Abstract
Many diseases that were considered major affliction of mankind in the past have been successfully eradicated with introduction of appropriate vaccine strategies. In order to expedite new challenges coming up to deal with various infectious diseases, nano-particulate-based subunit vaccines seem to be the demand of ordeal. The nano-vaccines can find better scope for the diseases that were not rampant in the semi-advanced world few years back. For example in present-day circumstances that corroborate with advancement in the field of medical sciences in terms of cancer chemotherapy, organ transplantation, therapy of autoimmune diseases, etc.; along with prevalence of altogether unheard diseases such as HIV infection, people are at risk of infliction with many more pathogens. In this regard, development of an effective prophylactic strategy against many opportunistic infections primarily caused by fungal pathogens needs better understanding of host pathogen relation and role of active immunity against pathogenic fungi. In the present study, we have tried to decipher effectiveness of a nano-sized vaccine delivery system in imparting protection against fungal pathogens.
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Church D, Elsayed S, Reid O et al (2006) Burn wound infections. Clin Microbiol Rev 19:403–434
Vivier E, Ugolini S (2011) Natural killer cells: from basic research to treatments. Front Immunol. doi:10.3389/fimmu.2011.00018
Buchacz K, Baker K, Palella J Jr et al (2007) AIDS-defining opportunistic illnesses in US patients, 1994-2007: a cohort study. AIDS 24:1549–1559
Leena VG, Ravi D, Abhay S (2005) Review of Health care in India. CEHAT, Mumbai. ISBN: 81-89042-40-8
Moghimi M, Hunter C, Murray C (2005) Nanomedicine: current status and future prospects. FASEB J 19:311–330
Couvreur P, Vauthier C (2006) Nanotechnology: intelligent design to treat complex disease. Pharm Res 23:1417–1450
Bangham AD, Standish MM, Miller N (1965) Cation permeability of phospholipid model membranes: effect of narcotics. Nature 208:1295–1297
Liechty B, Kryscio R, Slaughter V, Peppas A (2010) Polymers for drug delivery systems. Annu Rev Chem Biomol Eng 1:149–173
Moghimi M, Hunter C (2001) Capture of stealth nanoparticles by the body’s defences. Crit Rev Ther Drug Carrier Syst 18:527–550
Panyam J, Lof J, O'Leary E, Labhasetwar V (2002) Efficiency of dispatch and infiltrator cardiac infusion catheters in arterial localization of nanoparticles in a porcine coronary model of restenosis. J Drug Target 10:515–523
Quintana A, Raczka E, Piehler L et al (2002) Design and function of a dendrimer-based therapeutic nanodevice targeted to tumor cells through the folate receptor. Pharm Res 19:1310–1316
Allen TM, Cullis PR (2004) Drug delivery systems: entering the mainstream. Science 303:1818–1822
Sahoo SK, Labhasetwar V (2003) Nanotech approaches to drug delivery and imaging. Drug Discov Today 8:1112–1120
Sudimack J, Lee J (2000) Targeted drug delivery via the folate receptor. Adv Drug Deliv Rev 41:147–146
Sinico C, Fadda M (2009) Vesicular carriers for dermal drug delivery. Expert Opin Drug Deliv 6:813–825
Biju S, Sushama T, Mishra R et al (2006) Vesicular systems: an overview. Indian J Pharma Sci 68:141–153
Vollmar B, Menger D (2009) The hepatic microcirculation: mechanistic contributions and therapeutic targets in liver injury and repair. Physiol Rev 89:1269–1339
Singh S (2011) Membrane permeability in biological systems: a systems biology perspective. J Comput Sci Syst Biol 4:27–32
Copland J, Rades T, Davies M et al (2005) Lipid based particulate formulations for the delivery of antigen. Immunol Cell Biol 83:97–105
Semple C, Harasym O, Clow A et al (2005) Immunogenicity and rapid blood clearance of liposomes containing polyethylene glycol-lipid conjugates and nucleic acid. J Pharmacol Exp Ther 312:1020–1026
Syed M, Khan A, Nasti H et al (2003) Antigen entrapped in the escheriosomes leads to the generation of CD4(+) helper and CD8(+) cytotoxic T cell response. Vaccine 21:2383–2393
Ahmed A, Dare V, Hincke M (2008) Fibrin: a versatile scaffold for tissue engineering applications. Tissue Eng Part B Rev 14:199–215
Mosesson W (2005) Fibrinogen and fibrin structure and functions. J Thromb Haemost 3:1894–1904
Mosesson W, Siebenlist R, Meh A (2001) The structure and biological features of fibrinogen and fibrin. Ann N Y Acad Sci 936:11–30
Horan T, Francis W (2001) Fibrin degradation products, fibrin monomer and soluble fibrin in disseminated intravascular coagulation. Semin Thromb Hemost 27:657–666
Doolittle F, Chen R, Lau F (1971) Hybrid fibrin: proof of the intermolecular nature of- crosslinking units. Biochem Biophys Res Commun 44:94–100
Schense C, Hubbell A (1999) Cross-linking exogenous bifunctional peptides into fibrin gels with factor XIIIa. Bioconjug Chem 10:75–81
Gorodetsky R, Clark RA, An J et al (1999) Fibrin microbeads (FMB) as biodegradable carriers for culturing cells and for accelerating wound healing. J Invest Dermatol 112:866–872
Marx G, Mou X, Hotovely-Salomon A et al (2008) Heat denaturation of fibrinogen to develop a biomedical matrix. J Biomed Mater Res B Appl Biomater 84(1):49–57
Shimony N, Gorodetsky R, Marx G et al (2006) Fibrin microbeads (FMB) as a 3D platform for kidney gene and cell therapy. Kidney Int 69:625–633
Gurevich O, Vexler A, Marx G et al (2002) Fibrin microbeads for isolating and growing bone marrow-derived progenitor cells capable of forming bone tissue. Tissue Eng 8:661–672
Redl H, Schlag G, Stanek G, Hirschl A et al (1983) In vitro properties of mixtures of fibrin seal and antibiotics. Biomaterials 4:29–32
Tsourvakas S, Hatzigrigoris P, Tsibinos A et al (1995) Pharmacokinetic study of fibrin clot ciprofloxacin complex: an in vitro and in vivo experimental investigation. Arch Orthop Trauma Surg 114:295–297
Senderoff I, Sheu T, Sokoloski D (1991) Fibrin based drug delivery systems. J Parenter Sci Technol 45:2–6
Yoshida H, Yamaoka Y, Shinoyama M et al (2000) Novel drug delivery system using autologous fibrin glue--release properties of anti-cancer drugs. Biol Pharm Bull 23:371–374
Woolverton J, Fulton A, Salstrom J et al (2001) Tetracycline delivery from fibrin controls peritoneal infection without measurable systemic antibiotic. J Antimicrob Chemother 48:861–867
Kumar R, Vasantha Bai M, Krishnan K (2004) A freeze-dried fibrin disc as a biodegradable drug release matrix. Biologicals 32:49–55
Itokazu M, Yamamoto K, Yang Y et al (1997) The sustained release of antibiotic from freeze-dried fibrin-antibiotic compound and efficacies in a rat model of osteomyelitis. Infection 25:359–363
Simpson E, Gilbert A, Rudnick E et al (2002) Transscleral diffusion of carboplatin: an in vitro and in vivo study. Arch Ophthalmol 120:1069–1074
Pardue T, Hejny C, Gilbert A et al (2004) Retinal function after subconjunctival injection of carboplatin in fibrin sealant. Retina 24:776–782
Häfeli O, Pauer J, Unnithan J et al (2007) Fibrin glue system for adjuvant brachytherapy of brain tumors with 188Re and 186Re-labeled microspheres. Eur J Pharm Biopharm 65:282–288
Hou T, Xu J, Li Q et al (2008) In vitro evaluation of a fibrin gel antibiotic delivery system containing mesenchymal stem cells and vancomycin alginate beads for treating bone infections and facilitating bone formation. Tissue Eng Part A 14:1173–1182
Janmey A, McCormick E, Rammensee S et al (2007) Negative normal stress in semiflexible biopolymer gels. Nat Mater 6:48–51
Smidsrød O, Skjåk-Braek G (1990) Alginate as immobilization matrix for cells. Trends Biotechnol 8:71–78
Atala A, Kim W, Paige T et al (1994) Endoscopic treatment of vesicoureteral reflux with a chondrocyte-alginate suspension. J Urol 152:641–643
Wee S, Gombotz R (1998) Protein release from alginate matrices. Adv Drug Deliv Rev 31:267–285
Silva A (2006) Nanomedicine: seeing the benefits of ceria. Nat Nanotechnol 1:92–94
Kolambkar M, Peister A, Ekaputra K et al (2010) Colonization and osteogenic differentiation of different stem cell sources on electrospun nanofiber meshes. Tissue Eng Part A 16:3219–3230
Chen M, Wu F, Wang T et al (2005) Preparation of recombinant human bone morphogenetic protein-2 loaded dextran-based microspheres and their characteristics. Acta Pharmacol Sin 26:1093–1103
Bachelder M, Beaudette T, Broaders E et al (2010) In vitro analysis of acetalated dextran microparticles as a potent delivery platform for vaccine adjuvants. Mol Pharm 7:826–835
Qi J, Yao P, He F et al (2010) Nanoparticles with dextran/chitosan shell and BSA/chitosan core--doxorubicin loading and delivery. Int J Pharm 393:176–184
Müller E (2003) The origin of metazoan complexity: porifera as integrated animals. Integr Comp Biol 43:3–10
Di Lullo A, Sweeney M, Korkko J et al (2002) Mapping the ligand-binding sites and disease-associated mutations on the most abundant protein in the human, type I collagen. J Biol Chem 277:4223–4231
Wallace D, McPherson J, Ellingsworth L et al (1988) Injectable collagen for tissue augmentation. Collagen, Biotechnology 3:118–144
Wallace D, Rhee W, Reihanian H et al (1989) Injectable cross-linked collagen with improved flow properties. J Biomed Mater Res 23:931–945
Rosenblatt J, Devereux B, Wallace D (1993) Dynamic rheological studies of hydrophobic interactions in injectable collagen biomaterials. J Appl Polym Sci 50:953–963
Chow A, Fuller G, Wallace D et al (1985) Rheo-optical response of rod-like chains subject to transient shear flow:2. Two-color birefringence measurements on collagen protein. Macromolecule 18:793–804
Kligman M (1988) Histologic responses to collagen implants in human volunteers: comparison of Zyderm collagen with Zyplast implant. J Dermatol Surg Oncol 14:35–38
Stegman J, Chu S, Bensch K et al (1987) A light and electron microscopic evaluation of Zyderm collagen and Zyplast implants in aging human facial skin. A pilot study. Arch Dermatol 123:1644–1169
Wallace G, Rosenblatt J (2003) Collagen gel systems for sustained delivery and tissue engineering. Adv Drug Deliv Rev 55:1631–1649
Koch-Weser J, Sellers M (1976) Drug therapy. Binding of drugs to serum albumin (second of two parts). N Engl J Med 294:526–531
Kragh-Hansen U, Minchiotti L, Brennan O et al (1990) Hormone binding to natural mutants of human serum albumin. Eur J Biochem 193:169–174
Prinsen H, de Sain-van der Velden G (2004) Albumin turnover: experimental approach and its application in health and renal diseases. Clin Chim Acta 347:1–14
Nair S, Laurencin T (2006) Polymers as biomaterials for tissue engineering and controlled drug delivery. Adv Biochem Eng Biotechnol 102:47–90
Eldridge H, Staas K, Meulbroek A et al (1991) Biodegradable and biocompatible poly(DL-lactide-co-glycolide) microspheres as an adjuvant for staphylococcal enterotoxin B toxoid which enhances the level of toxin-neutralizing antibodies. Infect Immun 59:2978–2986
O'Hagan T, McGee P, Holmgren J et al (1993) Biodegradable microparticles for oral immunization. Vaccine 11:149–154
Pistner H, Gutwald R, Ordung R et al (1993) Poly(L-lactide): a long-term degradation study in vivo. I Biological results. Biomaterials 14:671–677
Marten L (2002) Encyclopedia of polymer science and technology. John Wiley & Sons, Inc., New York. doi:10.1002/0471440264.pst384
Lee Y, Soon Y (2007) Polymeric protein delivery systems. Prog Polym Sci 32:669–697
Mandal K, Bostanian A, Graves A et al (2002) Poly(D,L-lactide-co-glycolide) encapsulated poly(vinyl alcohol) hydrogel as a drug delivery system. Pharm Res 19:1713–1719
Yeo Y, Namjin B, Kinam P (2001) Microencapsulation methods for delivery of protein drugs. Biotechnol Bioprocess Eng 6:213–230
Middleton C, Tipton J (2000) Synthetic biodegradable polymers as orthopedic devices. Biomaterials 21:2335–2346
Makadia K, Siegel J (2011) Poly lactic-co-glycolic acid (PLGA) as biodegradable controlled drug delivery carrier. Polymers (Basel) 3:1377–1397
Visscher E, Robison A, Argentieri J (1987) Tissue response to biodegradable injectable microcapsules. J Biomater Appl 2:118–131
Cleland L, Powell F, Shire J (1993) The development of stable protein formulations: a close look at protein aggregation, deamidation, and oxidation. Crit Rev Ther Drug Carrier Syst 10:307–377
Denning W, Bromley J (2015) Infectious disease. How to bolster the antifungal pipeline. Science 347:1414–1416
Veerareddy R, Vobalaboina V (2004) Lipid-based formulations of amphotericin B. Drugs Today (Barc) 40:133–145
Agrawal K, Gupta M (2000) Tuftsin-bearing liposomes in treatment of macrophage-based infections. Adv Drug Deliv Rev 41:135–146
Shadkchan Y, Keisari Y, Segal E (2004) Cytokines in mice treated with amphotericin B-intralipid. Med Mycol 42:123–128
Owais M, Ahmed I, Krishnakumar B et al (1993) Tuftsin-bearing liposomes as drug vehicles in the treatment of experimental aspergillosis. FEBS Lett 326:56–58
Masood K, Feroz M, Rukhsana J et al (2004) Prophylactic role of liposomised chloroquine against murine cryptococcosis less susceptible to fluconazole. Pharm Res 21:2207–2212
Arellano M, Lonial S (2008) Clinical uses of GM-CSF, a critical appraisal and update. Biologics 2:13–27
Blanco L, Garcia E (2008) Immune response to fungal infections. Vet Immunol Immunopathol 125:47–70
Polonelli L, Casadevall A, Han Y et al (2000) The efficacy of acquired humoral and cellular immunity in the prevention and therapy of experimental fungal infections. Med Mycol 38:281–292
Romani L (2011) Immunity to fungal infections. Nat Rev Immunol 11:275–288
Wüthrich M, Deepe S Jr, Klein B (2012) Adaptive immunity to fungi. Annu Rev Immunol 30:115–148
van de Veerdonk L, Netea G (2010) T-cell subsets and antifungal host defenses. Curr Fungal Infect Rep 4:238–243
Gibson F, Johnston A (2015) Immunity to Cryptococcus neoformans and C. gattii during cryptococcosis. Fungal Genet Biol 78:76–86
Spellberg B (2011) Vaccines for invasive fungal infections. F1000 Med Rep 3:13
Paramythiotou E, Frantzeskaki F, Flevari A et al (2014) Invasive fungal infections in the ICU: how to approach, how to treat. Molecules 19:1085–1119
Medici P, Del Poeta M (2015) New insights on the development of fungal vaccines: from immunity to recent challenges. Mem Inst Oswaldo Cruz 110:966–973
Anaissie E (1992) Opportunistic mycoses in the immunocompromised host: experience at a cancer center and review. Clin Infect Dis 14:S43–S53
Pfaller M, Wenzel R (1992) Impact of the changing epidemiology of fungal infections in the 1990s. Eur J Clin Microbiol Infect Dis 11:287–1291
Richardson D (1991) Opportunistic and pathogenic fungi. J Antimicrob Chemother 28:1–11
Walsh J (1992) Emerging targets in antibacterial and antifungal. Chapman & Hall, New York, pp 249–373
Banerjee N, Emori G, Culver H et al (1991) Secular trends in nosocomial primary bloodstream infections in the United States, 1980-1989. National Nosocomial Infections Surveillance System. Am J Med 91:86S–89S
Emori G, Gaynes P (1993) An overview of nosocomial infections, including the role of the microbiology laboratory. Clin Microbiol Rev 6:428–442
Goff A, Koletar L, Buesching J et al (1995) Isolation of flucanozole-resistant Candida albicans from HIV negativepatients never treated with azoles. Clin Infect Dis 20:77–83
Nolte S, Parkinson T, Falconer J (1997) Isolation and charecterisation of flucanazole and amphoterecin B resistant Candida albicans from blood of two patients with leukemia. Antimicrob Agents Chemother 41:196–199
Nguyen H, Peacock E Jr, Morris J et al (1996) The changing face of candidemia: emergence of non-Candida albicans species and antifungal resistance. Am J Med 100:617–623
Iannitti G, Carvalho A, Romani L (2012) From memory to antifungal vaccine design. Trends Immunol 33:467–474
Behnsen J, Hartmann A, Schmaler J et al (2008) The opportunistic human pathogenic fungus Aspergillus fumigatus evades the host complement system. Infect Immun 76:820–827
Nanjappa G, Klein S (2014) Vaccine immunity against fungal infections. Curr Opin Immunol 28:27–33
Del Poeta M, Casadevall A (2012) Ten challenges on Cryptococcus and cryptococcosis. Mycopathologia 173:303–310
Shapiro S, Robbins N, Cowen E (2011) Regulatory circuitry governing fungal development, drug resistance, and disease. Microbiol Mol Biol Rev 75:213–267
Kirkpatrick H (1989) Chronic mucocutaneous candidiasis. Eur J Clin Microbiol Infect Dis 8:448–456
Bodey GP (1993) Hematogenous and major organ candidiasis. In: Bodey GP (ed) Candidiasis: pathogenesis, diagnosis and treatment. Raven, New York, pp 279–329
Casanova M, Martínez P, Chaffin L (1990) Fab fragments from a monoclonal antibody against a germ tube mannoprotein block the yeast-to-mycelium transition in Candida albicans. Infect Immun 58:3810–38112
Buckley H, Lucas J, Hattler G Jr et al (1968) Defective cellular immunity associated with chronic mucocutaneous moniliasis and recurrent staphylococcal botryomycosis: immunological reconstitution by allogeneic bone marrow. Clin Exp Immunol 3:153–169
Hoh C, Lin P, Chan L et al (1996) Successful allogeneic bone marrow transplantation in severe chronic mucocutaneous candidiasis syndrome. Bone Marrow Transplant 18:797–800
Cutler E (1976) Acute systemic candidiasis in normal and congenitally thymic-deficient (nude) mice. J Reticuloendothel Soc 19:121–124
Jones-Carson J, Vazquez-Torres A, Warner T et al (2000) Disparate requirement for T cells in resistance to mucosal and acute systemic candidiasis. Infect Immun 68:2363–2365
Tabeta H, Mikami Y, Abe F et al (1984) Studies on defense mechanisms against Candida albicans infection in congenitally athymic nude (nu/nu) mice. Mycopathologia 84:107–113
Romani L, Cenci E, Menacci A et al (1995) T helper cell dichotomy to Candida albicans: implications for pathology, therapy, and vaccine design. Immunol Res 14:148–162
Bistoni F, Cenci E, Mencacci A et al (1993) Mucosal and systemic T helper cell function after intragastric colonization of adult mice with Candida albicans. J Infect Dis 168:1449–1157
Ashman B, Fulurija A, Papadimitriou M (1999) Both CD4+ and CD8+ lymphocytes reduce the severity of tissue lesions in murine systemic cadidiasis, and CD4+ cells also demonstrate strain-specific immunopathological effects. Microbiology 145:1631–1640
Bodey P (1986) Infection in cancer patients. A continuing association. Am J Med 81:11–26
Nasser M, Melgar R, Longworth L et al (1997) Incidence and risk of developing fungal prosthetic valve endocarditis after nosocomial candidemia. Am J Med 103:25–32
Bross J, Talbot GH, Maislin G et al (1989) Risk factors for nosocomial candidemia: a case-control study in adults without leukemia. Am J Med 87:614–620
Wey B, Mori M, Pfaller A et al (1989) Risk factors for hospital-acquired candidemia. A matched case-control study. Arch Intern Med 149:2349–2353
MacDonald L, Baker C, Chenoweth C (1998) Risk factors for candidemia in a children's hospital. Clin Infect Dis 26:642–645
Lopez-Berestein G, Bodey GP, Fainstein V et al (1989) Treatment of systemic fungal infections with liposomal amphotericin B. Arch Intern Med 149:2533–2536
Ruhnke M, Schmidt-Westhausen A, Trautmann M (1997) In vitro activities of voriconazole (UK-109,496) against fluconazole-susceptible and -resistant Candida albicans isolates from oral cavities of patients with human immunodeficiency virus infection. Antimicrob Agents Chemother 41:575–577
Sanati H, Belanger P, Fratti R et al (1997) A new triazole, voriconazole (UK-109,496), blocks sterol biosynthesis in Candida albicans and Candida krusei. Antimicrob Agents Chemother 41:2492–2496
Hazen C, Baron J, Colombo L et al (2003) Comparison of the susceptibilities of Candida spp. to fluconazole and voriconazole in a 4-year global evaluation using disk diffusion. J Clin Microbiol 41:5623–5632
Anderson B (2005) Evolution of antifungal-drug resistance: mechanisms and pathogen fitness. Nat Rev Microbiol 3:547–556
Richardson D (2005) Changing patterns and trends in systemic fungal infections. J Antimicrob Chemother 56:i5–i11
Sangeorzan A, Bradley F, He X et al (1994) Epidemiology of oral candidiasis in HIV-infected patients: colonization, infection, treatment, and emergence of fluconazole resistance. Am J Med 97:339–346
Johnson M, Warnock W (1995) Azole drug resistance in yeasts. J Antimicrob Chemother 36:751–755
Meunier F, Aoun M, Bitar N (1992) Candidemia in immunocompromised patients. Clin Infect Dis 14:S120–S125
White J, Habib R, Vanthuyne A et al (2001) Combined topical flucytosine and amphotericin B for refractory vaginal Candida glabrata infections. Sex Transm Infect 77:212–213
Kojic M, Darouiche O (2004) Candida infections of medical devices. Clin Microbiol Rev 17:255–267
Ada G (1991) Vaccine development. Real and imagined dangers. Nature 349:369
Mochon B, Cutler E (2005) Is a vaccine needed against Candida albicans? Med Mycol 43:97–115
Huang C, Lin Y, Leu S et al (1998) Yeast carriage on hands of hospital personnel working in intensive care units. J Hosp Infect 39:47–55
Hilleman R (2002) Overview of the needs and realities for developing new and improved vaccines in the 21st century. Intervirology 45:199–211
Milstien J, Lambert S (2002) Emergency response vaccines--a challenge for the public sector and the vaccine industry. Vaccine 21:146–154
Owais M, Massod K, Agrewala N et al (2001) Use of liposome as an immunopotentiating delivery system: in perspective of vaccine development. Scand J Immunol 54:125–132
Naider F, Shenbagamurthi P, Steinfeld S et al (1983) Synthesis and biological activity of tripeptidyl polyoxins as antifungal agents. Antimicrob Agents Chemother 24:787–796
Denning W (2003) Echinocandin antifungal drugs. Lancet 362:1142–1151
Farah S, Ashman B, Challacombe J (2000) Oral candidosis. Clin Dermatol 18:553–562
Fidel L Jr (2004) History and new insights into host defense against vaginal candidiasis. Trends Microbiol 12:220–227
Nucci M, Colombo AL, Spector N et al (1997) Breakthrough candidemia in neutropenic patients. Clin Infect Dis 24:275–276
Casadevall A (1995) Antibody immunity and invasive fungal infections. Infect Immun 63:4211–4218
Hannula J, Saarela M, Jousimies-Somer H et al (1999) Age-related acquisition of oral and nasopharyngeal yeast species and stability of colonization in young children. Oral Microbiol Immunol 14:176–182
Chauhan A, Zubair S, Nadeem A et al (2014) Escheriosome-mediated cytosolic delivery of PLK1-specific siRNA: potential in treatment of liver cancer in BALB/c mice. Nanomedicine (Lond) 9:407–420
Singha H, Mallick I, Jana C et al (2008) Escheriosomes entrapped DNA vaccine co-expressing Cu-Zn superoxide dismutase and IL-18 confers protection against Brucella abortus. Microbes Infect 10:1089–1096
Loftus J, Fung E, Roncaglia P et al (2005) The genome of the basidiomycetous yeast and human pathogen Cryptococcus neoformans. Science 307:1321–1324
Dadachova E, Bryan RA, Huang X et al (2007) Ionizing radiation changes the electronic properties of melanin and enhances the growth of melanized fungi. PLoS One 2:e457
Joseph H, Thomas K, Kyung K et al (1998) Book ISBN: 978-1-55581-501-1
Alvarez M, Burn T, Luo Y et al (2009) The outcome of Cryptococcus neoformans intracellular pathogenesis in human monocytes. BMC Microbiol 9:51. doi:10.1186/1471-2180-9-51
Saag MS, Graybill RJ, Larsen RA et al (2000) Practice guidelines for the management of cryptococcal disease. Infectious Diseases Society of America. Clin Infect Dis 30:710–718
Martínez P, Gil L, López-Ribot L et al (1998) Serologic response to cell wall mannoproteins and proteins of Candida albicans. Clin Microbiol Rev 11:121–141
Vibhagool A, Sungkanuparph S, Mootsikapun P et al (2003) Discontinuation of secondary prophylaxis for cryptococcal meningitis in human immunodeficiency virus-infected patients treated with highly active antiretroviral therapy: a prospective, multicenter, randomized study. Clin Infect Dis 36:1329–1331
Schaars F, Meintjes A, Morroni C et al (2006) Outcome of AIDS-associated cryptococcal meningitis initially treated with 200 mg/day or 400 mg/day of fluconazole. BMC Infect Dis 6:118
Ahmad E, Fatima T, Owais M et al (2011) Beaded plasma clot: a potent sustained-release, drug-delivery system. Ther Deliv 2:573–583
Wingfield T (2001) Protein precipitation using ammonium sulfate. Curr Protoc Protein Sci. doi:10.1002/0471140864.psa03fs13
Ahmad N, Masood K, Owais M (2001) Fusogenic potential of prokaryotic membrane lipids. Implication in vaccine development. Eur J Biochem 268:5667–5675
Pietrella D, Mazzolla R, Lupo P et al (2002) Mannoprotein from Cryptococcus neoformans promotes T-helper type 1 anticandidal responses in mice. Infect Immun 70:6621–6627
Acknowledgment
We thank the coordinator of the department for allowing us to avail required facilities of the department to complete this study. Asim Azhar is thankful to UGC for providing financial assistance in terms of Kothari postdoctoral fellowship.
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Zubair, S., Azhar, A., Khan, N., Ahmad, E., Ajmal, M., Owais, M. (2017). Nanoparticle-Based Mycosis Vaccine. In: Kalkum, M., Semis, M. (eds) Vaccines for Invasive Fungal Infections. Methods in Molecular Biology, vol 1625. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7104-6_13
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