Division of Immunology, Department of Pediatrics, Boston Children's Hospital, Boston, MA, United States.
Department of Pediatrics, Harvard Medical School, Boston, MA, United States.
Front Immunol. 2020 Dec 11;11:603050. doi: 10.3389/fimmu.2020.603050. eCollection 2020.
Food allergy is a major health issue, affecting the lives of 8% of U.S. children and their families. There is an urgent need to identify the environmental and endogenous signals that induce and sustain allergic responses to ingested allergens. Acute reactions to foods are triggered by the activation of mast cells and basophils, both of which release inflammatory mediators that lead to a range of clinical manifestations, including gastrointestinal, cutaneous, and respiratory reactions as well as systemic anaphylaxis. Both of these innate effector cell types express the high affinity IgE receptor, FcϵRI, on their surface and are armed for adaptive antigen recognition by very-tightly bound IgE antibodies which, when cross-linked by polyvalent allergen, trigger degranulation. These cells also express inhibitory receptors, including the IgG Fc receptor, FcγRIIb, that suppress their IgE-mediated activation. Recent studies have shown that natural resolution of food allergies is associated with increasing food-specific IgG levels. Furthermore, oral immunotherapy, the sequential administration of incrementally increasing doses of food allergen, is accompanied by the strong induction of allergen-specific IgG antibodies in both human subjects and murine models. These can deliver inhibitory signals FcγRIIb that block IgE-induced immediate food reactions. In addition to their role in mediating immediate hypersensitivity reactions, mast cells and basophils serve separate but critical functions as adjuvants for type 2 immunity in food allergy. Mast cells and basophils, activated by IgE, are key sources of IL-4 that tilts the immune balance away from tolerance and towards type 2 immunity by promoting the induction of Th2 cells along with the innate effectors of type 2 immunity, ILC2s, while suppressing the development of regulatory T cells and driving their subversion to a pathogenic pro-Th2 phenotype. This adjuvant effect of mast cells and basophils is suppressed when inhibitory signals are delivered by IgG antibodies signaling FcγRIIb. This review summarizes current understanding of the immunoregulatory effects of mast cells and basophils and how these functions are modulated by IgE and IgG antibodies. Understanding these pathways could provide important insights into innovative strategies for preventing and/or reversing food allergy in patients.
食物过敏是一个主要的健康问题,影响着美国 8%的儿童及其家庭的生活。目前迫切需要确定诱导和维持对摄入过敏原的过敏反应的环境和内源性信号。食物的急性反应是由肥大细胞和嗜碱性粒细胞的激活触发的,这两种细胞都释放炎症介质,导致一系列临床表现,包括胃肠道、皮肤和呼吸道反应以及全身性过敏反应。这两种先天效应细胞类型在其表面表达高亲和力 IgE 受体 FcεRI,并通过非常紧密结合的 IgE 抗体武装进行适应性抗原识别,当多价过敏原交联时,触发脱粒。这些细胞还表达抑制性受体,包括 IgG Fc 受体 FcγRIIb,抑制它们的 IgE 介导的激活。最近的研究表明,食物过敏的自然缓解与食物特异性 IgG 水平的增加有关。此外,口服免疫疗法,即序贯给予递增剂量的食物过敏原,伴随着人类和鼠模型中食物特异性 IgG 抗体的强烈诱导。这些可以提供抑制性信号 FcγRIIb,阻断 IgE 诱导的即时食物反应。除了在介导即刻超敏反应中的作用外,肥大细胞和嗜碱性粒细胞在食物过敏的 2 型免疫中作为佐剂发挥着单独但关键的作用。通过 IgE 激活的肥大细胞和嗜碱性粒细胞是 IL-4 的主要来源,通过促进 Th2 细胞的诱导以及 2 型免疫的先天效应细胞 ILC2,同时抑制调节性 T 细胞的发育并驱动其向致病性 pro-Th2 表型的转化,使免疫平衡从耐受转向 2 型免疫。当 IgG 抗体信号 FcγRIIb 传递抑制信号时,肥大细胞和嗜碱性粒细胞的这种佐剂作用受到抑制。这篇综述总结了目前对肥大细胞和嗜碱性粒细胞免疫调节作用的理解,以及 IgE 和 IgG 抗体如何调节这些功能。了解这些途径可以为预防和/或逆转患者食物过敏的创新策略提供重要的见解。