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首页> 外文期刊>Antimicrobial agents and chemotherapy. >In vitro and in vivo activities of novel fluoroquinolones alone and in combination with clarithromycin against clinically isolated Mycobacterium avium complex strains in Japan.
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In vitro and in vivo activities of novel fluoroquinolones alone and in combination with clarithromycin against clinically isolated Mycobacterium avium complex strains in Japan.

机译:新型氟喹诺酮类药物单独或与克拉霉素联用对日本临床分离的鸟分枝杆菌复杂菌株的体外和体内活性。

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摘要

The recommended treatments for Mycobacterium avium complex (MAC) infectious disease are combination regimens of clarithromycin (CLR) or azithromycin with ethambutol and rifamycin. However, these chemotherapy regimens are sometimes unsuccessful. Recently developed antimicrobial agents, such as newer fluoroquinolones (FQs) containing C-8 methoxy quinolone (moxifloxacin [MXF] and gatifloxacin [GAT]), are expected to be novel antimycobacterial agents. Here, we evaluated the in vitro and in vivo antimycobacterial activities of three FQs (MXF, GAT, and levofloxacin) and CLR against clinically isolated MAC strains. Subsequently, the in vitro and in vivo synergic activities of FQ-CLR combinations against MAC strains were investigated. CLR and the individual FQs alone showed promising activity against MAC strains in vitro, and the bacterial counts in organs (lungs, liver, and spleen) of MAC-infected mice treated with single agents were significantly reduced compared to control mice. CLR showed the best anti-MACeffect in vivo. When the three FQs were individually combined with CLR in vitro, mild antagonism was observed for 53 to 57% of the tested isolates. Moreover, mice were infected with MAC strains showing mild antagonism for FQ-CLR combinations in vitro, and the anti-MAC effects of the FQ-CLR combinations were evaluated by counting the viable bacteria in their organs and by histopathological examination after 28 days of treatment. Several FQ-CLR combinations exhibited bacterial counts in organs significantly higher than those in mice treated with CLR alone. Our results indicate that the activity of CLR is occasionally attenuated by combination with an FQ both in vitro and in vivo and that this effect seems to be MAC strain dependent. Careful combination chemotherapy using these agents against MAC infectious disease may be required.
机译:鸟分枝杆菌复合物(MAC)传染病的推荐治疗方法是克拉霉素(CLR)或阿奇霉素与乙胺丁醇和利福霉素的联合治疗。但是,这些化疗方案有时不成功。预期最近开发的抗菌剂,例如含有C-8甲氧基喹诺酮(莫西沙星[MXF]和加替沙星[GAT])的较新的氟喹诺酮类(FQs)是新型的抗分枝杆菌药。在这里,我们评估了三种FQ(MXF,GAT和左氧氟沙星)和CLR对临床分离出的MAC菌株的体外和体内抗分枝杆菌活性。随后,研究了FQ-CLR组合对MAC菌株的体外和体内协同活性。 CLR和单独的FQs在体外对MAC菌株显示出有希望的活性,并且与对照小鼠相比,用单一药物处理的MAC感染小鼠的器官(肺,肝和脾脏)细菌计数显着降低。 CLR在体内显示出最佳的抗MAC效应。当三个FQ在体外分别与CLR结合使用时,对53%至57%的测试分离株观察到轻度拮抗作用。此外,小鼠感染了对FQ-CLR组合具有轻度拮抗作用的MAC株,并通过计数其器官中的活细菌并在治疗28天后进行了组织病理学检查来评估FQ-CLR组合的抗MAC作用。几种FQ-CLR组合在器官中的细菌计数显着高于单独使用CLR治疗的小鼠。我们的结果表明,在体外和体内,与FQ联合使用均会降低CLR的活性,这种作用似乎是MAC菌株依赖性的。可能需要使用这些药物针对MAC传染病进行仔细的联合化疗。

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