首页> 外文期刊>Transfusion and apheresis science: official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis >The contact system at the crossroads of various key patho- physiological functions: Update on present understanding, laboratory exploration and future perspectives
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The contact system at the crossroads of various key patho- physiological functions: Update on present understanding, laboratory exploration and future perspectives

机译:各种关键良理生理功能的十字路口的接触系统:关于现有理解,实验室探索和未来观点的更新

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The contact system initiates the intrinsic pathway of coagulation and is started by Factor XII activation, which then activates prekallicrein to kallicrein and Factor XI to Factor XIa and, in the presence of high molecular weight kininogen, forms a "contact phase activation loop", that amplifies Factor XII activation. FXII deficiency is not associated with bleeding tendencies, but when the blood clots, the thrombus is less dense, thus favoring antithrombotic protection. Activated Factor XII inhibition emerges as an efficient target for preventing thromboembolic diseases without inducing a hemorrhagic risk. Activated Factor XII exhibits other activities, in that it can activate complement and provoke inflammation, contributing to innate immunity. It also stimulates fibrinolysis through uPA activation from scu-PA. Among the other components of the contact phase, Factor XI has a more important role in coagulation pathways and can directly activate FX, FVIII and FV, in a FIX independent pathway. Its deficiency is associated with a mild bleeding diathesis ("pseudo-hemophilia" or hemophilia C), with a variable incidence among kindreds. Recently, the occurrence of thrombotic events the same day following infusion of immunoglobulin concentrates has been demonstrated to be caused by the presence of trace amounts of activated Factor XI, pointing out the key role of this factor for thrombogenicity. Prekallicrein can be activated at the endothelial surface in the presence of high molecular weight kininogen, whose cleavage generates bra-dykinins and contributes to vessel tonicity and inflammation. The contact phase, through its activation loop, is then an important physiological system, which can initiate and regulate various biological functions and is at the crossroads of various biological activities. Many of the body's physiological functions are intimately linked between them, making the global approach of special usefulness for understanding the interactions which can result from any abnormality of one of them. New pharmaceutical drugs targeting a defined activity need to be investigated for all the possible interferences or side effects. In this article we aim to present and summarize the present understanding of contact phase system activation and regulation, its involvement in various physiological functions, and the laboratory tools for its exploration.
机译:接触系统启动凝血的内在途径,并通过因子XII活化开始,然后激活前Kallicrein至Kallicrein和因子Xi以因子XIA,并且在高分子量激动学的存在中,形成“接触相活化环”,形成“接触期活化环”放大因子XII激活。 FXII缺乏与出血倾向无关,但是当血凝块时,血栓较少,因此有利于抗血栓形成保护。活化因子XII抑制作为预防血栓栓塞疾病而不引起出血风险的有效靶标。激活因子XII展示其他活动,因为它可以激活补体和挑衅炎症,有助于先天免疫力。它还通过SCU-PA的UPA活化刺激纤维蛋白溶解。在接触阶段的其他组分中,因子XI在凝血途径中具有更重要的作用,并且可以在固定的独立途径中直接激活FX,FVIII和Fv。它的缺陷与轻度血液化素质(“伪血友病”或血友病C)有关,可变性的粘性发生率。最近,已经证明了在输注免疫球蛋白浓缩物后的同一天的发生血栓形成的发生是由痕量活性因子XI的存在引起的,指出该因素的血栓形成性的关键作用。在高分子量激动学的存在下,可以在内皮表面活化前kallicrein,其裂解产生BRA-脊柱蛋白并有助于血管张力和炎症。通过其活化环,接触阶段是一个重要的生理系统,可以启动和调节各种生物学功能,并且是各种生物活性的十字路口。许多身体的生理功能与它们之间密切相关,使得全球特殊用途的方法,了解可能因其中一个异常而导致的相互作用。需要针对所有可能的干扰或副作用调查靶向定义活性的新药物药物。在本文中,我们的目标是展示和总结对联系期系统激活和监管的现状,其参与各种生理功能,以及其勘探的实验室工具。

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