The Transcription Factor T-Bet Is Required for Optimal Type I Follicular Helper T Cell Maintenance During Acute Viral Infection

Follicular helper T cells (TFH cells), known as the primary "helpers" of the germinal center (GC) reaction, promote the humoral immune response to defend against various pathogens. Under conditions of infection by different types of pathogens, many shared transcription factors (TFs), such...

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Published inFrontiers in immunology Vol. 10; p. 606
Main Authors Wang, Pengcheng, Wang, Youping, Xie, Luoyingzi, Xiao, Minglu, Wu, Jialin, Xu, Lifan, Bai, Qiang, Hao, Yaxing, Huang, Qizhao, Chen, Xiangyu, He, Ran, Li, Baohua, Yang, Sen, Chen, Yaokai, Wu, Yuzhang, Ye, Lilin
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 29.03.2019
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Summary:Follicular helper T cells (TFH cells), known as the primary "helpers" of the germinal center (GC) reaction, promote the humoral immune response to defend against various pathogens. Under conditions of infection by different types of pathogens, many shared transcription factors (TFs), such as Bcl-6, TCF-1, and Maf, are selectively enriched in pathogen-specific TFH cells, orchestrating TFH cell differentiation and function. In addition, TFH cells also coexpress environmentally associated TFs as their conventional T cell counterparts (such as T-bet, GATA-3, or ROR-γt, which are expressed in Th1, Th2, or Th17 cells, respectively). These features likely indicate both the lineage-specificity and environmental adaption of the TFH cell responses. However, the extent to which the TFH cell response relies on these environmentally specific TFs is not completely understood. Here, we found that T-bet was specifically expressed in Type I TFH cells but not Type II TFH cells. While dispensable for the early fate commitment of TFH cells, T-bet was essential for the maintenance of differentiated TFH cells, promoting their proliferation, and inhibiting their apoptosis during acute viral infection. Microarray analysis showed both similarities and differences in transcriptome dependency on T-bet in TFH and TH1 cells, suggesting the distinctive role of T-bet in TFH cells. Collectively, our findings reveal an important and specific supporting role for T-bet in type I TFH cell response, which can help us gain a deeper understanding of TFH cell subsets.
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Edited by: Georgia Fousteri, San Raffaele Hospital (IRCCS), Italy
These authors have contributed equally to this work
Reviewed by: Masato Kubo, Tokyo University of Science, Japan; Colleen Jean Winstead, Merck Sharp & Dohme Corp, United States
This article was submitted to T Cell Biology, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2019.00606