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本文引用的文献

1
Unexpected high prevalence of resistance-associated Rv0678 variants in MDR-TB patients without documented prior use of clofazimine or bedaquiline.在未记录有先前使用氯法齐明或贝达喹啉情况的耐多药结核病患者中,与耐药相关的Rv0678变体意外地具有高流行率。
J Antimicrob Chemother. 2017 Mar 1;72(3):684-690. doi: 10.1093/jac/dkw502.
2
Mutations in pepQ Confer Low-Level Resistance to Bedaquiline and Clofazimine in Mycobacterium tuberculosis.pepQ基因突变赋予结核分枝杆菌对贝达喹啉和氯法齐明的低水平耐药性。
Antimicrob Agents Chemother. 2016 Jul 22;60(8):4590-9. doi: 10.1128/AAC.00753-16. Print 2016 Aug.
3
Mycobacterium tuberculosis whole genome sequencing and protein structure modelling provides insights into anti-tuberculosis drug resistance.结核分枝杆菌全基因组测序和蛋白质结构建模为深入了解抗结核药物耐药性提供了线索。
BMC Med. 2016 Mar 23;14:31. doi: 10.1186/s12916-016-0575-9.
4
Acquired Resistance to Bedaquiline and Delamanid in Therapy for Tuberculosis.结核病治疗中对贝达喹啉和地拉马尼的获得性耐药性。
N Engl J Med. 2015 Nov 12;373(20):1986-8. doi: 10.1056/NEJMc1505196.
5
Identification of novel mutations associated with clofazimine resistance in Mycobacterium tuberculosis.结核分枝杆菌中与氯法齐明耐药相关的新突变的鉴定
J Antimicrob Chemother. 2015 Sep;70(9):2507-10. doi: 10.1093/jac/dkv150. Epub 2015 Jun 4.
6
Bedaquiline susceptibility testing of Mycobacterium tuberculosis in an automated liquid culture system.在自动化液体培养系统中对结核分枝杆菌进行贝达喹啉药敏试验。
J Antimicrob Chemother. 2015 Aug;70(8):2300-5. doi: 10.1093/jac/dkv117. Epub 2015 May 14.
7
Clofazimine for the treatment of multidrug-resistant tuberculosis: prospective, multicenter, randomized controlled study in China.氯法齐明治疗耐多药结核病的前瞻性、多中心、随机对照研究在中国进行。
Clin Infect Dis. 2015 May 1;60(9):1361-7. doi: 10.1093/cid/civ027. Epub 2015 Jan 20.
8
Clofazimine shortens the duration of the first-line treatment regimen for experimental chemotherapy of tuberculosis.氯法齐明可缩短结核病实验性化疗一线治疗方案的疗程。
Proc Natl Acad Sci U S A. 2015 Jan 20;112(3):869-74. doi: 10.1073/pnas.1416951112. Epub 2015 Jan 5.
9
A mutation associated with clofazimine and bedaquiline cross-resistance in MDR-TB following bedaquiline treatment.在使用贝达喹啉治疗后,与耐多药结核病中氯法齐明和贝达喹啉交叉耐药相关的一种突变。
Eur Respir J. 2015 Feb;45(2):554-7. doi: 10.1183/09031936.00142914. Epub 2014 Oct 30.
10
Acquired resistance of Mycobacterium tuberculosis to bedaquiline.结核分枝杆菌对贝达喹啉的获得性耐药性。
PLoS One. 2014 Jul 10;9(7):e102135. doi: 10.1371/journal.pone.0102135. eCollection 2014.

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.

DOI:10.1128/AAC.00239-17
PMID:28320727
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5444180/
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。