CTLA4Ig-induced linked regulation of allogeneic T cell responses

被引:25
作者
Lee, RS
Rusche, JR
Maloney, ME
Sachs, DH
Sayegh, MH
Madsen, JC
机构
[1] Massachusetts Gen Hosp, Dept Surg, Div Cardiac Surg, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Transplantat Biol Res Ctr, Boston, MA 02114 USA
[3] Repligen Corp, Needham, MA 02494 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Renal Div,Lab Immunogenet & Transplantat, Boston, MA 02115 USA
关键词
D O I
10.4049/jimmunol.166.3.1572
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The mechanisms by which CTLA4Ig exerts its powerful immunomodulatory effects are not clear. We show here that CTLA4Ig can induce linked regulation of allogeneic porcine T cell responses in vitro. Naive miniature swine SLA(dd) T cells were rendered hyporesponsive to specific allogeneic Ag after coculturing with MHC-mismatched SLA(cc) stimulators in the presence of CTLA4Ig, These Ag-specific hyporesponsive T cells were subsequently able to actively inhibit the allogeneic responses of naive syngeneic T cells in an MHC-linked fashion, as the responses of naive SLA(dd) responders against specific SLA(cc) and (SLA(ac))F-1 stimulators were inhibited, but allogeneic responses against a 1:1 mixture of SLA(aa) (I-a, IIa) and SLA(cc) (I-c, IIc) were maintained. This inhibition could be generated against either class I or class II Ags, was radiosensitive, and required cell-cell contact. Furthermore, the mechanism of inhibition was not dependent upon a deletional, apoptotic pathway, but it was reversed by anti-IL-10 mAb. These data suggest that CTLA4Ig-induced inhibition of naive allogeneic T cell responses can be mediated through the generation of regulatory T cells via an IL-10-dependent mechanism.
引用
收藏
页码:1572 / 1582
页数:11
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[31]   Regulation of CTLA-4 expression during T cell activation [J].
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Wang, YS ;
Walunas, T ;
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Listman, J ;
Finn, PW .
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[32]   Lymphocyte activation: T-cell regulation by CTLA-4 [J].
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[33]   Negative regulation of human T cell activation by CTLA-4. [J].
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Chai, N. -N. ;
Jordan, S. ;
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