Chiocchia G, Boissier M C, Manoury B, Fournier C
INSERM U 283, Hôpital Cochin, Paris, France.
Eur J Immunol. 1993 Feb;23(2):327-32. doi: 10.1002/eji.1830230204.
Injection of native type II collagen (CII) to susceptible strains of mice (H-2q) induces a rheumatoid arthritis-like disease. To study the role of CD8+ T cells in the collagen-induced arthritis (CIA), we generated CII-specific T cell hybridomas by fusion of cells from arthritic C3H. Q mice and an AKR thymoma. Two hybrid clones (P3G8 and P2D9) were selected for their ability to lyse syngeneic CII-pulsed macrophages and recognize different antigenic epitopes in association with Kq molecules. When these T cell clones were irradiated and inoculated into (C3H.Q x AKR)F1 mice 21 days prior to priming with native CII/complete Freund's adjuvant, the incidence and the duration of CIA were significantly reduced in comparison to groups receiving saline or control T cell hybridoma. Furthermore, both anti-CII T cell hybridomas were able to attenuate CIA in highly susceptible inbred strains of mice and this suppression was antigen and disease specific. The protective activity seems to require intact cells as neither membrane fractions nor cytosolic preparations of the hybridoma T cells retained the vaccinating activity. Most importantly, one of the hybrid clones (P3G8) had a therapeutic effect on CIA since its administration to arthritic DBA/1 mice on day 30 after priming down-regulated the ongoing disease. Taken together, these findings suggest that anti-CII cytotoxic T cell clones can vaccinate against CIA and even reverse the disease.
向易感性小鼠品系(H-2q)注射天然II型胶原蛋白(CII)可诱发类风湿性关节炎样疾病。为研究CD8 + T细胞在胶原蛋白诱导的关节炎(CIA)中的作用,我们通过将关节炎C3H.Q小鼠的细胞与AKR胸腺瘤细胞融合,生成了CII特异性T细胞杂交瘤。选择了两个杂交克隆(P3G8和P2D9),因其能够裂解同基因CII刺激的巨噬细胞,并识别与Kq分子相关的不同抗原表位。在用天然CII/完全弗氏佐剂致敏前21天,将这些T细胞克隆进行照射并接种到(C3H.Q×AKR)F1小鼠中,与接受生理盐水或对照T细胞杂交瘤的组相比,CIA的发病率和持续时间显著降低。此外,两种抗CII T细胞杂交瘤均能够减轻高度易感性近交系小鼠的CIA,且这种抑制作用具有抗原和疾病特异性。保护活性似乎需要完整细胞,因为杂交瘤T细胞的膜组分和胞质制剂均不保留接种活性。最重要的是,其中一个杂交克隆(P3G8)对CIA具有治疗作用,因为在致敏后第30天给予关节炎DBA/1小鼠该克隆可下调正在发生的疾病。综上所述,这些发现表明抗CII细胞毒性T细胞克隆可预防CIA,甚至可使疾病逆转。