Kamada H, Nakagami K
Third Laboratory for Pharmacological Research, Asahi Chemical Industry Co., Ltd., Shizuoka, Japan.
Jpn J Pharmacol. 1996 Feb;70(2):169-75. doi: 10.1254/jjp.70.169.
This study examines the effect of mizoribine (MZR), an immunosuppressant, on collagen-induced arthritis in mice. DBA/1J mice, immunized on days 0 and 21 with 200 micrograms of type II collagen in complete Freund adjuvant, were treated with various doses of MZR for 12 weeks, beginning on the day after the primary immunization. MZR reduced the arthritis score in a dose-dependent fashion, showing significant suppression, even at a dose of 10 mg/kg. At doses of more than 20 mg/kg, MZR also significantly suppressed bone damage in the hind limbs. MZR significantly suppressed the delayed-type hypersensitivity response to type II collagen, but only slightly decreased anti-type II collagen antibody levels. MZR restored the L3T4+/Lyt-2+ ratio, which was increased in arthritic mice, to the level found in normal mice. These findings show that MZR suppresses collagen-induced arthritis and bone damage in mice, and suggest that the inhibitory effect of MZR is based on its suppression of cellular immunity. These results provide a theoretical basis for the clinical use of MZR in rheumatoid arthritis.
本研究考察了免疫抑制剂咪唑立宾(MZR)对小鼠胶原诱导性关节炎的作用。DBA/1J小鼠在第0天和第21天用200微克Ⅱ型胶原与完全弗氏佐剂进行免疫,自初次免疫后次日起,用不同剂量的MZR治疗12周。MZR以剂量依赖性方式降低关节炎评分,即使在10毫克/千克的剂量下也显示出显著抑制作用。在剂量超过20毫克/千克时,MZR还显著抑制后肢的骨损伤。MZR显著抑制对Ⅱ型胶原的迟发型超敏反应,但仅轻微降低抗Ⅱ型胶原抗体水平。MZR使关节炎小鼠中升高的L3T4+/Lyt-2+比值恢复到正常小鼠的水平。这些发现表明MZR抑制小鼠胶原诱导性关节炎和骨损伤,并提示MZR的抑制作用基于其对细胞免疫的抑制。这些结果为MZR在类风湿关节炎临床应用中提供了理论依据。