Brough Helen A, Kim Edwin H, Anagnostou Aikaterini, Lanser Bruce J, Chinthrajah R Sharon, Sindher Sayantani B
Department of Women and Children's Health (Pediatric Allergy), School of Life Course Sciences, Faculty of Life Sciences and Medicine and Peter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, United Kingdom; Children's Allergy Service and Evelina Children's Hospital, Guy's and St Thomas's NHS Foundation Trust, London, United Kingdom.
Department of Pediatrics, University of North Carolina, Chapel Hill, NC.
J Allergy Clin Immunol Pract. 2025 Apr;13(4):731-739. doi: 10.1016/j.jaip.2024.12.011. Epub 2024 Dec 17.
Food allergy is a common disease that has substantial impacts on the quality of life of patients and their families, and all reactions have the potential for causing life-threatening anaphylaxis. Food-allergic individuals currently have 2 Food and Drug Administration- approved therapeutic options available to them aside from life-long allergen avoidance: oral immunotherapy (OIT) and omalizumab. OIT for food allergy has been extensively studied in clinical trials and currently provides the greatest level of protection; however, it also has a high burden of treatment. Studies suggest that more successful OIT outcomes may be attained with earlier intervention; however, early OIT presents its own challenges. Omalizumab, recently Food and Drug Administration-approved, is a biologic targeting IgE, a major driver of allergic reactions. In contrast to OIT, omalizumab monotherapy offers a low treatment burden therapeutic option that provides a safety net against reactions to accidental ingestion of multiple allergens. In addition, omalizumab has been investigated as an adjunct to OIT, improving the speed and safety of single-allergen or multiallergen OIT. Here, we discuss the clinical use of these therapeutic options and provide a guide for shared decision making between patients and physicians about what therapeutic option might be more appropriate.
食物过敏是一种常见疾病,对患者及其家人的生活质量有重大影响,所有反应都有可能引发危及生命的过敏反应。目前,除了终身避免接触过敏原外,食物过敏患者还有两种获得美国食品药品监督管理局(Food and Drug Administration)批准的治疗选择:口服免疫疗法(OIT)和奥马珠单抗。食物过敏的口服免疫疗法已在临床试验中得到广泛研究,目前提供了最高水平的保护;然而,它的治疗负担也很高。研究表明,早期干预可能会取得更成功的口服免疫疗法效果;然而,早期口服免疫疗法也有其自身的挑战。最近获得美国食品药品监督管理局批准的奥马珠单抗是一种靶向免疫球蛋白E(IgE)的生物制剂,免疫球蛋白E是过敏反应的主要驱动因素。与口服免疫疗法不同,奥马珠单抗单药治疗提供了一种治疗负担低的治疗选择,为意外摄入多种过敏原引发的反应提供了安全保障。此外,奥马珠单抗已被研究作为口服免疫疗法的辅助药物,可提高单过敏原或多过敏原口服免疫疗法的速度和安全性。在此,我们讨论这些治疗选择的临床应用,并为患者和医生之间关于哪种治疗选择可能更合适的共同决策提供指导。