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Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development

An effective vaccine for the hepatitis C virus (HCV) is a major unmet medical and public health need, and it requires an antigen that elicits immune responses to multiple key conserved epitopes. Decades of research have generated a number of vaccine candidates; based on these data and research throu...

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Autores principales: Toth, Eric A., Chagas, Andrezza, Pierce, Brian G., Fuerst, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227786/
https://www.ncbi.nlm.nih.gov/pubmed/34072451
http://dx.doi.org/10.3390/v13061027
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author Toth, Eric A.
Chagas, Andrezza
Pierce, Brian G.
Fuerst, Thomas R.
author_facet Toth, Eric A.
Chagas, Andrezza
Pierce, Brian G.
Fuerst, Thomas R.
author_sort Toth, Eric A.
collection PubMed
description An effective vaccine for the hepatitis C virus (HCV) is a major unmet medical and public health need, and it requires an antigen that elicits immune responses to multiple key conserved epitopes. Decades of research have generated a number of vaccine candidates; based on these data and research through clinical development, a vaccine antigen based on the E1E2 glycoprotein complex appears to be the best choice. One bottleneck in the development of an E1E2-based vaccine is that the antigen is challenging to produce in large quantities and at high levels of purity and antigenic/functional integrity. This review describes the production and characterization of E1E2-based vaccine antigens, both membrane-associated and a novel secreted form of E1E2, with a particular emphasis on the major challenges facing the field and how those challenges can be addressed.
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spelling pubmed-82277862021-06-26 Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development Toth, Eric A. Chagas, Andrezza Pierce, Brian G. Fuerst, Thomas R. Viruses Review An effective vaccine for the hepatitis C virus (HCV) is a major unmet medical and public health need, and it requires an antigen that elicits immune responses to multiple key conserved epitopes. Decades of research have generated a number of vaccine candidates; based on these data and research through clinical development, a vaccine antigen based on the E1E2 glycoprotein complex appears to be the best choice. One bottleneck in the development of an E1E2-based vaccine is that the antigen is challenging to produce in large quantities and at high levels of purity and antigenic/functional integrity. This review describes the production and characterization of E1E2-based vaccine antigens, both membrane-associated and a novel secreted form of E1E2, with a particular emphasis on the major challenges facing the field and how those challenges can be addressed. MDPI 2021-05-29 /pmc/articles/PMC8227786/ /pubmed/34072451 http://dx.doi.org/10.3390/v13061027 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Toth, Eric A.
Chagas, Andrezza
Pierce, Brian G.
Fuerst, Thomas R.
Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development
title Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development
title_full Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development
title_fullStr Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development
title_full_unstemmed Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development
title_short Structural and Biophysical Characterization of the HCV E1E2 Heterodimer for Vaccine Development
title_sort structural and biophysical characterization of the hcv e1e2 heterodimer for vaccine development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227786/
https://www.ncbi.nlm.nih.gov/pubmed/34072451
http://dx.doi.org/10.3390/v13061027
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