Synergistic tolerance induced by LF15-0195 and anti-CD45RB monoclonal antibody through suppressive dendritic cells

被引:25
作者
Min, WP
Zhou, DJ
Ichim, TE
Xia, XP
Zhang, X
Yang, JM
Huang, XY
Garcia, B
Dutartre, P
Jevnikar, AM
Strejan, GH
Zhong, R
机构
[1] Univ Western Ontario, Dept Surg, London, ON N6A 3K7, Canada
[2] Univ Western Ontario, Dept Med, London, ON, Canada
[3] Univ Western Ontario, Dept Pathol, London, ON, Canada
[4] Univ Western Ontario, Dept Microbiol, London, ON, Canada
[5] Univ Western Ontario, Dept Immunol, London, ON, Canada
[6] London Hlth Sci Ctr, Multiorgan Transplant Program, London, ON, Canada
[7] Lawson Hlth Res Inst, London, ON, Canada
[8] Robarts Res Inst, Transplant Grp, London, ON N6A 5C1, Canada
[9] Fournier Lab, Daix, France
关键词
D O I
10.1097/01.TP.0000061792.78914.52
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. LF 15-0195 (LF), a novel analogue of 15-deoxyspergualin (DSG), inhibits maturation of dendritic cells (DC). Anti-CD45RB is a monoclonal antibody (mAb) that blocks activation of T-helper (Th) 1 cells and generates T-regulatory cells. This study addressed whether these two reagents act synergistically to inducing tolerance, and investigated associated cellular mechanisms. Methods. BALB/c recipients were treated by a short course of mAb alone, LF alone, or the combination of both agents. Mice that accepted a C57BL/6 cardiac allograft for more than 100 days were considered tolerant. Splenic DC were purified using positive selection for CD11c. Bone marrow DC were generated by culture with interleukin-4 and granulocyte-macrophage colony-stimulating factor. Surface marker expression was determined by fluorescence-activated cell sorter analysis. DC function was assessed by the ability to stimulate or inhibit T cells in vitro. Results. Although monotherapy with LF or mAb failed to induce tolerance, combination therapy resulted in long-lasting acceptance of allogeneic hearts (>200 days) and secondary donor skin grafts (>100 days). DC from tolerant recipients possessed lower major histocompatibility complex class II and CD40 expression, and were poorer co-stimulators for T-cell proliferation than control DC. Furthermore, DC from tolerant mice induced Th2 differentiation, suppressed overall T-cell proliferation, and were poor presenters of T cells specific for antigen to pigeon cytochrome c 81-104. Conclusions. The combination of LF and anti-CD45RB mAb induced stable tolerance. The synergy of these two approaches appears to be mediated through formation of tolerogenic DC and T-regulatory cells.
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收藏
页码:1160 / 1165
页数:6
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