Bachmann Martin F, Krenger Pascal S, Mohsen Mona O, Kramer Matthias F, Starchenka Sviatlana, Whitehead Piers, Vogel Monique, Heath Matthew D
Department of Rheumatology and Immunology, University Hospital of Bern, Bern, Switzerland.
Department for Biomedical Research Bern (DBMR), University of Bern, Bern, Switzerland.
Allergy. 2025 Jan;80(1):37-46. doi: 10.1111/all.16248. Epub 2024 Aug 27.
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.
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。