先天性淋巴细胞
生物
免疫学
免疫疗法
过敏原
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,Clémence Henon,Rachael C. Y. Li,Suzanne M. Bal,Balthasar A. Heesters,Gemma Vila‐Nadal,Oliver Hunewald,Guillem Montamat,Feng He,Markus Ollert,Oleksandra Fedina,Mongkol Lao‐Araya,Susanne Vijverberg,Anke‐Hilse Maitland‐van der Zee,Cornelis M. van Drunen,Wytske J. Fokkens,Stephen R. Durham,Hergen Spits,Mohamed H. Shamji
出处
期刊:Immunity
[Elsevier]
日期:2021-02-01
卷期号:54 (2): 291-307.e7
被引量:143
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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