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皮肤试验对预测链格孢菌鼻腔激发试验反应的作用

Skin testing in predicting response to nasal provocation with alternaria.

作者信息

Krouse John H, Shah Anand G, Kerswill Kristy

机构信息

Department of Otolaryngology, Wayne State University, Detroit, MI 48201, USA.

出版信息

Laryngoscope. 2004 Aug;114(8):1389-93. doi: 10.1097/00005537-200408000-00013.

DOI:10.1097/00005537-200408000-00013
PMID:15280713
Abstract

OBJECTIVE

Examine the efficacy of epicutaneous and intradermal testing in predicting response to nasal provocation with Alternaria antigen.

STUDY DESIGN AND SETTING

Prospective study. Subjects were tested with the Multi-Test II (MT) epicutaneous testing device. Subjects with negative wheals were then tested with a 1:500 weight:volume intradermal injection of Alternaria. They had baseline assessment of nasal cross-sectional area (CSA) using acoustic rhinometry and underwent nasal provocation with increasing Alternaria concentrations. CSA was assessed at each concentration. A nasal allergen provocation score (NAP) of nasal symptoms as well as a nasal visual analogue scale (VAS) were also completed with each concentration.

RESULTS

Sensitivity and specificity of MT in predicting nasal response to Alternaria were poor at 42% and 44%, respectively. The addition of intradermal testing increased sensitivity only modestly to 58%. hierarchical linear modeling analysis demonstrated that subjects positive to Alternaria on skin testing did not show a significant reduction in nasal CSA on acoustic rhinometry or significant elevations in two nasal symptom scores with direct nasal provocation.

CONCLUSION AND SIGNIFICANCE

Skin testing with either epicutaneous or intradermal testing may not be an accurate or sufficient technique in the assessment of Alternaria reactivity. These results suggest that mold allergies may involve more complex immune mechanisms than simply an immunoglobulin (Ig)E mediated type I immediate hypersensitivity response alone. An alternate model for mold sensitivity, as well as modifications in testing methods, may be required in the evaluation of mold allergy.

摘要

目的

研究表皮试验和皮内试验在预测对链格孢菌抗原鼻腔激发反应中的疗效。

研究设计与环境

前瞻性研究。受试者使用Multi-Test II(MT)表皮试验装置进行检测。风团反应阴性的受试者随后接受1:500重量/体积的链格孢菌皮内注射。使用声反射鼻测量法对鼻腔横截面积(CSA)进行基线评估,并对受试者进行浓度递增的链格孢菌鼻腔激发试验。在每个浓度下评估CSA。在每个浓度下还完成了鼻腔症状的鼻腔过敏原激发评分(NAP)以及鼻腔视觉模拟量表(VAS)。

结果

MT预测鼻腔对链格孢菌反应的敏感性和特异性较差,分别为42%和44%。添加皮内试验后,敏感性仅适度提高至58%。分层线性模型分析表明,皮肤试验对链格孢菌呈阳性的受试者在声反射鼻测量中鼻腔CSA没有显著降低,直接鼻腔激发试验中两个鼻腔症状评分也没有显著升高。

结论与意义

表皮试验或皮内试验进行皮肤检测在评估链格孢菌反应性时可能不是一种准确或充分的技术。这些结果表明,霉菌过敏可能涉及比单纯免疫球蛋白(Ig)E介导的I型速发型超敏反应更复杂的免疫机制。在评估霉菌过敏时,可能需要一种替代的霉菌敏感性模型以及检测方法的改进。

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