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一种新型、耐受性良好的螨变应原皮下免疫治疗:临床和免疫疗效的证据。

A novel and well tolerated mite allergoid subcutaneous immunotherapy: evidence of clinical and immunologic efficacy.

机构信息

Hospital Universitari Germans Trias Pujol, Unitat d'Al.lèrgia Barcelona, Catalonia, Spain.

Allergy Therapeutics East Worthing, BN14 8SA, UK.

出版信息

Immun Inflamm Dis. 2014 Aug;2(2):92-8. doi: 10.1002/iid3.23. Epub 2014 May 29.

Abstract

Allergy to house dust mite is one of the most common causes of allergic rhinitis. A novel tyrosine-adsorbed, modified allergen product, Acarovac Plus, developed for the treatment of perennial mite allergy seeks to address the underlying cause of allergic rhinitis in this instance. One of two dosing regimens may be used, either the Conventional Regimen or the Cluster Regimen. We sought to compare the efficacy and safety of a specific immunotherapy, developed for the treatment of perennial mite allergy, administered under a Conventional and Clustered dosing schedule in patients with persistent allergic rhinitis. Thirty adult patients, between 18 and 65 years old, with allergic rhinitis and/or asthma secondary to hypersensitivity to Dermatophagoides pteronyssinus were administered with either conventional or cluster initial regime, with a final visit one week after the last dose administration. The efficacy to the Conventional and Cluster regimens was measured using a Nasal Challenge Test monitoring clinical symptoms and peak nasal inspiratory flow. Total IgE, serum-specific inmunoglobulins (IgE and IgG4) to Dermatophagoides pteronyssinus and relevant cytokines (IFN-γ, IL-4, IL-5, IL-10 and IL-13) were assessed. A Satisfaction Questionnaire (TSQM) was completed after each patient's final visit. The tolerability of the vaccine was assessed monitoring adverse reactions. No adverse events were recorded in either conventional or cluster regime. The specific Nasal Challenge Test led to a decrease in symptom scores and a significant decrease in mean nasal peak inspiratory flow drop was recorded in both dosing regimen groups. A significant increase in IgG4-specific antibody titres was assessed. No significant changes were observed in concentrations of total IgE, specific IgE or cytokines (IFN-γ, IL-4, IL-5, IL-10 and IL-13). Patients declared themselves most satisfied in relation to "Secondary effects", with high overall satisfaction in both groups. Cluster and conventional specific immunotherapy resulted in no adverse reaction(s) and led to similar improvements in immunological parameters, clinical efficacy (Nasal Challenge Test) and high overall satisfaction.

摘要

屋尘螨过敏是过敏性鼻炎最常见的原因之一。一种新型的酪氨酸吸附、改良的过敏原产品 Acarovac Plus 被开发用于治疗常年性螨过敏,旨在解决这种情况下过敏性鼻炎的根本原因。可以使用两种剂量方案之一,即常规方案或群集方案。我们旨在比较针对常年性螨过敏开发的特定免疫疗法在常规和群集剂量方案下治疗持续性过敏性鼻炎患者的疗效和安全性。30 名年龄在 18 至 65 岁之间的成年患者,因对屋尘螨过敏而患有过敏性鼻炎和/或哮喘,给予常规或群集初始方案治疗,最后一次给药后一周进行最后一次就诊。使用鼻激发试验监测临床症状和最大鼻吸气流量来评估常规和群集方案的疗效。总 IgE、血清特异性免疫球蛋白(IgE 和 IgG4)对屋尘螨和相关细胞因子(IFN-γ、IL-4、IL-5、IL-10 和 IL-13)进行评估。每位患者最后一次就诊后完成满意度问卷(TSQM)。通过监测不良反应评估疫苗的耐受性。常规或群集方案均未记录到不良事件。特定的鼻激发试验导致症状评分降低,并且在两个剂量方案组中均记录到平均鼻峰吸气流量下降显著降低。评估了 IgG4 特异性抗体滴度的显著增加。总 IgE、特异性 IgE 或细胞因子(IFN-γ、IL-4、IL-5、IL-10 和 IL-13)的浓度没有观察到显著变化。患者在“次要作用”方面表示最满意,两组总体满意度均很高。群集和常规特异性免疫疗法均无不良反应,并导致免疫参数、临床疗效(鼻激发试验)和总体高满意度的相似改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd59/4217550/36c63e6d350e/iid30002-0092-f1.jpg

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