TL1A is an epithelial alarmin that cooperates with IL-33 for initiation of allergic airway inflammation

被引:12
作者
Schmitt, Pauline [1 ]
Duval, Anais [1 ]
Camus, Mylene [1 ]
Lefrancais, Emma [1 ]
Roga, Stephane [1 ]
Dedieu, Cecile [1 ]
Ortega, Nathalie [1 ]
Bellard, Elisabeth [1 ]
Mirey, Emilie [1 ]
Mouton-Barbosa, Emmanuelle [1 ]
Burlet-Schiltz, Odile [1 ]
Gonzalez-de-Peredo, Anne [1 ]
Cayrol, Corinne [1 ]
Girard, Jean-Philippe [1 ]
机构
[1] Univ Toulouse, Univ Toulouse III Paul Sabatier UPS, Inst Pharmacol & Biol Structurale IPBS, CNRS, Toulouse, France
关键词
INNATE LYMPHOID-CELLS; LUNG; ALTERNARIA; CYTOKINE; PROMOTES; ASTHMA; TRANSCRIPTION; IMMUNITY; DR3; TEZEPELUMAB;
D O I
10.1084/jem.20231236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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-9(high) ILC2s during the initiation of allergic airway inflammation. Upon synergistic activation by IL-33 and TL1A, lung ILC2s acquire a transient IL-9(high)GATA3(low) "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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页数:32
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