Sano C, Shimizu T, Sato K, Kawauchi H, Kawahara S, Tomioka H
Department of Microbiology and Immunology, Shimane Medical University, Japan.
Antimicrob Agents Chemother. 1999 Feb;43(2):360-4. doi: 10.1128/AAC.43.2.360.
The effects of half-sized secretory leukocyte protease inhibitor or diclofenac sodium administered alone or in combination with the benzoxazinorifamycin KRM-1648 on the therapeutic efficacy of KRM-1648 against Mycobacterium avium complex (MAC) in mice were studied. Neither of the two anti-inflammatory drugs affected the efficacy of KRM-1648, while they exerted significant modulating effects on tumor necrosis factor alpha production by MAC-infected macrophages.
研究了单独给予或与苯并恶嗪诺利福霉素KRM - 1648联合给予半量分泌型白细胞蛋白酶抑制剂或双氯芬酸钠对KRM - 1648抗小鼠鸟分枝杆菌复合群(MAC)治疗效果的影响。这两种抗炎药均未影响KRM - 1648的疗效,但它们对MAC感染的巨噬细胞产生肿瘤坏死因子α具有显著的调节作用。