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The ins and outs of mycobacterium tuberculosis drug susceptibility testing: Themed review 'Therapeutic efficiency in the presence of resistance mechanisms: (when) to give-or not to give?'

机译:结核分枝杆菌药敏试验的来龙去脉:主题综述“在存在耐药机制的情况下的治疗效率:(何时)给予或不给予?”

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摘要

Clin Microbiol Infect ABSTRACT: Drug susceptibility testing of Mycobacterium tuberculosis in the diagnostic laboratory classifies clinical isolates as either drug-'resistant' or drug-'susceptible', on the basis of their ability to grow in the presence of a 'critical concentration' of the test compound. From knowledge of the mechanisms that underlie drug resistance, it has become evident that drug resistance in M. tuberculosis is quite heterogeneous and involves low-level, moderate-level and high-level drug resistance phenotypes. Different mutations are associated with different levels of phenotypic resistance, and the acquisition of a genetic alteration leading to a decrease in drug susceptibility does not inevitably exclude the affected compound from treatment regimens. As a result, the simple categorization of clinical M. tuberculosis isolates as 'resistant' on the basis of susceptibility testing at 'critical concentrations' may need to be revised and supplemented by quantitative measures of resistance testing to reflect the biological complexity of drug resistance, with the view of optimally exploiting the compounds available for treatment.
机译:Clin Microbiol Infect摘要:在诊断实验室中,结核分枝杆菌的药敏测试将临床分离株根据其在“临界浓度”的浓度下生长的能力分类为“耐药”或“易感”。测试化合物。从对抗药性的基础机理的认识来看,结核分枝杆菌的抗药性非常不均一,涉及低,中,高水平的抗药性表型。不同的突变与不同水平的表型抗性相关,获得导致药物敏感性降低的遗传改变并不能不可避免地将受影响的化合物排除在治疗方案之外。结果,可能需要对基于``关键浓度''的药敏试验将临床结核分枝杆菌分离为``耐药''的简单分类进行补充,并通过定量的耐药性检测方法加以补充,以反映耐药性的生物学复杂性,为了最佳地利用可用于治疗的化合物。

著录项

  • 作者

    Böttger, E C;

  • 作者单位
  • 年度 2011
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  • 原文格式 PDF
  • 正文语种 eng
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