TL1A is an epithelial alarmin that cooperates with IL-33 for initiation of allergic airway inflammation.
Pauline SchmittAnais DuvalMylène CamusEmma LefrançaisStéphane RogaCécile DedieuNathalie OrtegaElisabeth BellardEmilie MireyEmmanuelle Mouton-BarbosaOdile Burlet-SchiltzAnne Gonzalez de PeredoCorinne CayrolJean-Philippe GirardPublished in: The Journal of experimental medicine (2024)
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.
Keyphrases
- stem cells
- chronic obstructive pulmonary disease
- cystic fibrosis
- endothelial cells
- induced apoptosis
- rheumatoid arthritis
- drug delivery
- bone marrow
- mass spectrometry
- mesenchymal stem cells
- single cell
- blood brain barrier
- metabolic syndrome
- single molecule
- oxidative stress
- cancer therapy
- allergic rhinitis
- binding protein
- cell cycle arrest
- air pollution
- subarachnoid hemorrhage
- induced pluripotent stem cells