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补体因子及其抑制剂在心肌梗死中的可能作用:一项免疫组织化学研究。

Possible role of complement factors and their inhibitors in the myocardial infarction: an immunohistochemical study.

作者信息

Ilczuk Tomasz, Wasiutynski Aleksander, Wilczek Ewa, Gornicka Barbara

机构信息

Department of Pathology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Cent Eur J Immunol. 2014;39(2):253-9. doi: 10.5114/ceji.2014.43731. Epub 2014 Jun 27.

Abstract

Ongoing development of our civilization is accompanied by a marked increase of incidence of cardiovascular diseases and cardiovascular mortality. Ischemic heart disease with its extreme form - myocardial infarction - is one of the main problems of modern medicine. Despite much research devoted to this disease entity, its pathomechanism remains incompletely understood. Basing on research reports, more and more emphasis is put on immune reactions in the myocardium. Available literature lacks detailed studies examining the role of complement system and its inhibitors in the development and pathogenesis of myocardial infarction. Cells of ischemic myocardium were proven to become foreign antigens for the immune system of the patient's body. This results in complement activation of formation of so called membrane attacking complex that injures myocardial cells. By binding to its surface, it extends the myocardial destruction caused by the infarction itself. Results of immunochemistry studies presented in this paper have demonstrated the existence colocalization of complement components (C4d, C9) and membrane inhibitors (CD55, CD59) as well as soluble inhibitors (factor H) of the complement in the examined muscle tissue that underwent ischemic necrosis. Positive immunohistochemical reaction was found in the myocardial cells, intercellular matrix and blood vessels.

摘要

我们文明的不断发展伴随着心血管疾病发病率和心血管死亡率的显著上升。缺血性心脏病及其极端形式——心肌梗死——是现代医学的主要问题之一。尽管对这种疾病实体进行了大量研究,但其发病机制仍未完全明了。基于研究报告,越来越多的重点放在心肌中的免疫反应上。现有文献缺乏对补体系统及其抑制剂在心肌梗死发生发展过程中作用的详细研究。缺血心肌细胞被证明会成为患者机体免疫系统的外来抗原。这会导致补体激活,形成所谓的膜攻击复合物,从而损伤心肌细胞。通过与心肌细胞表面结合,它会加剧梗死本身所造成的心肌破坏。本文所呈现的免疫化学研究结果表明,在经历缺血坏死的被检查肌肉组织中,补体成分(C4d、C9)与膜抑制剂(CD55、CD59)以及补体的可溶性抑制剂(H因子)存在共定位现象。在心肌细胞、细胞间基质和血管中发现了阳性免疫组化反应。

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