Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection
T follicular helper CD4 cells (Tfh) are essential for the development and maintenance of germinal center (GC) reactions, a critical process that promotes the generation of long-lived high affinity humoral immunity. It is becoming increasingly evident that GC-Tfh cells are heterogeneous in nature wit...
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doaj-53457e95c1bd4e03a0690fa8108442c52020-11-24T23:34:29ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-06-01910.3389/fimmu.2018.01272363861Tfh1 Cells in Germinal Centers During Chronic HIV/SIV InfectionVijayakumar Velu0Vijayakumar Velu1Geetha Mylvaganam2Chris Ibegbu3Chris Ibegbu4Rama Rao Amara5Rama Rao Amara6Emory Vaccine Center, Emory University, Atlanta, GA, United StatesYerkes National Primate Research Center, Emory University, Atlanta, GA, United StatesRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, Harvard, Cambridge, MA, United StatesEmory Vaccine Center, Emory University, Atlanta, GA, United StatesYerkes National Primate Research Center, Emory University, Atlanta, GA, United StatesEmory Vaccine Center, Emory University, Atlanta, GA, United StatesYerkes National Primate Research Center, Emory University, Atlanta, GA, United StatesT follicular helper CD4 cells (Tfh) are essential for the development and maintenance of germinal center (GC) reactions, a critical process that promotes the generation of long-lived high affinity humoral immunity. It is becoming increasingly evident that GC-Tfh cells are heterogeneous in nature with some cellular characteristics associated with a Th1, Th2, and Th17 phenotype. Emerging studies suggest that GC-Tfh cells are directed to differentiate into distinct phenotypes during chronic HIV/SIV infection and these changes in GC-Tfh cells can greatly impact the B cell response and subclass of antibodies generated. Studies in HIV-infected humans have shown that certain Tfh phenotypes are associated with the generation of broadly neutralizing antibody responses. Moreover, the susceptibility of particular GC-Tfh subsets to HIV infection within the secondary lymphoid sites can also impact GC-Tfh/B cell interactions. In this review, we discuss the recent advances that show Tfh heterogeneity during chronic HIV/SIV infection. In particular, we will discuss the dynamics of GC-Tfh cells, their altered differentiation state and function, and their impact on B cell responses during HIV/SIV infection. In addition, we will also discuss the potential role of a recently described novel subset of follicular homing CXCR5+ CD8 T cells (Tfc) and their importance in contributing to control of chronic HIV/SIV infection. A better understanding of the mechanistic role of follicular homing CD4 and CD8 T cells during HIV/SIV infection will aid in the design of vaccines and therapeutic strategies to prevent and treat HIV/AIDS.https://www.frontiersin.org/article/10.3389/fimmu.2018.01272/fullTfh1 cellsgerminal centersHIV/SIV reservoirsfollicular CD8 T cellsTfh cellsHIV/SIV infection |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vijayakumar Velu Vijayakumar Velu Geetha Mylvaganam Chris Ibegbu Chris Ibegbu Rama Rao Amara Rama Rao Amara |
spellingShingle |
Vijayakumar Velu Vijayakumar Velu Geetha Mylvaganam Chris Ibegbu Chris Ibegbu Rama Rao Amara Rama Rao Amara Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection Frontiers in Immunology Tfh1 cells germinal centers HIV/SIV reservoirs follicular CD8 T cells Tfh cells HIV/SIV infection |
author_facet |
Vijayakumar Velu Vijayakumar Velu Geetha Mylvaganam Chris Ibegbu Chris Ibegbu Rama Rao Amara Rama Rao Amara |
author_sort |
Vijayakumar Velu |
title |
Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection |
title_short |
Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection |
title_full |
Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection |
title_fullStr |
Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection |
title_full_unstemmed |
Tfh1 Cells in Germinal Centers During Chronic HIV/SIV Infection |
title_sort |
tfh1 cells in germinal centers during chronic hiv/siv infection |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2018-06-01 |
description |
T follicular helper CD4 cells (Tfh) are essential for the development and maintenance of germinal center (GC) reactions, a critical process that promotes the generation of long-lived high affinity humoral immunity. It is becoming increasingly evident that GC-Tfh cells are heterogeneous in nature with some cellular characteristics associated with a Th1, Th2, and Th17 phenotype. Emerging studies suggest that GC-Tfh cells are directed to differentiate into distinct phenotypes during chronic HIV/SIV infection and these changes in GC-Tfh cells can greatly impact the B cell response and subclass of antibodies generated. Studies in HIV-infected humans have shown that certain Tfh phenotypes are associated with the generation of broadly neutralizing antibody responses. Moreover, the susceptibility of particular GC-Tfh subsets to HIV infection within the secondary lymphoid sites can also impact GC-Tfh/B cell interactions. In this review, we discuss the recent advances that show Tfh heterogeneity during chronic HIV/SIV infection. In particular, we will discuss the dynamics of GC-Tfh cells, their altered differentiation state and function, and their impact on B cell responses during HIV/SIV infection. In addition, we will also discuss the potential role of a recently described novel subset of follicular homing CXCR5+ CD8 T cells (Tfc) and their importance in contributing to control of chronic HIV/SIV infection. A better understanding of the mechanistic role of follicular homing CD4 and CD8 T cells during HIV/SIV infection will aid in the design of vaccines and therapeutic strategies to prevent and treat HIV/AIDS. |
topic |
Tfh1 cells germinal centers HIV/SIV reservoirs follicular CD8 T cells Tfh cells HIV/SIV infection |
url |
https://www.frontiersin.org/article/10.3389/fimmu.2018.01272/full |
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