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接受水性疫苗特异性变应原免疫疗法的特应性犬中针对粉尘螨的IgG反应。

Dermatophagoides farinae-specific IgG responses in atopic dogs undergoing allergen-specific immunotherapy with aqueous vaccines.

作者信息

Hou Chia-Chun, Griffin Craig E, Hill Peter B

机构信息

The Royal Dick School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.

出版信息

Vet Dermatol. 2008 Aug;19(4):215-20. doi: 10.1111/j.1365-3164.2008.00682.x.

Abstract

The molecular and immunologic mechanisms associated with successful allergen-specific immunotherapy (ASIT) have not been completely elucidated. The aim of this study was to characterize the changes in Dermatophagoides farinae-specific IgG in atopic dogs undergoing ASIT using aqueous vaccines. Fifteen atopic dogs with a positive skin test reaction to D. farinae were treated with aqueous vaccines for a minimum of 2 months following a standard protocol. Serum samples were collected before and during therapy and used to probe Western blots containing separated proteins of D. farinae. IgG responses were detected using a polyclonal goat anticanine IgG antibody and a chromogenic substrate 3,3'-diaminobenzidine. The blots were analysed using a semiquantitative digital image analysis system that evaluated the number and molecular weight of bands, as well as their intensity, which was related to IgG concentration. Prior to ASIT, all dogs showed allergen-specific IgG responses to various antigens of D. farinae. During ASIT, there was a significant increase in the total quantity of D. farinae-specific IgG antibodies to various antigens from the mite (P = 0.015). Significant increases were observed for a 98-kDa band (P = 0.015), likely to be Der f 15; bands with molecular weights between 50 and 70kDa (P=0.012); and bands between 30 and 45 kDa (P = 0.035). These findings provide support for the hypothesis that ASIT induces IgG blocking antibodies to allergens known to be relevant in canine atopic dermatitis.

摘要

与成功的变应原特异性免疫疗法(ASIT)相关的分子和免疫机制尚未完全阐明。本研究的目的是表征使用水性疫苗进行ASIT的特应性犬中,针对粉尘螨的特异性IgG的变化。15只对粉尘螨皮肤试验反应呈阳性的特应性犬,按照标准方案接受水性疫苗治疗至少2个月。在治疗前和治疗期间采集血清样本,用于探测含有粉尘螨分离蛋白的蛋白质印迹。使用多克隆山羊抗犬IgG抗体和显色底物3,3'-二氨基联苯胺检测IgG反应。使用半定量数字图像分析系统分析印迹,该系统评估条带的数量、分子量及其强度,强度与IgG浓度相关。在ASIT之前,所有犬对粉尘螨的各种抗原均表现出变应原特异性IgG反应。在ASIT期间,针对螨的各种抗原的粉尘螨特异性IgG抗体总量显著增加(P = 0.015)。观察到一条98 kDa条带(P = 0.015)显著增加,可能是Der f 15;分子量在50至70 kDa之间的条带(P = 0.012);以及30至45 kDa之间的条带(P = 0.035)显著增加。这些发现为以下假设提供了支持,即ASIT诱导针对已知与犬特应性皮炎相关的变应原的IgG阻断抗体。

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