van den Berg W B, Joosten L A, Helsen M, van de Loo F A
Department of Rheumatology, University Hospital Nijmegen, The Netherlands.
Clin Exp Immunol. 1994 Feb;95(2):237-43. doi: 10.1111/j.1365-2249.1994.tb06517.x.
Inflammatory cytokines have been implicated in the pathogenesis of rheumatoid arthritis. To validate a key role for IL-1 in arthritic processes we have studied the protective effect of neutralizing antimurine IL-1 antibodies in the murine collagen-induced arthritis (CIA) model. Combination of anti-IL-1 alpha and anti-IL-1 beta given before onset of arthritis was shown to prevent disease completely. Remarkably, a single treatment was also highly effective in the established phase of arthritis, reducing both inflammation as well as cartilage destruction. Suppression was most pronounced with the combination, but anti-IL-1 beta alone also induced significant relief. Finally, we studied the protective effect of IL-1 neutralization on cartilage metabolism in a unilateral expression model of collagen arthritis. To this end zymosan was injected in one knee joint before onset of disease, resulting in accelerated expression in that particular joint and the draining paw. Anti-IL-1 treatment started after accelerated expression of arthritis was able to fully normalize chondrocyte synthetic function, which was highly suppressed in the control group. It is concluded that IL-1 is an important determinant in both inflammation and cartilage destruction in collagen arthritis, and this may have implications for therapy in human arthritis.
炎症细胞因子与类风湿性关节炎的发病机制有关。为了验证白细胞介素-1(IL-1)在关节炎进程中的关键作用,我们在小鼠胶原诱导性关节炎(CIA)模型中研究了中和抗小鼠IL-1抗体的保护作用。在关节炎发作前给予抗IL-1α和抗IL-1β的组合可完全预防疾病。值得注意的是,单次治疗在关节炎的既定阶段也非常有效,可减轻炎症以及软骨破坏。联合使用时抑制作用最为明显,但单独使用抗IL-1β也能显著缓解症状。最后,我们在胶原性关节炎的单侧表达模型中研究了IL-1中和对软骨代谢的保护作用。为此,在疾病发作前向一个膝关节注射酵母聚糖,导致该特定关节和引流爪中的表达加速。在关节炎加速表达后开始的抗IL-1治疗能够使软骨细胞合成功能完全恢复正常,而在对照组中该功能受到高度抑制。结论是,IL-1是胶原性关节炎炎症和软骨破坏的重要决定因素,这可能对人类关节炎的治疗有启示意义。