Key points are not available for this paper at this time.
A fundamental function of CD4+ helper T (T(H)) cells is the regulation of B cell-mediated humoral immunity. Development of T follicular helper (T(FH)) cells that provide help to B cells is mediated by the cytokines interleukin-6 and interleukin-21 but is independent of TH1, TH2, and TH17 effector cell lineages. Here, we characterize the function of Bcl6, a transcription factor selectively expressed in T(FH) cells. Bcl6 expression is regulated by interleukin-6 and interleukin-21. Bcl6 overexpression induced T(FH)-related gene expression and inhibited other T(H) lineage cell differentiation in a DNA binding-dependent manner. Moreover, Bcl6 deficiency in T cells resulted in impaired T(FH) cell development and germinal center reactions, and altered production of other effector T cell subsets. Our data thus illustrate that Bcl6 is required for programming of T(FH) cell generation.
Building similarity graph...
Analyzing shared references across papers
Loading...
Roza Nurieva
The University of Texas MD Anderson Cancer Center
Yeonseok Chung
Seoul National University
Gustavo Martínez
Q Therapeutics (United States)
Science
The University of Texas MD Anderson Cancer Center
Building similarity graph...
Analyzing shared references across papers
Loading...
Nurieva et al. (Fri,) studied this question.
synapsesocial.com/papers/68f8b01e24b0bc2d859006a9 — DOI: https://doi.org/10.1126/science.1176676
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: