Brewer T F, Colditz G A
Infectious Disease Unit, Massachusetts General Hospital, Boston.
Clin Infect Dis. 1995 Jan;20(1):126-35. doi: 10.1093/clinids/20.1.126.
Bacille Calmette-Guérin (BCG) vaccination for the prevention of tuberculosis has been used in humans since 1921. Furthermore, for > 60 years it has been possible to separate BCG strains (defined here as a BCG vaccine maintained in a particular laboratory and used in a particular trial or set of trials) on the basis of in vitro and in vivo tests. Investigators have concluded that differences in the BCG strains used in efficacy trials on humans may be responsible for the wide range in levels of protection from tuberculosis reported in those trials. We review the development of the separate strains used in the trials included in a recent meta-analysis and examine data for and against the protective efficacy of different BCG strains. The difficulties in correlating results of in vitro and in vivo tests with protective efficacy in humans are discussed. The limited data available from human studies suggest that the BCG strain used for vaccination is not a significant determinant of the overall efficacy in the prevention of tuberculosis.
自1921年以来,卡介苗(BCG)一直用于预防人类结核病。此外,60多年来,基于体外和体内试验,已能够区分卡介苗菌株(在此定义为保存在特定实验室并用于特定试验或一系列试验的卡介苗疫苗)。研究人员得出结论,在人体疗效试验中使用的卡介苗菌株差异可能是这些试验中报道的结核病保护水平差异很大的原因。我们回顾了最近一项荟萃分析中所纳入试验中使用的不同菌株的发展情况,并研究了支持和反对不同卡介苗菌株保护效力的数据。讨论了将体外和体内试验结果与人体保护效力相关联时存在的困难。人体研究中可用的数据有限,这表明用于接种的卡介苗菌株并非预防结核病总体效力的重要决定因素。