Yamashita Kosei, Nakamura Toshinori, Imai Takanori, Honda Aiko, Okada Yuki, Maeda Mayu, Kamiya Taro
Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan.
Asia Pac Allergy. 2023 Sep;13(3):97-104. doi: 10.5415/apallergy.0000000000000110. Epub 2023 Sep 7.
Oral immunotherapy (OIT) can help children with persistent food allergies achieve sustained unresponsiveness (SU). However, the optimal therapeutic period for obtaining SU remains unclear.
We aimed to retrospectively investigate the association between the OIT treatment period and achievement of SU.
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.
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.
OIT for at least 2.7 PY can increase the rate of SU achievement. The protocol No. 3107.
口服免疫疗法(OIT)可帮助患有持续性食物过敏的儿童实现持续无反应(SU)。然而,获得SU的最佳治疗期仍不清楚。
我们旨在回顾性研究OIT治疗期与SU实现之间的关联。
我们纳入了2018年1月1日至2022年12月31日期间接受花生过敏OIT治疗的患者。OIT包括累积期、维持期、完全回避期以及用于确认SU的口服食物激发试验(OFC)。OFC中的花生剂量逐渐增加至3000毫克(花生蛋白:795毫克),随后维持≥5个月。SU定义为在完全回避≥2周后对795毫克花生蛋白呈阴性反应。我们使用Kaplan-Meier分析评估实现SU的治疗OIT期。
48名患者接受了花生OIT治疗。开始OIT治疗的起始年龄为8岁(四分位间距[IQR],7 - 10岁)。41名(85%)患者有过敏反应病史。开始OIT治疗时,对花生和Ara h 2的特异性免疫球蛋白E浓度中位数分别为85.3(IQR,33.7 - 100)和57.6(IQR,21.9 - 100)UA/mL。中位观察期为2.1(IQR,1.6 - 3.0)人年(PY)。34名(71%)患者实现了SU,SU实现率随治疗期逐渐增加。实现SU的中位时间为2.1(95%置信区间,1.6 - 2.5)PY。2.7 PY后SU实现率放缓。
OIT治疗至少2.7 PY可提高SU实现率。方案编号3107。