O'Callaghan J W, Forrest M J, Brooks P M
Department of Rheumatology, University of Sydney, Australia.
Rheumatol Int. 1988;8(1):41-5. doi: 10.1007/BF00541349.
Polymorphonuclear cell (PMN) chemotaxis was assessed using the in vitro under agarose assay in ten rheumatoid arthritis patients prior to and following a single 10-mg dose of methotrexate (MTX). PMNs obtained from patients after MTX showed a decreased chemotactic migration response to both zymosan activated serum (P less than 0.005) and N-formyl-L-methionyl-L-phenylalanine (P less than 0.01). In similar conditions, no significant difference in chemotactic migration could be detected in six rheumatoid arthritis patients not on MTX. In contrast to the in vivo effects of MTX, there was no inhibition of normal PMN chemotactic migration following a 30-min in vitro incubation of the cells with MTX (P less than 0.99).
在10例类风湿关节炎患者单次服用10毫克甲氨蝶呤(MTX)之前和之后,采用琼脂糖下体外试验评估多形核细胞(PMN)趋化性。服用MTX后从患者获取的PMN对酵母聚糖激活血清(P<0.005)和N-甲酰-L-蛋氨酰-L-苯丙氨酸(P<0.01)的趋化迁移反应均降低。在类似条件下,6例未服用MTX的类风湿关节炎患者的趋化迁移未检测到显著差异。与MTX的体内作用相反,细胞与MTX体外孵育30分钟后,正常PMN趋化迁移未受抑制(P<0.99)。