CD86 and CD80 differentially modulate the suppressive function of human regulatory T cells.

نویسندگان

  • Yong Zheng
  • Claire N Manzotti
  • Michael Liu
  • Fiona Burke
  • Karen I Mead
  • David M Sansom
چکیده

Regulatory T cells (Treg) are important in maintaining tolerance to self tissues. As both CD28 and CTLA-4 molecules are implicated in the function of Treg, we investigated the ability of their two natural ligands, CD80 and CD86, to influence the Treg-suppressive capacity. During T cell responses to alloantigens expressed on dendritic cells, we observed that Abs against CD86 potently enhanced suppression by CD4(+)CD25(+) Treg. In contrast, blocking CD80 enhanced proliferative responses by impairing Treg suppression. Intriguingly, the relative expression levels of CD80 and CD86 on dendritic cells are modulated during progression from an immature to a mature state, and this correlates with the ability of Treg to suppress responses. Our data show that CD80 and CD86 have opposing functions through CD28 and CTLA-4 on Treg, an observation that has significant implications for manipulation of immune responses and tolerance in vivo.

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عنوان ژورنال:
  • Journal of immunology

دوره 172 5  شماره 

صفحات  -

تاریخ انتشار 2004