Gastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
J Crohns Colitis. 2023 Jun 16;17(6):995-1009. doi: 10.1093/ecco-jcc/jjad005.
Biological agents cross the placenta, resulting in detectable blood levels in the neonate. Neonatal vaccinations are essential to prevent serious infections.
To review the effectiveness and safety of vaccines in children exposed to biological drugs in utero and/or those whose mothers received biological agents during lactation.
A systematic bibliographic search was performed.
Infants exposed in utero to anti-tumour necrosis factor drugs [anti-TNFs], vedolizumab or ustekinumab mount adequate serological responses to vaccines. No relevant adverse events for non-live inactivated vaccines have been reported in newborns exposed in utero to biologics. Studies assessing the safety of live-attenuated vaccines administered to infants exposed to biologics in utero have not observed, in general, serious adverse events. However, although no severe complications have been reported with rotavirus live vaccination, several fatal disseminated tuberculosis infections after administration of the BCG live vaccine in infants exposed to anti-TNFs in utero have been reported. Infliximab, adalimumab, and probably also vedolizumab and ustekinumab treatments are considered compatible with breastfeeding, although minuscule amounts of these biologics have been detected in breast milk of treated nursing mothers. Based on the literature available, the benefits from breastfeeding while receiving infliximab [or any other anti-TNF] and at the same time adhering to national infant immunization programmes probably outweigh any hypothetical risk for the infant.
Vaccines appear to be effective in infants exposed to biologics in utero. Inactivated vaccines are probably safe, whereas live-attenuated vaccines should be avoided while the children have detectable levels of biological drugs. Vaccines [non-live and live] are probably safe in children breastfed by mothers treated with biologics.
生物制剂可穿过胎盘,导致新生儿血液中可检测到药物水平。新生儿疫苗接种对于预防严重感染至关重要。
评估在子宫内接触生物药物或其母亲在哺乳期接受生物制剂的儿童使用疫苗的有效性和安全性。
系统地进行文献检索。
在子宫内暴露于抗肿瘤坏死因子药物[抗 TNFs]、vedolizumab 或 ustekinumab 的婴儿对疫苗产生足够的血清学反应。在子宫内暴露于生物制剂的新生儿未报告与非活减毒疫苗相关的不良事件。评估在子宫内暴露于生物制剂的婴儿接种活减毒疫苗安全性的研究通常未观察到严重不良事件。然而,虽然 rotavirus 活疫苗接种未报告严重并发症,但在子宫内暴露于抗 TNFs 的婴儿中接种 BCG 活疫苗后,已报告几例致命播散性结核感染。尽管在接受治疗的哺乳期母亲的母乳中检测到这些生物制剂的微量,但认为 infliximab、adalimumab 以及可能还有 vedolizumab 和 ustekinumab 治疗与母乳喂养兼容。根据现有文献,在接受 infliximab[或任何其他抗 TNF]治疗的同时母乳喂养,并同时遵守国家婴儿免疫接种计划,可能会给婴儿带来更大的益处,而不是任何假设的风险。
疫苗似乎对在子宫内接触生物制剂的婴儿有效。灭活疫苗可能是安全的,而在儿童体内可检测到生物药物水平时,应避免使用活减毒疫苗。对于由接受生物制剂治疗的母亲母乳喂养的儿童,疫苗[非活和活]可能是安全的。