{"title":"Natural antigen landscape shaping intestinal Treg cells: Self, diet, and microbiota.","authors":"Jaeu Yi","doi":"10.1080/08830185.2026.2677909","DOIUrl":null,"url":null,"abstract":"<p><p>The gut represents a melting pot of distinct classes of antigens derived from self antigens, dietary components, and the commensal microbiota. To maintain tolerance to innocuous antigens while preserving the capacity to respond to potentially harmful microorganisms, the immune system has evolved tightly regulated mechanisms centered on the generation of Foxp3<sup>+</sup> regulatory T (Treg) cells at mucosal surfaces. Although early insights into intestinal Treg development were largely derived from studies using model dietary antigens or selected microbial species, a substantial gap remains in our understanding of the natural antigen landscape that elicits Treg responses <i>in vivo</i>. In this review, we discuss recent advances based on TCR classification approaches that define intestinal Treg T cell receptor (TCR) responses according to <i>in vivo</i> antigen reactivity, and we highlight key future directions for elucidating the functional roles of antigen-presenting cell subsets and their associated peptide landscapes in shaping intestinal Treg biology.</p>","PeriodicalId":14333,"journal":{"name":"International Reviews of Immunology","volume":" ","pages":"304-312"},"PeriodicalIF":5.4000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Reviews of Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/08830185.2026.2677909","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/25 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The gut represents a melting pot of distinct classes of antigens derived from self antigens, dietary components, and the commensal microbiota. To maintain tolerance to innocuous antigens while preserving the capacity to respond to potentially harmful microorganisms, the immune system has evolved tightly regulated mechanisms centered on the generation of Foxp3+ regulatory T (Treg) cells at mucosal surfaces. Although early insights into intestinal Treg development were largely derived from studies using model dietary antigens or selected microbial species, a substantial gap remains in our understanding of the natural antigen landscape that elicits Treg responses in vivo. In this review, we discuss recent advances based on TCR classification approaches that define intestinal Treg T cell receptor (TCR) responses according to in vivo antigen reactivity, and we highlight key future directions for elucidating the functional roles of antigen-presenting cell subsets and their associated peptide landscapes in shaping intestinal Treg biology.
期刊介绍:
This review journal provides the most current information on basic and translational research in immunology and related fields. In addition to invited reviews, the journal accepts for publication articles and editorials on relevant topics proposed by contributors. Each issue of International Reviews of Immunology contains both solicited and unsolicited review articles, editorials, and ''In-this-Issue'' highlights. The journal also hosts reviews that position the authors'' original work relative to advances in a given field, bridging the gap between annual reviews and the original research articles.
This review series is relevant to all immunologists, molecular biologists, microbiologists, translational scientists, industry researchers, and physicians who work in basic and clinical immunology, inflammatory and allergic diseases, vaccines, and additional topics relevant to medical research and drug development that connect immunology to disciplines such as oncology, cardiovascular disease, and metabolic disorders.
Covered in International Reviews of Immunology: Basic and developmental immunology (innate and adaptive immunity; inflammation; and tumor and microbial immunology); Clinical research (mechanisms of disease in man pertaining to infectious diseases, autoimmunity, allergy, oncology / immunology); and Translational research (relevant to biomarkers, diagnostics, vaccines, and drug development).