Infant and Toddler Peanut Oral Immunotherapy: Initiation Before Age 2 Increases Ad Libitum Peanut Consumption

IF 6.6 1区 医学 Q1 ALLERGY Journal of Allergy and Clinical Immunology-In Practice Pub Date : 2025-04-01 Epub Date: 2025-02-05 DOI:10.1016/j.jaip.2025.01.032
S. Shahzad Mustafa MD , Peter Capucilli MD , Linh-An Tuong MD, MSc , Denise Sanchez-Tejera MD , Karthik Vadamalai MD , Allison Ramsey MD
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Abstract

Background

Peanut oral immunotherapy (POIT) has promising potential of disease modification, but there are no studies to date evaluating high-dose POIT, leading to ad libitum (ad lib) consumption of peanut products, especially in children 6 months to 4 years of age.

Objective

To report real-world outcomes of high-dose POIT in children 6 months to 4 years of age, including adverse events, achievement of ad lib consumption, and the impact of age on these outcome measures.

Methods

Patients 6 months to 4 years of age with a diagnosis of peanut allergy were enrolled in a POIT protocol with a goal dose of 3000 mg. Demographics along with POIT and clinical outcomes 6 months after POIT are reported.

Results

Sixty children, with a median age of 16 months, started POIT. Three (5%) were lost to follow-up, and 6 (10%) discontinued POIT because of recurrent adverse events or the inability to consume daily peanut protein. Fifty-one (85%) children completed POIT in a median of 7 months and were consuming ad lib peanut products for a duration of 6 months after completion of the POIT protocol. Sixteen (26.7%) children experienced a total of 22 adverse reactions during POIT. Initiating POIT before 24 months of age increased the likelihood of ad lib peanut consumption by an odds ratio of 11.69 (1.19-114.31, P = .035).

Conclusions

Our study demonstrates that high-dose POIT in infants and toddlers is well tolerated and can lead to ad lib introduction of dietary peanut products into the diet, especially if initiated before 2 years of age.
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婴幼儿花生口服免疫治疗:2岁前开始增加花生的摄入量。
背景:花生口服免疫疗法(POIT)具有改善疾病的潜力,但迄今为止还没有研究评估高剂量POIT导致花生制品的即食消费,特别是6个月至4岁的儿童。目的:报告6个月至4岁儿童使用高剂量POIT的真实结局,包括不良事件、实现自用药以及年龄对这些结局指标的影响。方法:6个月至4岁诊断为花生过敏(PA)的患者加入POIT方案,目标剂量为3000 mg。报告了人口统计数据,以及POIT和POIT后6个月的临床结果。结果:60名儿童开始使用POIT,中位年龄为16个月。3名(5%)患者失去随访,6名(10%)患者因复发性不良事件或无法每日摄入花生蛋白而停止服用POIT。51名(85%)儿童在中位7个月内完成了POIT,并在POIT方案完成后的6个月内食用了即席花生产品。16例(26.7%)患儿在POIT期间共发生22次不良反应。在24月龄之前启动POIT会增加即食花生食用的可能性,优势比为11.69 (1.19-114.31,p=0.035)。结论:我们的研究表明,婴幼儿对高剂量的POIT具有良好的耐受性,并且可以导致在饮食中引入即食花生产品,特别是如果在两岁之前开始。
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来源期刊
CiteScore
11.10
自引率
9.60%
发文量
683
审稿时长
50 days
期刊介绍: JACI: In Practice is an official publication of the American Academy of Allergy, Asthma & Immunology (AAAAI). It is a companion title to The Journal of Allergy and Clinical Immunology, and it aims to provide timely clinical papers, case reports, and management recommendations to clinical allergists and other physicians dealing with allergic and immunologic diseases in their practice. The mission of JACI: In Practice is to offer valid and impactful information that supports evidence-based clinical decisions in the diagnosis and management of asthma, allergies, immunologic conditions, and related diseases. This journal publishes articles on various conditions treated by allergist-immunologists, including food allergy, respiratory disorders (such as asthma, rhinitis, nasal polyps, sinusitis, cough, ABPA, and hypersensitivity pneumonitis), drug allergy, insect sting allergy, anaphylaxis, dermatologic disorders (such as atopic dermatitis, contact dermatitis, urticaria, angioedema, and HAE), immunodeficiency, autoinflammatory syndromes, eosinophilic disorders, and mast cell disorders. The focus of the journal is on providing cutting-edge clinical information that practitioners can use in their everyday practice or to acquire new knowledge and skills for the benefit of their patients. However, mechanistic or translational studies without immediate or near future clinical relevance, as well as animal studies, are not within the scope of the journal.
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