The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection

Tissue-resident memory T cells (TRM) were first described in 2009. While initially the major focus was on CD8<sup>+</sup> TRM, there has recently been increased interest in defining the phenotype and the role of CD4<sup>+</sup> TRM in diseases. Circulating CD4<sup>+<...

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Main Authors: Thomas R. O’Neil, Kevin Hu, Naomi R. Truong, Sana Arshad, Barbara L. Shacklett, Anthony L. Cunningham, Najla Nasr
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/3/359
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author Thomas R. O’Neil
Kevin Hu
Naomi R. Truong
Sana Arshad
Barbara L. Shacklett
Anthony L. Cunningham
Najla Nasr
author_facet Thomas R. O’Neil
Kevin Hu
Naomi R. Truong
Sana Arshad
Barbara L. Shacklett
Anthony L. Cunningham
Najla Nasr
author_sort Thomas R. O’Neil
collection DOAJ
description Tissue-resident memory T cells (TRM) were first described in 2009. While initially the major focus was on CD8<sup>+</sup> TRM, there has recently been increased interest in defining the phenotype and the role of CD4<sup>+</sup> TRM in diseases. Circulating CD4<sup>+</sup> T cells seed CD4<sup>+</sup> TRM, but there also appears to be an equilibrium between CD4<sup>+</sup> TRM and blood CD4<sup>+</sup> T cells. CD4<sup>+</sup> TRM are more mobile than CD8<sup>+</sup> TRM, usually localized deeper within the dermis/lamina propria and yet may exhibit synergy with CD8<sup>+</sup> TRM in disease control. This has been demonstrated in herpes simplex infections in mice. In human recurrent herpes infections, both CD4<sup>+</sup> and CD8<sup>+</sup> TRM persisting between lesions may control asymptomatic shedding through interferon-gamma secretion, although this has been more clearly shown for CD8<sup>+</sup> T cells. The exact role of the CD4<sup>+</sup>/CD8<sup>+</sup> TRM axis in the trigeminal ganglia and/or cornea in controlling recurrent herpetic keratitis is unknown. In HIV, CD4<sup>+</sup> TRM have now been shown to be a major target for productive and latent infection in the cervix. In HSV and HIV co-infections, CD4<sup>+</sup> TRM persisting in the dermis support HIV replication. Further understanding of the role of CD4<sup>+</sup> TRM and their induction by vaccines may help control sexual transmission by both viruses.
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spelling doaj.art-0df9304bb510409fb5bbd48137c6f05a2023-12-11T18:21:29ZengMDPI AGViruses1999-49152021-02-0113335910.3390/v13030359The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV InfectionThomas R. O’Neil0Kevin Hu1Naomi R. Truong2Sana Arshad3Barbara L. Shacklett4Anthony L. Cunningham5Najla Nasr6Centre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW 2145, AustraliaCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW 2145, AustraliaCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW 2145, AustraliaCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW 2145, AustraliaDepartment of Medical Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USACentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW 2145, AustraliaCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW 2145, AustraliaTissue-resident memory T cells (TRM) were first described in 2009. While initially the major focus was on CD8<sup>+</sup> TRM, there has recently been increased interest in defining the phenotype and the role of CD4<sup>+</sup> TRM in diseases. Circulating CD4<sup>+</sup> T cells seed CD4<sup>+</sup> TRM, but there also appears to be an equilibrium between CD4<sup>+</sup> TRM and blood CD4<sup>+</sup> T cells. CD4<sup>+</sup> TRM are more mobile than CD8<sup>+</sup> TRM, usually localized deeper within the dermis/lamina propria and yet may exhibit synergy with CD8<sup>+</sup> TRM in disease control. This has been demonstrated in herpes simplex infections in mice. In human recurrent herpes infections, both CD4<sup>+</sup> and CD8<sup>+</sup> TRM persisting between lesions may control asymptomatic shedding through interferon-gamma secretion, although this has been more clearly shown for CD8<sup>+</sup> T cells. The exact role of the CD4<sup>+</sup>/CD8<sup>+</sup> TRM axis in the trigeminal ganglia and/or cornea in controlling recurrent herpetic keratitis is unknown. In HIV, CD4<sup>+</sup> TRM have now been shown to be a major target for productive and latent infection in the cervix. In HSV and HIV co-infections, CD4<sup>+</sup> TRM persisting in the dermis support HIV replication. Further understanding of the role of CD4<sup>+</sup> TRM and their induction by vaccines may help control sexual transmission by both viruses.https://www.mdpi.com/1999-4915/13/3/359HIV-1HSV-1/2tissue resident CD4<sup>+</sup>CD8<sup>+</sup>vaccinesinfection
spellingShingle Thomas R. O’Neil
Kevin Hu
Naomi R. Truong
Sana Arshad
Barbara L. Shacklett
Anthony L. Cunningham
Najla Nasr
The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection
Viruses
HIV-1
HSV-1/2
tissue resident CD4<sup>+</sup>
CD8<sup>+</sup>
vaccines
infection
title The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection
title_full The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection
title_fullStr The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection
title_full_unstemmed The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection
title_short The Role of Tissue Resident Memory CD4 T Cells in Herpes Simplex Viral and HIV Infection
title_sort role of tissue resident memory cd4 t cells in herpes simplex viral and hiv infection
topic HIV-1
HSV-1/2
tissue resident CD4<sup>+</sup>
CD8<sup>+</sup>
vaccines
infection
url https://www.mdpi.com/1999-4915/13/3/359
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