首页    期刊浏览 2024年12月04日 星期三
登录注册

文章基本信息

  • 标题:Designer covalent heterobivalent inhibitors prevent IgE-dependent responses to peanut allergen
  • 本地全文:下载
  • 作者:Peter E. Deak ; Baksun Kim ; Amina Abdul Qayum
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2019
  • 卷号:116
  • 期号:18
  • 页码:8966-8974
  • DOI:10.1073/pnas.1820417116
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Allergies are a result of allergen proteins cross-linking allergen-specific IgE (sIgE) on the surface of mast cells and basophils. The diversity and complexity of allergen epitopes, and high-affinity of the sIgE–allergen interaction have impaired the development of allergen-specific inhibitors of allergic responses. This study presents a design of food allergen-specific sIgE inhibitors named covalent heterobivalent inhibitors (cHBIs) that selectively form covalent bonds to only sIgEs, thereby permanently inhibiting them. Using screening reagents termed nanoallergens, we identified two immunodominant epitopes in peanuts that were common in a population of 16 allergic patients. Two cHBIs designed to inhibit only these two epitopes completely abrogated the allergic response in 14 of the 16 patients in an in vitro assay and inhibited basophil activation in an allergic patient ex vivo analysis. The efficacy of the cHBI design has valuable clinical implications for many allergen-specific responses and more broadly for any antibody-based disease.
  • 关键词:IgE ; allergy ; epitope ; selective inhibition ; peanut
国家哲学社会科学文献中心版权所有