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一种用于儿童过敏测试的基于新型玻璃微纤维的组胺分析方法。结果与传统白细胞组胺释放试验、皮肤点刺试验、支气管激发试验及放射变应原吸附试验进行比较。

A new glass microfibre-based histamine analysis for allergy testing in children. Results compared with conventional leukocyte histamine release assay, skin prick test, bronchial provocation test and RAST.

作者信息

Nolte H, Schiøtz O, Skov P S

出版信息

Allergy. 1987 Jul;42(5):366-73. doi: 10.1111/j.1398-9995.1987.tb02223.x.

Abstract

A new microfibre method for allergy testing measuring histamine release from human basophil leukocytes is described. Samples of 50 microliter washed blood are challenged with the suspected allergens. Released histamine is bound to microfibres and measured by a spectrofluorometrical method after removal of interfering substances by washing. The microfibre method (HR-MM) was compared to the conventional histamine release assay using the Ficoll-Hypaque gradient method (HR-FH) in 19 allergic children tested with one of three allergens. In addition, a comparison was made between the microfibre method and in vivo provocation tests, i.e. skin prick test (SPT), bronchial provocation test (BPT) and allergen specific serum IgE (RAST). It was found that the same individuals responded with histamine release to the same allergens in both histamine release assays, and the dose-response curves were almost identical. A positive correlation was found between the in vivo and in vitro tests. Thus it is concluded that the new method can provide reproducible, analytically precise (at the nanogram level) histamine release results in pediatric cases where: a positive SPT does not correlate with case history; BPT may be considered too hazardous or inconvenient; confirmation of negative or inconclusive SPT or RAST is needed. In contrast to other histamine release assays it is a convenient diagnostic tool in children since only small amounts of blood are needed and at least 96 tests can be carried out in 2 1/2 h.

摘要

本文描述了一种用于过敏测试的新型微纤维方法,该方法可测量人嗜碱性白细胞释放组胺的情况。用50微升洗涤后的血液样本与可疑过敏原进行反应。释放出的组胺与微纤维结合,在通过洗涤去除干扰物质后,采用荧光分光光度法进行测量。在19名对三种过敏原之一进行测试的过敏性儿童中,将微纤维方法(HR-MM)与使用Ficoll-Hypaque梯度法的传统组胺释放试验(HR-FH)进行了比较。此外,还对微纤维方法与体内激发试验,即皮肤点刺试验(SPT)、支气管激发试验(BPT)和过敏原特异性血清IgE(RAST)进行了比较。结果发现,在两种组胺释放试验中,相同个体对相同过敏原的组胺释放反应相同,且剂量反应曲线几乎一致。体内试验和体外试验之间存在正相关。因此得出结论,在以下儿科病例中,新方法能够提供可重复的、分析精确(纳克水平)的组胺释放结果:SPT阳性与病史不相关;BPT可能被认为过于危险或不方便;需要确认SPT或RAST阴性或不确定的情况。与其他组胺释放试验不同,该方法对儿童来说是一种方便的诊断工具,因为只需要少量血液,并且在2个半小时内至少可以进行96次检测。

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