Department of Biochemistry and Molecular Biology, School of Chemistry, Complutense University of Madrid, Spain.
J Investig Allergol Clin Immunol. 2013;23(6):371-82; quiz 2 p preceding 382.
Immunoglobulin (Ig) E-mediated food allergy is a type 2 helper T cell (TH2)-dependent disease whose prevalence is increasing in industrialized countries as a direct consequence of reduced tolerance to food antigens. The generation of regulatory T cells (Treg) is a key component of oral tolerance, and compelling experimental evidence has demonstrated that functional allergen-specific Treg cells play a major role in healthy immune responses to allergens and clinically successful allergen-specific immunotherapy. In the particular case of IgE-mediated food allergy, further investigations are required to firmly demonstrate the role of Treg cells during desensitization, induction of tolerance, or both, and several studies have also suggested a key role for these cells in healthy responses to food allergens. Treg cells are able to suppress the sensitization and effector phases of allergic reactions via several mechanisms of action based on multiple soluble and surface-binding molecules. Our knowledge of the mechanisms governing the generation of food allergen-specific Treg cells in the gastrointestinal mucosa, including the specific dendritic cell subsets involved in such processes, has increased significantly over the last decade. The identification of alternative tissues where oral tolerance to food allergens might occur in vive is crucial, not only for a better understanding of the pathophysiology of food allergy, but also for the development of alternative therapeutic interventions. Recent findings demonstrate that oral tolerance can be induced in the tonsils through generation and maintenance of functional allergen-specificTreg cells. Further investigation in this area could pave the way for novel treatments of food allergy and other immune tolerance-related diseases.
免疫球蛋白(Ig)E 介导的食物过敏是一种 2 型辅助 T 细胞(TH2)依赖性疾病,其在工业化国家的患病率正在增加,这是对食物抗原耐受性降低的直接后果。调节性 T 细胞(Treg)的产生是口服耐受的关键组成部分,强有力的实验证据表明,功能性过敏原特异性 Treg 细胞在健康的免疫应答中起主要作用过敏原和临床上成功的过敏原特异性免疫疗法。在 IgE 介导的食物过敏的特殊情况下,需要进一步研究来确定 Treg 细胞在脱敏、诱导耐受或两者兼而有之时的作用,并且一些研究还表明这些细胞在健康的食物过敏反应中起关键作用。Treg 细胞能够通过多种基于多种可溶性和表面结合分子的作用机制来抑制过敏反应的致敏和效应阶段。在过去的十年中,我们对胃肠道黏膜中产生食物过敏原特异性 Treg 细胞的机制的认识,包括参与这些过程的特定树突状细胞亚群,已经有了显著的提高。鉴定替代性组织中食物过敏原口服耐受可能发生的机制,不仅对于更好地理解食物过敏的病理生理学至关重要,而且对于开发替代性治疗干预措施也至关重要。最近的研究结果表明,口服耐受可以通过生成和维持功能性过敏原特异性 Treg 细胞在扁桃体中诱导。在这一领域的进一步研究可能为食物过敏和其他免疫耐受相关疾病的新治疗方法铺平道路。