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A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target

Antibodies that can neutralize diverse HIV-1 strains develop in ~10–20% of HIV-1 infected individuals, and their elicitation is a goal of vaccine design. Such antibodies can also serve as therapeutics for those who have already been infected with the virus. Structural characterizations of broadly re...

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Detalles Bibliográficos
Autores principales: Parker Miller, Emma, Finkelstein, Maxwell T., Erdman, Molly C., Seth, Paul C., Fera, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472920/
https://www.ncbi.nlm.nih.gov/pubmed/34578355
http://dx.doi.org/10.3390/v13091774
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author Parker Miller, Emma
Finkelstein, Maxwell T.
Erdman, Molly C.
Seth, Paul C.
Fera, Daniela
author_facet Parker Miller, Emma
Finkelstein, Maxwell T.
Erdman, Molly C.
Seth, Paul C.
Fera, Daniela
author_sort Parker Miller, Emma
collection PubMed
description Antibodies that can neutralize diverse HIV-1 strains develop in ~10–20% of HIV-1 infected individuals, and their elicitation is a goal of vaccine design. Such antibodies can also serve as therapeutics for those who have already been infected with the virus. Structural characterizations of broadly reactive antibodies in complex with the HIV-1 spike indicate that there are a limited number of sites of vulnerability on the spike. Analysis of their structures can help reveal commonalities that would be useful in vaccine design and provide insights on combinations of antibodies that can be used to minimize the incidence of viral resistance mutations. In this review, we give an update on recent structures determined of the spike in complex with broadly neutralizing antibodies in the context of all epitopes on the HIV-1 spike identified to date.
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spelling pubmed-84729202021-09-28 A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target Parker Miller, Emma Finkelstein, Maxwell T. Erdman, Molly C. Seth, Paul C. Fera, Daniela Viruses Review Antibodies that can neutralize diverse HIV-1 strains develop in ~10–20% of HIV-1 infected individuals, and their elicitation is a goal of vaccine design. Such antibodies can also serve as therapeutics for those who have already been infected with the virus. Structural characterizations of broadly reactive antibodies in complex with the HIV-1 spike indicate that there are a limited number of sites of vulnerability on the spike. Analysis of their structures can help reveal commonalities that would be useful in vaccine design and provide insights on combinations of antibodies that can be used to minimize the incidence of viral resistance mutations. In this review, we give an update on recent structures determined of the spike in complex with broadly neutralizing antibodies in the context of all epitopes on the HIV-1 spike identified to date. MDPI 2021-09-05 /pmc/articles/PMC8472920/ /pubmed/34578355 http://dx.doi.org/10.3390/v13091774 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
Parker Miller, Emma
Finkelstein, Maxwell T.
Erdman, Molly C.
Seth, Paul C.
Fera, Daniela
A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target
title A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target
title_full A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target
title_fullStr A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target
title_full_unstemmed A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target
title_short A Structural Update of Neutralizing Epitopes on the HIV Envelope, a Moving Target
title_sort structural update of neutralizing epitopes on the hiv envelope, a moving target
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472920/
https://www.ncbi.nlm.nih.gov/pubmed/34578355
http://dx.doi.org/10.3390/v13091774
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