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114 VLPs and particle vaccines

VLPs represent a powerful tool for vaccine development, representing the closest strategy to the native viruses for displaying and delivering conformational epitopes, with improved induction of antibodies and immune response in its whole. Moreover, the lack of genetic material makes VLPs the “safer...

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Autor principal: Buonaguro, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAIDS Journal of Acquired Immune Deficiency Syndromes 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149636/
http://dx.doi.org/10.1097/01.qai.0000446694.46916.e0
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author Buonaguro, Luigi
author_facet Buonaguro, Luigi
author_sort Buonaguro, Luigi
collection PubMed
description VLPs represent a powerful tool for vaccine development, representing the closest strategy to the native viruses for displaying and delivering conformational epitopes, with improved induction of antibodies and immune response in its whole. Moreover, the lack of genetic material makes VLPs the “safer counterpart” of live attenuated or killed viral vaccines which, indeed, may induce limited but possible undesired effects. VLP-based vaccines have been developed from both enveloped and non-enveloped viruses to target infectious and non-infectious diseases and are in various stages of development spanning preclinical evaluation to market. In particular, the only 2 preventive cancer vaccines licensed are based on VLP approach (HBV and HPV vaccines). Overall, pre-clinical and clinical trials with different VLP-based vaccines have shown they are well tolerated and can be administered by a number of routes, including intramuscular, subcutaneous, oral or intranasal. VLP vaccines have also been demonstrated to be highly immunogenic and capable of stimulating protective immunity in a number of instances when administered with or without adjuvants. Their potent immunogenicity is a result of several factors, including the ability to incorporate key immunogenic properties of viruses into a single entity and to hit the cells relevant for initiate an effective adaptive immune response.
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spelling pubmed-41496362014-09-24 114 VLPs and particle vaccines Buonaguro, Luigi J Acquir Immune Defic Syndr Abstract VLPs represent a powerful tool for vaccine development, representing the closest strategy to the native viruses for displaying and delivering conformational epitopes, with improved induction of antibodies and immune response in its whole. Moreover, the lack of genetic material makes VLPs the “safer counterpart” of live attenuated or killed viral vaccines which, indeed, may induce limited but possible undesired effects. VLP-based vaccines have been developed from both enveloped and non-enveloped viruses to target infectious and non-infectious diseases and are in various stages of development spanning preclinical evaluation to market. In particular, the only 2 preventive cancer vaccines licensed are based on VLP approach (HBV and HPV vaccines). Overall, pre-clinical and clinical trials with different VLP-based vaccines have shown they are well tolerated and can be administered by a number of routes, including intramuscular, subcutaneous, oral or intranasal. VLP vaccines have also been demonstrated to be highly immunogenic and capable of stimulating protective immunity in a number of instances when administered with or without adjuvants. Their potent immunogenicity is a result of several factors, including the ability to incorporate key immunogenic properties of viruses into a single entity and to hit the cells relevant for initiate an effective adaptive immune response. JAIDS Journal of Acquired Immune Deficiency Syndromes 2014-04 2014-03-07 /pmc/articles/PMC4149636/ http://dx.doi.org/10.1097/01.qai.0000446694.46916.e0 Text en Copyright © 2014 by Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Abstract
Buonaguro, Luigi
114 VLPs and particle vaccines
title 114 VLPs and particle vaccines
title_full 114 VLPs and particle vaccines
title_fullStr 114 VLPs and particle vaccines
title_full_unstemmed 114 VLPs and particle vaccines
title_short 114 VLPs and particle vaccines
title_sort 114 vlps and particle vaccines
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149636/
http://dx.doi.org/10.1097/01.qai.0000446694.46916.e0
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