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Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation

HIV-1 is known to show a high degree of genetic diversity, which may have major implications for disease pathogenesis and prevention. If every divergent isolate represented a distinct serotype, then effective vaccination might be impossible. However, using a sensitive new plaque- forming assay for H...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189498/
https://www.ncbi.nlm.nih.gov/pubmed/2478654
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collection PubMed
description HIV-1 is known to show a high degree of genetic diversity, which may have major implications for disease pathogenesis and prevention. If every divergent isolate represented a distinct serotype, then effective vaccination might be impossible. However, using a sensitive new plaque- forming assay for HIV-1, we have found that most infected patients make neutralizing antibodies, predominantly to a group-specific epitope shared among three highly divergent isolates. This epitope persists among divergent isolates and rarely mutates, despite the rapid overall mutation rate of HIV-1, suggesting that it may participate in an essential viral function. These findings, plus the rarity of reinfections among these patients, suggest that HIV-1 may be more susceptible to a vaccine strategy based on a group-specific neutralizing epitope than was previously suspected.
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spelling pubmed-21894982008-04-17 Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation J Exp Med Articles HIV-1 is known to show a high degree of genetic diversity, which may have major implications for disease pathogenesis and prevention. If every divergent isolate represented a distinct serotype, then effective vaccination might be impossible. However, using a sensitive new plaque- forming assay for HIV-1, we have found that most infected patients make neutralizing antibodies, predominantly to a group-specific epitope shared among three highly divergent isolates. This epitope persists among divergent isolates and rarely mutates, despite the rapid overall mutation rate of HIV-1, suggesting that it may participate in an essential viral function. These findings, plus the rarity of reinfections among these patients, suggest that HIV-1 may be more susceptible to a vaccine strategy based on a group-specific neutralizing epitope than was previously suspected. The Rockefeller University Press 1989-11-01 /pmc/articles/PMC2189498/ /pubmed/2478654 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation
title Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation
title_full Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation
title_fullStr Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation
title_full_unstemmed Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation
title_short Human immunodeficiency virus 1. Predominance of a group-specific neutralizing epitope that persists despite genetic variation
title_sort human immunodeficiency virus 1. predominance of a group-specific neutralizing epitope that persists despite genetic variation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189498/
https://www.ncbi.nlm.nih.gov/pubmed/2478654