23号公路
过敏原
免疫球蛋白E
免疫学
人口
医学
生物
过敏
抗体
环境卫生
作者
Joshua F. E. Koenig,Niels Peter Hell Knudsen,Allyssa Phelps,Kelly Bruton,Ilka Hoof,G. Lund,Danielle Della Libera,Anders Lund,Lars Harder Christensen,David R. Glass,Tina D. Walker,Allison Fang,Susan Waserman,Manel Jordana,Peter S. Andersen
出处
期刊:Science Translational Medicine
[American Association for the Advancement of Science (AAAS)]
日期:2024-02-07
卷期号:16 (733)
被引量:19
标识
DOI:10.1126/scitranslmed.adi0944
摘要
Allergen-specific immunoglobulin E (IgE) antibodies mediate pathology in diseases such as allergic rhinitis and food allergy. Memory B cells (MBCs) contribute to circulating IgE by regenerating IgE-producing plasma cells upon allergen encounter. Here, we report a population of type 2–polarized MBCs defined as CD23 hi , IL-4Rα hi , and CD32 low at both the transcriptional and surface protein levels. These MBC2s are enriched in IgG1- and IgG4-expressing cells while constitutively expressing germline transcripts for IgE. Allergen-specific B cells from patients with allergic rhinitis and food allergy were enriched in MBC2s. Furthermore, MBC2s generated allergen-specific IgE during sublingual immunotherapy, thereby identifying these cells as a major reservoir for IgE. The identification of MBC2s provides insights into the maintenance of IgE memory, which is detrimental in allergic diseases but could be beneficial in protection against venoms and helminths.
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