志贺样毒素ⅰ型和ⅱ型检测酶免疫分析法的建立

G. V. Kuklina, D. Pechenkin, S. S. Ipatov, Andrei Valentinovich Eremkin, Aleksei Aleksandrovich Kytmanov, O. V. Tikhvinskaya
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摘要

介绍。本研究的目的是建立一种检测ⅰ型和ⅱ型志贺样毒素的酶免疫分析法,并评估其诊断特性。材料和方法。在这项研究中,我们使用的杂交瘤产生单克隆抗体的志贺样毒素的I型和II型,从俄罗斯联邦国防部的联邦国家预算机构“48中央研究所”的分支机构(基洛夫)获得;BALB / c小鼠;志贺样I型和II型毒素。在培养瓶和BALB/c小鼠腹腔内培养杂交瘤细胞。采用饱和硫酸铵沉淀法从腹水中分离单克隆抗体,并用离子交换色谱法纯化。所得单克隆抗体用于ⅰ型和ⅱ型志贺样毒素的酶免疫检测。酶免疫测定的特定组分在保护环境中冷冻干燥。结果。通过研究,获得并纯化了抗ⅰ型和ⅱ型志贺样毒素的单克隆抗体;选择单克隆抗体用于固相吸附和免疫过氧化物酶偶联物的合成。结论。建立了“三明治”中1 ng/ml I型和II型志贺样毒素的实验酶免疫分析法-ELISA法。
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Development of enzyme immunoassay for detecting I and II types of shiga-like toxins
Introduction. The aim of the work was development of enzyme immunoassay for detecting I and II types of shiga-like toxins and assessment of it diagnostic properties. Materials and methods. For the research, we used hybridomas producing monoclonal antibodies to shiga-like toxins of types I and II, obtained at the branch of the Federal State Budgetary Institution “48 Central Research Institute” of the Ministry of Defense of Russian Federation (Kirov); BALB/c mice; shiga-like toxins of types I and II. Hybridoma cells were cultured in culture flasks and in the peritoneal cavity of BALB/c mice. Monoclonal antibodies were isolated from ascitic fluids by precipitation with a saturated solution of ammonium sulfate, followed by purification by ion exchange chromatography. The obtained preparations of monoclonal antibodies were used to develop enzyme immunoassay for the detection of shiga-like toxins of types I and II. Specific components of enzyme immunoassay were freeze-dried in a protective environment. Results. As a result of research, preparative quantities of monoclonal antibodies against I and II types of shiga-like toxins were obtained and purified; selection of monoclonal antibodies for sorption on the solid phase and for the synthesis of immunoperoxidase conjugates was carried out. Conclusion. experimental enzyme immunoassay allowing to identify 1 ng/ml I and II types of shiga-like toxins in «sandwich»-ELISA was developed.
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