Wraith David C, Krishna Mamidipudi T
Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Department of Allergy and Immunology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Clin Exp Allergy. 2021 Jun;51(6):751-769. doi: 10.1111/cea.13840. Epub 2021 Feb 17.
Allergen-specific immunotherapy (AIT) is the only means of altering the natural immunological course of allergic diseases and achieving long-term remission. Pharmacological measures are able to suppress the immune response and/or ameliorate the symptoms but there is a risk of relapse soon after these measures are withdrawn. Current AIT approaches depend on the administration of intact allergens, often comprising crude extracts of the allergen. We propose that the challenges arising from current approaches, including the risk of serious side-effects, burdensome duration of treatment, poor compliance and high cost, are overcome by application of peptides based on CD4 T cell epitopes rather than whole allergens. Here we describe evolving approaches, summarize clinical trials involving peptide AIT in allergic rhinitis and asthma, discuss the putative mechanisms involved in their action, address gaps in evidence and propose future directions for research and clinical development.
变应原特异性免疫疗法(AIT)是改变过敏性疾病自然免疫进程并实现长期缓解的唯一手段。药物治疗措施能够抑制免疫反应和/或缓解症状,但在这些措施停止后很快就有复发的风险。当前的AIT方法依赖于给予完整的变应原,通常包括变应原的粗提物。我们认为,基于CD4 T细胞表位的肽段而非完整变应原的应用,能够克服当前方法所带来的挑战,包括严重副作用风险、治疗时间长、依从性差和成本高。在此,我们描述不断发展的方法,总结涉及肽段AIT治疗过敏性鼻炎和哮喘的临床试验,讨论其作用的推定机制,指出证据空白,并提出未来研究和临床发展的方向。