Yamaki Kouya, Uchida Hiroyuki, Harada Yoshiki, Li Xiaojuan, Yanagisawa Rie, Takano Hirohisa, Hayashi Hideyuki, Taneda Shinji, Mori Yoki, Yoshino Shin
Department of Pharmacology, Kobe Pharmaceutical University, Kobe, Hyogo 658-8558, Japan.
J Pharm Pharmacol. 2003 Dec;55(12):1661-6. doi: 10.1211/0022357022269.
We investigated the effect of the anti-rheumatic drug methotrexate (MTX) on Th1 and Th2 immune responses in mice. For this investigation, mice were immunized subcutaneously at the base of the tail with ovalbumin (OVA) emulsified with complete Freund's adjuvant (day 0). Varying doses of MTX were orally administered daily from days 0 to 20. On day 21, anti-OVA IgG2a and interferon-gamma (IFN-gamma) as indicators of Th1 responses and anti-OVA IgG1 and interleukin-10 (IL-10) as those of Th2 responses were measured. The results showed that treatment with MTX was followed by decreases in OVA-specific IgG and proliferation of spleen cells to the antigen. The anti-rheumatic drug inhibited both anti-OVA IgG2a and IgG1 production, although the inhibitory effect of MTX on the antigen-specific IgG2a production appeared to be greater than that on IgG1 production. IFN-gamma, but not IL-10, secretion was markedly downregulated by MTX. Administration of MTX resulted in suppression of antigen (OVA)-induced arthritis in mice. The suppression of the joint inflammation by MTX was associated with inhibition of OVA-specific proliferative responses of spleen cells, anti-OVA IgG, IgG2a and IgG1 production, and IFN-gamma and IL-10 secretion, although more pronounced decreases in IgG2a and IFN-gamma were observed compared with those in IgG1 and IL-10 in MTX-treated mice. These results indicate that MTX appears to suppress Th1 and, to a lesser extent, Th2 immune responses and its anti-arthritic effect on human rheumatoid arthritis might be at least in part explained by down-regulation of Th1 responses involved in the disease.
我们研究了抗风湿药物甲氨蝶呤(MTX)对小鼠Th1和Th2免疫反应的影响。为此项研究,在小鼠尾巴根部皮下注射用完全弗氏佐剂乳化的卵清蛋白(OVA)(第0天)。从第0天至第20天,每天口服不同剂量的MTX。在第21天,检测作为Th1反应指标的抗OVA IgG2a和干扰素-γ(IFN-γ)以及作为Th2反应指标的抗OVA IgG1和白细胞介素-10(IL-10)。结果显示,MTX治疗后OVA特异性IgG减少,脾细胞对抗原的增殖也减少。该抗风湿药物抑制了抗OVA IgG2a和IgG1的产生,尽管MTX对抗原特异性IgG2a产生的抑制作用似乎大于对IgG1产生的抑制作用。MTX显著下调了IFN-γ的分泌,但未下调IL-10的分泌。MTX给药导致小鼠抗原(OVA)诱导的关节炎受到抑制。MTX对关节炎症的抑制与脾细胞OVA特异性增殖反应、抗OVA IgG、IgG2a和IgG1产生以及IFN-γ和IL-10分泌的抑制有关,尽管在MTX治疗的小鼠中观察到IgG2a和IFN-γ的下降比IgG1和IL-10更明显。这些结果表明,MTX似乎抑制Th1免疫反应,在较小程度上也抑制Th2免疫反应,其对人类类风湿性关节炎的抗关节炎作用可能至少部分是由于下调了该疾病中涉及的Th1反应。