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Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway
Lifelong persistent infection by herpesviruses depends on the balance between host immune responses and viral immune evasion. CD4 T cells responding to antigens presented on major histocompatibility complex class II (MHC-II) molecules are known to play an important role in controlling herpesvirus in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446767/ https://www.ncbi.nlm.nih.gov/pubmed/23012630 http://dx.doi.org/10.3390/v4081335 |
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author | Zuo, Jianmin Rowe, Martin |
author_facet | Zuo, Jianmin Rowe, Martin |
author_sort | Zuo, Jianmin |
collection | PubMed |
description | Lifelong persistent infection by herpesviruses depends on the balance between host immune responses and viral immune evasion. CD4 T cells responding to antigens presented on major histocompatibility complex class II (MHC-II) molecules are known to play an important role in controlling herpesvirus infections. Here we review, with emphasis on human herpesvirus infections, the strategies evolved to evade CD4 T cell immunity. These viruses target multiple points on the MHC class II antigen presentation pathway. The mechanisms include: suppression of CIITA to inhibit the synthesis of MHC class II molecules, diversion or degradation of HLA-DR molecules during membrane transport, and direct targeting of the invariant chain chaperone of HLA-DR. |
format | Online Article Text |
id | pubmed-3446767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-34467672012-09-25 Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway Zuo, Jianmin Rowe, Martin Viruses Review Lifelong persistent infection by herpesviruses depends on the balance between host immune responses and viral immune evasion. CD4 T cells responding to antigens presented on major histocompatibility complex class II (MHC-II) molecules are known to play an important role in controlling herpesvirus infections. Here we review, with emphasis on human herpesvirus infections, the strategies evolved to evade CD4 T cell immunity. These viruses target multiple points on the MHC class II antigen presentation pathway. The mechanisms include: suppression of CIITA to inhibit the synthesis of MHC class II molecules, diversion or degradation of HLA-DR molecules during membrane transport, and direct targeting of the invariant chain chaperone of HLA-DR. MDPI 2012-08-22 /pmc/articles/PMC3446767/ /pubmed/23012630 http://dx.doi.org/10.3390/v4081335 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (Lhttp://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Zuo, Jianmin Rowe, Martin Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway |
title | Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway |
title_full | Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway |
title_fullStr | Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway |
title_full_unstemmed | Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway |
title_short | Herpesviruses Placating the Unwilling Host: Manipulation of the MHC Class II Antigen Presentation Pathway |
title_sort | herpesviruses placating the unwilling host: manipulation of the mhc class ii antigen presentation pathway |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446767/ https://www.ncbi.nlm.nih.gov/pubmed/23012630 http://dx.doi.org/10.3390/v4081335 |
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