产前流感疫苗接种与儿童过敏和自身免疫性疾病:一项纵向、基于人群的相关队列研究

IF 10.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL PLoS Medicine Pub Date : 2022-04-01 DOI:10.1371/journal.pmed.1003963
Damien Foo, M. Sarna, G. Pereira, H. Moore, A. Regan
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引用次数: 0

摘要

背景很少有研究评估母亲接种流感疫苗对6个月以上儿童过敏性和自身免疫性疾病发展的影响。我们旨在研究子宫内接触季节性灭活流感疫苗(IIV)与随后诊断过敏性和自身免疫性疾病之间的关系。方法和发现这项基于人群的纵向关联队列研究包括来自西澳大利亚州106206名母亲的124760名单胎活产儿童,这些儿童于2012年4月至2016年7月出生,从出生起随访长达5年。在我们的研究队列中,64169名(51.4%)为男性,6566名(5.3%)为原住民和/或托雷斯海峡岛民儿童,随访结束时的平均年龄为3.0岁(标准差,1.3)。暴露是在妊娠期间接受季节性IIV。结果是从医院和/或急诊科(ED)记录中确定的过敏性或自身免疫性疾病的诊断,包括哮喘和过敏反应。根据母亲年龄、原住民和/或托雷斯海峡岛民身份、社会经济地位、体重指数、产次、医疗条件、妊娠并发症、产前吸烟和产前护理,治疗权重的反向概率(IPTW)说明了接种疫苗的基线概率。模型还根据儿童的土著和/或托雷斯海峡岛民身份进行了调整。有14396名(11.5%)母亲接种疫苗的儿童;913名(6.3%)母亲接种过疫苗的儿童和7655名(6.9%)母亲未接种疫苗的儿童分别被诊断为过敏性或自身免疫性疾病。总体而言,母体流感疫苗接种与过敏性或自身免疫性疾病的诊断无关(调整后的危险比[aHR],1.02;95%置信区间[CI],0.95至1.09),我们确定了妊娠晚期流感疫苗接种与哮喘(n=40;aHR,0.70;95%CI,0.50至0.97)和过敏反应(n=36;aHR为0.67;95%CI为0.47至0.95)的诊断之间的负相关;因此,我们的研究结果只能推广到需要住院治疗或急诊科就诊的更严重事件。由于细胞大小较小(即<5),无法确定分层后所有结果的估计值。结论在本研究中,我们观察到子宫内接触流感疫苗与过敏性或自身免疫性疾病的诊断之间没有关联。尽管我们在妊娠后期使用季节性IIV时发现哮喘和过敏反应诊断呈负相关,但还需要更多的研究来证实这一点。总的来说,我们的研究结果支持季节性流感灭活疫苗在妊娠期间与儿童早期过敏性和自身免疫性疾病相关的安全性,并支持当前全球孕产妇疫苗计划和政策的延续。
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Prenatal influenza vaccination and allergic and autoimmune diseases in childhood: A longitudinal, population-based linked cohort study
Background Few studies have evaluated the effect of maternal influenza vaccination on the development of allergic and autoimmune diseases in children beyond 6 months of age. We aimed to investigate the association between in utero exposure to seasonal inactivated influenza vaccine (IIV) and subsequent diagnosis of allergic and autoimmune diseases. Methods and findings This longitudinal, population-based linked cohort study included 124,760 singleton, live-born children from 106,206 mothers in Western Australia (WA) born between April 2012 and July 2016, with up to 5 years of follow-up from birth. In our study cohort, 64,169 (51.4%) were male, 6,566 (5.3%) were Aboriginal and/or Torres Strait Islander children, and the mean age at the end of follow-up was 3.0 (standard deviation, 1.3) years. The exposure was receipt of seasonal IIV during pregnancy. The outcomes were diagnosis of an allergic or autoimmune disease, including asthma and anaphylaxis, identified from hospital and/or emergency department (ED) records. Inverse probability of treatment weights (IPTWs) accounted for baseline probability of vaccination by maternal age, Aboriginal and/or Torres Strait Islander status, socioeconomic status, body mass index, parity, medical conditions, pregnancy complications, prenatal smoking, and prenatal care. The models additionally adjusted for the Aboriginal and/or Torres Strait Islander status of the child. There were 14,396 (11.5%) maternally vaccinated children; 913 (6.3%) maternally vaccinated and 7,655 (6.9%) maternally unvaccinated children had a diagnosis of allergic or autoimmune disease, respectively. Overall, maternal influenza vaccination was not associated with diagnosis of an allergic or autoimmune disease (adjusted hazard ratio [aHR], 1.02; 95% confidence interval [CI], 0.95 to 1.09). In trimester-specific analyses, we identified a negative association between third trimester influenza vaccination and the diagnosis of asthma (n = 40; aHR, 0.70; 95% CI, 0.50 to 0.97) and anaphylaxis (n = 36; aHR, 0.67; 95% CI, 0.47 to 0.95).We did not capture outcomes diagnosed in a primary care setting; therefore, our findings are only generalizable to more severe events requiring hospitalization or presentation to the ED. Due to small cell sizes (i.e., <5), estimates could not be determined for all outcomes after stratification. Conclusions In this study, we observed no association between in utero exposure to influenza vaccine and diagnosis of allergic or autoimmune diseases. Although we identified a negative association of asthma and anaphylaxis diagnosis when seasonal IIV was administered later in pregnancy, additional studies are needed to confirm this. Overall, our findings support the safety of seasonal inactivated influenza vaccine during pregnancy in relation to allergic and autoimmune diseases in early childhood and support the continuation of current global maternal vaccine programs and policies.
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来源期刊
PLoS Medicine
PLoS Medicine 医学-医学:内科
CiteScore
21.60
自引率
0.60%
发文量
227
审稿时长
3 months
期刊介绍: PLOS Medicine aims to be a leading platform for research and analysis on the global health challenges faced by humanity. The journal covers a wide range of topics, including biomedicine, the environment, society, and politics, that affect the well-being of individuals worldwide. It particularly highlights studies that contribute to clinical practice, health policy, or our understanding of disease mechanisms, with the ultimate goal of improving health outcomes in diverse settings. Unwavering in its commitment to ethical standards, PLOS Medicine ensures integrity in medical publishing. This includes actively managing and transparently disclosing any conflicts of interest during the reporting, peer review, and publication processes. The journal promotes transparency by providing visibility into the review and publication procedures. It also encourages data sharing and the reuse of published work. Author rights are upheld, allowing them to retain copyright. Furthermore, PLOS Medicine strongly supports Open Access publishing, making research articles freely available to all without restrictions, facilitating widespread dissemination of knowledge. The journal does not endorse drug or medical device advertising and refrains from exclusive sales of reprints to avoid conflicts of interest.
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