γδ T‐cell responses during HIV infection and antiretroviral therapy

Abstract 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 advance...

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Main Authors: Jennifer A Juno, Emily M Eriksson
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Clinical & Translational Immunology
Subjects:
Online Access:https://doi.org/10.1002/cti2.1069
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author Jennifer A Juno
Emily M Eriksson
author_facet Jennifer A Juno
Emily M Eriksson
author_sort Jennifer A Juno
collection DOAJ
description Abstract 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 doaj.art-dc30bfd4ffc84f3eb56e4208265ca5ee2022-12-21T23:16:05ZengWileyClinical & Translational Immunology2050-00682019-01-0187n/an/a10.1002/cti2.1069γδ T‐cell responses during HIV infection and antiretroviral therapyJennifer A Juno0Emily M Eriksson1Department of Microbiology and Immunology The University of Melbourne at The Peter Doherty Institute for Infection and Immunity Melbourne VIC AustraliaDivision of Population Health and Immunity Walter and Eliza Hall Institute of Medical Science Melbourne VIC AustraliaAbstract 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.https://doi.org/10.1002/cti2.1069γδgutHIVSIVVδ1Vδ2
spellingShingle Jennifer A Juno
Emily M Eriksson
γδ T‐cell responses during HIV infection and antiretroviral therapy
Clinical & Translational Immunology
γδ
gut
HIV
SIV
Vδ1
Vδ2
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 γδ
gut
HIV
SIV
Vδ1
Vδ2
url https://doi.org/10.1002/cti2.1069
work_keys_str_mv AT jenniferajuno gdtcellresponsesduringhivinfectionandantiretroviraltherapy
AT emilymeriksson gdtcellresponsesduringhivinfectionandantiretroviraltherapy