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评估一种用于检测特应性犬过敏原特异性IgE抗体的商业酶联免疫吸附测定(ELISA)试验。

Evaluation of a commercial ELISA test for the detection of allergen-specific IgE antibodies in atopic dogs.

作者信息

Ginel P J, Riaño C, Lucena R

机构信息

Department of Veterinary Clinical Pathology, Faculty of Veterinary Medicine, University of Córdoba, Spain.

出版信息

Zentralbl Veterinarmed B. 1998 Sep;45(7):421-5. doi: 10.1111/j.1439-0450.1998.tb00811.x.

Abstract

A commercial enzyme-linked immunosorbent assay (ELISA) designed to detect allergen-specific immunoglobulin (Ig)E antibodies were evaluated in 36 atopic dogs and in 12 normal dogs. The test showed a sensitivity of 72.23% and a specificity of 41.6%. Positive and negative predictive values were 76.47 and 35.71% respectively. Correlation between the ELISA kit results and intradermal skin testing varied depending on the allergen and ranged from 47.1 to 80.4%, although positive correlation (i.e. allergens positive in both tests) ranged rom 2.7 to 19.4%. In conclusion, this serological test gave both false positive and false negative results. Sensitivity, specificity and predictive values indicate that this ELISA may not be useful in canine atopy. Although correlation studies were hampered by the impossibility of using the same allergenic extracts, the correlation observed between intradermal and serological testing indicates that results from both tests are not interchangeable.

摘要

一种旨在检测变应原特异性免疫球蛋白(Ig)E抗体的商业酶联免疫吸附测定(ELISA)在36只特应性犬和12只正常犬中进行了评估。该测试的敏感性为72.23%,特异性为41.6%。阳性和阴性预测值分别为76.47%和35.71%。ELISA试剂盒结果与皮内皮肤试验之间的相关性因变应原而异,范围为47.1%至80.4%,尽管阳性相关性(即两项试验均为阳性的变应原)范围为2.7%至19.4%。总之,这项血清学检测出现了假阳性和假阴性结果。敏感性、特异性和预测值表明,这种ELISA可能对犬特应性疾病无用。尽管由于无法使用相同的变应原提取物而妨碍了相关性研究,但皮内试验和血清学检测之间观察到的相关性表明,两项试验结果不可互换。

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