Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III-Paul Sabatier (UPS) , Toulouse, France.
J Exp Med. 2024 Jun 3;221(6). doi: 10.1084/jem.20231236. Epub 2024 Apr 10.
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.
上皮细胞衍生的细胞因子或警报素,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 TNF 样配体 1A (TL1A) 是一种上皮细胞警报素,在稳态下在小鼠和人类的肺泡上皮细胞中持续表达,它与 IL-33 合作,在过敏性气道炎症的起始阶段早期诱导 IL-9high ILC2s。在 IL-33 和 TL1A 的协同激活下,肺 ILC2s 获得短暂的 IL-9highGATA3low“ILC9”表型,并产生大量的 IL-9。大规模蛋白质组学分析、肺活体显微镜检查和 ILC9 细胞的过继转移的组合表明,高 IL-9 表达区分了具有增加启动 IL-5 依赖性过敏性气道炎症能力的多细胞因子产生的激活状态 ILC2s。与 IL-33 和 TSLP 相似,TL1A 在健康和哮喘人类肺部的气道基底细胞中表达。这些结果表明,TL1A 是一种上皮细胞衍生的细胞因子,是气道中 IL-33 的重要辅助因子。