Nishi H, Nishimura S, Higashiura M, Ikeya N, Ohta H, Tsuji T, Nishimura M, Ohnishi S, Higashi H
Diagnostic Science Division, Shionogi and Co., Ltd., 2-5-1 Mishima, Settsu-shi, Osaka, Japan.
J Immunol Methods. 2000 Jun 23;240(1-2):39-46. doi: 10.1016/s0022-1759(00)00169-1.
A new method for evaluating histamine release from purified basophils was developed. Basophil-containing leukocytes were directly purified from a small amount of peripheral blood using monoclonal antibody BA312-coated magnetic beads. The purified basophils still rosetted to magnetic beads maintained a normal response to anti-IgE and to dust mite allergen in comparison with the conventional method using washed leukocytes. This methodology facilitates the purification of basophils, anti-IgE- and allergen-induced histamine release, and subsequent histamine determination within only 3 h. The released histamine was analyzed by an enzyme-linked immunosorbent assay (ELISA) with a characteristic detection profile. Since all steps were performed in 96-well microplates, many clinical samples could be analyzed at the same time, permitting easy applications in routine laboratories.
开发了一种评估纯化嗜碱性粒细胞组胺释放的新方法。使用包被单克隆抗体BA312的磁珠直接从少量外周血中纯化含嗜碱性粒细胞的白细胞。与使用洗涤白细胞的传统方法相比,纯化的嗜碱性粒细胞仍与磁珠形成玫瑰花结,对抗IgE和尘螨过敏原保持正常反应。这种方法有助于嗜碱性粒细胞的纯化、抗IgE和过敏原诱导的组胺释放,以及仅在3小时内进行后续组胺测定。通过具有特征性检测谱的酶联免疫吸附测定(ELISA)分析释放的组胺。由于所有步骤均在96孔微孔板中进行,因此可同时分析许多临床样本,便于在常规实验室中应用。