Morgane Hilaire, Angélina Mimoun, Léonie Cagnet, Rémy Villette, Aristeidis Roubanis, Hugo Sentenac, Benoît L. Salomon
{"title":"新生儿调节性T细胞在多个组织中持续存在到成年,在皮肤中高度富集","authors":"Morgane Hilaire, Angélina Mimoun, Léonie Cagnet, Rémy Villette, Aristeidis Roubanis, Hugo Sentenac, Benoît L. Salomon","doi":"10.1126/sciadv.adx8037","DOIUrl":null,"url":null,"abstract":"<div >Foxp3<sup>+</sup> regulatory T cells (T<sub>regs</sub>) reside in both lymphoid and nonlymphoid organs, where they play a crucial role in immune tolerance and tissue homeostasis. In mice, T<sub>regs</sub> begin colonizing these tissues shortly after birth, contributing to long-term immune response regulation therein. However, the kinetics of T<sub>reg</sub> generation across different tissues remains unclear. Here, we investigate T<sub>reg</sub> ontogeny from birth to adulthood in various tissues. In lymphoid organs, the adult T<sub>reg</sub> pool is continuously replenished with cells generated at different ages. In contrast, the skin retains a large fraction of T<sub>regs</sub> that colonize the tissue during the neonatal period, with minimal turnover in adulthood. The liver, lungs, and colon exhibit intermediate T<sub>reg</sub> renewal dynamics. Notably, neonatal T<sub>regs</sub> that persist into adulthood display a more activated phenotype and express markers associated with tissue-resident T<sub>regs</sub> and type 2 immunity. Our findings reveal tissue-specific differences in T<sub>reg</sub> generation kinetics and highlight a major phenotypic shift between neonatal and adult-derived T<sub>regs</sub>.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 40","pages":""},"PeriodicalIF":12.5000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adx8037","citationCount":"0","resultStr":"{\"title\":\"Neonatal regulatory T cells persist into adulthood across multiple tissues with high enrichment in the skin\",\"authors\":\"Morgane Hilaire, Angélina Mimoun, Léonie Cagnet, Rémy Villette, Aristeidis Roubanis, Hugo Sentenac, Benoît L. Salomon\",\"doi\":\"10.1126/sciadv.adx8037\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div >Foxp3<sup>+</sup> regulatory T cells (T<sub>regs</sub>) reside in both lymphoid and nonlymphoid organs, where they play a crucial role in immune tolerance and tissue homeostasis. In mice, T<sub>regs</sub> begin colonizing these tissues shortly after birth, contributing to long-term immune response regulation therein. However, the kinetics of T<sub>reg</sub> generation across different tissues remains unclear. Here, we investigate T<sub>reg</sub> ontogeny from birth to adulthood in various tissues. In lymphoid organs, the adult T<sub>reg</sub> pool is continuously replenished with cells generated at different ages. In contrast, the skin retains a large fraction of T<sub>regs</sub> that colonize the tissue during the neonatal period, with minimal turnover in adulthood. The liver, lungs, and colon exhibit intermediate T<sub>reg</sub> renewal dynamics. Notably, neonatal T<sub>regs</sub> that persist into adulthood display a more activated phenotype and express markers associated with tissue-resident T<sub>regs</sub> and type 2 immunity. Our findings reveal tissue-specific differences in T<sub>reg</sub> generation kinetics and highlight a major phenotypic shift between neonatal and adult-derived T<sub>regs</sub>.</div>\",\"PeriodicalId\":21609,\"journal\":{\"name\":\"Science Advances\",\"volume\":\"11 40\",\"pages\":\"\"},\"PeriodicalIF\":12.5000,\"publicationDate\":\"2025-10-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.science.org/doi/reader/10.1126/sciadv.adx8037\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Advances\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.science.org/doi/10.1126/sciadv.adx8037\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adx8037","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Neonatal regulatory T cells persist into adulthood across multiple tissues with high enrichment in the skin
Foxp3+ regulatory T cells (Tregs) reside in both lymphoid and nonlymphoid organs, where they play a crucial role in immune tolerance and tissue homeostasis. In mice, Tregs begin colonizing these tissues shortly after birth, contributing to long-term immune response regulation therein. However, the kinetics of Treg generation across different tissues remains unclear. Here, we investigate Treg ontogeny from birth to adulthood in various tissues. In lymphoid organs, the adult Treg pool is continuously replenished with cells generated at different ages. In contrast, the skin retains a large fraction of Tregs that colonize the tissue during the neonatal period, with minimal turnover in adulthood. The liver, lungs, and colon exhibit intermediate Treg renewal dynamics. Notably, neonatal Tregs that persist into adulthood display a more activated phenotype and express markers associated with tissue-resident Tregs and type 2 immunity. Our findings reveal tissue-specific differences in Treg generation kinetics and highlight a major phenotypic shift between neonatal and adult-derived Tregs.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.