Dietert Rodney R
Department of Microbiology and Immunology, Cornell University, Ithaca, NY 14853, United States.
Reprod Toxicol. 2017 Mar;68:49-58. doi: 10.1016/j.reprotox.2016.04.026. Epub 2016 May 7.
Through its role as gatekeeper and filter to the external world, the microbiome affects developmental programming of physiological systems including the immune system. In turn, the immune system must tolerate, personalize, and prune the microbiome. Immune and host barrier status in early life significantly effects everything from embryo viability and pregnancy duration to the likelihood of misregulated inflammation, and risk of noncommunicable diseases (NCDs). Since the programming of and interactions among the microbiome, the host defense barrier, and the immune system can affect inflammation-driven health risks across the lifespan, a systems biology-type understanding of these three biological components may be useful. Here, I consider the potential utility of focusing on programming of a newly-defined systems biology unit termed the "microimmunosome."
通过作为通向外部世界的守门人和过滤器,微生物群影响包括免疫系统在内的生理系统的发育编程。反过来,免疫系统必须耐受、个性化并修剪微生物群。生命早期的免疫和宿主屏障状态显著影响从胚胎活力和孕期时长到炎症调节异常的可能性以及非传染性疾病(NCDs)风险的一切。由于微生物群、宿主防御屏障和免疫系统之间的编程及相互作用会影响一生中炎症驱动的健康风险,对这三个生物组成部分的系统生物学类型的理解可能会有所帮助。在此,我考虑专注于一个新定义的系统生物学单元——“微免疫体”的编程的潜在效用。