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[大环内酯类药物在肺部非结核分枝杆菌病中的治疗效果]

[Therapeutic efficacy of macrolide in pulmonary nontuberculous mycobacteriosis].

作者信息

Tomono K

机构信息

Second Department of Internal Medicine, Nagasaki University School of Medicine, Japan.

出版信息

Kekkaku. 1994 Nov;69(11):725-32.

PMID:7837727
Abstract

Clarithromycin (CAM) is semi-synthetic macrolide antimicrobial agent, differing from erythromycin by an O-methyl substitution at position 6 of the 14-membered lactate ring. CAM is one of the very few antimicrobial agents that show activity against that Mycobacterium avium complex (MAC) in vivo, in vitro, and in AIDS patients with disseminated infections. The purpose of the present study was to evaluate the therapeutic efficacy of CAM against MAC in patients with chronic pulmonary MAC infection. In vitro activity against clinically isolated MAC; MIC was evaluated by liquid medium dilution method. CAM was the most effective than other antitubercular drugs against M. avium, but less effective than RFP against M. intracellulare. Activity in animal model of infection; In vivo activity was evaluated by the murine models of hematogenous pulmonary MAC infection. A dose-related reduction in lung cell counts was noted with treatment at 10, 50, 150, and 300 mg/kg of body weight administrated daily. Histopathological examinations were revealed also the reduction of the numbers of granulomas in the lungs with treatment CAM at 300 mg/kg. Therapeutic efficacy of CAM in chronic pulmonary MAC infection; Thirty patients with chronic pulmonary MAC infection were given CAM with other antitubercular drugs. Nineteen of 30 patients had previously received combination antimycobacterial therapy. The overall efficacy rates were 23.3%, and ten patients (33.3%) had negative sputum culture for MAC. Eradication of MAC from sputum has been almost observed within 3 months of initiating treatment, and the patients those who had no cavitation were effective. In conclusion, CAM was considerably effective against chronic pulmonary MAC infection, and the effect was observed relatively rapid.

摘要

克拉霉素(CAM)是一种半合成大环内酯类抗菌剂,在14元内酯环的6位上有一个O-甲基取代基,与红霉素不同。CAM是极少数在体内、体外以及对播散性感染的艾滋病患者中对鸟分枝杆菌复合体(MAC)具有活性的抗菌剂之一。本研究的目的是评估CAM对慢性肺部MAC感染患者的治疗效果。对临床分离的MAC的体外活性;通过液体培养基稀释法评估最低抑菌浓度(MIC)。CAM对鸟分枝杆菌比其他抗结核药物最有效,但对细胞内分枝杆菌比利福平效果差。感染动物模型中的活性;通过血源性肺部MAC感染的小鼠模型评估体内活性。每天给予10、50、150和300mg/kg体重的治疗可使肺细胞计数出现剂量相关的减少。组织病理学检查还显示,给予300mg/kg的CAM治疗后,肺部肉芽肿数量减少。CAM在慢性肺部MAC感染中的治疗效果;30例慢性肺部MAC感染患者接受CAM与其他抗结核药物联合治疗。30例患者中有19例此前接受过联合抗分枝杆菌治疗。总有效率为23.3%,10例患者(33.3%)MAC痰培养转阴。在开始治疗后3个月内几乎观察到痰中MAC被清除,无空洞的患者有效。总之,CAM对慢性肺部MAC感染相当有效,且效果出现相对较快。

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