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北美成年人的猫尾草过敏免疫治疗片治疗的疗效和安全性。

Efficacy and safety of timothy grass allergy immunotherapy tablet treatment in North American adults.

机构信息

Department of Medicine, Division of Allergy and Immunology, National Jewish Health, Denver, Colo., USA.

出版信息

J Allergy Clin Immunol. 2011 Jan;127(1):72-80, 80.e1-2. doi: 10.1016/j.jaci.2010.11.035.

Abstract

BACKGROUND

Immunotherapy for allergic rhinoconjunctivitis (ARC) in North America is generally administered subcutaneously, but alternative formulations might be safer and more convenient. Trials of sublingual formulations in North America are needed to confirm European efficacy and safety data.

OBJECTIVE

We sought to investigate the efficacy and safety of timothy grass allergy immunotherapy tablet (AIT) treatment in North American subjects with ARC.

METHODS

Four hundred thirty-nine adults with grass pollen-induced ARC with or without asthma were randomized to once-daily 2,800 bioequivalent allergen units of standardized grass AIT (oral lyophilisate, Phleum pratense, 75,000 standardized quality tablet, containing approximately 15 μg of Phl p 5) or placebo approximately 16 weeks before the 2009 grass pollen season (GPS). The primary end point was the average total combined score of the daily symptom score and the daily medication score during the GPS. Rhinoconjunctivitis Quality of Life Questionnaire with standardized activities (RQLQ[S]) scores, Phl p 5-specific IgG4 levels, and IgE-blocking factor levels were additional end points. Adverse events (AEs) were monitored for safety.

RESULTS

Relative to placebo, grass AIT treatment improved total combined scores by 20% (P = .005), daily symptom scores by 18% (P = .02), and RQLQ(S) scores by 17% (P = .02). Daily medication scores were improved by 26% and trended toward significance (P = .08). Phl p 5-specific IgG4 and IgE-blocking factor levels were higher after grass AIT treatment compared with those after placebo at the end of the GPS (P < .001). Grass AIT treatment was safe and well tolerated. The majority of AEs were transient mild local reactions with no investigator-diagnosed grass AIT-related serious AEs or reports of anaphylactic shock/respiratory compromise. In the grass AIT group, 1 subject received epinephrine after experiencing a possible grade 1 systemic reaction (local site reactions, chest discomfort, and rash).

CONCLUSIONS

Timothy grass AIT treatment (cross-reactive with related Pooideae grasses) was demonstrated to be effective, generally safe, and well tolerated in North American adults with grass pollen-induced ARC.

摘要

背景

在北美,治疗变应性鼻结膜炎(ARC)的免疫疗法一般采用皮下注射,但替代制剂可能更安全、更方便。需要在北美开展舌下制剂的试验来验证欧洲的疗效和安全性数据。

目的

我们旨在研究 Timothy 草变应原免疫治疗片(AIT)治疗北美 ARC 患者的疗效和安全性。

方法

439 例患有花粉诱发的 ARC 伴或不伴哮喘的成年患者,随机分为每日一次接受 2800 个生物等效过敏原单位标准化草 AIT(口服冻干制剂,Phleum pratense,75000 个标准化质量片剂,含约 15μg Phl p 5)或安慰剂,治疗时间大约为 2009 年花粉季节(GPS)前 16 周。主要终点为 GPS 期间每日症状评分和每日用药评分的平均总分。 Rhinoconjunctivitis Quality of Life Questionnaire with standardized activities(RQLQ[S])评分、Phl p 5 特异性 IgG4 水平和 IgE 阻断因子水平为次要终点。监测不良事件(AE)以评估安全性。

结果

与安慰剂相比,草 AIT 治疗使总评分改善 20%(P =.005),每日症状评分改善 18%(P =.02),RQLQ[S]评分改善 17%(P =.02)。每日用药评分改善 26%,且有显著趋势(P =.08)。GPS 结束时,草 AIT 治疗组的 Phl p 5 特异性 IgG4 和 IgE 阻断因子水平高于安慰剂组(P <.001)。草 AIT 治疗安全且耐受性良好。大多数 AE 为短暂的轻度局部反应,无研究者诊断的草 AIT 相关严重 AE 或过敏反应/呼吸窘迫报告。在草 AIT 组中,1 例患者在经历可能为 1 级全身反应(局部反应部位、胸痛和皮疹)后接受了肾上腺素治疗。

结论

在北美花粉诱导的 ARC 成年患者中, Timothy 草 AIT 治疗(与相关 Pooideae 草交叉反应)被证实是有效、一般安全且耐受良好的。

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