Rastogi N, Labrousse V, Bryskier A
Unité de la Tuberculose et des Mycobactéries, Institut Pasteur, Pointe-à-Pitre, Guadeloupe, French West Indies.
Antimicrob Agents Chemother. 1995 Apr;39(4):976-8. doi: 10.1128/AAC.39.4.976.
Recent reports have shown that roxithromycin possesses significant activity against atypical mycobacteria, including the Mycobacterium avium complex (MAC), and that its extracellular anti-MAC activity is further enhanced in two- or three-drug combinations with ethambutol, rifampin, amikacin, ofloxacin, and clofazimine. In accordance with the above data, the anti-MAC potential of roxithromycin used alone and in combination with the above-mentioned antituberculous drugs was screened intracellularly against five clinical MAC isolates (from both human immunodeficiency virus-positive and human immunodeficiency virus-negative patients), phagocytized by human monocyte-derived macrophages. The results showed that roxithromycin used alone and within clinically achievable levels was active against all of the MAC isolates tested. Screening of two-drug combinations showed that both rifampin and clofazimine further increased the intracellular activity of roxithromycin against all five isolates by 35 to 80% (ethambutol, ofloxacin, and amikacin resulted in increased intracellular activity against one, two, and four isolates, respectively). For the three-drug combinations, the combination of roxithromycin plus ethambutol used with rifampin or clofazimine was the most uniformly active against all five MAC isolates, with activity increases of 42 to 90%, followed by roxithromycin plus ethambutol used with amikacin, which resulted in activity increases of 15 to 90%. The overall level of intracellular killing after 5 days of drug addition, in comparison with growth in untreated controls, varied from 1 to 3 log units depending on the individual MAC isolate and/or drug combination used.
近期报告显示,罗红霉素对非典型分枝杆菌具有显著活性,包括鸟分枝杆菌复合群(MAC),并且在与乙胺丁醇、利福平、阿米卡星、氧氟沙星和氯法齐明组成的二联或三联药物组合中,其细胞外抗MAC活性会进一步增强。根据上述数据,在细胞内针对五株临床MAC分离株(来自人类免疫缺陷病毒阳性和人类免疫缺陷病毒阴性患者)进行了单独使用罗红霉素以及与上述抗结核药物联合使用时抗MAC潜力的筛选,这些分离株由人单核细胞衍生的巨噬细胞吞噬。结果表明,单独使用且在临床可达到水平的罗红霉素对所有测试的MAC分离株均有活性。二联药物组合的筛选显示,利福平和氯法齐明均使罗红霉素对所有五株分离株的细胞内活性进一步提高了35%至80%(乙胺丁醇、氧氟沙星和阿米卡星分别使针对一株、两株和四株分离株的细胞内活性增加)。对于三联药物组合,罗红霉素加乙胺丁醇与利福平或氯法齐明联合使用对所有五株MAC分离株的活性最为一致,活性增加了42%至90%,其次是罗红霉素加乙胺丁醇与阿米卡星联合使用,活性增加了15%至90%。与未处理对照中的生长情况相比,添加药物5天后细胞内杀伤的总体水平因所用的个体MAC分离株和/或药物组合而异,从1至3个对数单位不等。