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耐多药结核病患者分离株中对氯法齐明和贝达喹啉的原发性耐药情况。

Primary Clofazimine and Bedaquiline Resistance among Isolates from Patients with Multidrug-Resistant Tuberculosis.

作者信息

Xu Jian, Wang Bin, Hu Minghao, Huo Fengmin, Guo Shaochen, Jing Wei, Nuermberger Eric, Lu Yu

机构信息

Beijing Key Laboratory of Drug Resistance Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, and Beijing Chest Hospital, Capital Medical University, Beijing, China.

Center for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Antimicrob Agents Chemother. 2017 May 24;61(6). doi: 10.1128/AAC.00239-17. Print 2017 Jun.

Abstract

Clofazimine has been repurposed for the treatment of tuberculosis, especially for multidrug-resistant tuberculosis (MDR-TB). To test the susceptibility to clofazimine of clinical isolates, MICs of clofazimine were determined using the microplate alamarBlue assay (MABA) method for 80 drug-resistant isolates and 10 drug-susceptible isolates for comparison. For five clofazimine-resistant strains isolated from previously treated pre-extensively drug-resistant TB (pre-XDR-TB) and XDR-TB patients without prior exposure to clofazimine or bedaquiline, clofazimine MICs were ≥1.2 μg/ml. Four isolates with cross-resistance to bedaquiline had mutations. The other isolate with no resistance to bedaquiline had an mutation. This study adds to a recent study showing that 6.3% of MDR-TB patients without prior clofazimine or bedaquiline exposure harbored isolates with mutations, which raises concern that preexisting resistance to these drugs may be associated with prior TB treatment. Furthermore, we propose a tentative breakpoint of 1.2 μg/ml for clofazimine resistance using the MABA method. More-widespread surveillance and individualized testing for clofazimine and bedaquiline resistance, together with assessment of their clinical usage, especially among previously treated and MDR-TB patients, are warranted.

摘要

氯法齐明已被重新用于治疗结核病,尤其是耐多药结核病(MDR-TB)。为了检测临床分离株对氯法齐明的敏感性,使用微孔板alamarBlue检测法(MABA)测定了80株耐药分离株和10株敏感分离株的氯法齐明最低抑菌浓度(MIC)以作比较。对于从先前治疗的广泛耐药结核病(pre-XDR-TB)和广泛耐药结核病(XDR-TB)患者中分离出的5株未接触过氯法齐明或贝达喹啉的耐氯法齐明菌株,氯法齐明的MIC≥1.2μg/ml。4株对贝达喹啉有交叉耐药性的分离株存在突变。另一株对贝达喹啉无耐药性的分离株存在一种突变。本研究补充了最近一项研究,该研究表明,6.3%未接触过氯法齐明或贝达喹啉的MDR-TB患者携带的分离株存在突变,这引发了人们对这些药物的预先存在的耐药性可能与先前的结核病治疗有关的担忧。此外,我们建议使用MABA方法将氯法齐明耐药性的暂定断点设定为1.2μg/ml。有必要对氯法齐明和贝达喹啉耐药性进行更广泛的监测和个体化检测,并评估它们的临床使用情况,尤其是在先前治疗的患者和MDR-TB患者中。

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