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The impact of HLA polymorphism on herpesvirus infection and disease
Human Leukocyte Antigens (HLA) are cell surface molecules, central in coordinating innate and adaptive immune responses, that are targets of strong diversifying natural selection by pathogens. Of these pathogens, human herpesviruses have a uniquely ancient relationship with our species, where coevol...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205880/ https://www.ncbi.nlm.nih.gov/pubmed/36595060 http://dx.doi.org/10.1007/s00251-022-01288-z |
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author | Palmer, William H. Norman, Paul J. |
author_facet | Palmer, William H. Norman, Paul J. |
author_sort | Palmer, William H. |
collection | PubMed |
description | Human Leukocyte Antigens (HLA) are cell surface molecules, central in coordinating innate and adaptive immune responses, that are targets of strong diversifying natural selection by pathogens. Of these pathogens, human herpesviruses have a uniquely ancient relationship with our species, where coevolution likely has reciprocating impact on HLA and viral genomic diversity. Consistent with this notion, genetic variation at multiple HLA loci is strongly associated with modulating immunity to herpesvirus infection. Here, we synthesize published genetic associations of HLA with herpesvirus infection and disease, both from case/control and genome-wide association studies. We analyze genetic associations across the eight human herpesviruses and identify HLA alleles that are associated with diverse herpesvirus-related phenotypes. We find that whereas most HLA genetic associations are virus- or disease-specific, HLA-A*01 and HLA-A*02 allotypes may be more generally associated with immune susceptibility and control, respectively, across multiple herpesviruses. Connecting genetic association data with functional corroboration, we discuss mechanisms by which diverse HLA and cognate receptor allotypes direct variable immune responses during herpesvirus infection and pathogenesis. Together, this review examines the complexity of HLA-herpesvirus interactions driven by differential T cell and Natural Killer cell immune responses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00251-022-01288-z. |
format | Online Article Text |
id | pubmed-10205880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-102058802023-05-25 The impact of HLA polymorphism on herpesvirus infection and disease Palmer, William H. Norman, Paul J. Immunogenetics Review Human Leukocyte Antigens (HLA) are cell surface molecules, central in coordinating innate and adaptive immune responses, that are targets of strong diversifying natural selection by pathogens. Of these pathogens, human herpesviruses have a uniquely ancient relationship with our species, where coevolution likely has reciprocating impact on HLA and viral genomic diversity. Consistent with this notion, genetic variation at multiple HLA loci is strongly associated with modulating immunity to herpesvirus infection. Here, we synthesize published genetic associations of HLA with herpesvirus infection and disease, both from case/control and genome-wide association studies. We analyze genetic associations across the eight human herpesviruses and identify HLA alleles that are associated with diverse herpesvirus-related phenotypes. We find that whereas most HLA genetic associations are virus- or disease-specific, HLA-A*01 and HLA-A*02 allotypes may be more generally associated with immune susceptibility and control, respectively, across multiple herpesviruses. Connecting genetic association data with functional corroboration, we discuss mechanisms by which diverse HLA and cognate receptor allotypes direct variable immune responses during herpesvirus infection and pathogenesis. Together, this review examines the complexity of HLA-herpesvirus interactions driven by differential T cell and Natural Killer cell immune responses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00251-022-01288-z. Springer Berlin Heidelberg 2023-01-03 2023 /pmc/articles/PMC10205880/ /pubmed/36595060 http://dx.doi.org/10.1007/s00251-022-01288-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Palmer, William H. Norman, Paul J. The impact of HLA polymorphism on herpesvirus infection and disease |
title | The impact of HLA polymorphism on herpesvirus infection and disease |
title_full | The impact of HLA polymorphism on herpesvirus infection and disease |
title_fullStr | The impact of HLA polymorphism on herpesvirus infection and disease |
title_full_unstemmed | The impact of HLA polymorphism on herpesvirus infection and disease |
title_short | The impact of HLA polymorphism on herpesvirus infection and disease |
title_sort | impact of hla polymorphism on herpesvirus infection and disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205880/ https://www.ncbi.nlm.nih.gov/pubmed/36595060 http://dx.doi.org/10.1007/s00251-022-01288-z |
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