CD 161 ( NKR - P 1 A ) Costimulation of CD 1 d - dependent Activation of Human T Cells Expressing Invariant V a 24 J a Q T Cell Receptor a Chains

نویسندگان

  • Mark Exley
  • Steven Porcelli
  • Margo Furman
  • Jorge Garcia
  • Steven Balk
چکیده

A population of human T cells expressing an invariant V a 24J a Q T cell antigen receptor (TCR) a chain and high levels of CD161 (NKR-P1A) appears to play an immunoregulatory role through production of both T helper (Th) type 1 and Th2 cytokines. Unlike other CD161 1 T cells, the major histocompatibility complex–like nonpolymorphic CD1d molecule is the target for the TCR expressed by these T cells (V a 24 invt T cells) and by the homologous murine NK1 (NKR-P1C) 1 T cell population. In this report, CD161 was shown to act as a specific costimulatory molecule for TCR-mediated proliferation and cytokine secretion by V a 24 invt T cells. However, in contrast to results in the mouse, ligation of CD161 in the absence of TCR stimulation did not result in V a 24 invt T cell activation, and costimulation through CD161 did not cause polarization of the cytokine secretion pattern. CD161 monoclonal antibodies specifically inhibited V a 24 invt T cell proliferation and cytokine secretion in response to CD1d 1 target cells, demonstrating a physiological accessory molecule function for CD161. However, CD1d-restricted target cell lysis by activated V a 24 invt T cells, which involved a granule-mediated exocytotic mechanism, was CD161-independent. In further contrast to the mouse, the signaling pathway involved in V a 24 invt T cell costimulation through CD161 did not appear to involve stable association with tyrosine kinase p56 Lck . These results demonstrate a role for CD161 as a novel costimulatory molecule for TCR-mediated recognition of CD1d by human V a 24 invt T cells.

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تاریخ انتشار 1998