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Generation and function of immunosuppressive human and murine CD8 + T cells by transforming growth factor‐β and retinoic acid
Author(s) -
Fleissner Diana,
Frede Annika,
Knott Markus,
Knuschke Torben,
Geffers Robert,
Hansen Wiebke,
Dobos Gustav,
Langhorst Jost,
Buer Jan,
Westendorf Astrid M.
Publication year - 2011
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/j.1365-2567.2011.03469.x
Subject(s) - foxp3 , il 2 receptor , regulatory t cell , cytotoxic t cell , biology , microbiology and biotechnology , cd8 , immune system , immunology , interleukin 21 , retinoic acid , t cell , in vitro , cell culture , biochemistry , genetics
Summary The intestinal immune system is constantly challenged by foreign antigens and commensal bacteria. Therefore, proper control of the intestinal microenvironment is required. One important arm of this regulatory network consists of regulatory T cells. In contrast to CD4 + Foxp3 + regulatory T cells, which have been well characterized, immunomodulatory CD8 + T cells that express Foxp3 are less well defined in terms of their generation and function. Failures of these regulatory mechanisms contribute to the development of inflammatory bowel disease. In this study we demonstrate that the frequency of CD8 + Foxp3 + T cells is reduced in the peripheral blood of patients with ulcerative colitis. As these cells might play a currently underestimated role in the maintenance of intestinal homeostasis, we have investigated human and murine CD8 + Foxp3 + T cells generated by stimulating naive CD8 + T cells in the presence of transforming growth factor‐β and retinoic acid, mediators that are abundantly produced in the intestinal mucosa. These CD8 + Foxp3 + fully competent regulatory T cells show strong expression of regulatory molecules CD25, Gpr83 and CTLA‐4 and exhibit cell–cell contact‐dependent immunosuppressive activity in vitro . Our study illustrates a previously unappreciated critical role of CD8 + Foxp3 + T cells in controlling potentially dangerous T cells and in the maintenance of intestinal homeostasis.