4.6 Article

Bach2 Negatively Regulates T Follicular Helper Cell Differentiation and Is Critical for CD4+ T Cell Memory

期刊

JOURNAL OF IMMUNOLOGY
卷 202, 期 10, 页码 2991-2998

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1801626

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资金

  1. National Institutes of Health [AI095439, AI103162, AI130232, AI116188, AI122842, AI133679]
  2. University of Alabama at Birmingham Center for AIDS Research Grant [P30AI027767-26]

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T follicular helper (Tfh) cells are essential for germinal center B cell responses. The molecular mechanism underlying the initial Tfh cell differentiation, however, is still incompletely understood. In this study, we show that in vivo, despite enhanced non-Tfh cell effector functions, the deletion of transcription factor Bach2 results in preferential Tfh cell differentiation. Mechanistically, the deletion of Bach2 leads to the induction of CXCR5 expression even before the upregulation of Asc12. Subsequently, we have identified a novel regulatory element in the murine CXCR5 locus that negatively regulates CXCR5 promoter activities in a Bach2-dependent manner. Bach2 deficiency eventually results in a collapsed CD4(+)T cell response with severely impaired CD4(+)T cell memory, including Tfh cell memory. Our results demonstrate that Bach2 critically regulates Tfh cell differentiation and CD4(+)T cell memory.

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