Cheifetz Talia R, Knoop Kathryn A
Department of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Mayo Graduate School of Biomedical Sciences, Rochester, Minnesota, USA.
Immunol Rev. 2024 Sep;326(1):17-34. doi: 10.1111/imr.13366. Epub 2024 Jul 13.
Oral tolerance promotes the suppression of immune responses to innocuous antigen and is primarily mediated by regulatory T cell (Tregs). The development of oral tolerance begins in early life during a "window of tolerance," which occurs around weaning and is mediated by components in breastmilk. Herein, we review the factors dictating this window and how Tregs are uniquely educated in early life. In early life, the translocation of luminal antigen for Treg induction is primarily dictated by goblet cell-associated antigen passages (GAPs). GAPs in the colon are negatively regulated by maternally-derived epidermal growth factor and the microbiota, restricting GAP formation to the "periweaning" period (postnatal day 11-21 in mice, 4-6 months in humans). The induction of solid food also promotes the diversification of the bacteria such that bacterially-derived metabolites known to promote Tregs-short-chain fatty acids, tryptophan metabolites, and bile acids-peak during the periweaning phase. Further, breastmilk immunoglobulins-IgA and IgG-regulate both microbial diversity and the interaction of microbes with the epithelium, further controlling which antigens are presented to T cells. Overall, these elements work in conjunction to induce a long-lived population of Tregs, around weaning, that are crucial for maintaining homeostasis in adults.
口服耐受促进对无害抗原的免疫反应抑制,主要由调节性T细胞(Tregs)介导。口服耐受的发展始于生命早期的一个“耐受窗口”,该窗口发生在断奶前后,由母乳中的成分介导。在此,我们回顾了决定这个窗口的因素以及Tregs在生命早期是如何被独特地塑造的。在生命早期,用于诱导Tregs的腔内抗原转运主要由杯状细胞相关抗原通道(GAPs)决定。结肠中的GAPs受到母体来源的表皮生长因子和微生物群的负调控,将GAP形成限制在“断奶前后”时期(小鼠出生后第11 - 21天,人类4 - 6个月)。固体食物的引入也促进了细菌的多样化,使得已知促进Tregs的细菌衍生代谢产物——短链脂肪酸、色氨酸代谢产物和胆汁酸——在断奶前后阶段达到峰值。此外,母乳中的免疫球蛋白——IgA和IgG——调节微生物多样性以及微生物与上皮细胞的相互作用,进一步控制呈递给T细胞的抗原。总体而言,这些因素共同作用,在断奶前后诱导产生一群长寿的Tregs,它们对于维持成年人的内环境稳定至关重要。