Research Advances in Mast Cell Biology and Their Translation Into Novel Therapies for Anaphylaxis

过敏反应 肥大细胞 免疫球蛋白E 免疫学 医学 过敏 免疫系统 抗体
作者
Melanie C. Dispenza,Dean D. Metcalfe,Ana Olivera
出处
期刊:The Journal of Allergy and Clinical Immunology: In Practice [Elsevier BV]
卷期号:11 (7): 2032-2042 被引量:14
标识
DOI:10.1016/j.jaip.2023.03.015
摘要

Anaphylaxis is an acute, potentially life-threatening systemic allergic reaction for which there are no known reliable preventative therapies. Its primary cell mediator, the mast cell, has several pathophysiologic roles and functions in IgE-mediated reactions that continue to be poorly understood. Recent advances in the understanding of allergic mechanisms have identified novel targets for inhibiting mast cell function and activation. The prevention of anaphylaxis is within reach with new drugs that could modulate immune tolerance, mast cell proliferation and differentiation, and IgE regulation and production. Several US Food and Drug Administration–approved drugs for chronic urticaria, mastocytosis, and cancer are also being repurposed to prevent anaphylaxis. New therapeutics have not only shown promise in potential efficacy for preventing IgE-mediated reactions, but in some cases, they are able to inform us about mast cell mechanisms in vivo. This review summarizes the most recent advances in the treatment of anaphylaxis that have arisen from new pharmacologic tools and our current understanding of mast cell biology. Anaphylaxis is an acute, potentially life-threatening systemic allergic reaction for which there are no known reliable preventative therapies. Its primary cell mediator, the mast cell, has several pathophysiologic roles and functions in IgE-mediated reactions that continue to be poorly understood. Recent advances in the understanding of allergic mechanisms have identified novel targets for inhibiting mast cell function and activation. The prevention of anaphylaxis is within reach with new drugs that could modulate immune tolerance, mast cell proliferation and differentiation, and IgE regulation and production. Several US Food and Drug Administration–approved drugs for chronic urticaria, mastocytosis, and cancer are also being repurposed to prevent anaphylaxis. New therapeutics have not only shown promise in potential efficacy for preventing IgE-mediated reactions, but in some cases, they are able to inform us about mast cell mechanisms in vivo. This review summarizes the most recent advances in the treatment of anaphylaxis that have arisen from new pharmacologic tools and our current understanding of mast cell biology. Anaphylaxis: Bench to BedsideThe Journal of Allergy and Clinical Immunology: In PracticeVol. 11Issue 7PreviewAnaphylaxis has long been a condition associated with extreme anxiety for patients and clinicians alike. We have begun to acquire a deeper understanding of the immunologic pathways, and the tools necessary to identify the risk factors that promote reactions and can serve as targets for preventative treatment. The articles in this theme issue of the Journal of Allergy and Clinical Immunology: In Practice reflect the accelerating pace of advances in this unique area within allergy-immunology. Full-Text PDF
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