花生口服益生菌免疫治疗与8周持续无反应和长期生活质量改善相关

P. Loke, Kuang-Chih Hsiao, A. Lozinsky, S. Ashley, M. Lloyd, Sigrid Pitkin, C. Axelrad, K. Jayawardana, D. Tey, E. Su, M. Robinson, A. Leung, A. Dunn Galvin, M. Tang
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引用次数: 3

摘要

花生过敏在大多数患者中会持续一生。目前的管理依赖于避免过敏原;然而,约50%的患者在1年内意外接触。花生口服免疫疗法(OIT)在诱导脱敏方面是有效的,并且可以在一部分接受治疗的患者中诱导持续无反应性(SU);然而,缺乏长期有效性和健康相关生活质量(HRQL)影响的数据。OIT诱导的SU可能是短暂的,高达67%的治疗应答者在12个月内失去SU。此外,一项荟萃分析发现花生OIT与频繁的不良事件(AE)相关,并且没有显著改善HRQL。我们之前报道了一项概念验证随机试验(PPOIT- 001)的结果,该试验显示,74.2%的1 - 10岁儿童在18个月的联合益生菌和花生口服免疫疗法(PPOIT)治疗后出现了2至6周的SU。对PPOIT- 001患者的长期随访显示,在70%的初始治疗应答者中,PPOIT诱导的SU在治疗后持续4年。亲本PPOIT- 001研究的不足之处包括参与者的选择是基于临床反应史和花生皮肤点针刺试验(SPT)或特异性IgE (sIgE)阳性,而不是双盲安慰剂对照食物挑战(DBPCFC),以及在治疗后2至6周而不是治疗后评估SU
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probiotic peanut oral immunotherapy is associated with long‐term persistence of 8‐week sustained unresponsiveness and long‐lasting quality‐of‐life improvement
Peanut allergy persists for life in the majority of patients. Current management relies on allergen avoidance; however, about 50% of patients have accidental exposures within 1 year. 1 Peanut oral im munotherapy (OIT) is effective at inducing desensitization and can induce sustained unresponsiveness (SU) in a subset of treated pa tients; however, data on long- term effectiveness and health- related quality- of- life (HRQL) impact are lacking. OIT- induced SU may be short- lived, with up to 67% of treatment responders losing their SU within 12 months. 2 Furthermore, a meta- analysis found that peanut OIT was associated with frequent adverse events (AE) and no signif icant improvement in HRQL. 3 We previously reported results from a proof- of- concept random ized trial (PPOIT- 001), which showed that 18- month treatment with combined probiotic and peanut oral immunotherapy (PPOIT) in duced 2- to 6- week SU in 74.2% of children aged 1– 10 years. 4 A long-term follow- up of PPOIT- 001 patients showed that PPOIT- induced SU persisted to 4- year post- treatment in 70% of initial treatment responders. 5 Weaknesses of the parent PPOIT- 001 study included participant selection based upon the clinical history of reaction and positive peanut skin prick test (SPT) or specific- IgE (sIgE) rather than double- blind placebo- controlled food challenge (DBPCFC), and the assessment of SU at 2- to 6- week post- treatment rather than after
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