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Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design

The degradation of HIV-derived proteins into epitopes displayed by MHC-I or MHC-II are the first events leading to the priming of HIV-specific immune responses and to the recognition of infected cells. Despite a wealth of information about peptidases involved in protein degradation, our knowledge of...

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Autores principales: Rucevic, Marijana, Boucau, Julie, Dinter, Jens, Kourjian, Georgio, Le Gall, Sylvie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147695/
https://www.ncbi.nlm.nih.gov/pubmed/25196483
http://dx.doi.org/10.3390/v6083271
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author Rucevic, Marijana
Boucau, Julie
Dinter, Jens
Kourjian, Georgio
Le Gall, Sylvie
author_facet Rucevic, Marijana
Boucau, Julie
Dinter, Jens
Kourjian, Georgio
Le Gall, Sylvie
author_sort Rucevic, Marijana
collection PubMed
description The degradation of HIV-derived proteins into epitopes displayed by MHC-I or MHC-II are the first events leading to the priming of HIV-specific immune responses and to the recognition of infected cells. Despite a wealth of information about peptidases involved in protein degradation, our knowledge of epitope presentation during HIV infection remains limited. Here we review current data on HIV protein degradation linking epitope production and immunodominance, viral evolution and impaired epitope presentation. We propose that an in-depth understanding of HIV antigen processing and presentation in relevant primary cells could be exploited to identify signatures leading to efficient or inefficient epitope presentation in HIV proteomes, and to improve the design of immunogens eliciting immune responses efficiently recognizing all infected cells.
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spelling pubmed-41476952014-08-28 Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design Rucevic, Marijana Boucau, Julie Dinter, Jens Kourjian, Georgio Le Gall, Sylvie Viruses Review The degradation of HIV-derived proteins into epitopes displayed by MHC-I or MHC-II are the first events leading to the priming of HIV-specific immune responses and to the recognition of infected cells. Despite a wealth of information about peptidases involved in protein degradation, our knowledge of epitope presentation during HIV infection remains limited. Here we review current data on HIV protein degradation linking epitope production and immunodominance, viral evolution and impaired epitope presentation. We propose that an in-depth understanding of HIV antigen processing and presentation in relevant primary cells could be exploited to identify signatures leading to efficient or inefficient epitope presentation in HIV proteomes, and to improve the design of immunogens eliciting immune responses efficiently recognizing all infected cells. MDPI 2014-08-21 /pmc/articles/PMC4147695/ /pubmed/25196483 http://dx.doi.org/10.3390/v6083271 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Rucevic, Marijana
Boucau, Julie
Dinter, Jens
Kourjian, Georgio
Le Gall, Sylvie
Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design
title Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design
title_full Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design
title_fullStr Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design
title_full_unstemmed Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design
title_short Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design
title_sort mechanisms of hiv protein degradation into epitopes: implications for vaccine design
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147695/
https://www.ncbi.nlm.nih.gov/pubmed/25196483
http://dx.doi.org/10.3390/v6083271
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