Chinthrajah R Sharon, Sindher Sayantani B, Nadeau Kari C, Leflein Jeffrey G, Spergel Jonathan M, Petroni Daniel H, Jones Stacie M, Casale Thomas B, Wang Julie, Carr Warner W, Shreffler Wayne G, Wood Robert A, Wambre Erik, Liu Jinzhong, Akinlade Bolanle, Atanasio Amanda, Orengo Jamie M, Hamilton Jennifer D, Kamal Mohamed A, Hooper Andrea T, Patel Kiran, Laws Elizabeth, Mannent Leda P, Adelman Daniel C, Ratnayake Anoshie, Radin Allen R
Sean N. Parker Center for Allergy and Asthma Research at Stanford University, Stanford, California, USA.
Harvard T.H. Chan School of Public Health, Harvard University, Boston, Massachusetts, USA.
Allergy. 2025 Mar;80(3):827-842. doi: 10.1111/all.16420. Epub 2024 Dec 14.
Peanut allergy is a common, life-threatening food allergy in children. We evaluated whether dupilumab, which blocks the activity of interleukin (IL)-4/IL-13, enhances the efficacy of oral immunotherapy (OIT) AR101 in pediatric patients with peanut allergy.
A Phase II, multicenter, randomized, double-blind study was conducted in the USA (NCT03682770) in pediatric patients (6-≤ 17 years old) with confirmed peanut allergy. Patients were randomized 2:1 to receive dupilumab + OIT or placebo + OIT during a 28-40-week up-dosing period. Patients in the dupilumab + OIT group were re-randomized 1:1 and received dupilumab + OIT or placebo + OIT during 24-week OIT maintenance, undergoing a 2044 mg (cumulative) of peanut protein double-blind, placebo-controlled food challenge (DBPCFC) following up-dosing, maintenance, and at 12-week post-treatment follow-up.
The study enrolled 148 patients, 123 of whom were included in the modified full analysis set, with a mean age of 11.1 years. Dupilumab + OIT treatment (n = 84) led to a 20.2% increase (p < 0.05) in the number of patients who passed a DBPCFC to 2044 mg (cumulative) of peanut protein following the up-dosing period versus placebo (OIT alone, n = 39). Following the OIT maintenance period, continuous dupilumab treatment improved the number of patients who passed a DBPCFC to 2044 mg (cumulative) of peanut protein versus patients continuously on OIT alone (16.6% difference [95% CI -9.7, 42.8], p = 0.2123). Safety was consistent with known dupilumab safety profile.
Dupilumab provided a modest increase efficacy of OIT in children and adolescents with peanut allergy, though it did not provide protection against OIT-related anaphylaxis.
ClinicalTrials.gov identifier: NCT03793608.
花生过敏是儿童中常见的、危及生命的食物过敏。我们评估了阻断白细胞介素(IL)-4/IL-13活性的度普利尤单抗是否能提高口服免疫疗法(OIT)AR101对花生过敏儿科患者的疗效。
在美国进行了一项II期、多中心、随机、双盲研究(NCT03682770),纳入确诊为花生过敏的儿科患者(6至≤17岁)。在28至40周的递增剂量期,患者按2:1随机分组,接受度普利尤单抗+OIT或安慰剂+OIT。度普利尤单抗+OIT组的患者在24周的OIT维持期再次按1:1随机分组,接受度普利尤单抗+OIT或安慰剂+OIT,在递增剂量期、维持期以及治疗后12周随访后接受2044毫克(累积)花生蛋白的双盲、安慰剂对照食物激发试验(DBPCFC)。
该研究共纳入148例患者,其中123例纳入改良全分析集,平均年龄11.1岁。与安慰剂(仅OIT,n = 39)相比,度普利尤单抗+OIT治疗组(n = 84)在递增剂量期后通过2044毫克(累积)花生蛋白DBPCFC的患者数量增加了20.2%(p < 0.05)。在OIT维持期后,持续使用度普利尤单抗治疗的患者通过2044毫克(累积)花生蛋白DBPCFC的数量高于仅持续接受OIT治疗的患者(差异为16.6% [95% CI -9.7, 42.8],p = 0.2123)。安全性与已知的度普利尤单抗安全性特征一致。
度普利尤单抗使花生过敏儿童和青少年的OIT疗效略有提高,但它不能预防与OIT相关的过敏反应。
ClinicalTrials.gov标识符:NCT03793608。