Chiocchia G, Boissier M C, Ronziere M C, Herbage D, Fournier C
INSERM U. 283, Hôpital Cochin, Paris, France.
J Immunol. 1990 Jul 15;145(2):519-25.
After immunization with native type II collagen (CII), susceptible strains of mice (H-2q) develop a polyarthritis that mimics rheumatoid arthritis. Although the underlying mechanisms are still undefined, T cells and particularly CD4+ lymphocytes seem to play a crucial role in the initiation of collagen-induced arthritis. To investigate whether CD8+ cells may participate in the pathogenesis of the disease, we have generated lines and clones of cytotoxic T cell hybridomas reactive to CII by fusion of lymph node and spleen cells from bovine native CII-primed C3H.Q (H-2q) mice and the AKR-derived thymoma cell line BW 5147. Clones were selected for their ability to lyse syngeneic macrophages pulsed with bovine native CII in an Ag-dependent manner. The two hybrid clones that were characterized, exhibited cell surface phenotypes of cytotoxic cells and reacted with CII purified from various species. However, each of them recognized different determinants on the CII molecule. P3G8 clone was specific for an epitope shared by CII and type XI collagen, whereas P2D9 clone reacted with CII and type IX collagen. Both hybridomas recognized CII-pulsed targets in association with H-2Kq molecules. These data indicate that the two CII-specific cytotoxic clones recognize different epitopes that are shared by other articular collagens and will allow us to test their influence on the development of arthritis in vivo.
用天然II型胶原蛋白(CII)免疫后,易感小鼠品系(H-2q)会发生类似于类风湿性关节炎的多关节炎。尽管其潜在机制仍不明确,但T细胞尤其是CD4+淋巴细胞似乎在胶原诱导的关节炎发病过程中起关键作用。为了研究CD8+细胞是否可能参与该疾病的发病机制,我们通过将来自用牛天然CII免疫的C3H.Q(H-2q)小鼠的淋巴结和脾细胞与AKR来源的胸腺瘤细胞系BW 5147融合,产生了对CII有反应的细胞毒性T细胞杂交瘤系和克隆。选择克隆是基于它们以抗原依赖的方式裂解用牛天然CII脉冲处理的同基因巨噬细胞的能力。经鉴定的两个杂交克隆表现出细胞毒性细胞的细胞表面表型,并与从各种物种纯化的CII发生反应。然而,它们各自识别CII分子上不同的决定簇。P3G8克隆对CII和XI型胶原蛋白共有的一个表位具有特异性,而P2D9克隆与CII和IX型胶原蛋白发生反应。两种杂交瘤都识别与H-2Kq分子相关的CII脉冲处理的靶细胞。这些数据表明,这两个CII特异性细胞毒性克隆识别其他关节胶原蛋白共有的不同表位,这将使我们能够在体内测试它们对关节炎发展的影响。