TL1A 是一种上皮警报蛋白,它与 IL-33 相互配合,共同引发过敏性气道炎症。

IF 12.6 1区 医学 Q1 IMMUNOLOGY Journal of Experimental Medicine Pub Date : 2024-06-03 Epub Date: 2024-04-10 DOI:10.1084/jem.20231236
Pauline Schmitt, Anais Duval, Mylène Camus, Emma Lefrançais, Stéphane Roga, Cécile Dedieu, Nathalie Ortega, Elisabeth Bellard, Emilie Mirey, Emmanuelle Mouton-Barbosa, Odile Burlet-Schiltz, Anne Gonzalez-de-Peredo, Corinne Cayrol, Jean-Philippe Girard
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引用次数: 0

摘要

上皮源性细胞因子或警报素,如白细胞介素-33(IL-33)和胸腺基质淋巴细胞生成素(TSLP),是 2 型免疫和哮喘的主要参与者。在这里,我们证明了 TNF 样配体 1A(TL1A)是一种上皮警戒素,在小鼠和人类肺泡上皮稳态时均为组成型表达,它与 IL-33 相互配合,在过敏性气道炎症的起始阶段早期诱导 IL-9 高的 ILC2。在 IL-33 和 TL1A 的协同激活下,肺部 ILC2 获得短暂的 IL-9highGATA3low "ILC9 "表型,并产生大量的 IL-9。结合大规模蛋白质组学分析、肺内显微镜和 ILC9 细胞的收养性转移发现,IL-9 的高表达区分了多细胞因子产生状态的活化 ILC2s,它们启动 IL-5 依赖性过敏性气道炎症的能力更强。与 IL-33 和 TSLP 相似,TL1A 也在健康和哮喘患者肺部的气道基础细胞中表达。这些结果表明,TL1A 是一种上皮源性细胞因子,也是 IL-33 在气道中的重要辅助因子。
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TL1A is an epithelial alarmin that cooperates with IL-33 for initiation of allergic airway inflammation.

Epithelium-derived cytokines or alarmins, such as interleukin-33 (IL-33) and thymic stromal lymphopoietin (TSLP), are major players in type 2 immunity and asthma. Here, we demonstrate that TNF-like ligand 1A (TL1A) is an epithelial alarmin, constitutively expressed in alveolar epithelium at steady state in both mice and humans, which cooperates with IL-33 for early induction of IL-9high ILC2s during the initiation of allergic airway inflammation. Upon synergistic activation by IL-33 and TL1A, lung ILC2s acquire a transient IL-9highGATA3low "ILC9" phenotype and produce prodigious amounts of IL-9. A combination of large-scale proteomic analyses, lung intravital microscopy, and adoptive transfer of ILC9 cells revealed that high IL-9 expression distinguishes a multicytokine-producing state-of-activated ILC2s with an increased capacity to initiate IL-5-dependent allergic airway inflammation. Similar to IL-33 and TSLP, TL1A is expressed in airway basal cells in healthy and asthmatic human lungs. Together, these results indicate that TL1A is an epithelium-derived cytokine and an important cofactor of IL-33 in the airways.

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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.
期刊最新文献
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