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抗体亲和力和亲合力在IgE介导的过敏反应中的作用

On the role of antibody affinity and avidity in the IgE-mediated allergic response.

作者信息

Bachmann Martin F, Krenger Pascal S, Mohsen Mona O, Kramer Matthias F, Starchenka Sviatlana, Whitehead Piers, Vogel Monique, Heath Matthew D

机构信息

Department of Rheumatology and Immunology, University Hospital of Bern, Bern, Switzerland.

Department for Biomedical Research Bern (DBMR), University of Bern, Bern, Switzerland.

出版信息

Allergy. 2025 Jan;80(1):37-46. doi: 10.1111/all.16248. Epub 2024 Aug 27.

Abstract

Type I hypersensitivity, also known as classical allergy, is mediated via allergen-specific IgE antibodies bound to type I FcR (FcεRI) on the surface of mast cells and basophils upon cross-linking by allergens. This IgE-mediated cellular activation may be blocked by allergen-specific IgG through multiple mechanisms, including direct neutralization of the allergen or engagement of the inhibitory receptor FcγRIIb which blocks IgE signal transduction. In addition, co-engagement of FcεRI and FcγRIIb by IgE-IgG-allergen immune complexes causes down regulation of receptor-bound IgE, resulting in desensitization of the cells. Both, activation of FcεRI by allergen-specific IgE and engagement of FcγRIIb by allergen-specific IgG are driven by allergen-binding. Here we delineate the distinct roles of antibody affinity versus avidity in driving these processes and discuss the role of IgG subclasses in inhibiting basophil and mast cell activation.

摘要

I型超敏反应,也称为经典过敏反应,是由变应原特异性IgE抗体介导的。这些抗体结合在肥大细胞和嗜碱性粒细胞表面的I型Fc受体(FcεRI)上,当变应原使其发生交联时即被激活。变应原特异性IgG可通过多种机制阻断这种IgE介导的细胞活化,包括直接中和变应原或激活抑制性受体FcγRIIb从而阻断IgE信号转导。此外,IgE-IgG-变应原免疫复合物共同激活FcεRI和FcγRIIb会导致受体结合型IgE下调,从而使细胞脱敏。变应原特异性IgE激活FcεRI以及变应原特异性IgG激活FcγRIIb均由变应原结合驱动。在此,我们阐述了抗体亲和力和avidity在驱动这些过程中的不同作用,并讨论了IgG亚类在抑制嗜碱性粒细胞和肥大细胞活化中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd13/11724228/5508ef727a3b/ALL-80-37-g004.jpg

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