单克隆抗体
发病机制
免疫学
类风湿性关节炎
T细胞
体内
关节炎
受体
生物
肿瘤坏死因子α
抗体
医学
免疫系统
内科学
生物技术
作者
Takeo Yoshioka,Atsuo Nakajima,Hisaya Akiba,Toshiyuki Ishiwata,Gorô Asano,Shinichi Yoshino,Hideo Yagita,Ko Okumura
标识
DOI:10.1002/1521-4141(200010)30:10<2815::aid-immu2815>3.0.co;2-
摘要
OX40 ligand (OX40L) and OX40 (CD134) are a pair of cell surface molecules belonging to the TNF/TNF receptor family. Interaction of OX40L with its receptor OX40 is thought to be important in T cell activation through T cell/antigen-presenting cell interaction. However, involvement of these molecules in the pathogenesis of rheumatoid arthritis (RA) remains unclear. To explore the contribution of OX40/OX40L interaction to the pathogenesis of RA in vivo, we evaluated the effect of a neutralizing anti-OX40L monoclonal antibody (mAb) on the development of collagen-induced arthritis (CIA) in DBA/1 mice as an animal model for RA. Administration of anti-OX40L mAb into type II collagen (CII) -immunized DBA/1 mice dramatically ameliorated the disease severity. In vivo treatment with anti-OX40L mAb did not inhibit the expansion of CII-reactive T cells, but suppressed IFN-gamma and anti-CII IgG2a production. Therefore, OX40/OX40L interaction appears to play a critical role in the development of CIA by enhancing Th1-type autoimmune response. In addition, T lymphocytes in synovial fluid and synovial tissue from RA patients expressed OX40, while OX40L was expressed on sublining cells in synovial tissue. These results indicate that OX40/OX40L interaction may play a critical role in the development of RA.
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