Rossi Renato E, Monasterolo Giorgio, Incorvaia Cristoforo, Moingeon Philippe, Frati Franco, Passalacqua Giovanni, Rossi Lucilla, Canonica Giorgio W
Allergy Unit, National Health Service, Rete di Allergologia Regione Piemonte, Cuneo 1, Italy.
Clin Mol Allergy. 2010 Mar 15;8:4. doi: 10.1186/1476-7961-8-4.
Some studies reported the possible induction of food allergy, caused by neo-sensitization to cross-reacting allergens, during immunotherapy with aeroallergens, while other studies ruled out such possibility.
The aim of this study was to evaluate the development of neo-sensitization to Pen a 1 (tropomyosin) as well as the appearance of reactions after ingestion of foods containing tropomyosin as a consequence of sublingual mite immunization.
Specific IgE to Tropomyosin (rPen a 1) before and after mite sublingual immunotherapy in 134 subjects were measured. IgE-specific antibodies for mite extract and recombinant allergen Pen a 1 were evaluated using the immunoenzymatic CAP system (Phadia Diagnostics, Milan, Italy).
All patients had rPen a 1 IgE negative results before and after mite SLIT and did not show positive shrimp extract skin reactivity and serological rPen a 1 IgE conversion after treatment. More important, no patient showed systemic reactions to crustacean ingestion.
Patients did not show neo-sensitization to tropomyosin, a component of the extract (namely mite group 10) administered. An assessment of a patient's possible pre-existing sensitisation to tropomyosin by skin test and/or specific IgE prior to start mite extract immunotherapy is recommended.
This trial is registered in EudraCT, with the ID number of 2010-02035531.
一些研究报告称,在气传变应原免疫治疗期间,对交叉反应性变应原的新致敏可能引发食物过敏,而其他研究则排除了这种可能性。
本研究旨在评估经舌下螨免疫治疗后对Pen a 1(原肌球蛋白)新致敏的发生情况,以及摄入含原肌球蛋白食物后反应的出现情况。
检测了134名受试者在螨舌下免疫治疗前后针对原肌球蛋白(重组Pen a 1)的特异性IgE。使用免疫酶联CAP系统(意大利米兰法迪亚诊断公司)评估螨提取物和重组变应原Pen a 1的IgE特异性抗体。
所有患者在螨舌下免疫治疗前后rPen a 1 IgE结果均为阴性,治疗后未出现虾提取物皮肤反应阳性及血清rPen a 1 IgE转换。更重要的是,没有患者在摄入甲壳类食物后出现全身反应。
患者未对所给予提取物(即螨第10组)的成分原肌球蛋白产生新致敏。建议在开始螨提取物免疫治疗前,通过皮肤试验和/或特异性IgE对患者可能预先存在的原肌球蛋白致敏情况进行评估。
本试验已在欧洲临床试验数据库(EudraCT)注册,注册号为2010 - 02035531。