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STAT4 and T-bet control follicular helper T cell development in viral infections.

Jason S WeinsteinBrian J LaidlawYisi LuJessica K WangVincent P SchulzNingcheng LiEdward I HermanSusan M KaechPatrick G GallagherJoseph E Craft
Published in: The Journal of experimental medicine (2017)
Follicular helper T (Tfh) cells promote germinal center (GC) B cell survival and proliferation and guide their differentiation and immunoglobulin isotype switching by delivering contact-dependent and soluble factors, including IL-21, IL-4, IL-9, and IFN-γ. IL-21 and IFN-γ are coexpressed by Tfh cells during viral infections, but transcriptional regulation of these cytokines is not completely understood. In this study, we show that the T helper type 1 cell (Th1 cell) transcriptional regulators T-bet and STAT4 are coexpressed with Bcl6 in Tfh cells after acute viral infection, with a temporal decline in T-bet in the waning response. T-bet is important for Tfh cell production of IFN-γ, but not IL-21, and for a robust GC reaction. STAT4, phosphorylated in Tfh cells upon infection, is required for expression of T-bet and Bcl6 and for IFN-γ and IL-21. These data indicate that T-bet is expressed with Bcl6 in Tfh cells and is required alongside STAT4 to coordinate Tfh cell IL-21 and IFN-γ production and for promotion of the GC response after acute viral challenge.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • dendritic cells
  • immune response
  • single cell
  • cell therapy
  • cell proliferation
  • sars cov
  • signaling pathway
  • cell death
  • gene expression
  • bone marrow
  • gas chromatography
  • heat shock