Cetero Research, Mississauga, ON, Canada.
Adiga Life Sciences Inc., Hamilton, ON, Canada.
Clin Exp Allergy. 2015 May;45(5):974-981. doi: 10.1111/cea.12488.
Cat-PAD, the first in a new class of synthetic peptide immuno-regulatory epitopes (SPIREs), was shown to significantly improve rhinoconjunctivitis symptoms in subjects with cat allergy up to 1 year after the start of a short course of treatment.
To evaluate the long-term effects of Cat-PAD on rhinoconjunctivitis symptoms following standardized allergen challenge 2 years after treatment.
In a randomized, double-blind, placebo-controlled, parallel group study, subjects were exposed to cat allergen in an environmental exposure chamber (EEC) before and after treatment with two regimens of Cat-PAD (either eight doses of 3 nmol or four doses of 6 nmol) given intradermally over a 3-month period. In this follow-up study, changes from baseline in rhinoconjunctivitis symptoms were reassessed 2 years after the start of treatment.
The primary endpoint showed a mean reduction in total rhinoconjunctivitis symptom scores of 3.85 units in the 4 × 6 nmol Cat-PAD group compared to placebo 2 years after the start of treatment (P = 0.13), and this difference was statistically significant in the secondary endpoint at the end of day 4 when the cumulative allergen challenge was greatest (P = 0.02). Consistent reductions in nasal symptoms of between 2 and 3 units were observed for 4 × 6 nmol Cat-PAD compared to placebo between the 2 and 3 h time points on days 1-4 of EEC challenge at 2 years (P < 0.05). The 8 × 3 nmol dose did not show a meaningful effect in this study.
A persistent, clinically meaningful reduction in rhinoconjunctivitis symptoms was observed on EEC challenge 2 years after the start of a short course of treatment with 4 × 6 nmol Cat-PAD. This study is the first to provide evidence of a long-term therapeutic effect with this new class of SPIREs.
Cat-PAD 是一类新型合成肽免疫调节表位(SPIREs)中的首个产品,研究显示,在接受为期 3 个月的 8 次 3 nmol 或 4 次 6 nmol 皮内注射治疗后,接受 Cat-PAD 治疗的猫过敏受试者在治疗开始后 1 年内可显著改善鼻结膜炎症状。
在治疗开始后 2 年,通过标准化过敏原挑战,评估 Cat-PAD 对鼻结膜炎症状的长期影响。
在一项随机、双盲、安慰剂对照、平行组研究中,受试者在接受两种 Cat-PAD 方案(8 次 3 nmol 或 4 次 6 nmol)皮内注射治疗 3 个月后,在环境暴露室(EEC)中暴露于猫过敏原之前和之后,通过 EEC 暴露评估治疗开始后 2 年时的鼻结膜炎症状从基线的变化。
主要终点显示,与安慰剂相比,4×6 nmol Cat-PAD 组在治疗开始后 2 年时的总鼻结膜炎症状评分平均降低 3.85 分(P = 0.13),次要终点在累积过敏原挑战最大时的第 4 天结束时具有统计学意义(P = 0.02)。在 EEC 挑战的第 1-4 天的 2-3 小时时间点,与安慰剂相比,4×6 nmol Cat-PAD 组观察到的鼻症状分别降低 2-3 个单位,差异具有统计学意义(P < 0.05)。在这项研究中,8×3 nmol 剂量没有显示出有意义的效果。
在 EEC 挑战开始后 2 年,接受 4×6 nmol Cat-PAD 短期治疗后,可观察到鼻结膜炎症状持续且具有临床意义的减轻。这项研究首次提供了这种新型 SPIRE 类药物具有长期治疗效果的证据。