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Design and Engineering of Deimmunized Vaccinia Viral Vectors

Vaccinia viral (VV) vectors are increasingly used in oncolytic virus therapy and vaccine development for cancer and infectious diseases. However, their effectiveness is hindered by the strong anti-viral immune response induced by the viral vector. In this review, we discuss the strategies to deimmun...

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Detalles Bibliográficos
Autores principales: Song, Kevin, Viskovska, Mariya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697509/
https://www.ncbi.nlm.nih.gov/pubmed/33187060
http://dx.doi.org/10.3390/biomedicines8110491
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author Song, Kevin
Viskovska, Mariya
author_facet Song, Kevin
Viskovska, Mariya
author_sort Song, Kevin
collection PubMed
description Vaccinia viral (VV) vectors are increasingly used in oncolytic virus therapy and vaccine development for cancer and infectious diseases. However, their effectiveness is hindered by the strong anti-viral immune response induced by the viral vector. In this review, we discuss the strategies to deimmunize vaccinia viral vector. One approach is to mask the virus from the neutralization antibody responses by mapping and eliminating of B-cell epitopes on the viral membrane proteins. The recombinant VVs contain one or more viral glycoproteins with mutations in the neutralizing antibody epitopes, resulting in viral escape from neutralization. In addition, a regulator of complement activation (e.g., CD55) can be expressed on the surface of the virus particle, leading to increased resistance to complement-mediated neutralization.
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spelling pubmed-76975092020-11-29 Design and Engineering of Deimmunized Vaccinia Viral Vectors Song, Kevin Viskovska, Mariya Biomedicines Review Vaccinia viral (VV) vectors are increasingly used in oncolytic virus therapy and vaccine development for cancer and infectious diseases. However, their effectiveness is hindered by the strong anti-viral immune response induced by the viral vector. In this review, we discuss the strategies to deimmunize vaccinia viral vector. One approach is to mask the virus from the neutralization antibody responses by mapping and eliminating of B-cell epitopes on the viral membrane proteins. The recombinant VVs contain one or more viral glycoproteins with mutations in the neutralizing antibody epitopes, resulting in viral escape from neutralization. In addition, a regulator of complement activation (e.g., CD55) can be expressed on the surface of the virus particle, leading to increased resistance to complement-mediated neutralization. MDPI 2020-11-11 /pmc/articles/PMC7697509/ /pubmed/33187060 http://dx.doi.org/10.3390/biomedicines8110491 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Song, Kevin
Viskovska, Mariya
Design and Engineering of Deimmunized Vaccinia Viral Vectors
title Design and Engineering of Deimmunized Vaccinia Viral Vectors
title_full Design and Engineering of Deimmunized Vaccinia Viral Vectors
title_fullStr Design and Engineering of Deimmunized Vaccinia Viral Vectors
title_full_unstemmed Design and Engineering of Deimmunized Vaccinia Viral Vectors
title_short Design and Engineering of Deimmunized Vaccinia Viral Vectors
title_sort design and engineering of deimmunized vaccinia viral vectors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697509/
https://www.ncbi.nlm.nih.gov/pubmed/33187060
http://dx.doi.org/10.3390/biomedicines8110491
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