Williams R O, Mauri C, Mason L J, Marinova-Mutafchieva L, Ross S E, Feldmann M, Maini R N
Kennedy Institute of Rheumatology, London, UK.
Arthritis Rheum. 1998 Oct;41(10):1806-12. doi: 10.1002/1529-0131(199810)41:10<1806::AID-ART12>3.0.CO;2-9.
To define the mechanisms of action of 2 novel drugs, cyclosporine and anti-tumor necrosis factor alpha (TNFalpha), in collagen-induced arthritis and to determine the effect of combination therapy.
Type II collagen-immunized DBA/1 mice with established arthritis were treated with cyclosporine alone, anti-TNFalpha alone, cyclosporine plus anti-TNFalpha, or saline.
Cyclosporine was found to ameliorate arthritis, suppress interferon-gamma (IFNgamma) production by CD4+ T cells, and reduce TNFalpha expression in arthritic joints. However, cyclosporine did not directly inhibit TNFalpha production by macrophages, indicating that the decrease in TNFalpha expression observed in vivo was probably an indirect consequence of the reduction in type 1 T helper cell activity. Anti-TNFalpha also reduced IFNgamma production by T cells, indicating that TNFalpha is involved in the cellular immune response to collagen. Combined treatment with cyclosporine plus anti-TNFalpha had an additive therapeutic effect.
Although cyclosporine and anti-TNFalpha target different points in the inflammatory pathway, there is an overlap in the consequences of their actions in vivo.
确定两种新型药物环孢素和抗肿瘤坏死因子α(TNFα)在胶原诱导性关节炎中的作用机制,并确定联合治疗的效果。
用Ⅱ型胶原免疫已患关节炎的DBA/1小鼠,分别单独给予环孢素、单独给予抗TNFα、联合给予环孢素加抗TNFα或给予生理盐水。
发现环孢素可改善关节炎,抑制CD4+T细胞产生干扰素γ(IFNγ),并降低关节炎关节中TNFα的表达。然而,环孢素并不直接抑制巨噬细胞产生TNFα,这表明体内观察到的TNFα表达降低可能是1型辅助性T细胞活性降低的间接结果。抗TNFα也降低了T细胞产生IFNγ,表明TNFα参与了对胶原的细胞免疫反应。环孢素加抗TNFα联合治疗具有相加的治疗效果。
虽然环孢素和抗TNFα作用于炎症途径的不同靶点,但它们在体内的作用结果存在重叠。