Department of Pediatrics, Baylor College of Medicine, Houston, Texas; Texas Children's Hospital, Section of Immunology, Allergy and Retrovirology, Houston, Texas.
Department of Pediatrics, Baylor College of Medicine, Houston, Texas; Texas Children's Hospital, Section of Immunology, Allergy and Retrovirology, Houston, Texas.
J Allergy Clin Immunol Pract. 2022 Feb;10(2):566-576.e6. doi: 10.1016/j.jaip.2021.10.074. Epub 2021 Dec 7.
The maximum tolerated dose of peanut protein following peanut oral immunotherapy (POIT) is unknown because most research studies have not examined very high thresholds.
To define the maximum dose tolerated by patients on POIT and severity of allergic reactions after a 1-month period of treatment discontinuation.
In a phase 2 3-year POIT open-label study, we enrolled participants age 5 to 13 years with a 1-year build-up period followed by a 2-year daily maintenance dose of 3900 mg with assessment of the maximum tolerated dose using double-blind placebo-controlled food challenges (DBPCFCs) of 26,225 mg cumulative dose of peanut protein. The DBPCFC was performed at baseline, after 12-month build-up, at 2 year of maintenance, and after a 1-month period of treatment discontinuation. Biomarkers were assessed every 6 weeks for the first 6 months of therapy. A general linear mixed model was used for analysis.
The mean maximum cumulative tolerated dose after 12 months increased by 12,063 mg (P < .001) (n = 12), slightly decreased during maintenance (n = 11), and significantly decreased by 7593 mg after avoidance for 1 month (P = .03) (n = 6). Biomarker analysis revealed decreases in cytokine expression within the first 6 weeks of initiation of POIT and decreased peanut-IgG and increased cytokine expression after 1 month of discontinuation. The DBPCFC reaction severity, examined through a symptom score with 1 point for each defined symptom, decreased after 12 months, but did not significantly change after 1 month of POIT discontinuation.
The evaluation of POIT and sustained unresponsiveness by maximum tolerated dose by DBPCFCs in this small phase 2 trial showed that desensitization is diminished, with 100% loss of tolerated dose after 1 month of avoidance following 3 years of treatment.
由于大多数研究并未检查非常高的阈值,因此,尚不清楚在进行花生口服免疫治疗(POIT)后,患者可耐受的最大剂量是多少。
确定 POIT 中断 1 个月后,患者可耐受的剂量上限和过敏反应的严重程度。
在一项为期 3 年的 2 期 POIT 开放性研究中,我们纳入了年龄在 5 至 13 岁之间的参与者,在为期 1 年的递增期后,每日接受 3900 mg 的维持剂量,使用 26,225 mg 累积剂量的花生蛋白进行双盲安慰剂对照食物挑战(DBPCFC)来评估最大耐受剂量。DBPCFC 在基线、12 个月递增期后、2 年维持期和 POIT 中断 1 个月后进行。在治疗的前 6 个月内,每 6 周评估一次生物标志物。使用一般线性混合模型进行分析。
12 个月时,最大累积耐受剂量平均增加了 12063 mg(P <.001)(n=12),在维持期略有下降(n=11),在 POIT 中断 1 个月后显著下降了 7593 mg(P=.03)(n=6)。生物标志物分析显示,在 POIT 启动的前 6 周内细胞因子表达减少,在 POIT 中断 1 个月后,花生 IgG 减少,细胞因子表达增加。通过每个定义症状得 1 分的症状评分来评估 DBPCFC 反应严重程度,在 12 个月后下降,但在 POIT 中断 1 个月后没有显著变化。
在这项小型 2 期试验中,通过 DBPCFC 评估 POIT 和最大耐受剂量下的持续无反应性表明,脱敏作用减弱,在经过 3 年治疗后,避免治疗 1 个月后,最大耐受剂量丧失 100%。