Adipose tissue harbors pathogenic T cells in obesity that exacerbate inflammatory arthritis.

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-09-01 Epub Date: 2025-07-07 DOI:10.1084/jem.20240677
Heather J Faust, Margaret H Chang, A Helena Jonsson, Erin Theisen, Nelson M LaMarche, William V Trim, Lydia Lynch, Peter A Nigrovic, Michael B Brenner
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引用次数: 0

Abstract

Obesity worsens inflammatory arthritis severity, even in non-load-bearing joints, but the mechanism is unknown. Here, we show that there is an immunological mechanism mediated by T cells in adipose tissue. Using an antigen-induced arthritis model with trackable, arthritis-inducing CD8+ OT-I T cells, we found that OT-I T cells home to visceral adipose tissue (VAT) and expand there in the obese high-fat diet (HFD) context. Transplant of VAT from arthritic mice increased arthritis severity in naïve recipient mice and was ameliorated by CD8 T cell depletion. Bulk RNA sequencing identified pro-inflammatory changes to OT-I T cells in VAT characterized by increased IFN α and γ signaling after HFD. Intraperitoneal injection of IFNα, but not IFNγ, expanded CD8 T cell numbers in VAT. HFD-induced expansion of VAT CD8 T cells was ameliorated with global Ifnar1 deletion, and importantly, genetic deletion of Ifnar1 in T cells decreased arthritis severity in obese mice. These results provide a mechanistic explanation of how obesity worsens autoimmunity.

肥胖的脂肪组织中含有致病性T细胞,会加剧炎症性关节炎。
肥胖会加重炎症性关节炎的严重程度,即使在非承重关节中也是如此,但其机制尚不清楚。在这里,我们表明在脂肪组织中存在由T细胞介导的免疫机制。利用抗原诱导的关节炎模型和可追踪的,诱导关节炎的CD8+ OT-I T细胞,我们发现OT-I T细胞回到内脏脂肪组织(VAT)并在肥胖高脂肪饮食(HFD)背景下在那里扩张。来自关节炎小鼠的VAT移植增加naïve受体小鼠的关节炎严重程度,并通过CD8 T细胞耗竭得到改善。大量RNA测序发现VAT中OT-I - T细胞的促炎变化,其特征是HFD后IFN α和γ信号的增加。腹腔注射IFNα,而非IFNγ,可增加VAT中CD8 T细胞的数量。hfd诱导的VAT CD8 T细胞扩增随着Ifnar1的缺失而得到改善,重要的是,T细胞中Ifnar1的基因缺失降低了肥胖小鼠关节炎的严重程度。这些结果为肥胖如何恶化自身免疫提供了机制上的解释。
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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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