Chowdhury Ehtesam A, Jadeja Olivia C
Department of General Surgery, Hereford County Hospital, Wye Valley NHS Trust, Hereford, United Kingdom.
Department of General Surgery, Southmead Hospital, North Bristol NHS Trust, Bristol, United Kingdom.
Front Allergy. 2025 May 20;6:1613237. doi: 10.3389/falgy.2025.1613237. eCollection 2025.
Peanut allergies result from a type 1 hypersensitivity reaction, with a prevalence of approximately 1% in children under 5 years of age. The allergens that instigate this reaction are the peanut proteins (Ara h 1-Ara h 8) for which IgE antibodies are specifically produced. Allergen immunotherapy (AIT), despite the uncertainty regarding its mode of action, has been increasingly utilised with the aim of desensitisation against these allergens. AIT encompasses various modes of administration, including epicutaneous immunotherapy (EPIT) and oral immunotherapy (OIT). The review adheres to Preferred Reporting Items for Systematic reviews and Meta-Analyses guidelines, with a comprehensive literature search conducted using databases including MEDLINE®, Embase™, PubMed®, and Google Scholar™. Search terms targeted OIT and EPIT in the desensitisation and management of peanut allergy in children, with studies spanning the past 20 years included based on predefined eligibility criteria. The extent of the immunotherapies' efficacy and safety in children is yet to be thoroughly established; however, OIT demonstrated increased desensitisation rates amongst children when compared to EPIT. The long-term efficacy has not been fully established, with sustained unresponsiveness not reported within most studies. Both modes of administration had a high proportion of participants experiencing adverse effects (AEs), with gastrointestinal symptoms more common with OIT and cutaneous reactions with EPIT. Serious AEs were observed less frequently, however, systemic reactions such as anaphylaxis were more apparent with OIT. Future research should focus on peanut EPIT, as the literature was relatively scarce. Furthermore, research studies should assess sustained unresponsiveness to fully gauge the long-term effects of AIT in children.
花生过敏是由1型超敏反应引起的,在5岁以下儿童中的患病率约为1%。引发这种反应的过敏原是花生蛋白(Ara h 1 - Ara h 8),针对这些蛋白会特异性产生IgE抗体。尽管过敏原免疫疗法(AIT)的作用机制尚不确定,但为了对这些过敏原进行脱敏,其使用越来越广泛。AIT包括多种给药方式,包括经皮免疫疗法(EPIT)和口服免疫疗法(OIT)。本综述遵循系统评价和Meta分析的首选报告项目指南,使用包括MEDLINE®、Embase™、PubMed®和Google Scholar™在内的数据库进行了全面的文献检索。检索词针对儿童花生过敏脱敏和管理中的OIT和EPIT,根据预先定义的纳入标准纳入了过去20年的研究。免疫疗法在儿童中的疗效和安全性程度尚未完全确立;然而,与EPIT相比,OIT在儿童中显示出更高的脱敏率。长期疗效尚未完全确立,大多数研究中未报告持续无反应情况。两种给药方式都有很大比例的参与者出现不良反应(AE),胃肠道症状在OIT中更常见,皮肤反应在EPIT中更常见。严重AE的观察频率较低,然而,全身性反应如过敏反应在OIT中更明显。未来的研究应聚焦于花生EPIT,因为相关文献相对较少。此外,研究应评估持续无反应情况,以全面衡量AIT对儿童的长期影响。