CD43 is a murine T cell costimulatory receptor that functions independently of CD28

  • Anne I. Sperling
  • , Jonathan M. Green
  • , R. Lee Mosley
  • , Peter L. Smith
  • , Richard J. DiPaolo
  • , John R. Klein
  • , Jeffrey A. Bluestone
  • , Craig B. Thompson

Research output: Contribution to journalArticlepeer-review

129 Scopus citations

Abstract

Costimulation mediated by the CD28 receptor has been shown to play an important role in the development of a vigorous T cell immune response. Nevertheless, CD28-deficient mice can mount effective T cell-dependent immune responses. These data suggest that other costimulatory molecules may play a role in T cell activation. In a search for other costimulatory receptors on T cells, we have characterized a monoclonal antibody (mAb) that can costimulate T cells in the absence of accessory cells. Similar to CD28 antibodies, this mAb, R2/60, was found to synergize with T cell receptor engagement in inducing proliferation. Independent ligation of CD3 and the ligand recognized by R2/60 results in T cell proliferation, suggesting that the two molecules do not have to colocalize to activate the R2/60 costimulatory pathway. R2/60 does not react with CD28, and furthermore, R2/60 costimulates in a CD28- independent fashion since the mAb costimulates T cells from the CD28- deficient mice as well as wild-type mice. Expression cloning of the R2/60 antigen identified the ligand as murine CD43. Together, these data demonstrate that CD43 can serve as a receptor on T cells that can provide CD28-independent costimulation.

Original languageEnglish
Pages (from-to)139-146
Number of pages8
JournalJournal of Experimental Medicine
Volume182
Issue number1
DOIs
StatePublished - Jul 1 1995

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