The Transcription Factor KLF2 Restrains CD4+ T Follicular Helper Cell Differentiation

June Yong Lee, Cara N. Skon, You Jeong Lee, Soohwan Oh, Justin J. Taylor, Deepali Malhotra, Marc K. Jenkins, M. Geoffrey Rosenfeld, Kristin A. Hogquist, Stephen C. Jameson

Research output: Contribution to journalArticlepeer-review

126 Scopus citations


T follicular helper (Tfh) cells are essential for efficient B cell responses, yet the factors that regulate differentiation of this CD4+ Tcell subset are incompletely understood. Here we found that the KLF2 transcription factor serves to restrain Tfh cell generation. Induced KLF2 deficiency in activated CD4+ Tcells led to increased Tfh cell generation and B cell priming, whereas KLF2 overexpression prevented Tfh cell production. KLF2 promotes expression of the trafficking receptor S1PR1, and S1PR1 downregulation is essential for efficient Tfh cell production. However, KLF2 also induced expression of the transcription factor Blimp-1, which repressed transcription factor Bcl-6 and thereby impaired Tfh cell differentiation. Furthermore, KLF2 induced expression of the transcription factors T-bet and GATA3 and enhanced Th1 differentiation. Hence, our data indicate KLF2 ispivotal for coordinating CD4+ Tcell differentiation through two distinct and complementary mechanisms: via control of Tcell localization and by regulation of lineage-defining transcription factors.

Original languageEnglish (US)
Pages (from-to)252-264
Number of pages13
Issue number2
StatePublished - Feb 17 2015

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© 2015 Elsevier Inc.


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