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氯法齐明和克拉霉素在感染雾化小鼠模型中的协同作用。

Synergistic Activity of Clofazimine and Clarithromycin in an Aerosol Mouse Model of Infection.

机构信息

AGIR EA 4294, University Center of Research and Health (CURS), Amiens, France

Department of Infectious Disease, University Hospital of Amiens-Picardie, Amiens, France.

出版信息

Antimicrob Agents Chemother. 2020 Apr 21;64(5). doi: 10.1128/AAC.02349-19.

Abstract

Infections with nontuberculous mycobacteria (NTM) have a poor prognosis in patients with underlying respiratory diseases. Clofazimine (CFZ) showed both experimental and clinical promising results against clinically relevant NTM. However, there are no data on CFZ in combination with the current recommended treatment; therefore, we aimed to study its activity in an aerosol mouse model of In an aerosol infection BALB/c mouse model using strain Chester, we treated 58 mice with four combinations of rifampin (RIF) at 10 mg/kg, CFZ at 25 mg/kg, and clarithromycin (CLR) and ethambutol (EMB) at 100 mg/kg. Treatment efficacy was assessed on the basis of lung CFU counts after 2 (M2) and 4 (M4) months of treatment. At M2, CLR-RIF-EMB was slightly but significantly more efficient than CFZ-RIF-EMB (3.02 ± 0.12 versus 3.55 ± 0.28, respectively, < 0.01), whereas CLR-CFZ-EMB and CLR-CFZ-RIF-EMB dramatically decreased lung CFU counts by 4.32 and 4.47 log, respectively, compared to untreated group. At M4, CLR-RIF-EMB was significantly more efficient than CFZ-RIF-EMB (2 ± 0.53 versus 2.66 ± 0.22, respectively, = 0.01). The addition of CLZ to CLR dramatically decreased the lung CFU count, with CFU counts 5.41 and 5.79 log lower in the CLR-CFZ-EMB and CLR-CFZ-RIF-EMB groups, respectively, than in the untreated group. The addition of CFZ to CLR seems to improve the efficacy of CLR as early as M2 and was confirmed at M4. CFZ, in addition to RIF and EMB, on the other hand, is less effective than CLR-RIF-EMB. These results need to be confirmed by similar studies along with CFZ potential for shortening treatment.

摘要

非结核分枝杆菌(NTM)感染在患有基础呼吸道疾病的患者中预后不良。氯法齐明(CFZ)在针对临床相关 NTM 的实验和临床研究中均显示出良好的效果。然而,目前尚无 CFZ 联合现有推荐治疗方案的数据,因此,我们旨在研究其在气溶胶感染 BALB/c 小鼠模型中的活性。

在使用 Chester 株进行的气溶胶感染 BALB/c 小鼠模型中,我们用四种组合的利福平(RIF)10mg/kg、CFZ 25mg/kg、克拉霉素(CLR)和乙胺丁醇(EMB)100mg/kg 治疗了 58 只小鼠。在治疗 2(M2)和 4(M4)个月后,根据肺部 CFU 计数评估治疗效果。在 M2 时,CLR-RIF-EMB 比 CFZ-RIF-EMB 略高,但差异有统计学意义(分别为 3.02±0.12 和 3.55±0.28, < 0.01),而 CLR-CFZ-EMB 和 CLR-CFZ-RIF-EMB 则分别使肺部 CFU 计数降低 4.32 和 4.47 log,与未治疗组相比差异有统计学意义。在 M4 时,CLR-RIF-EMB 比 CFZ-RIF-EMB 更有效(分别为 2±0.53 和 2.66±0.22, = 0.01)。CLZ 与 CLR 联合使用可显著降低肺部 CFU 计数,CLR-CFZ-EMB 和 CLR-CFZ-RIF-EMB 组的 CFU 计数比未治疗组低 5.41 和 5.79 log。CFZ 与 CLR 联合使用可在 M2 时就改善 CLR 的疗效,并在 M4 时得到证实。CFZ 联合 RIF 和 EMB 不如 CLR-RIF-EMB 有效。这些结果需要通过类似的研究以及 CFZ 缩短治疗时间的潜力来证实。

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