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硝基咪唑并吡喃类药物PA - 824在小鼠结核病模型中的杀菌活性

Bactericidal activity of the nitroimidazopyran PA-824 in a murine model of tuberculosis.

作者信息

Tyagi Sandeep, Nuermberger E, Yoshimatsu T, Williams K, Rosenthal I, Lounis N, Bishai W, Grosset J

机构信息

Center for Tuberculosis Research, Johns Hopkins University, 1503 East Jefferson St., Baltimore, MD 21231-1002, USA.

出版信息

Antimicrob Agents Chemother. 2005 Jun;49(6):2289-93. doi: 10.1128/AAC.49.6.2289-2293.2005.

Abstract

The nitroimidazopyran PA-824 has potent in vitro activity against Mycobacterium tuberculosis, a narrow spectrum of activity limited primarily to the M. tuberculosis complex, and no demonstrable cross-resistance to a variety of antituberculosis drugs. In a series of experiments, we sequentially characterized the activity of PA-824 in an experimental murine model of tuberculosis. The minimal effective dose was 12.5 mg/kg of body weight/day. The minimal bactericidal dose (MBD) was 100 mg/kg/day. When PA-824 was used as monotherapy at the MBD, it exhibited promising bactericidal activity during the initial intensive phase of therapy that was similar to that of the equipotent dose of isoniazid in humans. In combination with isoniazid, PA-824 prevented the selection of isoniazid-resistant mutants. Perhaps more importantly, PA-824 also demonstrated potent activity during the continuation phase of therapy, during which it targeted bacilli that had persisted through an initial 2-month intensive phase of treatment with rifampin, isoniazid, and pyrazinamide. Together, these data strongly support further evaluation of PA-824 in combination with first- or second-line antituberculosis drugs to determine its potential contribution to the treatment of drug-susceptible or multidrug-resistant tuberculosis, respectively.

摘要

硝基咪唑并吡喃类药物PA - 824对结核分枝杆菌具有强大的体外活性,其活性谱较窄,主要限于结核分枝杆菌复合群,并且对多种抗结核药物无明显交叉耐药性。在一系列实验中,我们在实验性小鼠结核病模型中对PA - 824的活性进行了连续表征。最小有效剂量为12.5毫克/千克体重/天。最小杀菌剂量(MBD)为100毫克/千克/天。当以MBD剂量将PA - 824用作单一疗法时,在治疗的初始强化阶段它表现出有前景的杀菌活性,这与人类中同等剂量的异烟肼相似。与异烟肼联合使用时,PA - 824可防止异烟肼耐药突变体的产生。也许更重要的是,PA - 824在治疗的延续阶段也表现出强大的活性,在此阶段它靶向那些在最初为期2个月的利福平、异烟肼和吡嗪酰胺强化治疗后仍持续存在的杆菌。总之,这些数据有力地支持进一步评估PA - 824与一线或二线抗结核药物联合使用,以分别确定其对治疗药物敏感或耐多药结核病的潜在贡献。

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