首页> 外国专利> METHOD FOR DETERMINING THE FUNCTIONAL ACTIVITY OF THE HUMAN COMPLEMENT SYSTEM FOR PREDICTING THE SEVERITY OF THE COURSE OF A SYSTEMIC INFLAMMATORY REACTION

METHOD FOR DETERMINING THE FUNCTIONAL ACTIVITY OF THE HUMAN COMPLEMENT SYSTEM FOR PREDICTING THE SEVERITY OF THE COURSE OF A SYSTEMIC INFLAMMATORY REACTION

机译:确定人体补体系统功能活性的方法,以预测全身炎症反应过程的严重程度

摘要

FIELD: diagnostics.;SUBSTANCE: invention relates to diagnostics, namely to a method for determining the functional activity of the classical pathway of the human complement system for predicting the severity of the course of the systemic inflammatory response. A method for determining the functional activity of the classical pathway of the human complement system for predicting the severity of the course of a systemic inflammatory reaction includes carrying out a lysis reaction of human erythrocytes of group A of the AB0 system (E(A)), sensitized with anti-A monoclonal IgM antibodies (E(A)mAb) and serum under conditions of veronal saline buffer (VBS2+), incubation of the obtained sample, then the reaction of complement-dependent lysis of E(A)mAb is evaluated turbidimetrically, by reducing the optical density of the suspension E(A)mAb at a wavelength of 620 nm determines the degree of erythrocyte lysis in experimental samples according to the calibration graph, where the control E(A)mAb represents 0% lysis, and the control of complete lysis E(A)mAb is 100% lysis, under certain conditions, while the increased functional activity of the classical pathway of the human complement system is noted with a degree of lysis of more than 60%, with a degree lysis from 31% to 59% as normal and with a degree of lysis less than 30% as reduced functional activity of the human complement system.;EFFECT: above-described method allows increasing the accuracy of the method for studying the functional activity of the classical pathway of the complement system, as well as to simplify the registration of the results of the analysis of the functional activity of the classical pathway of the complement system in routine studies and adaptation of the method for screening studies in the conditions of clinical diagnostic laboratories.;1 cl, 5 dwg, 2 tbl, 2 ex
机译:现场:诊断。;物质:发明涉及诊断诊断,即用于确定人体补体系统经典途径的功能活性,以预测全身炎症反应的过程的严重程度。用于确定人体补体系统的经典途径的功能活性,以预测全身炎症反应过程的严重程度,包括实施AB0系统的A组A的人红细胞的裂解反应(E(a)) ,用抗A单克隆IgM抗体(E(a)mAb)和血清在牛盐缓冲液(Vbs2 +)条件下敏化,评价所得样品的所得样品的培养,然后评估e(a)mab的补体依赖性溶解的反应通过减小悬浮液E(a)mab的光学密度在620nm的波长下确定根据校准图的实验样品中的红细胞裂解程度,其中控制e(a)mab表示0%裂解,和在某些条件下,对完全裂解e(a)mab的控制是100%裂解的,而人体补体系统的经典途径的官能活性增加的裂解程度超过60%,含有灰度从31%到59%的REE裂解,正常,裂解程度小于30%,降低人类补体系统的功能活性。;效果:上述方法允许增加用于研究功能活动的方法的准确性补体系统的经典途径,以及简化了常规研究中补体系统经典途径的功能活性的结果的登记,并适应临床诊断条件下的筛选研究方法实验室。; 1 cl,5 dwg,2 tbl,2前

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