[Study of functional activity of components and factors of the human complement system].

Voprosy meditsinskoi khimii Pub Date : 2002-11-01
L V Kozlov
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Abstract

Development suitable for clinical researches of hemolytic methods of determination of functional activity of the first components of a complement has allowed to show diagnostic value of testing activity of complement components in comparison with their contents as antigens. It has predetermined necessity for building modern ELISA tests-systems for quantitative determination of functional activity of complement components. Such methods built for the first time allow to determine activity of components C1q, C2, C3, C4 (and a ratio of isotypes C4A and C4B), C1-inhibitor, factors B and D. Addition of these tests-systems ELISA systems for quantitative determination of components, and in case of C1-inhibitor of presence IgG, IgA and IgM autoantibodies against C1-inhibitor frames opportunities of an evaluation complement status of the patient, hereditary predisposition to such diseases as a stomach ulcer, the glaucoma, a clamidiosis, bacteroidosis, allows to carry out differential diagnostics of angioedema. Inhibition of covalent linkage C4b or C3b various endogenic and exogenous effectors during formation C3- and C5-convertases allows to understand processes of a regulation of a homeostasis, and also the mechanism of action of drugs.

人体补体系统成分和因子的功能活性研究。
开发适合临床研究的溶血方法,测定补体第一组分的功能活性,可以显示补体组分的检测活性与其作为抗原的含量的诊断价值。建立现代酶联免疫吸附试验系统定量测定补体组分的功能活性,具有预先确定的必要性。这些首次建立的方法允许测定组分C1q、C2、C3、C4(以及同型C4A和C4B的比例)、c1抑制剂、因子B和d的活性。增加了这些检测系统——用于定量测定组分的ELISA系统,在c1抑制剂存在的情况下,针对c1抑制剂的IgG、IgA和IgM自身抗体框架有机会评估患者的补体状态,对胃溃疡、青光眼等疾病的遗传易感性。样杆菌病可以进行血管性水肿的鉴别诊断。在C3-和c5转化酶形成过程中,抑制共价连锁C4b或C3b各种内源性和外源性效应物,可以理解体内平衡的调节过程,以及药物的作用机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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