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来源于猫过敏原的合成肽免疫调节表位在猫过敏患者中有长期治疗效果。

Fel d 1-derived synthetic peptide immuno-regulatory epitopes show a long-term treatment effect in cat allergic subjects.

机构信息

Cetero Research, Mississauga, ON, Canada.

Adiga Life Sciences Inc., Hamilton, ON, Canada.

出版信息

Clin Exp Allergy. 2015 May;45(5):974-981. doi: 10.1111/cea.12488.

DOI:10.1111/cea.12488
PMID:25600085
Abstract

BACKGROUND

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.

OBJECTIVE

To evaluate the long-term effects of Cat-PAD on rhinoconjunctivitis symptoms following standardized allergen challenge 2 years after treatment.

METHODS

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.

RESULTS

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.

CONCLUSION AND CLINICAL RELEVANCE

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.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

结论和临床相关性

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。

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