Tsai J J, Wang T F, Wang S R
Section of Allergy and Clinical Immunology, Cathay General Hospital, Taipei, Taiwan.
Asian Pac J Allergy Immunol. 1994 Jun;12(1):65-71.
We have tested the effect of methotrexate (MTX) on platelet activating factor (PAF)-induced neutrophil and eosinophil locomotion, neutrophil leukotriene B4 (LTB4) generation and mononuclear cell DNA synthesis. Neutrophils from patients treated with low dose methotrexate showed reduced PAF-induced chemotactic responses (727.8 +/- 72.2/10 HPF vs 481.9 +/- 87.3/10 HPF, p < 0.05). Both MTX and the specific PAF antagonist BN-52021 significantly inhibited PAF-induced eosinophil and neutrophil locomotion in a dose-dependent manner. MTX also reduced calcium ionophore-driven LTB4 generation from the neutrophils of asthmatics (358.9 +/- 39.5 pg/10(6) cells vs 240.1 +/- 29.1 pg/10(6) cells, p < 0.05) and attenuated PHA-induced mononuclear DNA synthesis as shown by a reduction in 3H-thymidine uptake and propidium iodide staining. These findings support the view that the beneficial effects of MTX in asthma may be due not only to its anti-mitotic effects on the proliferation of mononuclear cells but also to direct effects on granulocyte locomotion and production of LTB4.
我们已经测试了甲氨蝶呤(MTX)对血小板活化因子(PAF)诱导的中性粒细胞和嗜酸性粒细胞运动、中性粒细胞白三烯B4(LTB4)生成以及单核细胞DNA合成的影响。接受低剂量甲氨蝶呤治疗的患者的中性粒细胞对PAF诱导的趋化反应降低(727.8±72.2/10高倍视野 vs 481.9±87.3/10高倍视野,p<0.05)。MTX和特异性PAF拮抗剂BN-52021均以剂量依赖性方式显著抑制PAF诱导的嗜酸性粒细胞和中性粒细胞运动。MTX还减少了钙离子载体驱动的哮喘患者中性粒细胞LTB4生成(358.9±39.5 pg/10⁶细胞 vs 240.1±29.1 pg/10⁶细胞,p<0.05),并减弱了PHA诱导的单核细胞DNA合成,这通过³H-胸腺嘧啶摄取减少和碘化丙啶染色得以体现。这些发现支持了这样一种观点,即MTX在哮喘中的有益作用可能不仅归因于其对单核细胞增殖的抗有丝分裂作用,还归因于对粒细胞运动和LTB4产生的直接作用。