Introduction

Since December 2019, a cluster of cases of “unknown viral pneumonia” linked to a local Huanan seafood wholesale market was reported in Wuhan, China. Scientists isolated a novel coronavirus (named Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)) that was identified as the cause of the unknown pneumonia in an infected patient in Wuhan [1]. Subsequently, the WHO officially named the disease as COVID-19.

Researchers have found that SARS‐CoV‐2 is closely linked to bat-derived SARS-like coronaviruses [2, 3], indicating probable animal-to-human transmission. Subsequently, more and more studies suggested that SARS‐CoV‐2 sustained human-to-human transmission [4,5,6]. A study indicated that hospital-related spread of SARS‐CoV‐2 was doubted in 41% of patients [7]. Furthermore, asymptomatic infection was suspected as a potential source of infection [8]. As of 18 January 2021, the ongoing infections have spread throughout China and numerous countries around the world [9,10,11,12,13]and have resulted in 99,026 cases in China and over 95 million cases in 216 other countries. It has overwhelmingly surpassed SARS and MERS in terms of both the number of infected cases and the spatial range of epidemic areas. So far, the accumulative confirmed cases have currently remained almost constant in China, on 18 January 2021, 232 cases were confirmed, while there still has been a striking rise in COVID-19 in other countries, 173,425 new cases were confirmed in the America and 38,598 in Brazil on 18 January 2021.

Recently, SARS-CoV­2 has become a pandemic, and the number of infected people is growing rapidly around the world. Nevertheless, the epidemic can still be stopped if nations are willing to take aggressive measures, as did China, whose current epidemic is under control. In this paper, we provide the updated comprehensive summary regarding COVID-19, from etiological characteristics to intervention and prevention experience from China, in the hopes of providing a reference for public health authorities and healthcare workers around the world.

Etiological Characteristics

Coronaviruses, a big family of single-stranded RNA viruses, can transmit animals and humans and can cause aspiratory, hepatic, digestive, and neurological diseases [14]. Coronaviruses are further divided into four genera: alpha-, beta-, gamma-, and delta-coronaviruses [15]. SARS‐CoV-2, as SARS-CoV in 2002 and MERS-CoV in 2012, belongs to a separate branch of the β-coronavirus family [1]. SARS­CoV-2 has been indicated to infect human aspiratory epithelial cells via an interaction between the viral spike (S-protein) and the angiotensin-converting enzyme 2 receptors on human cells, in the same manner as SARS-CoV [16]. A number of studies have shown that SARS­CoV­2 is most similar to SARS-like coronaviruses from horseshoe bats collected in Zhoushan, Zhejiang, with a nucleotide homology of 87.9–98.7% [17, 18], which is higher than SARS-CoV (~ 79%) and MERS-CoV (~ 50%) [2]; this indicates that bats are the most likely hosts of SARS-CoV-2. Moreover, Xiao et al. [19] found that one coronavirus isolated from a Malayan pangolin showed 100%, 98.6%, 97.8% and 90.7% amino acid identity with SARS-CoV-2 in the E, M, N and S genes, respectively, suggesting that pangolin may be a potential intermediate host. However, Lam et al. [20] expressed a different view, in which multiple lineages of pangolin coronavirus and their analogy to SARS-CoV-2 suggested that pangolins should be considered possible natural hosts. Shi et al. [21] found that SARS-CoV-2 replicates poorly in dogs, pigs, chickens, and ducks, but ferrets and cats were permissive to infection, moreover, cats were susceptible to airborne transmission. Additionally, Richard et al. [22] showed that SARS-CoV-2 was transmitted efficiently via direct contact and via the air between ferrets, 1 to 3 days and 3 to 7 days after exposure, respectively. To date, there is still no clear understanding regarding the natural and intermediate host of SARS­CoV­2, which warrants further research. What we can learn from SARS is that identifying the source of SARS­CoV­2 would help determine the transmission pattern of zoonosis and thus containing the ongoing global outbreak.

Epidemiology

In the beginning stages of the epidemic, a study by Li et al. [5] demonstrated that 55% of confirmed cases (425 patients) were related to the seafood market, unlike only 8.6% of the subsequent patients. The average incubation period was 5.1 days (95% CI 4.1–7.0), and the infection doubled in size every 7.4 days. According to the travel history and symptoms of 88 patients found outside Wuhan, the average incubation period was evaluated to be 6.4 days (95% CI 5.6–7.7) [23]. Foreign studies have also shown that the average incubation period of SARS-CoV-2 was 3.6 days (95% CI 1–9) [24]. Subsequently, Guan et al. reported that the median incubation period was 4.0 days (interquartile range: 3–7) in 1099 patients [6]. These estimates will help to provide a reasonable basis for the isolation and release of patients from medical observation. Taken together, China currently defines 14 days as a medical observation period.

At present, the estimated value of the mean basic reproduction rate (R0) of COVID-19 is still disputed. In a previous study, Li et al. [5] evaluated that R0 was 2.2 (95% CI 1.4–3.9), according to the mean continuous time interval of 7.6 days (95% CI 5.3–19). As the epidemic progressed, the analysis of the epidemiological data of 8866 patients showed that R0 was 3.77 (95% CI 3.51–4.05), based on the mean continuous time interval of 7 days [25]. Recently, Li et al. weighed five independent methods and found that the R0 of COVID-19 was 3.39 (95% CI 3.09–3.70) during the whole epidemic period, which was higher than that of SARS [26]. This may be one reason why more than 70 million people have been infected in more than 210 countries around the world in the last year with the number of confirmed cases growing rapidly and dramatically [27, 28]. Therefore, in the beginning stages of the epidemic, the value R0 = 2.2 (from 425 patients) may have been underestimated, as patients were not diagnosed in time due to a lack of medical resources.

SARS­CoV­2 has become a pandemic, and the number of infections is increasing dramatically. Epidemiological studies have indicated that SARS­CoV­2 is mainly spread by respiratory droplets, and can also be transmitted via direct or indirect contact with mucous membranes in the nose and mouth [29]. Furthermore, KIM et al. [30] found that a few naive indirect contacted confirmed ferrets were positive for viral RNA, suggesting airborne transmission. In addition, a considerable number of cases in the incubation period become a potential source of SARS­CoV­2 infection, as they exhibit atypical symptoms or are even asymptomatic [8]. Recently, besides nasopharyngeal swabs, viral RNA was also detected in patients’stool samples [31]. Luo et al. [32] showed that 16% of confirmed cases presented with gastrointestinal symptoms, suggesting that the digestive tract could be a potential SARS-CoV-2 infection route. Furthermore, positive viral RNA of the newborn at the age of 36 h suggested that SARS­CoV­2 might cause neonatal infection via mother-to-child transmission, but no reliable evidence is as yet available to support the possibility of vertical transmission of COVID-19 infection [33]. Recent studies have also found that SARS­CoV­2 can be transmitted via the ocular conjunctival route, which provides important theoretical support for virus prevention, especially for the protection of medical workers [34].

Clinical Features and Laboratory Findings

We summarized the clinical features and laboratory findings of cases with COVID-19 from four different studies (Table 1) [6, 10,11,12]. Males represented 55.2% (n = 899) of patients, and 38 healthcare workers had infections in Guan’s study [6]. The symptoms of COVID-19 are nonspecific and can range from asymptomatic to acute respiratory distress syndrome. Wang et al. [35] showed that asymptomatic carriers were more frequent amongst middle-aged individuals who had close contact with confirmed patients, which further increased the difficulty of epidemic intervention and prevention. In these four studies, there were a total of 1,628 cases; fever was the most common symptom (87.2%, n = 1420), followed by cough (59.6%, n = 971), fatigue (32.7%, n = 527), and atypical symptoms including diarrhea (3.8%, 3.2%), rhinorrhea (4.8%, 6.8%), and sore throat (13.9%, 6.4%), reported by Guan et al. [6] and Chen et al. [12], respectively. Notably, some digestive symptoms, including diarrhea, nausea, and vomiting, should not be overlooked in patients with COVID-19, and clinicians should be on high alert [32]. Besides, Dell’Era et al. [36] found that some infected people even had taste and smell disorders. Among COVID-19 infections, hypertension and cardiovascular and cerebrovascular diseases were the most common coexisting disorders, followed by diabetes. Patients who were transferred to intensive care units were more possible to have underlying diseases [7] and significantly longer durations of fever compared to those that did not require intensive care units [12]. Furthermore, Liu et al. [37] discovered that pregnant women were more likely to exhibit atypical clinical findings, which increased the difficulty of initial diagnosis. Qiu et al. [38] showed that all 36 children with infections exhibited moderate or mild symptoms, including asymptomatic cases, resulting in a dangerously infectious community situation. A mild respiratory tract infection was frequently the only clinical feature among the first 18 patients diagnosed with SARS-CoV-2 infection in Singapore [10]. However, if mild infections are not timely treated, they are likely to develop into severe cases and even death.

Table 1 Clinical Features and Laboratory Findings from four studies of 1628 patients with SARS-CoV-2 pneumonia in the World [6, 10,11,12]

Upon admission, Guan et al. showed that leukopenia, lymphocytopenia, and thrombocytopenia occurred in 33.7%, 83.2%, and 36.2% of cases, respectively, and many infected patients had elevated levels of C-reactive protein [6]. Zhang et al. [39] demonstrated that lymphopenia (75.4%) and eosinopenia (52.9%) were discovered in most patients. Liu et al. [40] found that patients with severe symptoms exhibited continuous and obvious decreases in lymphocyte counts and increases in neutrophil counts compared to patients with mild symptoms. Compared to the mild cases, severe cases exhibited significant decreases in T cell counts as well as increases in IL-2, IL-10, IL-6, and IFN-γ levels in peripheral blood. It seems that severe cases have more significant laboratory abnormalities than non-severe cases because of an obvious immunopathological process caused by a cytokine storm. Moreover, further research found that the viral clearance ratio was correlated with decreased serum lactate dehydrogenase and creatine kinase levels; such decreases may thus indicate that the infection is subsiding [41].

Imaging Findings

Chest computed tomography (CT) plays a vital role in the early diagnosis of COVID-19 [42, 43]. Herein, we summarized the imaging findings of three studies (Table 2) [44,45,46]. Upon admission of 225 cases, we found that typical CT findings consisted of bilateral pulmonary ground-glass opacity (84.4%, n = 190) and pulmonary consolidation (49.3%, n = 111); lesions were most likely to occur in the right lower lobe (76.9%, n = 173) and left lower lobe (75.6%, n = 170), and most patients had more than two lobes affected. Moreover, discrete pulmonary nodules, pleural effusion, pulmonary emphysema, pulmonary fibrosis and lymphadenopathy were rare symptoms [45]. Song et al. [47] showed that 44 of 51 (86%) patients had bilateral lung involvement; in 86% and 80% of patients, the peripheral and posterior part of the lungs were involved, respectively, patients older than 50 years old were more likely to have lung consolidation than patients younger than 50. Caruso et al. [48] discovered that 93% of confirmed cases had multilobe and posterior lung involvement; 91% of cases had bilateral pneumonia.

Table 2 Imaging findings at Chest CT from three studies of 225 patients with confirmed COVID-19 pneumonia [61,62,63]

Pan et al. [42] researched the time course of lung changes on chest CT during recovery from COVID-19, which consisted of the early stage (0–4 days), progressive stage (5–8 days), peak stage (9–13 days), and absorption stage (≥ 14 days). They found that small subpleural ground-glass opacities grew larger and exhibited crazy-paving patterns and consolidation up to two weeks after disease onset. After two weeks, the lesions were slowly absorbed, leaving extensive ground-glass opacity and subpleural parenchymal bands (the absorption stage). Meanwhile, Ai et al. [49] discovered that the accuracy rates of chest CT imaging and RT-PCR assay were 88% (888/1014) and 59% (601/1014) for the diagnosis of suspected cases with COVID-19, respectively, indicating that chest CT had a higher sensitivity for diagnosing COVID-19 than initial RT-PCR. However, Yang et al. [50] expressed a different view, as patients with RT-PCR-confirmed COVID-19 exhibit normal chest CT findings upon admission. This indicates that a normal chest CT result could not preclude COVID-19, especially for cases in the early stage.

Diagnosis of COVID-19

Diagnosis of COVID-19 needs a comprehensive analysis of epidemiological history and clinical presentation. Fever and dry cough were the common symptoms of a SARS-CoV-2 infection, while upper respiratory symptoms such as rhinorrhea were rare [6]. Furthermore, chest CT findings of COVID-19 presented multilobe involvement with typical ground-glass opacity and/or consolidation [51]. Finally, nasopharyngeal swabs with positive viral RNA remain the gold standard for the diagnosis of COVID-19 [52]. However, asymptomatic infections or normal chest CT findings followed by diagnosis can also often occur. In addition, RNA tests can also produce initially false negative results due to low viral load or the method of collecting nasopharyngeal swab specimens, so samples should be taken multiple times to confirm COVID-19 [53]. Besides, the serological testing of anti‐SARS‐CoV‐2 immunoglobulin G (IgG) and/or IgM was widely used as a complement method in the diagnosis of COVID‐19 [54]. Yu et al. [55] further discovered that different specimens had different viral loads in the different stages of infection, and the average viral load in sputum was confirmed to be significantly higher than in nasal swabs and throat swabs. Furthermore, the sputum sample viral load in the recovery stage was significantly lower than that in the early and progressive stages. As such, the eventual diagnosis of COVID-19 should be determined by a comprehensive analysis of CT imaging and blood test results.

Treatment

COVID-19 is a completely new disease that nobody knows how to treat it at first. Patients are generally on bed rest, maintained with a constant internal environment, receive supportive treatment and enough energy, and their vital signs are closely monitored. Up to now, over 1000 clinical studies have been conducted to treat COVID-19 infections in the world, including antiviral drugs, anti-inflammatories, corticosteroids, immunosuppressive agents and traditional Chinese medicine, and so on.

Antiviral Drugs

Although no antiviral treatment for COVID-19 has been proven effective, the antiretroviral drug lopinavir-ritonavir has been proposed [13], as it was previously effective in treating SARS and MERS [56, 57]. As these two viruses belong to the same branch as SARS-CoV-2, lopinavir-ritonavir may be effective against COVID-19. Cao et al. [58] found that no benefit was observed with lopinavir-ritonavir treatment beyond standard care in hospitalized patients with severe COVID-19. From the UK RECOVERY trial, 1616 patients were randomly allocated to receive lopinavir-ritonavir and 3424 patients to receive usual care, the results indicated that lopinavir-ritonavir was not supported in the treatment of hospitalized COVID-19 patients [59]. In another retrospective cohort study, arbidol combined with lopinavir-ritonavir had a better curative effect than only lopinavir-ritonavir in the treatment of COVID-19-induced pneumonia, this suggested that arbidol may be superior to lopinavir-ritonavir for COVID-19 patients [60]. However, in a retrospective study, Lian et al. [61] found that arbidol may not accelerate SARS-COV-2 clearance and improve prognosis in non-ICU patients, the efficacy of arbidol needs further evaluation. Furthermore, the anti-HIV drug nelfinavir is a potent inhibitor of cell fusion caused by the SARS-CoV-2, which need further study as an antiviral against COVID-19 infections [62]. Ianevski et al. [63] found that combinations of nelfinavir with amodiaquine was effective against seven SARS-CoV-2 strains. Moreover, favipiravir is a nucleoside drug used to block virus replication to suppress the effect of the virus, in a nonrandomized trial, a significant reduction in the median time to viral clearance using favipiravir was observed. However, patients were also treated with interferon-α1b, which makes it hard to estimate the antiviral effect of favipiravir, further trials need to be carried out to assess the efficacy of favipiravir against COVID-19 [64].

Meanwhile, Wang et al. [65] found that remdesivir, a novel nucleotide analog drug, could inhibit SARS­CoV­2 infection in vitro. Subsequently, the first case of SARS-COV-2 infection was given intravenously with remdesivir in the United States, most of the symptoms quickly subsided [31]. Sanville et al. [66] also used remdesivir to treat COVID-19 patients, which resulted in positive outcomes. In a recent study, a cohort of patients hospitalized for severe COVID-19 who were treated with compassionate-use remdesivir, clinical improvement was observed in 36 of 53 patients (68%) [67]. These findings are only retrospective descriptive studies, which are insufficient to support the clinical application of remdesivir. Other well-designed randomized trials of remdesivir treatment have also produced results. Beige et al. [68] suggested that patients treated with remdesivir had less time to recover than those treated with placebo. In another randomized clinical trial, at day 11, moderate COVID-19 patients in the 5-day Remdesivir group had a better clinical improvement than those receiving standard treatment [69].

Anti-inflammatories

Cortegiani et al. [70] summarized six studies and 23 ongoing clinical trials in China, and demonstrated that chloroquine was effective in restricting the replication of SARS-CoV-2 in vitro, but the clinical data were insufficient. In an observational study involving 1376 patients, the results showed that hydroxychloroquine was not associated with a significant reduction or increase in the risk of intubation composite endpoints or death [71]. Besides, preliminary findings suggested that the higher chloroquine dosage should not be recommended for critically ill patients with COVID-19 because of its potential safety hazards on a Randomized Clinical Trial [72]. Moreover, on one retrospective multicenter cohort study, patients hospitalized with COVID-19, treatment with hydroxychloroquine, azithromycin, compared with either treatment, or both, was not significantly associated with differences in in-hospital mortality [73]. Besides, on June 15, 2020, the US Food and Drug Administration (FDA) revoked the emergency authorization for chloroquine and hydroxychloroquine for the treatment of some COVID-19 patients due to poor efficacy and side effects. Drugs can cause serious adverse cardiac reactions and other potential side effects, and the known and potential risks of drug use outweigh the benefits. Besides, relevant studies have found that chloroquine and hydroxychloroquine have no significant antiviral effect on SARS-COV-2 infection in rhesus monkeys or human lung cells, and these studies do not support the use of hydroxychloroquine and chloroquine in the treatment of COVID-19 infected infections [74, 75]. Aditionally, Baron et al. [76] suggested that teicoplanin may potentially treat COVID-19 patients, as it had exhibited efficacy in inhibiting the initial stage of the MERS-CoV viral cycle in human cells. In a cohort of 21 patients, infections were complementarily treated with teicoplanin, none of the patients had adverse effects related to teicoplanin administration. The role of teicoplanin in the treatment of SARS-CoV-2 is required to further clinical investigation [77].

Corticosteroids

Meanwhile, corticosteroids have received worldwide attention as a potentially effective treatment for COVID-19, Angus et al. [78] showed that among patients with severe COVID-19, treatment with a 7-day fixed-dose course of hydrocortisone or shock-dependent dosing of hydrocortisone, compared with no hydrocortisone, resulted in 93% and 80% probabilities of superiority with regard to the odds of improvement in organ support-free days within 21 days. Tomazini et al. [79] also found that among patients with COVID-19 and moderate or severe ARDS, use of intravenous dexamethasone plus standard care compared with standard care alone resulted in a statistically significant increase in the number of ventilator-free days over 28 days, so corticosteroids are now a standard of therapy in severely ill patients with COVID-19 based on the RECOVERY trial.

Immunosuppressive Agents

Moreover, some clinical trials on the efficacy of immunosuppressive agents in the treatment of COVID-19 are being investigated. In one randomized clinical trial, researchers showed that participants who received colchicine had statistically significantly improved time to clinical deterioration [80]. Cao et al. [81] found significant chest computed tomography improvement, a faster recovery from lymphopenia, and favorable side-effect profile in the ruxolitinib group were encouraging and informative to future trials to test efficacy of ruxolitinib in a larger population. Stone et al. [82] found that tocilizumab was not effective for preventing intubation or death in moderately ill hospitalized patients with Covid-19 in a randomized, double-blind, placebo-controlled trial.

Traditional Chinese Medicine

Furthermore, traditional Chinese medicine (TCM) has played an extremely important role in the fight against COVID-19. In the third version COVID-19 treatment guidelines, the Chinese authorities announced that TCM was one of the recommended therapeutic options for COVID-19. In China, more than 30 TCM formulae were used in Hubei to fight the COVID-19. For example, in a multicenter, prospective, randomized controlled trial in confirmed cases with COVID-19, the recovery rate was significantly higher in treatment group with Lianhuaqingwen capsules (4 capsules, thrice daily) compared with control group (91.5% vs. 82.4%), the rate of improvement in chest computed tomographic images (83.8% vs. 64.1%) and clinical cure (78.9% vs. 66.2%) in treatment group was also higher than control group [83]. In total, TCM has been used in 91.5% of confirmed COVID-19 cases in China. Clinical observation showed that the total effective rate of TCM reached over 90%. TCM can effectively alleviate symptoms, reduce the development of mild and normal to severe, improve the cure rate, reduce the death rate, and promote the recovery of the body during the convalescent period (http://www.gov.cn/xinwen/2020-03/23/content_5494694.htm).

To sum up, corticosteroids, remdesivir and traditional Chinese medicine have shown to be clinically effective against COVID-19 in clinical trials so far. Lopinavir-ritonavir, chloroquine and hydroxychloroquine were initially promising are no longer being used because of lack of efficacy from clinical trials. Tocilizumab was not effective for preventing death in moderately ill hospitalized COVID-19 patients. The efficacy of arbidol, favipiravir, teicoplanin, ruxolitinib and colchicine are still undergoing further evaluation.

Vaccine

Vaccination is the most effective method for a long-term strategy for prevention and control of COVID-19 in the future. As of January 18, 2021, more than 214 vaccine candidates for COVID-19 had been reported and over 50 vaccine candidates were under clinical evaluation to treat COVID-19 around the world. At present, 15 vaccines from 5 technical routes are in clinical trials in China, and 6 of them are undergoing phase III clinical trials according to procedures and standards. Chen et al. [84, 85] has developed the world’s first recombinant coronavirus vaccine (AD5-NCOV) and completed phase I and II clinical trials, 4 weeks after vaccination, 99.5% of the subjects to produce specific antibodies, 89% of the subjects had a specific cellular immune response, the phase I and II clinical trials in general has reached the expected results. Chen’s team started phase III clinical trials of the COVID-19 vaccine in September this year in Mexico and expect to see preliminary phase III clinical results in three to six months. Besides, the Pfizer vaccine entered phase III trials on July 27, 43,538 people participated in the phase III trial, the results of the phase III clinical trial showed that a two-dose regimen of Pfizer vaccine (BNT162b2) conferred 95% protection against COVID-19 among people over the age of 16 [86]. On 2 December, the UK government announced that it had approved the Pfizer COVID-19 vaccine for its citizens, making the UK the first country in the world to do so, subsequently, the Pfizer vaccine was approved in Canada, the United States, Singapore and other countries. Besides, the Moderna vaccine entered phase III clinical trials on 27 July, and has enrolled roughly 30,000 people, making it the world’s first phase III clinical COVID-19 mRNA vaccine. On November 6, a preliminary Moderna data show that the immunization is 94% effective and seems to prevent severe infections, on the basis of an analysis of 95 cases in its ongoing phase III efficacy trial. Of these, 90 were in the group that received a placebo injection and 5 had received the vaccine, which equates to an efficacy of 94.5% [87]. On December 18, the US Food and Drug Administration (FDA) approved an emergency license for Moderna COVID-19 vaccine, the second COVID-19 vaccine to be approved in the US, following Pfizer vaccine. In addition, in an interim analysis of four randomised controlled trials in South Africa, Brazil, and the UK, they found that the efficacy of the Oxford vaccine (AZD1222) was 62.1% (in participants who received two standard doses) and 90.0% (in participants who received a low dose followed by a standard dose). Overall vaccine efficacy across both groups was 70.4% [88]. On December 30, the Oxford vaccine was officially approved for clinical use by the Medicines and Healthcare Products Regulatory Agency (MHRA). This is the second COVID-19 vaccine approved for use in the UK, after the Pfizer vaccine. Furthermore, On December 30, developed by Beijing biotechnology company COVID-19 vaccine phase III clinical trial data showed that the vaccine effectiveness was 79.34%, the data meet the world health organization-related technical standard, the vaccine has been approved by the State Food and Drug Administration for conditional marketing (http://www.bjbpi.com/news_list.asp?id=787). We expect more effective vaccines to be put on the market to fight the pandemic.

Intervention and Prevention Experience from China

At present, China’s epidemic prevention and control efforts have achieved steady success. To sum up, the stage of fighting the epidemic can be divided into the following four stages. In the first stage, at the end of December 2019, a case of pneumonia of unknown cause was discovered in Wuhan. The Chinese government immediately reported the outbreak and took prompt action to carry out etiological and epidemiological investigations.

In the second stage, that was, the outbreak period, began in late January, 2020. SARS-CoV-2 infection has been legally classified as a category B infectious disease but has been managed as a category A infectious disease by the Chinese authorities. With the number of confirmed cases rising rapidly across the country, China has adopted a key strategy to stop the spread of the virus. Wuhan as a largest city in central China (> 11 million inhabitants), the epicenter of the COVID­19 outbreak, and was locked down in an effort to curb rapid transmission on 23 January 2020, the lockdown of Wuhan’s public transportation, including trains, buses, subway, and airport, was also enforced to prevent the spread of the outbreak. Subsequently, other cities in Hubei province took similar measures, 30 other provinces also launched public health emergency response measures, many other cities also implemented the unprecedented intervention, and these effective experiences could improve public health response against the pandemic on global levels [89, 90]. At the same time, citizens leaving Wuhan must report to the local government and were required to be quarantined in designated places for 14 days. Due to the increasing number of infected cases in Wuhan, the medical resources in Hubei province were seriously insufficient; at the critical moment, the Chinese government has arranged more than 40,000 medical workers to support Hubei province [91]. At the same time, the Chinese government quickly constructed two designated hospitals (Huoshenshan and Leishenshan hospital) which could provide a total of over 2,000 beds for severe patients and more than a dozen Fangcang shelter hospitals for mild patients. Fangcang shelter hospitals quarantined thousands of confirmed cases, provided considerate medical services, and achieved an important triage function; it proved that the Fangcang shelter hospitals were the main reason for the success of epidemic prevention, other countries confronting the COVID-19 infection should also consider using Fangcang shelter hospitals as part of their public health response [92, 93].

For each individual, to further cut off potential transmission routes, Chinese authorities applied community­wide containment measures to reduce personal interactions; residents were asked to stay at home, and crowded areas such as schools and shopping malls were closed. Furthermore, all close contacts of confirmed patients and suspected patients were required for forced isolation in special places and received medical observation for 14 days. Due to the possibility of RNA tests turning positive again, the discharged patients were transferred to designated places to receive medical observation for another 14 days before returning home.

In the third stage, since late March, the number of newly confirmed cases in Wuhan has been reduced to zero, and the epidemic in China has achieved initial success. Subsequently, the control measures for leaving Wuhan were lifted, and the number of COVID-19 patients in hospitals in Wuhan was cleared, which marked that the spread of COVID-19 in Wuhan, the main battlefield in China, was basically interrupted. In order to find out Wuhan current situation of COVID-19, the Wuhan government decided to start novel Coronavirus nucleic acid screening for 10 million citizens within two weeks, screening results found no new symptomatic cases and 300 asymptomatic cases, and no positive cases were detected among 1,174 close contacts of asymptomatic cases, therefore, five to eight weeks after the lockdown ended, the infection rate of SARS-COV-2 in Wuhan was very low [94].

In the fourth stage, since 29 April 2020, the epidemic situation in China has been sporadic on the whole, imported cases from abroad have been basically brought under control, and the epidemic prevention and control across the country has entered a normal state. For example, confirmed cases have been found in Beijing, Qingdao, Shanghai, Xinjiang and Inner Mongolia one after the other; once there were confirmed cases in a locality, the local government will conduct nucleic acid tests for all personnel in the area, it took Qingdao five days to conduct nucleic acid tests on 7.5 million people in the city, full and thorough screening of possible infections.

On the whole, China’s response to the epidemic has been successful, this is due to strict epidemic prevention measures and people’s trust in the government. It proved that the early adoption of strict measures was of great significance for the control of COVID­19 outbreak, which could avoid local outbreaks caused by imported cases. But even when a local epidemic occurs, adopting high-intensity intervention and prevention measures in time, early detection and treatment of cases, suspected cases and close contacts to take strict medical quarantine and management, monitoring and screening of people who have moved in from the worst-affected areas, minimize public gathering activities, and also can effectively control the spread of the epidemic.

Conclusions

SARS­CoV­2 has become a pandemic, the number of infected people is still increasing rapidly, especially in some European and American countries. After three months of efforts, the epidemic in China has been effectively controlled, confirming that containment is viable. Other countries should take action immediately to reduce the spread of COVID­19. To date, the SARS-CoV-2 outbreak has lasted for a year, many issues remain unclear regarding COVID-19. First, the outbreak was first declared in Wuhan; however, this does not mean the source was there, and further investigation is needed. Second, it is unclear whether discharged patients can regain COVID-19 positivity and thus infectivity. Third, asymptomatic infections can transmit the disease, but the length and strength of the infectious period are to be determined, which is the focus and difficulty of formulation of containment measures at the present stage. The mechanism by which the virus causes asymptomatic infections and can still be transmitted is still unclear and requires further research. Finally, specific antiviral drugs are still not available and exist a lot of uncertainty about COVID-19 pneumonia. Although the domestic outbreak has been effectively controlled, the imported cases from abroad pose a new challenge to China. Thus, each of us still needs to be vigilant and not let down to prevent a second outbreak.