Optimal period for achieving sustained unresponsiveness in peanut oral immunotherapy.

IF 1.6 Q3 ALLERGY Asia Pacific Allergy Pub Date : 2023-09-01 Epub Date: 2023-09-07 DOI:10.5415/apallergy.0000000000000110
Kosei Yamashita, Toshinori Nakamura, Takanori Imai, Aiko Honda, Yuki Okada, Mayu Maeda, Taro Kamiya
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Abstract

Background: Oral immunotherapy (OIT) can help children with persistent food allergies achieve sustained unresponsiveness (SU). However, the optimal therapeutic period for obtaining SU remains unclear.

Objective: We aimed to retrospectively investigate the association between the OIT treatment period and achievement of SU.

Methods: We enrolled patients who received OIT for peanut allergy between January 1, 2018 and December 31, 2022. OIT comprised the build-up phase, maintenance phase, complete avoidance, and an oral food challenge (OFC) for confirming SU. The peanut dose in the OFC was gradually increased to 3,000 mg (peanut protein: 795 mg), which was subsequently maintained for ≥5 months. SU was defined as a negative response to 795 mg of peanut protein after ≥2 weeks of complete avoidance. We evaluated the therapeutic OIT period for achieving SU using Kaplan-Meier analysis.

Results: Forty-eight patients underwent peanut OIT. The starting age at OIT initiation was 8 (interquartile range [IQR], 7-10) years. Forty-one (85%) patients had a history of anaphylaxis. The median specific immunoglobulin E concentration to peanut and Ara h 2 at OIT initiation was 85.3 (IQR, 33.7-100) and 57.6 (IQR, 21.9-100) UA/mL, respectively. The median observational period was 2.1 (IQR, 1.6-3.0) person-years (PY). Thirty-four (71%) patients achieved SU, with the rate of SU achievement gradually increasing with the therapeutic period. The median period until SU achievement was 2.1 (95% confidence interval, 1.6-2.5) PY. The rate of SU achievement slowed down after 2.7 PY.

Conclusion: OIT for at least 2.7 PY can increase the rate of SU achievement. The protocol No. 3107.

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花生口服免疫疗法中实现持续无反应的最佳时期。
背景:口服免疫疗法(OIT)可以帮助持续性食物过敏的儿童实现持续无反应(SU)。然而,获得SU的最佳治疗期尚不清楚。目的:我们旨在回顾性研究OIT治疗期与SU成绩之间的关系。方法:我们招募了2018年1月1日至2022年12月31日期间因花生过敏接受OIT的患者。OIT包括建立阶段、维持阶段、完全避免和用于确认SU的口服食物挑战(OFC)。OFC中的花生剂量逐渐增加到3000 mg(花生蛋白:795 mg),随后维持≥5个月。SU被定义为对795的阴性反应 mg花生蛋白。我们使用Kaplan-Meier分析评估了实现SU的OIT治疗期。结果:48例患者接受花生OIT。OIT开始时的起始年龄为8岁(四分位间距[IQR],7-10)。四十一名(85%)患者有过敏反应史。在OIT开始时,花生和Ara H2的中位特异性免疫球蛋白E浓度分别为85.3(IQR,33.7-100)和57.6(IQR(21.9-100)UA/mL。中位观察期为2.1人年(IQR,1.6-3.0)。34例(71%)患者实现了SU,并且SU实现率随着治疗期的延长而逐渐增加。SU成就的中位期为2.1(95%置信区间,1.6-2.5)PY。2.7 PY后SU成就率减慢。结论:OIT至少2.7 PY可以提高SU成就率。协议编号3107。
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来源期刊
CiteScore
2.50
自引率
5.90%
发文量
33
期刊介绍: Asia Pacific Allergy (AP Allergy) is the official journal of the Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI). Although the primary aim of the journal is to promote communication between Asia Pacific scientists who are interested in allergy, asthma, and clinical immunology including immunodeficiency, the journal is intended to be available worldwide. To enable scientists and clinicians from emerging societies appreciate the scope and intent of the journal, early issues will contain more educational review material. For better communication and understanding, it will include rational concepts related to the diagnosis and management of asthma and other immunological conditions. Over time, the journal will increase the number of original research papers to become the foremost citation journal for allergy and clinical immunology information of the Asia Pacific in the future.
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