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Virus-like particles: Passport to immune recognition

Virus-like particles (VLPs) are formed by the self-assembly of envelope and/or capsid proteins from many viruses. In many cases such VLPs have structural characteristics and antigenicity similar to the parental virus, and some have already proven successful as vaccines against the cognate virus infe...

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Detalles Bibliográficos
Autores principales: Grgacic, Elizabeth V.L., Anderson, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128828/
https://www.ncbi.nlm.nih.gov/pubmed/16997714
http://dx.doi.org/10.1016/j.ymeth.2006.07.018
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author Grgacic, Elizabeth V.L.
Anderson, David A.
author_facet Grgacic, Elizabeth V.L.
Anderson, David A.
author_sort Grgacic, Elizabeth V.L.
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description Virus-like particles (VLPs) are formed by the self-assembly of envelope and/or capsid proteins from many viruses. In many cases such VLPs have structural characteristics and antigenicity similar to the parental virus, and some have already proven successful as vaccines against the cognate virus infection. The structural components of some VLPs have also proven amenable to the insertion or fusion of foreign antigenic sequences, allowing the production of chimeric VLPs exposing the foreign antigen on their surface. Other VLPs have been used as carriers for foreign antigens, including non-protein antigens, via chemical conjugation. This review outlines some of the advantages, disadvantages, and technical considerations for the use of a wide range of VLP systems in vaccine development.
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spelling pubmed-71288282020-04-08 Virus-like particles: Passport to immune recognition Grgacic, Elizabeth V.L. Anderson, David A. Methods Article Virus-like particles (VLPs) are formed by the self-assembly of envelope and/or capsid proteins from many viruses. In many cases such VLPs have structural characteristics and antigenicity similar to the parental virus, and some have already proven successful as vaccines against the cognate virus infection. The structural components of some VLPs have also proven amenable to the insertion or fusion of foreign antigenic sequences, allowing the production of chimeric VLPs exposing the foreign antigen on their surface. Other VLPs have been used as carriers for foreign antigens, including non-protein antigens, via chemical conjugation. This review outlines some of the advantages, disadvantages, and technical considerations for the use of a wide range of VLP systems in vaccine development. Elsevier Inc. 2006-09 2006-09-22 /pmc/articles/PMC7128828/ /pubmed/16997714 http://dx.doi.org/10.1016/j.ymeth.2006.07.018 Text en Copyright © 2006 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Grgacic, Elizabeth V.L.
Anderson, David A.
Virus-like particles: Passport to immune recognition
title Virus-like particles: Passport to immune recognition
title_full Virus-like particles: Passport to immune recognition
title_fullStr Virus-like particles: Passport to immune recognition
title_full_unstemmed Virus-like particles: Passport to immune recognition
title_short Virus-like particles: Passport to immune recognition
title_sort virus-like particles: passport to immune recognition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128828/
https://www.ncbi.nlm.nih.gov/pubmed/16997714
http://dx.doi.org/10.1016/j.ymeth.2006.07.018
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