Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection

The combination antiretroviral therapeutic (cART) regime effectively suppresses human immunodeficiency virus (HIV) replication and prevents progression to acquired immunodeficiency diseases. However, cART is not a cure, and viral rebound will occur immediately after treatment is interrupted largely...

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Main Authors: Minglu Xiao, Xiangyu Chen, Ran He, Lilin Ye
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-05-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.01095/full
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spelling doaj-5397ff50200e4fe9b5832ad0f204cee82020-11-24T20:41:21ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-05-01910.3389/fimmu.2018.01095362052Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus InfectionMinglu Xiao0Xiangyu Chen1Ran He2Lilin Ye3Institute of Immunology, Third Military Medical University, Chongqing, ChinaInstitute of Immunology, Third Military Medical University, Chongqing, ChinaDepartment of Immunology, School of Basic Medicine, Huazhong University of Science and Technology, Wuhan, ChinaInstitute of Immunology, Third Military Medical University, Chongqing, ChinaThe combination antiretroviral therapeutic (cART) regime effectively suppresses human immunodeficiency virus (HIV) replication and prevents progression to acquired immunodeficiency diseases. However, cART is not a cure, and viral rebound will occur immediately after treatment is interrupted largely due to the long-term presence of an HIV reservoir that is composed of latently infected target cells that maintain a quiescent state or persistently produce infectious viruses. CD4 T cells that reside in B-cell follicles within lymphoid tissues, called follicular helper T cells (TFH), have been identified as a major HIV reservoir. Due to their specialized anatomical structure, HIV-specific CD8 T cells are largely insulated from this TFH reservoir. It is increasingly clear that the elimination of TFH reservoirs is a key step toward a functional cure for HIV infection. Recently, several studies have suggested that a fraction of HIV-specific CD8 T cells can differentiate into a CXCR5-expressing subset, which are able to migrate into B-cell follicles and inhibit viral replication. In this review, we discuss the differentiation and functions of this newly identified CD8 T-cell subset and propose potential strategies for purging TFH HIV reservoirs by utilizing this unique population.https://www.frontiersin.org/article/10.3389/fimmu.2018.01095/fullfollicular CD8 T cellsB-cell follicleshuman immunodeficiency virus infectionshuman immunodeficiency virus reservoirCXCR5+CD8 T cells
collection DOAJ
language English
format Article
sources DOAJ
author Minglu Xiao
Xiangyu Chen
Ran He
Lilin Ye
spellingShingle Minglu Xiao
Xiangyu Chen
Ran He
Lilin Ye
Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection
Frontiers in Immunology
follicular CD8 T cells
B-cell follicles
human immunodeficiency virus infections
human immunodeficiency virus reservoir
CXCR5+CD8 T cells
author_facet Minglu Xiao
Xiangyu Chen
Ran He
Lilin Ye
author_sort Minglu Xiao
title Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection
title_short Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection
title_full Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection
title_fullStr Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection
title_full_unstemmed Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection
title_sort differentiation and function of follicular cd8 t cells during human immunodeficiency virus infection
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2018-05-01
description The combination antiretroviral therapeutic (cART) regime effectively suppresses human immunodeficiency virus (HIV) replication and prevents progression to acquired immunodeficiency diseases. However, cART is not a cure, and viral rebound will occur immediately after treatment is interrupted largely due to the long-term presence of an HIV reservoir that is composed of latently infected target cells that maintain a quiescent state or persistently produce infectious viruses. CD4 T cells that reside in B-cell follicles within lymphoid tissues, called follicular helper T cells (TFH), have been identified as a major HIV reservoir. Due to their specialized anatomical structure, HIV-specific CD8 T cells are largely insulated from this TFH reservoir. It is increasingly clear that the elimination of TFH reservoirs is a key step toward a functional cure for HIV infection. Recently, several studies have suggested that a fraction of HIV-specific CD8 T cells can differentiate into a CXCR5-expressing subset, which are able to migrate into B-cell follicles and inhibit viral replication. In this review, we discuss the differentiation and functions of this newly identified CD8 T-cell subset and propose potential strategies for purging TFH HIV reservoirs by utilizing this unique population.
topic follicular CD8 T cells
B-cell follicles
human immunodeficiency virus infections
human immunodeficiency virus reservoir
CXCR5+CD8 T cells
url https://www.frontiersin.org/article/10.3389/fimmu.2018.01095/full
work_keys_str_mv AT mingluxiao differentiationandfunctionoffollicularcd8tcellsduringhumanimmunodeficiencyvirusinfection
AT xiangyuchen differentiationandfunctionoffollicularcd8tcellsduringhumanimmunodeficiencyvirusinfection
AT ranhe differentiationandfunctionoffollicularcd8tcellsduringhumanimmunodeficiencyvirusinfection
AT lilinye differentiationandfunctionoffollicularcd8tcellsduringhumanimmunodeficiencyvirusinfection
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