From the, Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau.
Research Centre for Vitamins and Vaccines (CVIVA), Statens Serum Institute, Copenhagen S, Denmark.
J Intern Med. 2020 Dec;288(6):614-624. doi: 10.1111/joim.13084. Epub 2020 May 25.
Bacillus Calmette-Guérin (BCG) vaccine against tuberculosis (TB) is recommended at birth in TB-endemic areas. Currently, BCG vaccination programmes use "BCG vaccination coverage by 12 months of age" as the performance indicator. Previous studies suggest that BCG-vaccinated children, who develop a scar, have better overall survival compared with BCG-vaccinated children, who do not develop a scar. We summarized the available studies of BCG scarring and child survival. A structured literature search for studies with original data and analysis of BCG scarring and mortality were performed. Combined analyses on the effect of BCG scarring on overall mortality. We identified six studies covering seven cohorts, all from Guinea-Bissau, West Africa, with evaluation of BCG scarring amongst BCG-vaccinated children and follow-up for mortality. Determinants of BCG scarring were BCG strain, intradermal injection route, size of injection wheal, and co-administered vaccines and micronutrients. In a combined analysis, having a BCG scar vs. no BCG scar was associated with a mortality rate ratio (MRR) of 0.61 (95% CI: 0.51-0.74). The proportion with a BCG scar varied from 52 to 93%; the estimated effect of a BCG scar was not associated with the scar prevalence. The effect was strongest in the first (MRR = 0.48 (0.37-0.62)) and second (MRR = 0.63 (0.44-0.92)) year of life, and in children BCG-vaccinated in the neonatal period (MRR = 0.45 (0.36-0.55)). The effect was not explained by protection against TB. Confounding and genetic factors are unlikely to explain the strong association between BCG scarring and subsequent survival. Including "BCG scar prevalence" as a BCG vaccination programme performance indicator should be considered. The effect of revaccinating scar-negative children should be studied.
卡介苗(BCG)疫苗被推荐用于结核病(TB)流行地区的新生儿接种。目前,BCG 疫苗接种项目使用“12 月龄 BCG 接种覆盖率”作为绩效指标。既往研究提示,与未形成瘢痕的 BCG 接种儿童相比,形成瘢痕的 BCG 接种儿童的总体生存率更高。我们对有关 BCG 瘢痕形成与儿童生存的现有研究进行了总结。对具有原始数据的研究进行了结构化文献检索,并对 BCG 瘢痕形成与死亡率进行了分析。对 BCG 瘢痕形成对总体死亡率的影响进行了综合分析。我们共纳入了 6 项研究,共涉及 7 个队列,均来自于西非的几内亚比绍,评估了 BCG 接种儿童的 BCG 瘢痕形成情况,并随访其死亡率。影响 BCG 瘢痕形成的因素包括 BCG 菌株、皮内注射途径、注射丘疹大小、同时使用的疫苗和微量营养素。综合分析结果显示,与无 BCG 瘢痕相比,有 BCG 瘢痕与死亡率的比值比(MRR)为 0.61(95%CI:0.51-0.74)。有 BCG 瘢痕的比例为 52%~93%;估计的 BCG 瘢痕效应与瘢痕流行率无关。该效应在生命的前(MRR=0.48(0.37-0.62))和第二年(MRR=0.63(0.44-0.92))以及新生儿期(MRR=0.45(0.36-0.55))接种 BCG 的儿童中最强。该效应不能用预防结核病来解释。混杂因素和遗传因素不太可能解释 BCG 瘢痕形成与随后生存之间的强关联。将“BCG 瘢痕流行率”作为 BCG 疫苗接种项目的绩效指标应加以考虑。应该研究对瘢痕阴性儿童进行复种的效果。