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Subversion of the B-cell compartment during parasitic, bacterial, and viral infections

Recent studies on HIV infection have identified new human B-cell subsets with a potentially important impact on anti-viral immunity. Current work highlights the occurrence of similar B-cell alterations in other viral, bacterial, and parasitic infections, suggesting that common strategies have been d...

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Detalles Bibliográficos
Autores principales: Borhis, Gwenoline, Richard, Yolande
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374497/
https://www.ncbi.nlm.nih.gov/pubmed/25884828
http://dx.doi.org/10.1186/s12865-015-0079-y
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author Borhis, Gwenoline
Richard, Yolande
author_facet Borhis, Gwenoline
Richard, Yolande
author_sort Borhis, Gwenoline
collection PubMed
description Recent studies on HIV infection have identified new human B-cell subsets with a potentially important impact on anti-viral immunity. Current work highlights the occurrence of similar B-cell alterations in other viral, bacterial, and parasitic infections, suggesting that common strategies have been developed by pathogens to counteract protective immunity. For this review, we have selected key examples of human infections for which B-cell alterations have been described, to highlight the similarities and differences in the immune responses to a variety of pathogens. We believe that further comparisons between these models will lead to critical progress in the understanding of B-cell mechanisms and will open new target avenues for therapeutic interventions.
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spelling pubmed-43744972015-03-27 Subversion of the B-cell compartment during parasitic, bacterial, and viral infections Borhis, Gwenoline Richard, Yolande BMC Immunol Review Recent studies on HIV infection have identified new human B-cell subsets with a potentially important impact on anti-viral immunity. Current work highlights the occurrence of similar B-cell alterations in other viral, bacterial, and parasitic infections, suggesting that common strategies have been developed by pathogens to counteract protective immunity. For this review, we have selected key examples of human infections for which B-cell alterations have been described, to highlight the similarities and differences in the immune responses to a variety of pathogens. We believe that further comparisons between these models will lead to critical progress in the understanding of B-cell mechanisms and will open new target avenues for therapeutic interventions. BioMed Central 2015-03-26 /pmc/articles/PMC4374497/ /pubmed/25884828 http://dx.doi.org/10.1186/s12865-015-0079-y Text en © Borhis and Richard; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Borhis, Gwenoline
Richard, Yolande
Subversion of the B-cell compartment during parasitic, bacterial, and viral infections
title Subversion of the B-cell compartment during parasitic, bacterial, and viral infections
title_full Subversion of the B-cell compartment during parasitic, bacterial, and viral infections
title_fullStr Subversion of the B-cell compartment during parasitic, bacterial, and viral infections
title_full_unstemmed Subversion of the B-cell compartment during parasitic, bacterial, and viral infections
title_short Subversion of the B-cell compartment during parasitic, bacterial, and viral infections
title_sort subversion of the b-cell compartment during parasitic, bacterial, and viral infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374497/
https://www.ncbi.nlm.nih.gov/pubmed/25884828
http://dx.doi.org/10.1186/s12865-015-0079-y
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