Grüneberg R N, Emmerson A M, Cremer A W
Chemotherapy. 1985;31(4):324-8. doi: 10.1159/000238355.
Large populations of rifampicin-sensitive strains of Mycobacterium tuberculosis have been exposed in vitro to changing concentrations of rifampicin (RIF) in line with changes in the blood level of the drug observed during treatment, and to much lower concentrations. Experiments in which the organism was exposed to either 7 or 14 days of cyclically-changing rifampicin concentrations have resulted in the elimination of the M. tuberculosis test strains without the emergence of RIF resistance. The significance of these laboratory findings is discussed in relation to the debate as to whether rifampicin should be used in short courses for the treatment of non-tuberculous infections or whether it should be withheld for fear of inadvertently generating rifampicin-resistant strains of tubercle bacilli. It is argued that the evidence for withholding rifampicin from use in short courses against non-tuberculous infections is slight.
大量对利福平敏感的结核分枝杆菌菌株已在体外暴露于与治疗期间观察到的药物血药浓度变化一致的不断变化的利福平(RIF)浓度下,以及低得多的浓度下。将该生物体暴露于7天或14天周期性变化的利福平浓度的实验已导致结核分枝杆菌测试菌株被清除,且未出现利福平耐药性。结合关于利福平是否应用于非结核感染的短程治疗,或者是否应因担心无意中产生结核杆菌的利福平耐药菌株而停用的争论,讨论了这些实验室发现的意义。有人认为,不将利福平用于非结核感染短程治疗的证据不足。