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子宫内暴露于生物性疾病修正抗风湿药物与婴儿的影响:感染性并发症、疫苗反应和活疫苗接种的安全性。

In utero exposure to biologic disease-modifying anti-rheumatic drugs and effects to the infant: infectious complications, vaccine response, and safety of live vaccine administration.

机构信息

a Infection Management and Prevention Service, Queensland Children's Hospital , University of Queensland , Brisbane , Australia.

b The Queensland Children's Hospital , Brisbane , Australia.

出版信息

Expert Rev Vaccines. 2019 May;18(5):495-504. doi: 10.1080/14760584.2019.1599286. Epub 2019 Apr 5.

DOI:10.1080/14760584.2019.1599286
PMID:30916600
Abstract

Biologic disease-modifying anti-rheumatic drugs (bDMARDS) are increasingly used in clinical practice for a variety of conditions. Due to concerns surrounding persistence of drug levels and resulting immunosuppression, current case reports recommend against live vaccine administration in the first year of life for an infant exposed to perinatal bDMARDS. As a result, this significantly impacts receipt of rotavirus vaccination, a vaccine recommended in many countries' national immunization program. Area covered: We have reviewed all available published literature to explore the effect of peripartum bDMARDS exposure on infant immune responses, safety of live vaccines, and vaccine efficacy in the first year of life. Expert opinion: We recommend that otherwise healthy newborns with a history of perinatal exposure to bDMARDS should receive rotavirus vaccinations as per the recommended schedule. Bacille Calmette et Guerin vaccine should be withheld in the first year of life. No additional booster doses of inactivated vaccines are required as they appear to mount adequate immune responses to the routine schedule.

摘要

生物制剂类改善病情抗风湿药物(bDMARDs)在临床实践中越来越多地用于多种疾病。由于担心药物水平持续存在和由此产生的免疫抑制,目前的病例报告建议在接触围产期 bDMARDs 的婴儿出生后的第一年不接种活疫苗。因此,这严重影响了轮状病毒疫苗的接种,轮状病毒疫苗是许多国家国家免疫计划中推荐的疫苗。

涵盖领域

我们回顾了所有可用的已发表文献,以探讨围产期 bDMARDs 暴露对婴儿免疫反应、活疫苗安全性以及婴儿出生后第一年疫苗有效性的影响。

专家意见

我们建议,有围产期 bDMARDs 暴露史的健康新生儿应按推荐的时间表接种轮状病毒疫苗。卡介苗应在婴儿出生后的第一年中暂停使用。由于灭活疫苗似乎能对常规免疫程序产生足够的免疫反应,因此无需额外加强剂量。

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