Veziris Nicolas, Ibrahim Murad, Lounis Nacer, Chauffour Aurelie, Truffot-Pernot Chantal, Andries Koen, Jarlier Vincent
Laboratoire de Bactériologie-Hygiène, Université Pierre et Marie Curie, Paris, France.
Am J Respir Crit Care Med. 2009 Jan 1;179(1):75-9. doi: 10.1164/rccm.200711-1736OC. Epub 2008 Oct 23.
R207910 (TMC207 or J) is a member of the diarylquinolines, a new family of antituberculous drugs with high bactericidal activity when given daily in the murine model of tuberculosis. R207910 exhibits a long half-life and thus is a good candidate for once-weekly therapy of tuberculosis.
To study the activity of once-weekly R207910 monotherapy and combinations of R207910 with other antituberculous agents (isoniazid, rifapentine, moxifloxacin, and pyrazinamide).
The established infection model of murine tuberculosis was used. Colony counts were determined in the lungs.
Eight weeks of monotherapy reduced the bacillary load by 3 to 4 log(10) for rifapentine and by 5 to 6 log(10) for R207910 (P < 0.05). The addition of rifapentine and isoniazid or moxifloxacin did not improve the bactericidal activity of R207910 monotherapy. In contrast, the triple combination of R207910 plus rifapentine plus pyrazinamide given once weekly for 2 months (i.e., a total of only eight administrations), was significantly (P < 0.05) more active than R207910 monotherapy or other R207910 combinations, and led to lung culture negativity in 9 of 10 mice, whereas all lungs were culture positive in the groups treated with other drug combinations. Moreover, R207910 plus rifapentine plus pyrazinamide given once weekly was more active than the current standard regimen of rifampin plus isoniazid plus pyrazinamide given five times per week.
The unprecedented activity of the triple combination of R207910 plus rifapentine plus pyrazinamide suggests that it may be feasible to develop a fully intermittent once-weekly regimen.
R207910(TMC207或J)是二芳基喹啉类药物的一种,该类新型抗结核药物在小鼠结核病模型中每日给药时具有高杀菌活性。R207910半衰期长,因此是结核病每周一次治疗的理想候选药物。
研究R207910每周一次单药治疗以及R207910与其他抗结核药物(异烟肼、利福喷汀、莫西沙星和吡嗪酰胺)联合使用的活性。
采用已建立的小鼠结核病感染模型。测定肺内的菌落计数。
八周的单药治疗使利福喷汀的细菌载量降低3至4个对数(10),使R207910的细菌载量降低5至6个对数(10)(P<0.05)。添加利福喷汀和异烟肼或莫西沙星并未提高R207910单药治疗的杀菌活性。相比之下,R207910加利福喷汀加吡嗪酰胺三联组合每周给药一次,持续2个月(即总共仅给药八次),其活性显著高于(P<0.05)R207910单药治疗或其他R207910联合用药,并且使10只小鼠中有9只的肺培养转阴,而在接受其他药物联合治疗的组中,所有小鼠的肺培养均为阳性。此外,R207910加利福喷汀加吡嗪酰胺每周给药一次比目前的利福平加异烟肼加吡嗪酰胺每周给药五次的标准方案活性更高。
R207910加利福喷汀加吡嗪酰胺三联组合前所未有的活性表明,开发一种完全间歇性的每周一次治疗方案可能是可行的。