RORγt eTACs mediate oral tolerance and Treg induction.

IF 10.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-08-04 Epub Date: 2025-04-29 DOI:10.1084/jem.20250573
Im-Hong Sun, Anita E Qualls, Han S Yin, Jiaxi Wang, Matthew P Arvedson, Joe Germino, Nolan K Horner, Sheng Zhong, Juan Du, Martin Valdearcos, Vasilis Ntranos, Richard M Locksley, Roberto R Ricardo-Gonzalez, James M Gardner
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引用次数: 0

Abstract

The immune system must distinguish pathogens from innocuous dietary antigens, but the precise mechanisms and cellular actors remain unclear. Here, we demonstrate that RORγt-lineage APCs are required for oral tolerance. Using lineage tracing and single-cell sequencing, we show these APCs consist of three principal populations: type 3 innate lymphoid cells (ILC3s), RORγt-lineage dendritic cells, and cells expressing Aire called RORγt eTACs (R-eTACs)-also known as Janus or Thetis cells. We show that R-eTACs, but not ILC3s, are required for oral tolerance induction. We find R-eTACs are of probable myeloid origin and uniquely express integrin β8 (Itgb8). Both MHCII and Itgb8 expression in RORγt-lineage cells are necessary to induce food-specific regulatory T cells. Mice lacking R-eTACs or with deletion of MHCII or Itgb8 in the RORγt lineage fail to generate Tregs and instead develop a T-follicular helper response with elevated antigen-specific antibodies. These findings establish R-eTACs as critical mediators of oral tolerance and suggest novel cellular targets to modulate immune tolerance.

r γ - t eTACs介导口服耐受性和Treg诱导。
免疫系统必须将病原体与无害的膳食抗原区分开来,但确切的机制和细胞行为者仍不清楚。在这里,我们证明了rr γt谱系APCs是口服耐受性所必需的。通过谱系追踪和单细胞测序,我们发现这些apc由三个主要群体组成:3型先天淋巴样细胞(ILC3s)、RORγt谱系树突状细胞和表达Aire的RORγt eTACs细胞(R-eTACs)——也被称为Janus或Thetis细胞。我们发现R-eTACs,而不是ILC3s,是口服耐受诱导所必需的。我们发现R-eTACs可能起源于髓细胞,并独特表达整合素β8 (Itgb8)。MHCII和Itgb8在ror γ T细胞中的表达是诱导食物特异性调节性T细胞的必要条件。缺乏R-eTACs或缺失rorγ γt谱系中MHCII或Itgb8的小鼠不能产生Tregs,而是产生抗原特异性抗体升高的t滤泡辅助应答。这些发现证实R-eTACs是口服耐受的关键介质,并提示调节免疫耐受的新细胞靶点。
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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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