Sublingual Immunotherapy of Birch Pollen Associated Apple Allergy
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- allergen concentration to induce allergic reactions in the oral cavity as a measure of efficacy (oral provocation test)
研究概览
简要总结
More than 70% of birch pollen allergic patients suffer from allergic reactions to certain foods, e.g. stone fruits, hazelnut and some vegetables. However, specific immunotherapy (SIT) with birch pollen extract is not effective for the treatment of associated food allergy in a substantial number of patients. Based on our previous clinical and immunological investigations of birch pollen related food allergy (BPRFA) the investigators hypothesize that for effective SIT of this abundant food allergy the disease-eliciting food allergens should be employed. To prove this concept, the investigators aim to sublingually administer the major apple allergen, Mal d 1, to birch pollen-allergic patients with concomitant apple allergy and evaluate clinical and immunological effects of this treatment. The investigators choose Mal d 1 as model food allergen because (i) its cross-reactivity with Bet v 1 has been well characterized,(ii) apple is the most frequent trigger for BPRFA and (iii) recombinant(r)Mal d 1 was well tolerated after sublingual administration to 20 birch pollen-allergic patients in a previous study. Sublingual administration of a defined concentration of GMP-rMal d 1 will be compared with equal doses of GMP-rBet v 1 as a positive control and placebo-treatment. Clinical parameters will include skin prick tests (SPT) and objective and subjective assessment of apple and birch pollen-induced allergic symptoms. Immunological parameters will comprise the analysis of antibody and T cell responses to Mal d 1 and Bet v 1 as well as the evaluation of basophil activation.
The proposed pilot study will be a first investigation of the concept to specifically treat BPRFA with the involved food allergens and thus, represents an important step in the development of an efficient and safe therapy in the future.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •otherwise healthy persons between 18 und 50 years of age;
- •positive history of rhinoconjunctivitis to birch pollen
- •oral allergy syndrome(OAS) to apple
- •positive skin prick test (SPT) reaction to birch pollen and apple
- •specific IgE for Bet v 1 and Mal d 1
排除标准
- •Exclusion criteria
- •Persons who due to their physical or mental state are not able to provide informed consent.
- •Persons with underlying illnesses such as severe cardiopulmonary, malignant and/or autoimmune diseases
- •Persons suffering from Hyper-IgE syndrome
- •Persons receiving SIT during the past 5 years
- •persons suffering from severe allergic reactions to apple such as generalized urticaria, asthma and/or anaphylaxis
- •persons suffering from severe bronchial asthma to birch pollen
- •persons suffering from pathological alterations of the lips and oral mucosa
- •persons who are prescribed a treatment with immune-suppressive drugs, anti-histamines, leukotriene-antagonists or psychotropic drugs with anti-histaminic effects
- •persons using ß-blockers
- •Pregnant woman
研究组 & 干预措施
treatment with rMal d 1
these apple and birch pollen allergic patients are treated with daily sublingual application of 25µg recombinant Major apple allergen, Mal d 1 during 4 months
干预措施: rMal d 1 (Drug)
treatment with rBet v 1
These apple and birch pollen allergic patients are treated with daily sublingual application of 25µg recombinant Major birch pollen allergen,Bet v 1 during 4 months
干预措施: rBet v 1 (Drug)
treatment with placebo drops
These apple and birch pollen allergic patients are treated daily with placebo applied sublingually during 4 months
干预措施: placebo drops (Other)
结局指标
主要结局
allergen concentration to induce allergic reactions in the oral cavity as a measure of efficacy (oral provocation test)
时间窗: 1 year
To measure the clinical effects on apple-induced OAS, open food challenges (OFC) with every 30 minutes increasing doses of GMP-rMal d 1 will be performed before and after the treatment period.
次要结局
- T cell proliferation and cytokine production as a measure of tolerance induction(1 year)
- allergen specific antibody response(1)
研究者
Tamar Kinaciyan, MD
MD, Ass.Prof.
Medical University of Vienna
