Fu Liuhui, Littman Dan R
Department of Cell Biology, New York University School of Medicine, New York, New York, USA.
Howard Hughes Medical Institute, New York, New York, USA.
Immunol Rev. 2026 Jan;337(1):e70082. doi: 10.1111/imr.70082.
The immune system is tasked with mounting effective responses to pathogens while preventing inflammation triggered by innocuous antigens, including those derived from self, food, and commensal microbes. This balance is especially critical in the intestine, where dietary and microbial antigens are constantly encountered. Peripherally induced regulatory T cells (pTreg or iTreg) play a key role in suppressing inappropriate immune activation and maintaining gut homeostasis. Elucidating how pTreg cells are generated along the gastrointestinal tract is therefore critical to understanding peripheral tolerance. Recent studies have revealed that intestinal antigen-specific pTreg cell differentiation is induced by a distinct lineage of antigen-presenting cells (APCs) requiring expression of the transcription factors RORγt and PRDM16. Genetic perturbation of these APCs results not only in microbiota-specific proinflammatory T cell responses but also in the breakdown of oral tolerance, which in turn predisposes to allergic inflammation. In this review, we summarize the discovery of these tolerance-inducing APCs, highlight their role in instructing pTreg cell differentiation in response to microbiota and dietary antigens, and discuss the regulatory networks that support their function during intestinal immune tolerance.
免疫系统的任务是对病原体发起有效的免疫反应,同时防止由无害抗原引发的炎症,这些无害抗原包括来自自身、食物和共生微生物的抗原。这种平衡在肠道中尤为关键,因为在肠道中会不断接触到饮食和微生物抗原。外周诱导调节性T细胞(pTreg或iTreg)在抑制不适当的免疫激活和维持肠道内环境稳定方面发挥着关键作用。因此,阐明胃肠道中pTreg细胞是如何产生的对于理解外周耐受至关重要。最近的研究表明,肠道抗原特异性pTreg细胞的分化是由一类独特的抗原呈递细胞(APC)诱导的,这类细胞需要表达转录因子RORγt和PRDM16。这些APC的基因扰动不仅会导致微生物群特异性促炎T细胞反应,还会导致口服耐受的破坏,进而易引发过敏性炎症。在这篇综述中,我们总结了这些诱导耐受的APC的发现,强调了它们在指导pTreg细胞针对微生物群和饮食抗原进行分化中的作用,并讨论了在肠道免疫耐受过程中支持其功能的调控网络。