Molecular basis of T cell inactivation by CTLA-4

  • Kyung Mi Lee
  • , Ellen Chuang
  • , Matthew Griffin
  • , Roli Khattri
  • , David K. Hong
  • , Weiguo Zhang
  • , David Straus
  • , Lawrence E. Samelson
  • , Craig B. Thompson
  • , Jeffrey A. Bluestone

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

599 Citations (Scopus)

Abstract

CTLA-4, a negative regulator of T cell function, was found to associate with the T cell receptor (TCR) complex ζ chain in primary T cells. The association of TCRζ with CTLA-4, reconstituted in 293 transfectants, was enhanced by p56(lck)-induced tyrosine phosphorylation. Coexpression of the CTLA-4-associated tyrosine phosphatase, SHP-2, resulted in dephosphorylation of TCRζ bound to CTLA-4 and abolished the p56(lck)-inducible TCRζ-CTLA-4 interaction. Thus, CTLA-4 inhibits TCR signal transduction by binding to TCRζ and inhibiting tyrosine phosphorylation after T cell activation. These findings have broad implications for the negative regulation of T cell function and T cell tolerance.

Original languageEnglish
Pages (from-to)2263-2266
Number of pages4
JournalScience
Volume282
Issue number5397
DOIs
Publication statusPublished - 18 Dec 1998
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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