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γδ T‐cell responses during HIV infection and antiretroviral therapy

HIV infection is associated with a rapid and sustained inversion of the Vδ1:Vδ2 T‐cell ratio in peripheral blood. Studies of antiretroviral therapy (ART)‐treated cohorts suggest that ART is insufficient to reconstitute either the frequency or function of the γδ T‐cell subset. Recent advances are now...

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Detalles Bibliográficos
Autores principales: Juno, Jennifer A, Eriksson, Emily M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636517/
https://www.ncbi.nlm.nih.gov/pubmed/31321033
http://dx.doi.org/10.1002/cti2.1069
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author Juno, Jennifer A
Eriksson, Emily M
author_facet Juno, Jennifer A
Eriksson, Emily M
author_sort Juno, Jennifer A
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description HIV infection is associated with a rapid and sustained inversion of the Vδ1:Vδ2 T‐cell ratio in peripheral blood. Studies of antiretroviral therapy (ART)‐treated cohorts suggest that ART is insufficient to reconstitute either the frequency or function of the γδ T‐cell subset. Recent advances are now beginning to shed light on the relationship between microbial translocation, chronic inflammation, immune ageing and γδ T‐cell immunology. Here, we review the impact of acute, chronic untreated and treated HIV infection on circulating and mucosal γδ T‐cell subsets and highlight novel approaches to harness γδ T cells as components of anti‐HIV immunotherapy.
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spelling pubmed-66365172019-07-18 γδ T‐cell responses during HIV infection and antiretroviral therapy Juno, Jennifer A Eriksson, Emily M Clin Transl Immunology Special Feature Reviews HIV infection is associated with a rapid and sustained inversion of the Vδ1:Vδ2 T‐cell ratio in peripheral blood. Studies of antiretroviral therapy (ART)‐treated cohorts suggest that ART is insufficient to reconstitute either the frequency or function of the γδ T‐cell subset. Recent advances are now beginning to shed light on the relationship between microbial translocation, chronic inflammation, immune ageing and γδ T‐cell immunology. Here, we review the impact of acute, chronic untreated and treated HIV infection on circulating and mucosal γδ T‐cell subsets and highlight novel approaches to harness γδ T cells as components of anti‐HIV immunotherapy. John Wiley and Sons Inc. 2019-07-17 /pmc/articles/PMC6636517/ /pubmed/31321033 http://dx.doi.org/10.1002/cti2.1069 Text en © 2019 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/3.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Feature Reviews
Juno, Jennifer A
Eriksson, Emily M
γδ T‐cell responses during HIV infection and antiretroviral therapy
title γδ T‐cell responses during HIV infection and antiretroviral therapy
title_full γδ T‐cell responses during HIV infection and antiretroviral therapy
title_fullStr γδ T‐cell responses during HIV infection and antiretroviral therapy
title_full_unstemmed γδ T‐cell responses during HIV infection and antiretroviral therapy
title_short γδ T‐cell responses during HIV infection and antiretroviral therapy
title_sort γδ t‐cell responses during hiv infection and antiretroviral therapy
topic Special Feature Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636517/
https://www.ncbi.nlm.nih.gov/pubmed/31321033
http://dx.doi.org/10.1002/cti2.1069
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