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HLA-G Molecules in Autoimmune Diseases and Infections
Human leukocyte antigen (HLA)-G molecule, a non-classical HLA-Ib molecule, is less polymorphic when compared to classical HLA class I molecules. Human leukocyte antigen-G (HLA-G) was first detected on cytotrophoblast cells at the feto-maternal interface but its expression is prevalent during viral i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235267/ https://www.ncbi.nlm.nih.gov/pubmed/25477881 http://dx.doi.org/10.3389/fimmu.2014.00592 |
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author | Rizzo, Roberta Bortolotti, Daria Bolzani, Silvia Fainardi, Enrico |
author_facet | Rizzo, Roberta Bortolotti, Daria Bolzani, Silvia Fainardi, Enrico |
author_sort | Rizzo, Roberta |
collection | PubMed |
description | Human leukocyte antigen (HLA)-G molecule, a non-classical HLA-Ib molecule, is less polymorphic when compared to classical HLA class I molecules. Human leukocyte antigen-G (HLA-G) was first detected on cytotrophoblast cells at the feto-maternal interface but its expression is prevalent during viral infections and several autoimmune diseases. HLA-G gene is characterized by polymorphisms at the 3′ un-translated region and 5′ upstream regulatory region that regulate its expression and are associated with autoimmune diseases and viral infection susceptibility, creating an unbalanced and pathologic environment. This review focuses on the role of HLA-G genetic polymorphisms, mRNA, and protein expression in autoimmune conditions and viral infections. |
format | Online Article Text |
id | pubmed-4235267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42352672014-12-04 HLA-G Molecules in Autoimmune Diseases and Infections Rizzo, Roberta Bortolotti, Daria Bolzani, Silvia Fainardi, Enrico Front Immunol Immunology Human leukocyte antigen (HLA)-G molecule, a non-classical HLA-Ib molecule, is less polymorphic when compared to classical HLA class I molecules. Human leukocyte antigen-G (HLA-G) was first detected on cytotrophoblast cells at the feto-maternal interface but its expression is prevalent during viral infections and several autoimmune diseases. HLA-G gene is characterized by polymorphisms at the 3′ un-translated region and 5′ upstream regulatory region that regulate its expression and are associated with autoimmune diseases and viral infection susceptibility, creating an unbalanced and pathologic environment. This review focuses on the role of HLA-G genetic polymorphisms, mRNA, and protein expression in autoimmune conditions and viral infections. Frontiers Media S.A. 2014-11-18 /pmc/articles/PMC4235267/ /pubmed/25477881 http://dx.doi.org/10.3389/fimmu.2014.00592 Text en Copyright © 2014 Rizzo, Bortolotti, Bolzani and Fainardi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Rizzo, Roberta Bortolotti, Daria Bolzani, Silvia Fainardi, Enrico HLA-G Molecules in Autoimmune Diseases and Infections |
title | HLA-G Molecules in Autoimmune Diseases and Infections |
title_full | HLA-G Molecules in Autoimmune Diseases and Infections |
title_fullStr | HLA-G Molecules in Autoimmune Diseases and Infections |
title_full_unstemmed | HLA-G Molecules in Autoimmune Diseases and Infections |
title_short | HLA-G Molecules in Autoimmune Diseases and Infections |
title_sort | hla-g molecules in autoimmune diseases and infections |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235267/ https://www.ncbi.nlm.nih.gov/pubmed/25477881 http://dx.doi.org/10.3389/fimmu.2014.00592 |
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