Virus-like Particles as Antiviral Vaccine: Mechanism, Design, and Application
Virus-like particles (VLPs) are viral structural protein that are noninfectious as they do not contain viral genetic materials. They are safe and effective immune stimulators and play important roles in vaccine development because of their intrinsic immunogenicity to induce cellular and humoral immu...
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Published in | Biotechnology and bioprocess engineering Vol. 28; no. 1; pp. 1 - 16 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Seoul
The Korean Society for Biotechnology and Bioengineering
01.02.2023
Springer Nature B.V 한국생물공학회 |
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Abstract | Virus-like particles (VLPs) are viral structural protein that are noninfectious as they do not contain viral genetic materials. They are safe and effective immune stimulators and play important roles in vaccine development because of their intrinsic immunogenicity to induce cellular and humoral immune responses. In the design of antiviral vaccine, VLPs based vaccines are appealing multifunctional candidates with the advantages such as self-assembling nanoscaled structures, repetitive surface epitopes, ease of genetic and chemical modifications, versatility as antigen presenting platforms, intrinsic immunogenicity, higher safety profile in comparison with live-attenuated vaccines and inactivated vaccines. In this review, we discuss the mechanism of VLPs vaccine inducing cellular and humoral immune responses. We outline the impact of size, shape, surface charge, antigen presentation, genetic and chemical modification, and expression systems when constructing effective VLPs based vaccines. Recent applications of antiviral VLPs vaccines and their clinical trials are summarized. |
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AbstractList | Virus-like particles (VLPs) are viral structural protein that are noninfectious as they do not contain viral genetic materials. They are safe and effective immune stimulators and play important roles in vaccine development because of their intrinsic immunogenicity to induce cellular and humoral immune responses. In the design of antiviral vaccine, VLPs based vaccines are appealing multifunctional candidates with the advantages such as self-assembling nanoscaled structures, repetitive surface epitopes, ease of genetic and chemical modifications, versatility as antigen presenting platforms, intrinsic immunogenicity, higher safety profile in comparison with live-attenuated vaccines and inactivated vaccines. In this review, we discuss the mechanism of VLPs vaccine inducing cellular and humoral immune responses. We outline the impact of size, shape, surface charge, antigen presentation, genetic and chemical modification, and expression systems when constructing effective VLPs based vaccines. Recent applications of antiviral VLPs vaccines and their clinical trials are summarized. Virus-like particles (VLPs) are viral structural protein that are noninfectious as they do not contain viral genetic materials. They are safe and effective immune stimulators and play important roles in vaccine development because of their intrinsic immunogenicity to induce cellular and humoral immune responses. In the design of antiviral vaccine, VLPs based vaccines are appealing multifunctional candidates with the advantages such as self-assembling nanoscaled structures, repetitive surface epitopes, ease of genetic and chemical modifications, versatility as antigen presenting platforms, intrinsic immunogenicity, higher safety profile in comparison with live-attenuated vaccines and inactivated vaccines. In this review, we discuss the mechanism of VLPs vaccine inducing cellular and humoral immune responses. We outline the impact of size, shape, surface charge, antigen presentation, genetic and chemical modification, and expression systems when constructing effective VLPs based vaccines. Recent applications of antiviral VLPs vaccines and their clinical trials are summarized. KCI Citation Count: 0 Virus-like particles (VLPs) are viral structural protein that are noninfectious as they do not contain viral genetic materials. They are safe and effective immune stimulators and play important roles in vaccine development because of their intrinsic immunogenicity to induce cellular and humoral immune responses. In the design of antiviral vaccine, VLPs based vaccines are appealing multifunctional candidates with the advantages such as self-assembling nanoscaled structures, repetitive surface epitopes, ease of genetic and chemical modifications, versatility as antigen presenting platforms, intrinsic immunogenicity, higher safety profile in comparison with live-attenuated vaccines and inactivated vaccines. In this review, we discuss the mechanism of VLPs vaccine inducing cellular and humoral immune responses. We outline the impact of size, shape, surface charge, antigen presentation, genetic and chemical modification, and expression systems when constructing effective VLPs based vaccines. Recent applications of antiviral VLPs vaccines and their clinical trials are summarized.Virus-like particles (VLPs) are viral structural protein that are noninfectious as they do not contain viral genetic materials. They are safe and effective immune stimulators and play important roles in vaccine development because of their intrinsic immunogenicity to induce cellular and humoral immune responses. In the design of antiviral vaccine, VLPs based vaccines are appealing multifunctional candidates with the advantages such as self-assembling nanoscaled structures, repetitive surface epitopes, ease of genetic and chemical modifications, versatility as antigen presenting platforms, intrinsic immunogenicity, higher safety profile in comparison with live-attenuated vaccines and inactivated vaccines. In this review, we discuss the mechanism of VLPs vaccine inducing cellular and humoral immune responses. We outline the impact of size, shape, surface charge, antigen presentation, genetic and chemical modification, and expression systems when constructing effective VLPs based vaccines. Recent applications of antiviral VLPs vaccines and their clinical trials are summarized. |
Author | Fan, JinBo Wang, Yang Xu, Wen Ma, Xi Zhang, Lei Sun, XiaoJing |
Author_xml | – sequence: 1 givenname: Lei surname: Zhang fullname: Zhang, Lei organization: Xi’an Key Laboratory of Pathogenic Microorganism and Tumor Immunity, Department of Basic Medicine, Xi’an Medical University – sequence: 2 givenname: Wen surname: Xu fullname: Xu, Wen organization: Xi’an Key Laboratory of Pathogenic Microorganism and Tumor Immunity, Department of Basic Medicine, Xi’an Medical University – sequence: 3 givenname: Xi surname: Ma fullname: Ma, Xi organization: Xi’an Key Laboratory of Pathogenic Microorganism and Tumor Immunity, Department of Basic Medicine, Xi’an Medical University – sequence: 4 givenname: XiaoJing surname: Sun fullname: Sun, XiaoJing organization: Xi’an Key Laboratory of Pathogenic Microorganism and Tumor Immunity, Department of Basic Medicine, Xi’an Medical University – sequence: 5 givenname: JinBo surname: Fan fullname: Fan, JinBo organization: Xi’an Key Laboratory of Pathogenic Microorganism and Tumor Immunity, Department of Basic Medicine, Xi’an Medical University – sequence: 6 givenname: Yang surname: Wang fullname: Wang, Yang email: yang.wang@xiyi.edu.cn organization: Xi’an Key Laboratory of Pathogenic Microorganism and Tumor Immunity, Department of Basic Medicine, Xi’an Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36627930$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002940876$$DAccess content in National Research Foundation of Korea (NRF) |
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SubjectTerms | Antibodies Antigen presentation Antigens Antiviral drugs Biotechnology Chemical modification Chemistry Chemistry and Materials Science Clinical trials Cytokines Cytotoxicity Epitopes Genomes Hepatitis Immune response Immune response (humoral) Immunogenicity Industrial and Production Engineering live vaccines Lymphocytes Pathogens Pattern recognition Proteins Review Paper Self-assembly Stimulators structural proteins Surface charge System effectiveness T cell receptors Vaccine development Vaccines Viral infections Virus-like particles Viruses 생물공학 |
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Title | Virus-like Particles as Antiviral Vaccine: Mechanism, Design, and Application |
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ispartofPNX | Biotechnology and Bioprocess Engineering, 2023, 28(1), , pp.1-16 |
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