Ragon Institute of MGH, MIT and Harvard, Cambridge, MA, 02139, USA.
Vaccine Evaluation Center, BC Children's Hospital, Department of Pediatrics, Division of Infectious Diseases, University of British Columbia, Vancouver, BC, Canada.
Semin Immunopathol. 2017 Nov;39(6):605-613. doi: 10.1007/s00281-017-0653-x. Epub 2017 Oct 2.
As placental mammals, the pregnant women and the fetus have intense and prolonged interactions during gestation. There is increasing evidence that multiple molecular as well as cellular components originating in pregnant women are transferred to the fetus. The transfer of maternal antibodies has long been recognized as a central component of newborn immunity against pathogens. More recent studies indicate that inflammatory mediators, micronutrients, microbial products and maternal cells are transferred in utero and influence the fetal immune system. Together, these multiple signals are likely to form a complex network of interactions that program the neonatal immune system and tune its homeostatic regulation. Maternal disorders, in particular infectious diseases, modify these signals and may thereby alter immunity in early life. Understanding maternal programming of the newborn immune system could provide a basis for interventions promoting child health.
作为胎盘哺乳动物,孕妇和胎儿在妊娠期间会进行强烈而持久的相互作用。越来越多的证据表明,源自孕妇的多种分子和细胞成分被转移到胎儿中。母体抗体的转移早已被认为是新生儿对病原体产生免疫力的核心组成部分。最近的研究表明,炎症介质、微量营养素、微生物产物和母体细胞都在子宫内转移,并影响胎儿的免疫系统。这些多种信号共同构成了一个复杂的相互作用网络,为新生儿的免疫系统编程并调节其体内平衡调节。母体疾病,特别是传染病,会改变这些信号,并可能因此改变生命早期的免疫。了解母体对新生儿免疫系统的编程可能为促进儿童健康的干预措施提供基础。