新生儿接种卡介苗预防哮喘:来自MIS BAIR随机对照试验的结果。

IF 4.5
Laure F Pittet, Emily K Forbes, Susan Donath, Kate L Francis, Kaya Gardiner, Katie L Flanagan, Anne-Louise Ponsonby, Roy Robins-Browne, Frank Shann, Mike South, Peter Vuillermin, Dan Casalaz, Nigel Curtis, Nicole L Messina
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引用次数: 0

摘要

背景:哮喘在世界范围内具有重大影响,但预防策略仍然有限。我们的目的是评估新生儿卡介苗接种通过调节早期免疫预防哮喘的功效。方法:墨尔本婴儿研究:减少卡介苗过敏和感染(MIS BAIR)是澳大利亚维多利亚州的一项3期多中心随机对照试验。婴儿在出生后10天内被随机分配接受bcg -丹麦疫苗或不进行干预。5岁时哮喘的发病率是根据国际儿童哮喘和过敏研究的问题来估计的。临床试验:gov (NCT01906853)。结果:共有1272名婴儿被随机化。BCG组哮喘校正发病率为14.4%,对照组为16.0%(校正风险差[aRD] -1.7个百分点;95%ci -7.4, 3.9)。次要结局,包括严重哮喘和使用预防药物,显示出类似的趋势,aRD分别为-3.9 (95%CI -7.7, 0.0)和-5.6 (95%CI -10.9, -0.4),有利于卡介苗组。在父母一方或双方均患有哮喘的参与者中,BCG组的哮喘发生率(17.6%)也低于对照组(24.7%;aRD -7.2;95%CI -15.9, 1.5),但相互作用的检验无统计学意义(p = .07)。结论:虽然点估计表明卡介苗接种可能预防哮喘,但估计的广泛不确定性意味着需要进一步的更大样本量的研究来评估卡介苗接种在其主要适应症之外的长期益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neonatal BCG vaccination to prevent asthma: Results from the MIS BAIR randomized controlled trial.

Background: Asthma has a significant impact worldwide, but prevention strategies remain limited. We aimed to evaluate the efficacy of neonatal BCG vaccination in preventing asthma by modulating early-life immunity.

Methods: The Melbourne Infant Study: BCG for Allergy and Infection Reduction (MIS BAIR) was a phase 3 multicentre randomized controlled trial in Victoria, Australia. Infants were randomly assigned to receive the BCG-Denmark vaccine or no intervention within 10 days of birth. The incidence of asthma at 5 years of age was estimated using the International Study of Asthma and Allergies in Childhood questions.

Clinicaltrial: gov (NCT01906853).

Results: A total of 1272 infants were randomized. The adjusted incidence of asthma was 14.4% in the BCG group compared to 16.0% in the control group (adjusted risk difference [aRD] -1.7 percentage points; 95%CI -7.4, 3.9). Secondary outcomes, including severe asthma and use of preventer medication, showed similar trends, with an aRD of -3.9 (95%CI -7.7, 0.0), and -5.6 (95%CI -10.9, -0.4), respectively, favoring the BCG group. Among participants with one or both parents asthmatic, the rate of asthma was also lower in the BCG group (17.6%) compared with the control group (24.7%; aRD -7.2; 95%CI -15.9, 1.5), although a test for interaction was not significant (p = .07).

Conclusions: While the point estimates suggested BCG vaccination might protect against asthma, the wide uncertainty around the estimates means further studies with larger sample sizes are needed to evaluate the long-term benefits of BCG vaccination beyond its primary indication.

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