表位
免疫球蛋白E
免疫学
免疫原性
免疫疗法
生物
口服免疫疗法
抗体
过敏原
病毒学
过敏
免疫系统
作者
Genghao Chen,Ellen Shrock,Mamie Z. Li,Jonathan M. Spergel,Kari C. Nadeau,Jacqueline A. Pongracic,Dale T. Umetsu,Rima Rachid,Andrew J. MacGinnitie,Wanda Phipatanakul,Lynda C. Schneider,Hans C. Oettgen,Stephen J. Elledge
标识
DOI:10.1016/j.xcrm.2021.100410
摘要
Peanut allergy can result in life-threatening reactions and is a major public health concern. Oral immunotherapy (OIT) induces desensitization to food allergens through administration of increasing amounts of allergen. To dissect peanut-specific immunoglobulin E (IgE) and IgG responses in subjects undergoing OIT, we have developed AllerScan, a method that leverages phage-display and next-generation sequencing to identify the epitope targets of peanut-specific antibodies. We observe a striking diversification and boosting of the peanut-specific IgG repertoire after OIT and a reduction in pre-existing IgE levels against individual epitopes. High-resolution epitope mapping reveals shared recognition of public epitopes in Ara h 1, 2, 3, and 7. In individual subjects, OIT-induced IgG specificities overlap extensively with IgE and exhibit strikingly similar antibody footprints, suggesting related clonal lineages or convergent evolution of peanut-specific IgE and IgG B cells. Individual differences in epitope recognition identified via AllerScan could inform safer and more effective personalized immunotherapy.
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