脱颗粒
医学
免疫学
受体
肥大细胞
生物
细胞生物学
白细胞介素33
细胞因子
生物化学
白细胞介素
作者
Pavel Kolkhir,Daniel Elieh Ali Komi,Martin Metz,Frank Siebenhaar,Marcus Maurer
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2021-10-05
卷期号:22 (5): 294-308
被引量:108
标识
DOI:10.1038/s41577-021-00622-y
摘要
Mast cells have crucial roles in allergic and other inflammatory diseases. Preclinical approaches provide circumstantial evidence for mast cell involvement in many diseases, but these studies have major limitations - for example, there is still a lack of suitable mouse models for some mast cell-driven diseases such as urticaria. Some approaches for studying mast cells are invasive or can induce severe reactions, and very few mediators or receptors are specific for mast cells. Recently, several drugs that target human mast cells have been developed. These include monoclonal antibodies and small molecules that can specifically inhibit mast cell degranulation via key receptors (such as FcεRI), that block specific signal transduction pathways involved in mast cell activation (for example, BTK), that silence mast cells via inhibitory receptors (such as Siglec-8) or that reduce mast cell numbers and prevent their differentiation by acting on the mast/stem cell growth factor receptor KIT. In this Review, we discuss the existing and emerging therapies that target mast cells, and we consider how these treatments can help us to understand mast cell functions in disease.
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