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The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog

Epstein-Barr virus (EBV) infects most people and establishes life-long infection controlled by the host's immune system. The genetic stability of the virus, deep understanding of the viral antigens and immune epitopes recognized by the host's T-cell system and the fact that recent infectio...

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Autores principales: Long, Heather M., Meckiff, Benjamin J., Taylor, Graham S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759930/
https://www.ncbi.nlm.nih.gov/pubmed/31620125
http://dx.doi.org/10.3389/fimmu.2019.02193
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author Long, Heather M.
Meckiff, Benjamin J.
Taylor, Graham S.
author_facet Long, Heather M.
Meckiff, Benjamin J.
Taylor, Graham S.
author_sort Long, Heather M.
collection PubMed
description Epstein-Barr virus (EBV) infects most people and establishes life-long infection controlled by the host's immune system. The genetic stability of the virus, deep understanding of the viral antigens and immune epitopes recognized by the host's T-cell system and the fact that recent infection can be identified by the development of symptomatic infectious mononucleosis makes EBV a powerful system in which to study human immunology. The association between EBV and multiple cancers also means that the lessons learned have strong translational potential. Increasing evidence of a role for resident memory T-cells and non-conventional γδ T-cells in controlling EBV infection suggests new opportunities for research and means the virus will continue to provide exciting new insights into human biology and immunology into the future.
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spelling pubmed-67599302019-10-16 The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog Long, Heather M. Meckiff, Benjamin J. Taylor, Graham S. Front Immunol Immunology Epstein-Barr virus (EBV) infects most people and establishes life-long infection controlled by the host's immune system. The genetic stability of the virus, deep understanding of the viral antigens and immune epitopes recognized by the host's T-cell system and the fact that recent infection can be identified by the development of symptomatic infectious mononucleosis makes EBV a powerful system in which to study human immunology. The association between EBV and multiple cancers also means that the lessons learned have strong translational potential. Increasing evidence of a role for resident memory T-cells and non-conventional γδ T-cells in controlling EBV infection suggests new opportunities for research and means the virus will continue to provide exciting new insights into human biology and immunology into the future. Frontiers Media S.A. 2019-09-18 /pmc/articles/PMC6759930/ /pubmed/31620125 http://dx.doi.org/10.3389/fimmu.2019.02193 Text en Copyright © 2019 Long, Meckiff and Taylor. 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) and the copyright owner(s) 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
Long, Heather M.
Meckiff, Benjamin J.
Taylor, Graham S.
The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog
title The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog
title_full The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog
title_fullStr The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog
title_full_unstemmed The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog
title_short The T-cell Response to Epstein-Barr Virus–New Tricks From an Old Dog
title_sort t-cell response to epstein-barr virus–new tricks from an old dog
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759930/
https://www.ncbi.nlm.nih.gov/pubmed/31620125
http://dx.doi.org/10.3389/fimmu.2019.02193
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