CD200 immunoadhesin suppresses collagen-induced arthritis in mice

被引:83
作者
Gorczynski, RM
Chen, ZQ
Yu, K
Hu, J
机构
[1] Toronto Hosp, Transplant Res Div, Toronto, ON M5G 2C4, Canada
[2] Univ Toronto, Dept Surg, Toronto, ON M5G 2C4, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON M5G 2C4, Canada
基金
加拿大健康研究院;
关键词
CD20OFc; arthritis; cytokine production;
D O I
10.1006/clim.2001.5117
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DBA/1 mice immunized with 100 mug bovine collagen type II emulsified in Freund's adjuvant, followed by booster injection in incomplete adjuvant at 18 days, develop profound arthritis (> 50% of animals) by days postinjection. The molecule CD200 (previously called OX2), associated with, among others, follicular dendritic cells, is implicated in delivery of immunosuppressive signals to the immune system, and an immunoadhesin in which the extracellular domains of CD200 were linked to a mouse IgG2a. Fe region has been shown to promote renal allograft survival. DBA/1 mice receiving 15 mug/mouse CD200Fc at 3-day intervals following immunization with collagen did not develop arthritis in this model. Lymphocytes taken from CD200Fc-treated, collagen-immunized mice produced significantly lower levels of TNF alpha and IFN-gamma in culture supernatants after restimulation in vitro with collagen, in contrast to cells taken from control mice treated with PBS or normal mouse Ig. Serum from CD200Fc-treated mice contained less anti-collagen IgG (similar to 50% reduction), with relatively more IgG2b and IgG3, and lower levels of TNF alpha and IFN-gamma, than control mice. These data indicate that this immunoadhesin may have a potent role to play in the regulation of autoimmune disorders. (C) 2001 Elsevier Science.
引用
收藏
页码:328 / 334
页数:7
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