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Defective T cell activation and autoimmune disorder in Stra13-deficient mice

  • Hong Sun
  • , Binfeng Lu
  • , Rong Qin Li
  • , Richard A. Flavell
  • , Reshma Taneja
  • Icahn School of Medicine at Mount Sinai
  • Yale University

Research output: Contribution to journal › Article › peer-review

162 Scopus citations

Abstract

Stra13, a basic helix-loop-helix transcription factor, is up-regulated upon activation of CD4+ T cells. Here we show that Stra13-deficient mice exhibit defects in several phases of CD4+ T cell activation. In vivo, Stra13 deficiency results in ineffective elimination of activated T and B cells, which accumulate progressively, leading to lymphoid organ hyperplasia. Consequently, aging Stra13-/- mice develop autoimmune disease characterized by accumulation of spontaneously activated T and B cells, circulating autoantibodies, infiltration of T and B lymphocytes in several organs and immune complex deposition in glomeruli. Our studies identify Stra13 as a key regulator of lymphocyte activation that is vital for maintenance of self-tolerance and for constraint of autoimmunity.

Original languageEnglish
Pages (from-to)1040-1047
Number of pages8
JournalNature Immunology
Volume2
Issue number11
DOIs
StatePublished - 2001

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