https://doi.org/10.1080/14760584.2022.2113515.
Severe acute hepatitis of unknown aetiology in children - Multi-country n.d. https://www.who.int/emergencies/disease-outbreak-news/item/2022-DON394. Accessed 4 Sept 2022
Weaver AK, Head JR, Gould CF, Carlton EJ, Remais JV. Environmental factors influencing COVID-19 incidence and severity. Annu Rev Public Health. 2022;43:271–91. https://doi.org/10.1146/ANNUREV-PUBLHEALTH-052120-101420.
SARS-CoV-2 Variant Classifications and Definitions n.d. https://www.cdc.gov/coronavirus/2019-ncov/variants/variant-classifications.html. Accessed 8 Sept 2022
Vivek P. Chavda. Omicron variant (B.1.1.529) of SARS-CoV-2: Threat for the elderly? 2020.
Chavda VP, Hanuma Kumar Ghali EN, Yallapu MM. Apostolopoulos V. therapeutics to tackle omicron outbreak. Immunotherapy. 2022. https://doi.org/10.2217/imt-2022-0064.
Chavda VP, Patel AB, Vaghasiya DD. SARS-CoV-2 variants and vulnerability at the global level. J Med Virol. 2022;94:2986–3005. https://doi.org/10.1002/jmv.27717.
Basit A, Ali T, Ur Rehman S. Truncated human angiotensin converting enzyme 2; a potential inhibitor of SARS-CoV-2 spike glycoprotein and potent COVID-19 therapeutic agent. J Biomol Struct Dyn. 2020. https://doi.org/10.1080/07391102.2020.1768150.
Peacock TP, Brown JC, Zhou J, Thakur N, Newman J, Kugathasan R, et al. The SARS-CoV-2 variant, omicron, shows rapid replication in human primary nasal epithelial cultures and efficiently uses the endosomal route of entry. BioRxiv. 2022. https://doi.org/10.1101/2021.12.31.474653.
Willett BJ, Grove J, MacLean OA, Wilkie C, De Lorenzo G, Furnon W, et al. SARS-CoV-2 omicron is an immune escape variant with an altered cell entry pathway. Nat Microbiol. 2022;7:1161–79. https://doi.org/10.1038/s41564-022-01143-7.
Weekly epidemiological update on COVID-19 - 31 August 2022 n.d. https://www.who.int/publications/m/item/weekly-epidemiological-update-on-covid-19---31-august-2022. Accessed 8 Sept 2022
V’kovski P, Kratzel A, Steiner S, Stalder H, Thiel V. Coronavirus biology and replication: implications for SARS-CoV-2. Nat Rev Microbiol. 2021;19:155–70. https://doi.org/10.1038/s41579-020-00468-6.
Jones AN, Mourão A, Czarna A, Matsuda A, Fino R, Pyrc K, et al. Characterization of SARS-CoV-2 replication complex elongation and proofreading activity. Sci Rep. 2022;12:1–9. https://doi.org/10.1038/s41598-022-13380-1.
Manzanares-Meza LD, Medina-Contreras O. SARS-CoV-2 and influenza: a comparative overview and treatment implications. Bol Med Hosp Infant Mex. 2020;77:262–73. https://doi.org/10.24875/BMHIM.20000183.
Chavda VP, Chen Y, Dave J, Chen Z-S, Chauhan SC, Yallapu MM, et al. COVID-19 and vaccination: myths vs science. Expert Rev Vaccines. 2022. https://doi.org/10.1080/14760584.2022.2114900.
Rahimi F, TalebiBezmin Abadi A. Hybrid SARS-CoV-2 variants. Int J Surg. 2022. https://doi.org/10.1016/J.IJSU.2022.106656.
Tao K, Tzou PL, Nouhin J, Gupta RK, de Oliveira T, Kosakovsky Pond SL, et al. The biological and clinical significance of emerging SARS-CoV-2 variants. Nat Rev Genet. 2021;22:757. https://doi.org/10.1038/S41576-021-00408-X.
Amoutzias GD, Nikolaidis M, Tryfonopoulou E, Chlichlia K, Markoulatos P, Oliver SG. The remarkable evolutionary plasticity of coronaviruses by mutation and recombination: insights for the COVID-19 pandemic and the future evolutionary paths of SARS-CoV-2. Viruses. 2022;14:78. https://doi.org/10.3390/v14010078.
Beloukas A, Rampias T. Biological and clinical significance of adaptive evolution of coronaviruses. Life. 2021. https://doi.org/10.3390/LIFE11111129.
Rathnasinghe R, Jangra S, Ye C, Cupic A, Singh G, Martínez-Romero C, et al. Characterization of SARS-CoV-2 Spike mutations important for infection of mice and escape from human immune sera. Nat Commun. 2022;13:1–14. https://doi.org/10.1038/s41467-022-30763-0.
Novelli G, Colona V, Pandolfi P. A focus on the spread of the delta variant of SARS-CoV-2 in India. Indian J Med Res. 2021;153:537–41. https://doi.org/10.4103/IJMR.IJMR_1353_21.
Chavda VP. Apostolopoulos V. Global impact of delta plus variant and vaccination. Expert Rev Vaccines. 2022. https://doi.org/10.1080/14760584.2022.2044800.
Kumar S, Thambiraja TS, Karuppanan K, Subramaniam G. Omicron and delta variant of SARS-CoV-2: a comparative computational study of spike protein. J Med Virol. 2022;94:1641–9. https://doi.org/10.1002/JMV.27526.
Ellinghaus D, Degenhardt F, Bujanda L, Buti M, Albillos A, Invernizzi P, et al. Genomewide association study of severe covid-19 with respiratory failure. N Engl J Med. 2020;383:1522–34. https://doi.org/10.1056/NEJMOA2020283.
Callaway E. What omicron’s BA.4 and BA.5 variants mean for the pandemic. Nature. 2022. https://doi.org/10.1038/D41586-022-01730-Y.
Prakash V, Rajpurohit D, Suneetha V. Currency as a new mode of transmission of pathogens. Res J Pharm Biol Chem Sci. 2016;7:157–63. https://doi.org/10.14299/IJSER.2014.08.002.
Ciotti M, Ciccozzi M, Terrinoni A, Jiang W-C, Wang C-B, Bernardini S. The COVID-19 pandemic. Crit Rev Clin Lab Sci. 2020;57:365–88. https://doi.org/10.1080/10408363.2020.1783198.
Vijayasarathy S, Suneetha V. Un-noticed infections that affects public health: a brief study. Int J Res Pharm Sci. 2020;11:1343–7. https://doi.org/10.26452/IJRPS.V11I2.1995.
Krishnan A, Gangadaran P, Chavda VP, Jogalekar MP, Muthusamy R, Valu D, et al. Convalescent serum-derived exosomes: attractive niche as COVID-19 diagnostic tool and vehicle for mRNA delivery. Exp Biol Med (Maywood). 2022. https://doi.org/10.1177/15353702221092984.
Vandenberg O, Martiny D, Rochas O, van Belkum A, Kozlakidis Z. Considerations for diagnostic COVID-19 tests. Nat Rev Microbiol. 2021;19:171–83. https://doi.org/10.1038/s41579-020-00461-z.
Raoof S, Feigin D, Sung A, Raoof S, Irugulpati L, Rosenow EC. Interpretation of plain chest roentgenogram. Chest. 2012;141:545–58. https://doi.org/10.1378/CHEST.10-1302.
Shi H, Han X, Jiang N, Cao Y, Alwalid O, Gu J, et al. Radiological findings from 81 patients with COVID-19 pneumonia in Wuhan, China: a descriptive study. Lancet Infect Dis. 2020;20:425–34. https://doi.org/10.1016/S1473-3099(20)30086-4.
Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, et al. A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med. 2020;382:727–33. https://doi.org/10.1056/NEJMOA2001017.
Ufuk F. Three-dimensional CT of COVID-19 pneumonia. Radiology. 2020;296:E180. https://doi.org/10.1148/RADIOL.2020201183.
Freeman WM, Walker SJ, Vrana KE. Quantitative RT-PCR: pitfalls and potential. Biotechniques. 1999;26:112–25. https://doi.org/10.2144/99261RV01.
Corman VM, Landt O, Kaiser M, Molenkamp R, Meijer A, Chu DKW, et al. Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Eur Surv. 2019. https://doi.org/10.2807/1560-7917.ES.2020.25.3.2000045.
Bustin SA, Benes V, Garson JA, Hellemans J, Huggett J, Kubista M, et al. The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem. 2009;55:611–22. https://doi.org/10.1373/CLINCHEM.2008.112797.
Elledge SK, Zhou XX, Byrnes JR, Martinko AJ, Lui I, Pance K, et al. Engineering luminescent biosensors for point-of-care SARS-CoV-2 antibody detection. Nat Biotechnol. 2021;39:928–35. https://doi.org/10.1038/S41587-021-00878-8.
Teymouri M, Mollazadeh S, Mortazavi H, NaderiGhale-noie Z, Keyvani V, Aghababaei F, et al. Recent advances and challenges of RT-PCR tests for the diagnosis of COVID-19. Pathol Res Pract. 2021;221: 153443. https://doi.org/10.1016/J.PRP.2021.153443.
Ippoliti C, De Maio F, Santarelli G, Marchetti S, Vella A, Santangelo R, et al. Rapid detection of the omicron (B.1.1.529) SARS-CoV-2 variant using a COVID-19 diagnostic PCR assay. Microbiol Spectr. 2022. https://doi.org/10.1128/spectrum.00990-22.
Torrente-Rodríguez RM, Montero-Calle A, San Bartolomé C, Cano O, Vázquez M, Iglesias-Caballero M, et al. Towards control and oversight of SARS-CoV-2 diagnosis and monitoring through multiplexed quantitative electroanalytical immune response biosensors. Angew Chem. 2022. https://doi.org/10.1002/ange.202203662.
Wiersinga WJ, Rhodes A, Cheng AC, Peacock SJ, Prescott HC. Pathophysiology, transmission, diagnosis, and treatment of coronavirus disease 2019 (COVID-19): a review. JAMA. 2020;324:782–93. https://doi.org/10.1001/JAMA.2020.12839.
Basu D, Chavda VP, Mehta AA. Therapeutics for COVID-19 and post COVID-19 complications: an update. Curr Res Pharmacol Drug Discov. 2022. https://doi.org/10.1016/j.crphar.2022.100086.
Chavda VP, Gajjar N, Shah N, Dave DJ. Darunavir ethanolate: repurposing an anti-HIV drug in COVID-19 treatment. Eur J Med Chem Rep. 2021;3:100013. https://doi.org/10.1016/j.ejmcr.2021.100013.
Chavda VP, Kapadia C, Soni S, Prajapati R, Chauhan SC, Yallapu MM, et al. A global picture: therapeutic perspectives for COVID-19. Immunotherapy. 2022. https://doi.org/10.2217/imt-2021-0168.
Huang Z, Chavda VP, Vora LK, Gajjar N, Apostolopoulos V, Shah N, et al. 2-Deoxy-D-glucose and its derivatives for the COVID-19 treatment: an update. Front Pharmacol. 2022;13: 899633. https://doi.org/10.3389/fphar.2022.899633.
Angamo MT, Mohammed MA, Peterson GM. Efficacy and safety of remdesivir in hospitalised COVID-19 patients: a systematic review and meta-analysis. Infection. 2022;50:27–41. https://doi.org/10.1007/S15010-021-01671-0.
Beigel JH, Tomashek KM, Dodd LE, Mehta AK, Zingman BS, Kalil AC, et al. Remdesivir for the treatment of covid-19 — final report. N Engl J Med. 2020;383:1813–26. https://doi.org/10.1056/NEJMOA2007764/SUPPL_FILE/NEJMOA2007764_DATA-SHARING.PDF.
Chu CM, Cheng VCC, Hung IFN, Wong MML, Chan KH, Chan KS, et al. Role of lopinavir/ritonavir in the treatment of SARS: initial virological and clinical findings. Thorax. 2004;59:252–6. https://doi.org/10.1136/THORAX.2003.012658.
Yu M, Wang DC, Li S, Lei YH, Wei J, Huang LY. Meta-analysis of arbidol versus lopinavir/ritonavir in the treatment of coronavirus disease 2019. J Med Virol. 2022;94:1513–22. https://doi.org/10.1002/JMV.27481.
Axfors C, Schmitt AM, Janiaud P, van’t Hooft J, Abd-Elsalam S, Abdo EF, et al. Mortality outcomes with hydroxychloroquine and chloroquine in COVID-19 from an international collaborative meta-analysis of randomized trials. Nat Commun. 2021;12:1–13. https://doi.org/10.1038/s41467-021-22446-z.
Joshi S, Parkar J, Ansari A, Vora A, Talwar D, Tiwaskar M, et al. Role of favipiravir in the treatment of COVID-19. Int J Infect Dis. 2021;102:501–8. https://doi.org/10.1016/j.ijid.2020.10.069.
Fischer W, Eron JJ, Holman W, Cohen MS, Fang L, Szewczyk LJ, et al. Molnupiravir, an oral antiviral treatment for COVID-19. MedRxiv Prepr Serv Heal Sci. 2021. https://doi.org/10.1101/2021.06.17.21258639.
Saravolatz LD, Depcinski S, Sharma M. Molnupiravir and nirmatrelvir-ritonavir: oral COVID antiviral drugs. Clin Infect Dis. 2022. https://doi.org/10.1093/CID/CIAC180.
Vangeel L, Chiu W, De Jonghe S, Maes P, Slechten B, Raymenants J, et al. Remdesivir, molnupiravir and nirmatrelvir remain active against SARS-CoV-2 omicron and other variants of concern. Antiviral Res. 2022;198: 105252. https://doi.org/10.1016/j.antiviral.2022.105252.
Wahl A, Gralinski LE, Johnson CE, Yao W, Kovarova M, Dinnon KH, et al. SARS-CoV-2 infection is effectively treated and prevented by EIDD-2801. Nature. 2021;591:451–7. https://doi.org/10.1038/S41586-021-03312-W.
Wong CKH, Au ICH, Lau KTK, Lau EHY, Cowling BJ, Leung GM. Real-world effectiveness of early molnupiravir or nirmatrelvir–ritonavir in hospitalised patients with COVID-19 without supplemental oxygen requirement on admission during Hong Kong’s omicron BA.2 wave: a retrospective cohort study. Lancet Infect Dis. 2022. https://doi.org/10.1016/S1473-3099(22)00507-2.
Flisiak R, Zarębska-Michaluk D, Rogalska M, Kryńska JA, Kowalska J, Dutkiewicz E, et al. Real-world experience with molnupiravir during the period of SARS-CoV-2 omicron variant dominance. Pharmacol Rep. 2022. https://doi.org/10.1007/S43440-022-00408-6.
Marzi M, Vakil MK, Bahmanyar M, Zarenezhad E. Paxlovid: mechanism of action, synthesis, and in silico study. Biomed Res Int. 2022;2022:7341493. https://doi.org/10.1155/2022/7341493.
Chavda VP, Prajapati R, Lathigara D, Nagar B, Kukadiya J, Redwan EM, et al. Therapeutic monoclonal antibodies for COVID-19 management: an update. Expert Opin Biol Ther. 2022. https://doi.org/10.1080/14712598.2022.2078160.
Mathieu E, Ritchie H, Ortiz-Ospina E, Roser M, Hasell J, Appel C, et al. A global database of COVID-19 vaccinations. Nat Hum Behav. 2021;5:947–53. https://doi.org/10.1038/S41562-021-01122-8.
Chavda VP, Feehan J, Apostolopoulos V. A veterinary vaccine for SARS-CoV-2: the first COVID-19 vaccine for animals. Vaccines. 2021. https://doi.org/10.3390/vaccines9060631.
Chavda VP, Pandya R, Apostolopoulos V. DNA vaccines for SARS-CoV-2: toward third-generation vaccination era. Expert Rev Vaccines. 2021;20:1549–60. https://doi.org/10.1080/14760584.2021.1987223.
Clem AS. Fundamentals of vaccine immunology. J Glob Infect Dis. 2011;3:73. https://doi.org/10.4103/0974-777X.77299.
Vasireddy D, Atluri P, Malayala SV, Vanaparthy R, Mohan G. Review of COVID-19 vaccines approved in the United States of America for emergency use. J Clin Med Res. 2021;13:204–13. https://doi.org/10.14740/jocmr4490.
FDA Office of Media Affairs (2022) Coronavirus (COVID-19) update: FDA limits use of Janssen COVID-19 vaccine to certain individuals. FDA NEWS RELEASE 2022:For Immediate Release: May 05, 2022
Bernard NJ. Vaccine thrombosis. Nat Immunol. 2022;23:2. https://doi.org/10.1038/s41590-021-01111-z.
Capassoni M, Ketabchi S, Cassisa A, Caramelli R, Molinu AA, Galluccio F, et al. AstraZeneca (AZD1222) COVID-19 vaccine-associated adverse drug event: a case report. J Med Virol. 2021;93:5718. https://doi.org/10.1002/JMV.27175.
Muik A, Lui BG, Wallisch A-K, Bacher M, Mühl J, Reinholz J, et al. Neutralization of SARS-CoV-2 omicron by BNT162b2 mRNA vaccine-elicited human sera. Science (80-). 2022;375:678–80. https://doi.org/10.1126/science.abn7591.
Liu J, Chandrashekar A, Sellers D, Barrett J, Jacob-Dolan C, Lifton M, et al. Vaccines elicit highly conserved cellular immunity to SARS-CoV-2 omicron. Nature. 2022;603:493–6. https://doi.org/10.1038/s41586-022-04465-y.
Chavda VP, Apostolopoulos V. Is booster dose strategy sufficient for omicron variant of SARS-CoV-2? Vaccines. 2022;10:1–6. https://doi.org/10.3390/vaccines10030367.
Burki T. Understanding variants of SARS-CoV-2. Lancet (London, England). 2021;397:462. https://doi.org/10.1016/S0140-6736(21)00298-1.
Volz E, Mishra S, Chand M, Barrett JC, Johnson R, Geidelberg L, et al. Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England. Nature. 2021;593:266–9. https://doi.org/10.1038/s41586-021-03470-x.
Tian D, Sun Y, Xu H, Ye Q. The emergence and epidemic characteristics of the highly mutated SARS-CoV-2 omicron variant. J Med Virol. 2022;94:2376–83. https://doi.org/10.1002/JMV.27643.
Lauring AS, Tenforde MW, Chappell JD, Gaglani M, Ginde AA, Mcneal T, et al. Clinical severity of, and effectiveness of mRNA vaccines against, covid-19 from omicron, delta, and alpha SARS-CoV-2 variants in the United States: prospective observational study. BMJ. 2022. https://doi.org/10.1136/BMJ-2021-069761.
Mahadevaiah A, Doddamadaiah C, Sadananda KS, Cholenahalli NM. Study of immunogenicity, safety and efficacy of covishield vaccine among health care workers in a tertiary cardiac care centre. Indian J Med Microbiol. 2022;40:200–3. https://doi.org/10.1016/J.IJMMB.2022.03.003.
Kwok HF. Review of covid-19 vaccine clinical trials - a puzzle with missing pieces. Int J Biol Sci. 2021;17:1461. https://doi.org/10.7150/IJBS.59170.
Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine. N Engl J Med. 2021;384:403–16. https://doi.org/10.1056/NEJMOA2035389.
Ludvigsson JF. Systematic review of COVID-19 in children shows milder cases and a better prognosis than adults. Acta Paediatr. 2020;109:1088–95. https://doi.org/10.1111/apa.15270.
Çokuğraş H, Önal P. SARS-CoV-2 infection in children. Turkish Arch Pediatr Pediatr Arşivi. 2020;55:95. https://doi.org/10.14744/TURKPEDIATRIARS.2020.20270.
Bogunovic D, Merad M. Children and SARS-CoV-2. Cell Host Microbe. 2021;29:1040. https://doi.org/10.1016/J.CHOM.2021.06.015.
Liguoro I, Pilotto C, Bonanni M, Ferrari ME, Pusiol A, Nocerino A, et al. SARS-COV-2 infection in children and newborns: a systematic review. Eur J Pediatr. 2020;179:1029. https://doi.org/10.1007/S00431-020-03684-7.
Frutos AM, Kubale J, Kuan G, Ojeda S, Vydiswaran N, Sanchez N, et al. SARS-CoV-2 and endemic coronaviruses: comparing symptom presentation and severity of symptomatic illness among Nicaraguan children. PLOS Glob Public Heal. 2022;2: e0000414. https://doi.org/10.1371/JOURNAL.PGPH.0000414.
Gomez UT, Francisco RPV, Baptista FS, Gibelli MABC, Ibidi SM, de Carvalho WB, et al. Impact of SARS-CoV-2 on pregnancy and neonatal outcomes: an open prospective study of pregnant women in Brazil. Clinics (Sao Paulo). 2022. https://doi.org/10.1016/J.CLINSP.2022.100073.
Crovetto F, Crispi F, Llurba E, Pascal R, Larroya M, Trilla C, et al. Impact of severe acute respiratory syndrome coronavirus 2 infection on pregnancy outcomes: a population-based study. Clin Infect Dis. 2021;73:1768–75. https://doi.org/10.1093/CID/CIAB104.
Mosnino E, Bernardes LS, Mattern J, HipólitoMicheletti B, de Castro Maldonado AA, Vauloup-Fellous C, et al. Impact of SARS-CoV-2 alpha and gamma variants among symptomatic pregnant women: a two-center retrospective cohort study between France and Brazil. J Clin Med. 2022. https://doi.org/10.3390/JCM11092663.
Perrotta F, Corbi G, Mazzeo G, Boccia M, Aronne L, D’Agnano V, et al. COVID-19 and the elderly: insights into pathogenesis and clinical decision-making. Aging Clin Exp Res. 2020;32:1599. https://doi.org/10.1007/S40520-020-01631-Y.
Kim Y, Yu KM, Koh JY, Kim EH, Kim SM, Kim EJ, et al. Age-dependent pathogenic characteristics of SARS-CoV-2 infection in ferrets. Nat Commun. 2022;13:1–13. https://doi.org/10.1038/s41467-021-27717-3.
Mueller AL, Mcnamara MS, Sinclair DA. Why does COVID-19 disproportionately affect older people? Aging (Albany NY). 2020;12:9959. https://doi.org/10.18632/AGING.103344.
Belsky JA, Tullius BP, Lamb MG, Sayegh R, Stanek JR, Auletta JJ. COVID-19 in immunocompromised patients: a systematic review of cancer, hematopoietic cell and solid organ transplant patients. J Infect. 2021;82:329. https://doi.org/10.1016/J.JINF.2021.01.022.
Baek MS, Lee MT, Kim WY, Choi JC, Jung SY. COVID-19-related outcomes in immunocompromised patients: a nationwide study in Korea. PLoS One. 2021. https://doi.org/10.1371/JOURNAL.PONE.0257641.
Sanyaolu A, Okorie C, Marinkovic A, Patidar R, Younis K, Desai P, et al. Comorbidity and its impact on patients with COVID-19. SN Compr Clin Med. 2020;2:1069. https://doi.org/10.1007/S42399-020-00363-4.
WHO updates its treatment guidelines to include molnupiravir n.d. https://www.who.int/news/item/03-03-2022-molnupiravir. Accessed 8 Sept 2022
Coronavirus (COVID-19) update: FDA authorizes moderna and Pfizer-BioNTech COVID-19 vaccines for children down to 6 months of age | FDA n.d.
Monpara JD, Sodha SJ, Gupta PK. COVID-19 associated complications and potential therapeutic targets. Eur J Pharmacol. 2020;886: 173548. https://doi.org/10.1016/J.EJPHAR.2020.173548.
Arentz M, Yim E, Klaff L, Lokhandwala S, Riedo FX, Chong M, et al. Characteristics and outcomes of 21 critically Ill patients withCOVID-19 in Washington State. JAMA. 2020;323:1612. https://doi.org/10.1001/JAMA.2020.4326.
Yazdanpanah N, Rezaei N. Autoimmune complications of COVID-19. J Med Virol. 2022;94:54. https://doi.org/10.1002/JMV.27292.
Desai AD, Lavelle M, Boursiquot BC, Wan EY. Long-term complications of COVID-19. Am J Physiol - Cell Physiol. 2022;322:C1. https://doi.org/10.1152/AJPCELL.00375.2021.
Gu X, Cao B. In-hospital complications associated with COVID-19. Lancet (London, England). 2021;398:188. https://doi.org/10.1016/S0140-6736(21)00983-1.
Farshidfar F, Koleini N, Ardehali H. Cardiovascular complications of COVID-19. JCI Insight. 2021. https://doi.org/10.1172/JCI.INSIGHT.148980.
Yu WL, Toh HS, Te LC, Chang WT. Cardiovascular complications of COVID-19 and associated concerns: a review. Acta Cardiol Sin. 2021;37:9–17. https://doi.org/10.6515/ACS.202101_37(1).20200913A.
Holt NR, Neumann JT, McNeil JJ, Cheng AC. Implications of COVID-19 for an ageing population. Med J Aust. 2020;213:342-344.e1. https://doi.org/10.5694/MJA2.50785.
Hadj HI. Covid-19 vaccines and variants of concern: a review. Rev Med Virol. 2022;32: e2313. https://doi.org/10.1002/rmv.2313.
Sharma S, Grover M, Bhargava S, Samdani S, Kataria T. Post coronavirus disease mucormycosis: a deadly addition to the pandemic spectrum. J Laryngol Otol. 2021. https://doi.org/10.1017/S0022215121000992.
Forman R, Shah S, Jeurissen P, Jit M, Mossialos E. COVID-19 vaccine challenges: what have we learned so far and what remains to be done? Health Policy. 2021;125:553. https://doi.org/10.1016/J.HEALTHPOL.2021.03.013.
Capolongo S, Gola M, Brambilla A, Morganti A, Mosca EI, Barach P. COVID-19 and healthcare facilities: a decalogue of design strategies for resilient hospitals. Acta Bio Medica Atenei Parm. 2020;91:50. https://doi.org/10.23750/ABM.V91I9-S.10117.
Razu SR, Yasmin T, Arif TB, Islam MS, Islam SMS, Gesesew HA, et al. Challenges faced by healthcare professionals during the COVID-19 pandemic: a qualitative inquiry from Bangladesh. Front Public Heal. 2021;9: 647315. https://doi.org/10.3389/FPUBH.2021.647315/FULL.
Kumar H, Azad A, Gupta A, Sharma J, Bherwani H, Labhsetwar NK, et al. COVID-19 creating another problem? Sustainable solution for PPE disposal through LCA approach. Environ Dev Sustain. 2021;23:9418. https://doi.org/10.1007/S10668-020-01033-0.
Vanapalli KR, Sharma HB, Ranjan VP, Samal B, Bhattacharya J, Dubey BK, et al. Challenges and strategies for effective plastic waste management during and post COVID-19 pandemic. Sci Total Environ. 2021;750: 141514. https://doi.org/10.1016/J.SCITOTENV.2020.141514.
Wang Q, Guo Y, Iketani S, Nair MS, Li Z, Mohri H, et al. Antibody evasion by SARS-CoV-2 omicron subvariants BA.2.12.1, BA.4 and BA.5. Nature. 2022;608:603–8. https://doi.org/10.1038/s41586-022-05053-w.
Rahimi F, Talebi BAA. The omicron subvariant BA.2: birth of a new challenge during the COVID-19 pandemic. Int J Surg. 2022;99:106261. https://doi.org/10.1016/j.ijsu.2022.106261.
Madhi SA, Kwatra G, Myers JE, Jassat W, Dhar N, Mukendi CK, et al. Population immunity and covid-19 severity with omicron variant in South Africa. N Engl J Med. 2022;386:1314–26. https://doi.org/10.1056/NEJMOA2119658/SUPPL_FILE/NEJMOA2119658_DISCLOSURES.PDF.
Elliott P, Eales O, Steyn N, Tang D, Bodinier B, Wang H, et al. Twin peaks: the omicron SARS-CoV-2 BA.1 and BA.2 epidemics in England. Science (80-). 2022. https://doi.org/10.1126/SCIENCE.ABQ4411.
COVID-19 vaccines. World Heal Organ n.d. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/covid-19-vaccines (accessed September 21, 2022).
Zhavoronkov A, Aladinskiy V, Zhebrak A, Zagribelnyy B, Terentiev V, Bezrukov DS, et al. Potential COVID-2019 3C-like protease inhibitors designed using generative deep learning approaches 2020. Chemrxiv. 2020. https://doi.org/10.26434/CHEMRXIV.11829102.V2.
Gao K, Nguyen DD, Wang R, Wei G-W. Machine intelligence design of 2019-nCoV drugs. BioRxiv. 2020. https://doi.org/10.1101/2020.01.30.927889.
Beck BR, Shin B, Choi Y, Park S, Kang K. Predicting commercially available antiviral drugs that may act on the novel coronavirus (2019-nCoV), Wuhan, China through a drug-target interaction deep learning model. BioRxiv. 2020. https://doi.org/10.1101/2020.01.31.929547.
Chandra Kaushik A, Raj U. AI-driven drug discovery: a boon against COVID-19? AI Open. 2020;1:1–4. https://doi.org/10.1016/J.AIOPEN.2020.07.001.
Ke YY, Peng TT, Yeh TK, Huang WZ, Chang SE, Wu SH, et al. Artificial intelligence approach fighting COVID-19 with repurposing drugs. Biomed J. 2020;43:355–62. https://doi.org/10.1016/J.BJ.2020.05.001.
Goh GKM, Dunker AK, Foster JA, Uversky VN. A novel strategy for the development of vaccines for SARS-CoV-2 (COVID-19) and other viruses using ai and viral shell disorder. J Proteome Res. 2020;19:4355–63. https://doi.org/10.1021/ACS.JPROTEOME.0C00672/ASSET/IMAGES/LARGE/PR0C00672_0005.JPEG.
Arora N, Banerjee AK, Narasu ML. The role of artificial intelligence in tackling COVID-19. Future Virol. 2020;15:717–24. https://doi.org/10.2217/FVL-2020-0130.
Scherman D, Fetro C. Drug repositioning for rare diseases: knowledge-based success stories. Therapie. 2020;75:161–7. https://doi.org/10.1016/J.THERAP.2020.02.007.
Huang F, Zhang C, Liu Q, Zhao Y, Zhang Y, Qin Y, et al. Identification of amitriptyline HCl, flavin adenine dinucleotide, azacitidine and calcitriol as repurposing drugs for influenza A H5N1 virus-induced lung injury. PLoS Pathog. 2020. https://doi.org/10.1371/JOURNAL.PPAT.1008341.
Park K. A review of computational drug repurposing. Transl Clin Pharmacol. 2019;27:59–63. https://doi.org/10.12793/TCP.2019.27.2.59.
Pushpakom S, Iorio F, Eyers PA, Escott KJ, Hopper S, Wells A, et al. Drug repurposing: progress, challenges and recommendations. Nat Rev Drug Discov. 2019;18:41–58. https://doi.org/10.1038/NRD.2018.168.
Toniati P, Piva S, Cattalini M, Garrafa E, Regola F, Castelli F, et al. Tocilizumab for the treatment of severe COVID-19 pneumonia with hyperinflammatory syndrome and acute respiratory failure: a single center study of 100 patients in Brescia. Italy Autoimmun Rev. 2020. https://doi.org/10.1016/J.AUTREV.2020.102568.
Gordon CJ, Tchesnokov EP, Feng JY, Porter DP, Götte M. The antiviral compound remdesivir potently inhibits RNAdependent RNA polymerase from middle east respiratory syndrome coronavirus. J Biol Chem. 2020;295:4773–9. https://doi.org/10.1074/JBC.AC120.013056/ATTACHMENT/4909A17B-D857-478F-B458-44C88DC51D8A/MMC1.PDF.
Ansems K, Grundeis F, Dahms K, Mikolajewska A, Thieme V, Piechotta V, et al. Remdesivir for the treatment of COVID-19. Cochrane Database Syst Rev. 2021. https://doi.org/10.1002/14651858.CD014962.
Agostini ML, Andres EL, Sims AC, Graham RL, Sheahan TP, Lu X, et al. Coronavirus susceptibility to the antiviral remdesivir (GS-5734) is mediated by the viral polymerase and the proofreading exoribonuclease. MBio. 2018. https://doi.org/10.1128/MBIO.00221-18/ASSET/A3FF74B2-3D2F-4D32-8CFF-6F258D2C4B92/ASSETS/GRAPHIC/MBO0011837620007.JPEG.
Wang M, Cao R, Zhang L, Yang X, Liu J, Xu M, et al. Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro. Cell Res. 2020;30:269–71. https://doi.org/10.1038/s41422-020-0282-0.
Malin JJ, Suárez I, Priesner V, Fätkenheuer G, Rybniker J. Remdesivir against COVID-19 and other viral diseases. Clin Microbiol Rev. 2020;34:1–21. https://doi.org/10.1128/CMR.00162-20.
Nutho B, Mahalapbutr P, Hengphasatporn K, Pattaranggoon NC, Simanon N, Shigeta Y, et al. Why are lopinavir and ritonavir effective against the newly emerged coronavirus 2019? Atomistic insights into the inhibitory mechanisms. Biochemistry. 2020;59:1769–79. https://doi.org/10.1021/ACS.BIOCHEM.0C00160.
Kang CK, Seong MW, Choi SJ, Kim TS, Choe PG, Song SH, et al. In vitro activity of lopinavir/ritonavir and hydroxychloroquine against severe acute respiratory syndrome coronavirus 2 at concentrations achievable by usual doses. Korean J Intern Med. 2020;35:782–7. https://doi.org/10.3904/KJIM.2020.157.
George PM, Wells AU, Jenkins RG. Pulmonary fibrosis and COVID-19: the potential role for antifibrotic therapy. Lancet Respir Med. 2020;8:807–15. https://doi.org/10.1016/S2213-2600(20)30225-3.
Marwah V, Choudhary R, Malik V, Pemmaraju A, Peter D. Early experience of nintedanib in COVID-19 ARDS-related pulmonary fibrosis: a case series. Adv Respir Med. 2021;89:589–96. https://doi.org/10.5603/ARM.A2021.0113.
Choudhury A, Das NC, Patra R, Bhattacharya M, Ghosh P, Patra BC, et al. Exploring the binding efficacy of ivermectin against the key proteins of SARS-CoV-2 pathogenesis: an in silico approach. Future Virol. 2021;16:277–91. https://doi.org/10.2217/FVL-2020-0342.
Azam F, Taban IM, Eid EEM, Iqbal M, Alam O, Khan S, et al. An in-silico analysis of ivermectin interaction with potential SARS-CoV-2 targets and host nuclear importin α. J Biomol Struct Dyn. 2022;40:2851–64. https://doi.org/10.1080/07391102.2020.1841028.
Moore N. Chloroquine for COVID-19 infection. Drug Saf. 2020;43:393–4. https://doi.org/10.1007/S40264-020-00933-4.
Milane L, Amiji M. Clinical approval of nanotechnology-based SARS-CoV-2 mRNA vaccines: impact on translational nanomedicine. Drug Deliv Transl Res. 2021;11:1309–15. https://doi.org/10.1007/s13346-021-00911-y.
Bhutta ZA, Kanwal A, Ali M, Kulyar MFEA, Yao W, Shoaib M, et al. Emerging nanotechnology role in the development of innovative solutions against COVID-19 pandemic. Nanotechnology. 2021. https://doi.org/10.1088/1361-6528/ac189e.
Albaz AA, Rafeeq MM, Sain ZM, Almutairi WA, Alamri AS, Aloufi AH, et al. Nanotechnology-based approaches in the fight against SARS-CoV-2. AIMS Microbiol. 2021;7:368–98. https://doi.org/10.3934/microbiol.2021023.
Yang D. Application of nanotechnology in the COVID-19 pandemic. Int J Nanomed. 2021;16:623–49. https://doi.org/10.2147/IJN.S296383.
Dhama K, Dhawan M, Tiwari R, Emran TB, Mitra S, Rabaan AA, et al. COVID-19 intranasal vaccines: current progress advantages prospects, and challenges. Hum Vaccin Immunother. 2022. https://doi.org/10.1080/21645515.2022.2045853.
Americo JL, Cotter CA, Earl PL, Liu R, Moss B. Intranasal inoculation of an MVA-based vaccine induces IgA and protects the respiratory tract of hACE2 mice from SARS-CoV-2 infection. Proc Natl Acad Sci U S A. 2022. https://doi.org/10.1073/pnas.2202069119.
van der Ley PA, Zariri A, van Riet E, Oosterhoff D, Kruiswijk CP. An intranasal OMV-based vaccine induces high mucosal and systemic protecting immunity against a SARS-CoV-2 infection. Front Immunol. 2021. https://doi.org/10.3389/fimmu.2021.781280.
Topol EJ, Iwasaki A. Operation nasal vaccine—lightning speed to counter COVID-19. Sci Immunol. 2022. https://doi.org/10.1126/SCIIMMUNOL.ADD9947/ASSET/99E73652-A709-495C-92AA-1B8A0B05A7E5/ASSETS/IMAGES/LARGE/SCIIMMUNOL.ADD9947-FB.JPG.
To Evaluate Safety and Immunogenicity of DelNS1-2019-nCoV-RBD-OPT1 for COVID-19 in Healthy Adults Received 2 Doses of BNT162b2 - Full Text View - ClinicalTrials.gov n.d. https://clinicaltrials.gov/ct2/show/NCT05200741?term=DelNS1–2019-nCoV-RBD-OPT1&draw=2&rank=1. Accessed 21 Sept 2022
Nitric Oxide Nasal Spray (NONS) as Prevention for Treatment of Individuals at Risk of Exposure to COVID-19 Infection - Full Text View - ClinicalTrials.gov n.d. https://clinicaltrials.gov/ct2/show/NCT05109611. Accessed 21 Sept 2022
King RG, Silva-Sanchez A, Peel JN, Botta D, Dickson AM, Pinto AK, et al. Single-dose intranasal administration of AdCOVID elicits systemic and mucosal immunity against SARS-CoV-2 and fully protects mice from lethal challenge. Vaccines. 2021;9:881. https://doi.org/10.3390/VACCINES9080881.
Frank S, Brown SM, Capriotti JA, Westover JB, Pelletier JS, Tessema B. In vitro efficacy of a povidone-iodine nasal antiseptic for rapid inactivation of SARS-CoV-2. JAMA Otolaryngol Neck Surg. 2020;146:1054–8. https://doi.org/10.1001/JAMAOTO.2020.3053.
Stenseth NC, Dharmarajan G, Li R, Shi Z-L, Yang R, Gao GF. Lessons learnt from the COVID-19 pandemic. Front Public Heal. 2021. https://doi.org/10.3389/fpubh.2021.694705.
Pandey S, Yadav B, Pandey A, Tripathi T, Khawary M, Kant S, et al. Lessons from SARS-CoV-2 pandemic: evolution, disease dynamics and future. Biology. 2020. https://doi.org/10.3390/biology9060141.
Custódio TF, Das H, Sheward DJ, Hanke L, Pazicky S, Pieprzyk J, et al. Selection, biophysical and structural analysis of synthetic nanobodies that effectively neutralize SARS-CoV-2. Nat Commun. 2020;11:1–11. https://doi.org/10.1038/s41467-020-19204-y.
Barakat S, Berksöz M, Zahedimaram P, Piepoli S, Erman B. Nanobodies as molecular imaging probes. Free Radic Biol Med. 2022;182:260–75. https://doi.org/10.1016/J.FREERADBIOMED.2022.02.031.
Li T, Cai H, Yao H, Zhou B, Zhang N, van Vlissingen MF, et al. A synthetic nanobody targeting RBD protects hamsters from SARS-CoV-2 infection. Nat Commun. 2021;12:1–13. https://doi.org/10.1038/s41467-021-24905-z.
Cruickshank M, Shaban RZ. COVID-19: lessons to be learnt from a once-in-a-century global pandemic. J Clin Nurs. 2020;29:3901–4. https://doi.org/10.1111/jocn.15365.
Zhang H, Shaw R. Identifying research trends and gaps in the context of COVID-19. Int J Environ Res Public Health. 2020. https://doi.org/10.3390/ijerph17103370.
Yüce M, Filiztekin E, Özkaya KG. COVID-19 diagnosis—a review of current methods. Biosens Bioelectron. 2021. https://doi.org/10.1016/j.bios.2020.112752.
Overview of Testing for SARS-CoV-2, the virus that causes COVID-19 | CDC n.d. https://www.cdc.gov/coronavirus/2019-ncov/hcp/testing-overview.html. Accessed 8 Sept 2022
Robishaw JD, Alter SM, Solano JJ, Shih RD, DeMets DL, Maki DG, et al. Genomic surveillance to combat COVID-19: challenges and opportunities. Lancet Microbe. 2021;2:e481–4. https://doi.org/10.1016/S2666-5247(21)00121-X.
Search of: Recruiting, Not yet recruiting, Active, not recruiting, Enrolling by invitation, Unknown status Studies | Studies Without Results | COVID-19 - List Results - ClinicalTrials.gov n.d. https://clinicaltrials.gov/ct2/results?cond=COVID-19&Search=Apply&recrs=b&recrs=a&recrs=f&recrs=d&recrs=m&age_v=&gndr=&type=&rslt=Without. Accessed 8 Sept 2022
Tripathi R, Alqahtani SS, Albarraq AA, Meraya AM, Tripathi P, Banji D, et al. Awareness and preparedness of COVID-19 outbreak among healthcare workers and other residents of South-West Saudi Arabia: a cross-sectional survey. Front Public Health. 2020. https://doi.org/10.3389/fpubh.2020.00482.
Whitelaw S, Mamas MA, Topol E, Van Spall HGC. Applications of digital technology in COVID-19 pandemic planning and response. Lancet Digit Heal. 2020;2:e435–40. https://doi.org/10.1016/S2589-7500(20)30142-4.
Chaibun T, Puenpa J, Ngamdee T, Boonapatcharoen N, Athamanolap P, O’Mullane AP, et al. Rapid electrochemical detection of coronavirus SARS-CoV-2. Nat Commun. 2021. https://doi.org/10.1038/S41467-021-21121-7.
Tahamtan A, Ardebili A. Real-time RT-PCR in COVID-19 detection: issues affecting the results. Expert Rev Mol Diagn. 2020;20:1. https://doi.org/10.1080/14737159.2020.1757437.
Rong G, Zheng Y, Chen Y, Zhang Y, Zhu P, Sawan M. COVID-19 diagnostic methods and detection techniques: a review. Ref Modul Biomed Sci. 2021. https://doi.org/10.1016/B978-0-12-822548-6.00080-7.
Huang WE, Lim B, Hsu CC, Xiong D, Wu W, Yu Y, et al. RT-LAMP for rapid diagnosis of coronavirus SARS-CoV-2. Microb Biotechnol. 2020;13:950. https://doi.org/10.1111/1751-7915.13586.
Bustin SA, Nolan T. RT-qPCR testing of SARS-CoV-2: a primer. Int J Mol Sci. 2020. https://doi.org/10.3390/IJMS21083004.
Bustin S, Mueller R, Shipley G, Nolan T. COVID-19 and diagnostic testing for SARS-CoV-2 by RT-qPCR-Facts and fallacies. Int J Mol Sci. 2021;22:1–11. https://doi.org/10.3390/IJMS22052459.
Alcoba-Florez J, Gil-Campesino H, Artola DGG-MR, Valenzuela-Fernández ACL, Flores C. Sensitivity of different RT-qPCR solutions for SARS-CoV-2 detection. - Biospecimen research database. Int J Infect Dis. 2020. https://doi.org/10.1016/j.ijid.2020.07.058.
Leung RK-K, Cheng Q-X, Wu Z-L, Khan G, Liu Y, Xia H-Y, et al. CRISPR-Cas12-based nucleic acids detection systems. Methods. 2022;203:276–81. https://doi.org/10.1016/j.ymeth.2021.02.018.
Lee H, Suzuki T, Okada Y, Tanaka H, Okamori S, Kamata H, et al. Diagnostic performance of computed tomography imaging for COVID-19 in a region with low disease prevalence. Keio J Med. 2022;71:21–30. https://doi.org/10.2302/kjm.2021-0012-OA.
Vankadari N. Arbidol: a potential antiviral drug for the treatment of SARS-CoV-2 by blocking trimerization of the spike glycoprotein. Int J Antimicrob Agents. 2020;56:105998. https://doi.org/10.1016/j.ijantimicag.2020.105998.
AlaviDarazam I, Shokouhi S, Mardani M, Pourhoseingholi MA, Rabiei MM, Hatami F, et al. Umifenovir in hospitalized moderate to severe COVID-19 patients: a randomized clinical trial. Int Immunopharmacol. 2021;99: 107969. https://doi.org/10.1016/j.intimp.2021.107969.
Favipiravir manufacturers in India | Maithililifescience n.d.
Furuta Y, Gowen BB, Takahashi K, Shiraki K, Smee DF, Barnard DL. Favipiravir (T-705), a novel viral RNA polymerase inhibitor. Antiviral Res. 2013;100:446–54. https://doi.org/10.1016/j.antiviral.2013.09.015.
Özlüşen B, Kozan Ş, Akcan RE, Kalender M, Yaprak D, Peltek İB, et al. Effectiveness of favipiravir in COVID-19: a live systematic review. Eur J Clin Microbiol Infect Dis. 2021;40:2575–83. https://doi.org/10.1007/S10096-021-04307-1.
Lopez-Cortes LF, Ruiz-Valderas R, Sánchez-Rivas E, Lluch A, Gutierrez-Valencia A, Torres-Cornejo A, et al. Lopinavir plasma concentrations and virological outcome with lopinavir-ritonavir monotherapy in HIV-1-infected patients. Antimicrob Agents Chemother. 2013;57:3746–51. https://doi.org/10.1128/AAC.00315-13.
Spinner CD, Gottlieb RL, Criner GJ, Arribas López JR, Cattelan AM, Soriano Viladomiu A, et al. Effect of remdesivir vs standard care on clinical status at 11 days in patients with moderate COVID-19: a randomized clinical trial. JAMA - J Am Med Assoc. 2020;324:1048–57. https://doi.org/10.1001/jama.2020.16349.
Kokic G, Hillen HS, Tegunov D, Dienemann C, Seitz F, Schmitzova J, et al. Mechanism of SARS-CoV-2 polymerase stalling by remdesivir. Nat Commun. 2021;12:279. https://doi.org/10.1038/s41467-020-20542-0.
Te HS, Randall G, Jensen DM. Mechanism of action of ribavirin in the treatment of chronic hepatitis C. Gastroenterol Hepatol (N Y). 2007;3:218–25.
Tong S, Su Y, Yu Y, Wu C, Chen J, Wang S, et al. Ribavirin therapy for severe COVID-19: a retrospective cohort study. Int J Antimicrob Agents. 2020;56: 106114. https://doi.org/10.1016/j.ijantimicag.2020.106114.
Beaucourt S, Vignuzzi M. Ribavirin: a drug active against many viruses with multiple effects on virus replication and propagation. Molecular basis of ribavirin resistance. Curr Opin Virol. 2014;8:10–5. https://doi.org/10.1016/j.coviro.2014.04.011.
Delandre O, Gendrot M, Jardot P, Le Bideau M, Boxberger M, Boschi C, et al. Antiviral activity of repurposing ivermectin against a panel of 30 clinical SARS-CoV-2 strains belonging to 14 variants. Pharm. 2022. https://doi.org/10.3390/ph15040445.
Hoffmann M, Hofmann-Winkler H, Smith JC, Krüger N, Sørensen LK, Søgaard OS, et al. Camostat mesylate inhibits SARS-CoV-2 activation by TMPRSS2-related proteases and its metabolite GBPA exerts antiviral activity. BioRxiv Prepr Serv Biol. 2020. https://doi.org/10.1101/2020.08.05.237651.
Sakr Y, Bensasi H, Taha A, Bauer M, Ismail K. Camostat mesylate therapy in critically ill patients with COVID-19 pneumonia. Intensive Care Med. 2021;47:707–9. https://doi.org/10.1007/s00134-021-06395-1.
Takahashi W, Yoneda T, Koba H, Ueda T, Tsuji N, Ogawa H, et al. Potential mechanisms of nafamostat therapy for severe COVID-19 pneumonia with disseminated intravascular coagulation. Int J Infect Dis IJID Off Publ Int Soc Infect Dis. 2021;102:529–31. https://doi.org/10.1016/j.ijid.2020.10.093.
Mohseni M, Raissi V, Sharifan Y, Barikro K, Amiri S, Mohseni MS, et al. Therapeutic status of famotidine in COVID-19 patients: a review. Infect Disord Drug Targets. 2022;22: e070122200096. https://doi.org/10.2174/1871526522666220107125511.
Kabinger F, Stiller C, Schmitzová J, Dienemann C, Kokic G, Hillen HS, et al. Mechanism of molnupiravir-induced SARS-CoV-2 mutagenesis. Nat Struct Mol Biol. 2021;28:740–6. https://doi.org/10.1038/s41594-021-00651-0.
Singla S, Goyal S. Antiviral activity of molnupiravir against COVID-19: a schematic review of evidences. Bull Natl Res Cent. 2022;46:62. https://doi.org/10.1186/s42269-022-00753-9.
Taylor PC, Adams AC, Hufford MM, de la Torre I, Winthrop K, Gottlieb RL. Neutralizing monoclonal antibodies for treatment of COVID-19. Nat Rev Immunol. 2021;21:382–93. https://doi.org/10.1038/s41577-021-00542-x.
Dougan M, Nirula A, Azizad M, Mocherla B, Gottlieb RL, Chen P, et al. Bamlanivimab plus etesevimab in mild or moderate covid-19. N Engl J Med. 2021. https://doi.org/10.1056/NEJMoa2102685.
Joy AP, Augustine AT, Karattuthodi MS, Parambil JC, Chandrasekher D, Danisha P, et al. The impact of casirivimab-imdevimab antibody cocktail in patients amidst and post COVID 19 treatment: a retro-prospective comparative study in India. Clin Epidemiol Glob Heal. 2022;14: 100967. https://doi.org/10.1016/j.cegh.2022.100967.
Sherchan R, Cannady Preston J. Casirivimab., Treasure Island (FL): 2022.
Casirivimab and imdevimabCasirivimab and imdevimab for COVID-19. (2022). Aust Prescr, 45(2), 58–59. https://doi.org/10.18773/austprescr.2022.013
Elesdoudy A. Sotrovimab: is it effective in early treatment of mild and moderate COVID-19 infections? A retrospective study. Egypt J Bronchol. 2021. https://doi.org/10.1186/s43168-021-00104-8.
Sotrovimab for COVID-19. Aust Prescr 2021; 44: 175. https://doi.org/10.18773/austprescr.2021.051.
Yamasoba D, Kosugi Y, Kimura I, Fujita S, Uriu K, Ito J, et al. Neutralisation sensitivity of SARS-CoV-2 omicron subvariants to therapeutic monoclonal antibodies. Lancet Infect Dis. 2022;22:942–3. https://doi.org/10.1016/S1473-3099(22)00365-6.
Levin MJ, Ustianowski A, De Wit S, Launay O, Avila M, Templeton A, et al. Intramuscular AZD7442 (Tixagevimab-Cilgavimab) for prevention of covid-19. N Engl J Med. 2022;386:2188–200. https://doi.org/10.1056/NEJMoa2116620.
Horby PW, Mafham M, Bell JL, Linsell L, Staplin N, Emberson J, et al. Lopinavir–ritonavir in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial. Lancet. 2020;396:1345–52. https://doi.org/10.1016/S0140-6736(20)32013-4.
Faro-Viana J, Bergman ML, Gonçalves LA, Duarte N, Coutinho TP, Borges PC, et al. Population homogeneity for the antibody response to COVID-19 BNT162b2/comirnaty vaccine is only reached after the second dose across all adult age ranges. Nat Commun. 2022;13:1–8. https://doi.org/10.1038/s41467-021-27761-z.
Marta RA, Nakamura GEK, de Aquino BM, Bignardi PR. COVID-19 vaccines: update of the vaccines in use and under development. Vacunas. 2022. https://doi.org/10.1016/J.VACUN.2022.06.003.
Hammerschmidt SI, Thurm C, Bošnjak B, Bernhardt G, Reinhold A, Willenzon S, et al. Robust induction of neutralizing antibodies against the SARS-CoV-2 Delta variant after homologous spikevax or heterologous vaxzevria-spikevax vaccination. Eur J Immunol. 2022;52:356. https://doi.org/10.1002/EJI.202149645.
Dey A, ChozhavelRajanathan TM, Chandra H, Pericherla HPR, Kumar S, Choonia HS, et al. Immunogenic potential of DNA vaccine candidate, ZyCoV-D against SARS-CoV-2 in animal models. Vaccine. 2021;39:4108–16. https://doi.org/10.1016/J.VACCINE.2021.05.098.
Cazzola M, Rogliani P, Mazzeo F, Matera MG. Controversy surrounding the sputnik V vaccine. Respir Med. 2021;187: 106569. https://doi.org/10.1016/J.RMED.2021.106569.
Tukhvatulin AI, Dolzhikova IV, Shcheblyakov DV, Zubkova OV, Dzharullaeva AS, Kovyrshina AV, et al. An open, non-randomised, phase 1/2 trial on the safety, tolerability, and immunogenicity of single-dose vaccine “sputnik light” for prevention of coronavirus infection in healthy adults. Lancet Reg Heal - Eur. 2021;11: 100241. https://doi.org/10.1016/J.LANEPE.2021.100241.
Jin PI, Guo X, Chen W, Ma S, Pan H, Dai LI, et al. Safety and immunogenicity of heterologous boost immunization with an adenovirus type-5-vectored and protein-subunit-based COVID-19 vaccine (Convidecia/ZF2001): a randomized, observer-blinded, placebo-controlled trial. PLOS Med. 2022;19: e1003953. https://doi.org/10.1371/JOURNAL.PMED.1003953.
Yadav PD, Sapkal GN, Ella R, Sahay RR, Nyayanit DA, Patil DY, et al. Neutralization of beta and delta variant with sera of COVID-19 recovered cases and vaccinees of inactivated COVID-19 vaccine BBV152/covaxin. J Travel Med. 2021. https://doi.org/10.1093/JTM/TAAB104.
Elaidouni G, Chetouani Z, Merbouh CBM, Bkiyar H, Housni B. Acute ischemic stroke after first dose of inactivated COVID-19 vaccine: a case report. Radiol Case Rep. 2022;17:1942–5. https://doi.org/10.1016/J.RADCR.2022.02.082.
Tanriover MD, Doğanay HL, Akova M, Güner HR, Azap A, Akhan S, et al. Efficacy and safety of an inactivated whole-virion SARS-CoV-2 vaccine (CoronaVac): interim results of a double-blind, randomised, placebo-controlled, phase 3 trial in Turkey. Lancet. 2021;398:213–22. https://doi.org/10.1016/S0140-6736(21)01429-X.
Lazarus R, Taucher C, Brown C, Corbic I, Danon L, Dubischar K, et al. Safety and immunogenicity of the inactivated whole-virus adjuvanted vaccine VLA2001: a randomized, dose escalation, double-blind phase 1/2 clinical trial in healthy adults. J Infect. 2022. https://doi.org/10.1016/J.JINF.2022.06.009.
Zou S, Wu M, Ming F, Wu S, Guo W, Marley G, et al. Immune response and safety to inactivated COVID-19 vaccine: a comparison between people living with HIV and HIV-naive individuals. AIDS Res Ther. 2022;19:33. https://doi.org/10.1186/S12981-022-00459-Y.
Kozlovskaya LI, Piniaeva AN, Ignatyev GM, Gordeychuk IV, Volok VP, Rogova YV, et al. Long-term humoral immunogenicity, safety and protective efficacy of inactivated vaccine against COVID-19 (CoviVac) in preclinical studies. Emerg Microbes Infect. 2021;10:1790–806. https://doi.org/10.1080/22221751.2021.1971569/SUPPL_FILE/TEMI_A_1971569_SM4445.DOCX.
Nabirova D, Horth R, Smagul M, Nukenova G, Yesmagambetova A, Singer D, et al. Effectiveness of Sputnik V, Qazvac, Hayat-Vax, and coronavac vaccines in preventing COVID-19 in Kazakhstan, February-September 2021. SSRN Electron J. 2022. https://doi.org/10.2139/SSRN.4077889.
Liang Q, Li GF, Zhu FC. Vaccine profile of PPV23: Beijing minhai biotech 23-valent pneumococcal vaccine. Expert Rev Vaccines. 2016;15:1351–9. https://doi.org/10.1080/14760584.2016.1239536.
Fallahi MJ, EsmaeilzadehShahri N, Khodamoradi Z, Meymandi Nia M, Sehatpour F, Mahmoudi L. Case of possible encephalopathy following receiving the first dose of Iranian COVID-19Vaccine COVIran Barakat. Clin Case Rep. 2022. https://doi.org/10.1002/CCR3.5661.
Wang Y, Wang L, Cao H, Liu C. SARS-CoV-2 S1 is superior to the RBD as a COVID-19 subunit vaccine antigen. J Med Virol. 2021;93:892–8. https://doi.org/10.1002/JMV.26320.
Ghasemi S, Saffar KN, Ebrahimi F, Khatami P, Monazah A, Alizadeh GA, et al. Development of inactivated FAKHRAVAC ® vaccine against SARS-CoV-2 virus: preclinical study in animal models. Vaccines. 2021. https://doi.org/10.3390/VACCINES9111271.
Terkis S, Pavel I, Yetiskin H, Uygut MA, Aslan AF, Aydın G, et al. Development of an inactivated vaccine against SARS CoV-2. Vaccines. 2021;9:1266. https://doi.org/10.3390/VACCINES9111266.
Heath PT, Galiza EP, Baxter DN, Boffito M, Browne D, Burns F, et al. Safety and efficacy of NVX-CoV2373 covid-19 vaccine. N Engl J Med. 2021;385:1172–83. https://doi.org/10.1056/NEJMOA2107659.
Aguilar-Guerra TL, Fajardo-Díaz EM, Gorry CMA. Cuba’s national regulatory authority COVID-19: Olga Lidia Jacobo-Casanueva MS director center for state control of medicines and medical devices (CECMED). Medicc Rev. 2021;23:9–14. https://doi.org/10.37757/MR2021.V23.N3.3.
Hsieh SM, Liu MC, Chen YH, Sen LW, Hwang SJ, Cheng SH, et al. Safety and immunogenicity of CpG 1018 and aluminium hydroxide-adjuvanted SARS-CoV-2 S-2P protein vaccine MVC-COV1901: interim results of a large-scale, double-blind, randomised, placebo-controlled phase 2 trial in Taiwan. Lancet Respir Med. 2021;9:1396–406. https://doi.org/10.1016/S2213-2600(21)00402-1.
Smirnov VS, Lyalina LV, Milichkina AM, Khamitova IV, Zueva EV, Ivanov VA, et al. Longitudinal randomized cohort study of SARS-CoV-2 antibody seroprevalence in the St. Petersburg population. Viruses. 2022. https://doi.org/10.3390/V14050913.
Garib V, Katsamaki S, Turdikulova S, Levitskaya Y, Zahidova N, Bus G, et al. Milk of cow and goat, immunized by recombinant protein vaccine ZF-UZ-VAC2001(Zifivax), contains neutralizing antibodies against SARS-CoV-2 and remains active after standard milk pasteurization. Front Nutr. 2022. https://doi.org/10.3389/FNUT.2022.901871.
Thuluva S, Paradkar V, Turaga K, Gunneri S, Yerroju V, Mogulla R, et al. Selection of optimum formulation of RBD-based protein sub-unit covid19 vaccine (Corbevax) based on safety and immunogenicity in an open-label, randomized Phase-1 and 2 clinical studies. MedRxiv. 2022. https://doi.org/10.1101/2022.03.08.22271822.
Li L, Honda-Okubo Y, Huang Y, Jang H, Carlock MA, Baldwin J, et al. Immunisation of ferrets and mice with recombinant SARS-CoV-2 spike protein formulated with advax-SM adjuvant protects against COVID-19 infection. Vaccine. 2021;39:5940–53. https://doi.org/10.1016/J.VACCINE.2021.07.087.
Chavda VP, Vora LK, Vihol DR. COVAX-19Ⓡ vaccine: completely blocks virus transmission to non-immune individuals. Clin Complement Med Pharmacol. 2021;1:100004. https://doi.org/10.1016/j.ccmp.2021.100004.
Banihashemi SR, Es-haghi A, FallahMehrabadi MH, Nofeli M, Mokarram AR, Ranjbar A, et al. Safety and efficacy of combined intramuscular/intranasal RAZI-COV PARS vaccine candidate against SARS-CoV-2: a preclinical study in several animal models. Front Immunol. 2022. https://doi.org/10.3389/FIMMU.2022.836745.
Ferenci T, Sarkadi B. RBD-specific antibody responses after two doses of BBIBP-CorV (Sinopharm, Beijing CNBG) vaccine. BMC Infect Dis. 2022. https://doi.org/10.1186/S12879-022-07069-Z.
Reed G. Cuban COVID-19 vaccines for children: Rinaldo Puga MD MS principal investigator, pediatric clinical trials for soberana 02 and soberana plus. MEDICC Rev. 2022;24:14–8. https://doi.org/10.37757/MR2022.V24.N1.12.
Salimian J, Ahmadi A, Amani J, Olad G, Halabian R, Saffaei A, et al. Safety and immunogenicity of a recombinant receptor-binding domain-based protein subunit vaccine (Noora vaccine™) against COVID-19 in adults: a randomized, double-blind, placebo-controlled, phase 1 trial. J Med Virol. 2022. https://doi.org/10.1002/JMV.28097.
Immunogenicity and Safety Study of SK SARS-CoV-2 Recombinant Nanoparticle Vaccine (GBP510) Adjuvanted With AS03 (COVID-19) - Full Text View - ClinicalTrials.gov n.d. https://clinicaltrials.gov/ct2/show/NCT05007951. Accessed 21 Sept 2022
Li JJ, Luo XX, Huang XB. Initiation timing of veno-arterial extracorporeal membrane oxygenation. Zhonghua Yi Xue Za Zhi. 2022;102:1874–7. https://doi.org/10.3760/CMA.J.CN112137-20220415-00817.
Acute Respiratory Distress Syndrome - What Is Acute Respiratory Distress Syndrome? | NHLBI, NIH n.d. https://www.nhlbi.nih.gov/health/ards. Accessed 12 July 2022
Jiang Y, Rubin L, Peng T, Liu L, Xing X, Lazarovici P, et al. Cytokine storm in COVID-19: from viral infection to immune responses, diagnosis and therapy. Int J Biol Sci. 2022;18:459. https://doi.org/10.7150/IJBS.59272.
Zaim S, Chong JH, Sankaranarayanan V, Harky A. COVID-19 and multiorgan response. Curr Probl Cardiol. 2020;45: 100618. https://doi.org/10.1016/J.CPCARDIOL.2020.100618.
Liu Y, Sawalha AH, Lu Q. COVID-19 and autoimmune diseases. Curr Opin Rheumatol. 2021;33:155. https://doi.org/10.1097/BOR.0000000000000776.
VPC wants to dedicate this work to L M College of pharmacy as a part of the 75th year celebration of the college. Dr. Suneetha Vuppu and her students want to acknowledge honorable Chancellor Dr. G Viswanathan, Vellore Institute of Technology for his constant support and encouragement.
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Chavda, V.P., Vuppu, S., Mishra, T. et al. Recent review of COVID-19 management: diagnosis, treatment and vaccination. Pharmacol. Rep 74, 1120–1148 (2022). https://doi.org/10.1007/s43440-022-00425-5
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