Siraganian R P, Brodsky M J
J Allergy Clin Immunol. 1976 Jun;57(6):525-40. doi: 10.1016/0091-6749(76)90003-8.
A sensitive, automated, histamine assay system has been developed and applied for in vitro allergy testing. Nine common pollen and environmental allergens were used at three log dilutions for in vivo studies utilizing small volumes of blood (15-20 ml). The clinical evaluation was correlated with the results of the histamine release. two different procedures were utilized. The first is the commonly used histamine release from washed leukocytes. There was excellent correlation between the clinical evaluation and the results of histamine release from washed leukocytes in 17 different individuals. The second and simpler method utilized whole heparinized blood which might better reflect the immunologic reaction which occurs in vivo. Aliquots of blood and allergen were incubated for 1 hr at 37 degrees C and each supernatant was then analyzed for histamine release. There was excellent correlation between the two tests in 29 patients tested by both the whole blood and washed leukocyte methods. There was also good correlation between the clinical evaluation of the patients amd the intro tests. The precision, accuracy, and sensitivity of the automated histamine assay make feasible its routine application in the clinical study of allergic patients.
一种灵敏的、自动化的组胺检测系统已被开发出来并应用于体外过敏测试。在利用少量血液(15 - 20毫升)进行的体内研究中,对9种常见花粉和环境过敏原进行了三个对数稀释度的测试。临床评估与组胺释放结果相关。采用了两种不同的程序。第一种是常用的从洗涤过的白细胞中释放组胺的方法。在17名不同个体中,临床评估与从洗涤过的白细胞中释放组胺的结果之间存在极好的相关性。第二种更简单的方法使用全肝素化血液,这可能更好地反映体内发生的免疫反应。将血液和过敏原的等分试样在37℃下孵育1小时,然后对每个上清液进行组胺释放分析。在通过全血和洗涤白细胞方法进行测试的29名患者中,两种测试之间存在极好的相关性。患者的临床评估与体内测试之间也存在良好的相关性。自动化组胺检测的精密度、准确性和灵敏度使其在过敏患者的临床研究中的常规应用成为可能。