Clinical Research Advancement Section, Research Institute, National Center for Global Health and Medicine, Tokyo 162-8655, Japan; Division of Biochemistry, Faculty of Pharmacy and Graduate School of Pharmaceutical Science, Keio University, Tokyo 105-8512, Japan.
Division of Biochemistry, Faculty of Pharmacy and Graduate School of Pharmaceutical Science, Keio University, Tokyo 105-8512, Japan.
Cell Rep. 2024 Jul 23;43(7):114490. doi: 10.1016/j.celrep.2024.114490. Epub 2024 Jul 10.
Although oral tolerance is a critical system in regulating allergic disorders, the mechanisms by which dietary factors regulate the induction and maintenance of oral tolerance remain unclear. To address this, we explored the differentiation and function of various immune cells in the intestinal immune system under fasting and ad libitum-fed conditions before oral ovalbumin (OVA) administration. Fasting mitigated OVA-specific Treg expansion, which is essential for oral tolerance induction. This abnormality mainly resulted from functional defects in the CX3CR1 cells responsible for the uptake of luminal OVA and reduction of tolerogenic CD103 dendritic cells. Eventually, fasting impaired the preventive effect of oral OVA administration on asthma and allergic rhinitis development. Specific food ingredients, namely carbohydrates and arginine, were indispensable for oral tolerance induction by activating glycolysis and mTOR signaling. Overall, prior food intake and nutritional signals are critical for maintaining immune homeostasis by inducing tolerance to ingested food antigens.
尽管口服耐受是调节过敏疾病的关键系统,但膳食因素如何调节口服耐受的诱导和维持仍不清楚。为了解决这个问题,我们在给予口服卵清蛋白(OVA)之前,研究了空腹和随意进食条件下肠道免疫系统中各种免疫细胞的分化和功能。禁食减轻了对口服耐受诱导至关重要的 OVA 特异性 Treg 扩增。这种异常主要是由于负责摄取腔内分泌物 OVA 和减少耐受 CD103 树突状细胞的 CX3CR1 细胞的功能缺陷所致。最终,禁食损害了口服 OVA 给药对哮喘和过敏性鼻炎发展的预防作用。特定的食物成分,即碳水化合物和精氨酸,通过激活糖酵解和 mTOR 信号通路,对口服耐受诱导是必不可少的。总的来说,先前的食物摄入和营养信号对于通过诱导对摄入食物抗原的耐受来维持免疫稳态是至关重要的。