先天性淋巴细胞
生物
免疫学
免疫疗法
细胞因子
胸腺基质淋巴细胞生成素
免疫系统
先天免疫系统
过敏
作者
Korneliusz Golebski,Janice A. Layhadi,Ümit Murat Şahiner,Esther Helen Steveling,Madison M. Lenormand,Rachael C. Y. Li,Suzanne M. Bal,Balthasar A. Heesters,Gemma Vilà-Nadal,Oliver Hunewald,Guillem Montamat,Feng He,Markus Ollert,Oleksandra Fedina,Mongkol Lao‐Araya,Susanne J. H. Vijverberg,Anke H. Maitland‐van der Zee,Cornelis M. van Drunen,Wytske J. Fokkens,Stephen R. Durham
出处
期刊:Immunity
[Elsevier]
日期:2021-01-15
卷期号:54 (2): 291-307.e7
被引量:198
标识
DOI:10.1016/j.immuni.2020.12.013
摘要
Summary
The role of innate immune cells in allergen immunotherapy that confers immune tolerance to the sensitizing allergen is unclear. Here, we report a role of interleukin-10-producing type 2 innate lymphoid cells (IL-10+ ILC2s) in modulating grass-pollen allergy. We demonstrate that KLRG1+ but not KLRG1– ILC2 produced IL-10 upon activation with IL-33 and retinoic acid. These cells attenuated Th responses and maintained epithelial cell integrity. IL-10+ KLRG1+ ILC2s were lower in patients with grass-pollen allergy when compared to healthy subjects. In a prospective, double-blind, placebo-controlled trial, we demonstrated that the competence of ILC2 to produce IL-10 was restored in patients who received grass-pollen sublingual immunotherapy. The underpinning mechanisms were associated with the modification of retinol metabolic pathway, cytokine-cytokine receptor interaction, and JAK-STAT signaling pathways in the ILCs. Altogether, our findings underscore the contribution of IL-10+ ILC2s in the disease-modifying effect by allergen immunotherapy.
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