生物
免疫系统
免疫学
先天性淋巴细胞
嗜酸性粒细胞
获得性免疫系统
再生(生物学)
先天免疫系统
细胞生物学
细胞因子
免疫
CCL11型
癌症研究
趋化因子
嗜酸性粒细胞趋化因子
哮喘
作者
Emilie J. Cosway,Andrea J. White,Sonia M. Parnell,Edina Schweighoffer,Helen E. Jolin,Andrea Bacon,Hans‐Reimer Rodewald,Victor L. J. Tybulewicz,Andrew N. J. McKenzie,William E. Jenkinson,Graham Anderson
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2022-03-11
卷期号:7 (69): eabn3286-eabn3286
被引量:51
标识
DOI:10.1126/sciimmunol.abn3286
摘要
Therapeutic interventions used for cancer treatment provoke thymus damage and limit the recovery of protective immunity. Here, we show that eosinophils are an essential part of an intrathymic type 2 immune network that enables thymus recovery after ablative therapy. Within hours of damage, the thymus undergoes CCR3-dependent colonization by peripheral eosinophils, which reestablishes the epithelial microenvironments that control thymopoiesis. Eosinophil regulation of thymus regeneration occurs via the concerted action of NKT cells that trigger CCL11 production via IL4 receptor signaling in thymic stroma, and ILC2 that represent an intrathymic source of IL5, a cytokine that therapeutically boosts thymus regeneration after damage. Collectively, our findings identify an intrathymic network composed of multiple innate immune cells that restores thymus function during reestablishment of the adaptive immune system.
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