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Timothy 草花粉舌下免疫治疗片对桦树花粉诱发的变应性鼻结膜炎在环境暴露单元中的作用缺失。

Lack of effect of Timothy grass pollen sublingual immunotherapy tablet on birch pollen-induced allergic rhinoconjunctivitis in an environmental exposure unit.

机构信息

Department of Medicine, Queen's University, Kingston, Ontario, Canada; Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada; Allergy Research Unit, Kingston General Health Research Institute, Kingston, Ontario, Canada.

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada; Allergy Research Unit, Kingston General Health Research Institute, Kingston, Ontario, Canada.

出版信息

Ann Allergy Asthma Immunol. 2018 May;120(5):495-503.e2. doi: 10.1016/j.anai.2018.02.003. Epub 2018 Feb 9.

Abstract

BACKGROUND

Timothy grass pollen allergen extract tablets (Grastek) are standardized sublingual immunotherapy tablets (SLIT-T) approved for the treatment of grass pollen-induced allergic rhinitis (AR) and conjunctivitis. Many grass allergic patients are also cosensitized to birch pollen. Whether Timothy grass SLIT-T can confer symptomatic benefits for birch pollen-induced AR symptoms is unknown.

OBJECTIVE

To evaluate the treatment effect of Timothy grass SLIT-T for birch pollen-induced AR in participants sensitized to both grass and birch pollen using an environmental exposure unit (EEU).

METHODS

This study was a phase 4, randomized, double-blind, placebo-controlled, parallel-group study that enrolled participants aged 18 to 65 years allergic to both timothy grass and birch pollen. After a baseline EEU birch pollen challenge, in which a minimum total nasal symptom score (TNSS) of 6 of 12 was required for enrollment, participants were randomized to receive Timothy grass SLIT-T or placebo taken once daily for 4 months. No confirmatory grass pollen challenge was performed. The primary end point was the change in TNSS averaged from assessments from hours 2 to 5 during the posttreatment birch pollen challenge compared with baseline. The secondary and exploratory end points included temporally identical changes in total ocular symptom score (TOSS), total rhinoconjunctivitis symptom score (TRSS), and individual symptom scores.

RESULTS

The difference in TNSS reduction after 4 months of therapy between the Timothy grass SLIT-T and placebo group was not significant (P = .83). Reductions in TOSS (P = .19) and TRSS (P = .67) were also comparable between groups. Findings between groups for individual symptom scores were similar (all P > .40), except for watery eyes, in which symptom reduction was slightly better in the placebo arm (P = .01). Timothy grass SLIT-T was well tolerated, and no serious adverse effects occurred.

CONCLUSION

A bystander effect of grass SLIT-T on birch pollen-induced AR symptoms was not detected. Symptomatic benefits of grass SLIT-T are likely allergen specific.

TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT02394600.

摘要

背景

Timothy 草花粉过敏原舌下免疫治疗片剂(Grastek)是一种经批准用于治疗草花粉引起的过敏性鼻炎(AR)和结膜炎的标准化舌下免疫治疗片剂(SLIT-T)。许多草过敏患者也对桦树花粉过敏。 Timothy 草 SLIT-T 是否能为桦树花粉引起的 AR 症状带来症状改善尚不清楚。

目的

使用环境暴露单元(EEU)评估 Timothy 草 SLIT-T 对同时对 Timothy 草和桦树花粉过敏的患者的桦树花粉诱导 AR 的治疗效果。

方法

这是一项 4 期、随机、双盲、安慰剂对照、平行分组研究,共纳入了 18 至 65 岁同时对 Timothy 草和桦树花粉过敏的患者。在基线 EEU 桦树花粉挑战中,需要至少 12 个总鼻症状评分(TNSS)中的 6 个才能入组,之后患者随机接受 Timothy 草 SLIT-T 或安慰剂,每日一次,持续 4 个月。未进行确认性草花粉挑战。主要终点是与基线相比,治疗后桦树花粉挑战期间从第 2 小时到第 5 小时平均 TNSS 的变化。次要和探索性终点包括时间相同的总眼部症状评分(TOSS)、总鼻结膜炎症状评分(TRSS)和各个症状评分的变化。

结果

Timothy 草 SLIT-T 治疗 4 个月后 TNSS 降低的差异在治疗组和安慰剂组之间无统计学意义(P = .83)。两组间 TOSS(P = .19)和 TRSS(P = .67)的降低也相似。组间各个症状评分的结果相似(均 P > .40),除了流泪症状,在安慰剂组中症状减轻稍好(P = .01)。 Timothy 草 SLIT-T 耐受性良好,未发生严重不良事件。

结论

未检测到草 SLIT-T 对桦树花粉诱导的 AR 症状的旁观者效应。草 SLIT-T 的症状改善可能是过敏原特异性的。

试验注册

ClinicalTrials.gov 标识符:NCT02394600。

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