ALYATEC Environmental Exposure Chamber, Strasbourg, France; Chest Diseases Department, Strasbourg University Hospital, Strasbourg, France; Federation of Translational Medicine EA 3070, University of Strasbourg, Strasbourg, France.
ALYATEC Environmental Exposure Chamber, Strasbourg, France.
J Allergy Clin Immunol. 2022 Dec;150(6):1437-1446. doi: 10.1016/j.jaci.2022.06.025. Epub 2022 Aug 4.
The dominant allergen in cat dander, Felis domesticus allergen 1 (Fel d 1), is a persistent trigger for allergic rhinitis and asthma symptoms.
We evaluated the efficacy of Fel d 1 monoclonal antibodies (REGN1908/1909) in preventing cat allergen-induced early asthmatic responses (EARs) in cat-allergic patients with mild asthma.
Patients were randomized to single-dose REGN1908/1909 600 mg (n = 29) or placebo (n = 27). The FEV was measured for up to 4 hours in a cat allergen environmental exposure unit up to 85 days after dosing. Assessments included between-group differences in change from baseline in FEV area under the curve (AUC; 0-2 hours) and incidence of EAR (FEV reduction ≥20%).
NCT03838731.
Single-dose REGN1908/1909 significantly prevented reductions in FEV on days 8, 29, 57, and 85. Most REGN1908/1909 patients did not have an EAR by 4 hours (the last time point tested). In contrast, placebo-treated patients experienced a ≥20% mean FEV reduction on days 8, 29, 57, and 85 after dosing, with most experiencing an EAR within 1 hour. REGN1908/1909-treated patients tolerated 3-fold higher allergen quantities (P < .05 at all time points) versus placebo. REGN1908/1909 substantially reduced skin test reactivity to cat allergen versus placebo at all time points tested (nominal P < .001). REGN1908/1909 was generally well tolerated; no serious adverse events or deaths were reported.
Single-dose REGN1908/1909 significantly prevented reductions in FEV in cat-allergic patients with mild asthma on cat allergen environmental exposure unit exposure at 8 days and up to 85 days after dose.
猫皮屑中的主要过敏原,即家猫过敏原 1(Fel d 1),是引发过敏性鼻炎和哮喘症状的持续性触发因素。
我们评估了 Fel d 1 单克隆抗体(REGN1908/1909)预防轻度哮喘的猫过敏患者发生猫过敏原诱导的早期哮喘反应(EARs)的疗效。
患者随机接受单剂量 REGN1908/1909 600mg(n=29)或安慰剂(n=27)治疗。在给药后长达 85 天内,在猫过敏原环境暴露单元中最多测量 4 小时的 FEV。评估包括从基线变化的组间差异,即 FEV 曲线下面积(AUC;0-2 小时)和 EAR 发生率(FEV 下降≥20%)。
NCT03838731。
单剂量 REGN1908/1909 显著预防了第 8、29、57 和 85 天 FEV 的下降。大多数 REGN1908/1909 患者在 4 小时内(最后一次测试时间点)未发生 EAR。相比之下,安慰剂治疗的患者在给药后第 8、29、57 和 85 天出现了≥20%的平均 FEV 下降,其中大多数在 1 小时内发生了 EAR。REGN1908/1909 治疗的患者耐受的过敏原量是安慰剂的 3 倍(所有时间点均 P<.05)。与安慰剂相比,REGN1908/1909 大大降低了在所有测试时间点的猫过敏原皮肤试验反应性(名义 P<.001)。REGN1908/1909 通常具有良好的耐受性;未报告严重不良事件或死亡。
在猫过敏原环境暴露单元暴露 8 天和给药后长达 85 天内,单剂量 REGN1908/1909 显著预防了轻度哮喘的猫过敏患者的 FEV 下降。