In vitro generation of interleukin 10-producing regulatory CD4+ T cells is induced by immunosuppressive drugs and inhibited by T helper type 1 (Th1)- and Th2-inducing cytokines

被引:872
作者
Barrat, FJ
Cua, DJ
Boonstra, A
Richards, DF
Crain, C
Savelkoul, HF
de Waal-Malefyt, R
Coffman, RL
Hawrylowicz, CM
O'Garra, A
机构
[1] DNAX Res Inst Molec & Cellular Biol Inc, Dept Immunol, Palo Alto, CA 94304 USA
[2] Erasmus Univ, Dept Immunol, NL-3000 DR Rotterdam, Netherlands
[3] GKT Sch Med, Dept Resp Med & Allergy, London SE1 9RT, England
关键词
experimental autoimmune encephalomyelitis; vitamin D3; Dexamethasone; T regulatory lymphocyte; autoimmumity;
D O I
10.1084/jem.20011629
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We show that a combination of the immunosuppressive drugs, vitamin D3 and Dexamethasone, induced human and mouse naive CD4(+) T cells to differentiate in vitro into regulatory T cells. In contrast to the previously described in vitro derived CD4(+) T cells, these cells produced only interleukin (IL)-10, but no IL-5 and interferon (IFN)-gamma, and furthermore retained strong proliferative capacity. The development of these IL-10-producing cells was enhanced by neutralization of the T helper type 1 (Th1)- and Th2-inducing cytokines IL-4, IL-12, and IFN-gamma. These immunosuppressive drugs also induced the development of IL-10-producing T cells in the absence of antigen-presenting cells, with IL-10 acting as a positive autocrine factor for these T cells. Furthermore, nuclear factor (NF)-kappaB and activator protein (AP)-1 activities were inhibited in the IL-10-producing cells described here as well as key transcription factors involved in Th1 and Th2 subset differentiation. The regulatory function of these in vitro generated IL-10-producing T cells was demonstrated by their ability to prevent central nervous system inflammation, when targeted to the site of inflammation, and this function was shown to be IL-10 dependent. Generating homogeneous populations of IL-10-producing T cells in vitro will thus facilitate the use of regulatory T cells in immunotherapy.
引用
收藏
页码:603 / 616
页数:14
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