López-Sanz Celia, Jiménez-Saiz Rodrigo, Esteban Vanesa, Delgado-Dolset María Isabel, Perales-Chorda Carolina, Villaseñor Alma, Barber Domingo, Escribese María M
Department of Immunology, Instituto de Investigación Sanitaria Hospital Universitario de La Princesa (IIS-Princesa), Madrid, Spain.
Department of Immunology and Oncology, Centro Nacional de Biotecnología (CNB)-CSIC, Madrid, Spain.
Front Allergy. 2022 Jun 16;3:898494. doi: 10.3389/falgy.2022.898494. eCollection 2022.
Allergen immunotherapy (AIT) is the only treatment with disease-transforming potential for allergic disorders. The immunological mechanisms associated with AIT can be divided along time in two phases: short-term, involving mast cell (MC) desensitization; and long-term, with a regulatory T cell (Treg) response with significant reduction of eosinophilia. This regulatory response is induced in about 70% of patients and lasts up to 3 years after AIT cessation. MC desensitization is characteristic of the initial phase of AIT and it is often related to its success. Yet, the molecular mechanisms involved in allergen-specific MC desensitization, or the connection between MC desensitization and the development of a Treg arm, are poorly understood. The major AIT challenges are its long duration, the development of allergic reactions during AIT, and the lack of efficacy in a considerable proportion of patients. Therefore, reaching a better understanding of the immunology of AIT will help to tackle these short-comings and, particularly, to predict responder-patients. In this regard, omics strategies are empowering the identification of predictive and follow-up biomarkers in AIT. Here, we review the immunological mechanisms underlying AIT with a focus on MC desensitization and AIT-induced adverse reactions. Also, we discuss the identification of novel biomarkers with predictive potential that could improve the rational use of AIT.
变应原免疫疗法(AIT)是唯一具有改变过敏性疾病病情潜力的治疗方法。与AIT相关的免疫机制可随时间分为两个阶段:短期阶段,涉及肥大细胞(MC)脱敏;长期阶段,出现调节性T细胞(Treg)反应,嗜酸性粒细胞显著减少。约70%的患者会诱导产生这种调节性反应,且在AIT停止后可持续长达3年。MC脱敏是AIT初始阶段的特征,且通常与其成功与否相关。然而,目前对变应原特异性MC脱敏所涉及的分子机制,或MC脱敏与Treg分支形成之间的联系了解甚少。AIT面临的主要挑战包括疗程长、AIT期间发生过敏反应以及相当一部分患者治疗无效。因此,更好地理解AIT的免疫学将有助于克服这些不足,特别是有助于预测哪些患者会对治疗有反应。在这方面,组学策略有助于识别AIT中的预测性和随访生物标志物。在此,我们综述AIT的免疫机制,重点关注MC脱敏和AIT诱导的不良反应。此外,我们还讨论了具有预测潜力的新型生物标志物的识别,这些标志物可改善AIT的合理应用。