Bellanti Joseph A
Department of Pediatrics, Georgetown University Medical Center, Washington, District of Columbia; Department of Microbiology-Immunology, Georgetown University Medical Center, Washington, District of Columbia; International Center for Interdisciplinary Studies of Immunology (ICISI), Georgetown University Medical Center, Washington, District of Columbia.
Ann Allergy Asthma Immunol. 2025 May 29. doi: 10.1016/j.anai.2025.05.024.
Food allergies and inborn errors of immunity (IEIs) were once viewed as distinct disorders-hypersensitivity vs infection susceptibility. However, IEIs are now recognized to include immune dysregulation with autoimmunity, autoinflammation, lymphoproliferation, and severe atopy. Understanding the overlap between food allergies and IEIs is critical, given that allergic inflammation often complicates immune deficiencies.
To evaluate the shared immunologic mechanisms linking food allergies and IEIs, with a focus on immune dysregulation, barrier defects, microbial dysbiosis, and impaired regulatory T cell (Treg) function.
A comprehensive literature review was conducted using PubMed applying search terms including food allergy, primary immunodeficiency, IEI, Treg cells, immune dysregulation, autoimmunity, autoinflammation, epithelial barrier dysfunction, and microbiome. Particular focus was placed on identifying studies describing monogenic IEIs characterized by severe allergic phenotypes and elevated IgE levels. Articles were selected on the basis of relevance to the themes of the review, quality of study design, and their contribution to advancing understanding in the field. Priority was given to original research articles, systematic reviews, meta-analyses, and key historical studies.
Allergic symptoms, including food allergy and atopic dermatitis, frequently present early in IEIs and may precede infection susceptibility. Common features include Treg dysfunction, cytokine signaling defects, epithelial barrier compromise, and microbiome alterations. Recognition of these pathways has enhanced diagnosis and led to targeted therapies such as biologics and gene therapy.
Treg cells are central to maintaining immune tolerance across allergic, autoimmune, and immunodeficient states. Advances in understanding dysregulated immunity and barrier defects are driving personalized treatment strategies for patients with both food allergy and IEIs.
食物过敏和先天性免疫缺陷(IEIs)曾被视为截然不同的病症——超敏反应与感染易感性。然而,如今IEIs被认为包括伴有自身免疫、自身炎症、淋巴细胞增殖和严重特应性的免疫失调。鉴于过敏性炎症常常使免疫缺陷复杂化,了解食物过敏与IEIs之间的重叠至关重要。
评估连接食物过敏和IEIs的共同免疫机制,重点关注免疫失调、屏障缺陷、微生物群失调以及调节性T细胞(Treg)功能受损。
使用PubMed进行了全面的文献综述,应用的检索词包括食物过敏、原发性免疫缺陷、IEI、Treg细胞、免疫失调、自身免疫、自身炎症、上皮屏障功能障碍和微生物群。特别关注识别描述以严重过敏表型和IgE水平升高为特征的单基因IEIs的研究。根据与综述主题的相关性、研究设计质量及其对该领域认识进展的贡献来选择文章。优先选择原创研究文章、系统评价、荟萃分析和关键的历史研究。
包括食物过敏和特应性皮炎在内的过敏症状在IEIs中常常早期出现,并且可能先于感染易感性出现。共同特征包括Treg功能障碍、细胞因子信号缺陷、上皮屏障受损和微生物群改变。对这些途径的认识提高了诊断水平,并导致了如生物制剂和基因治疗等靶向治疗。
Treg细胞对于维持过敏、自身免疫和免疫缺陷状态下的免疫耐受至关重要。对免疫失调和屏障缺陷认识的进展正在推动针对食物过敏和IEIs患者的个性化治疗策略。