期刊论文详细信息
ENDOGENOUS FIBRINOLYTIC SYSTEM IN CHRONIC LARGE-VESSEL THROMBOEMBOLIC PULMONARY-HYPERTENSION
Note
关键词: PLASMINOGEN-ACTIVATOR INHIBITOR;    HUMAN-ENDOTHELIAL CELLS;    FAST-ACTING INHIBITOR;    DEEP-VEIN THROMBOSIS;    HUMAN-PLASMA;    VENOUS THROMBOEMBOLISM;    MONOCLONAL-ANTIBODY;    PROTEIN-S;    TISSUE;    PURIFICATION;   
DOI  :  10.1161/01.CIR.86.4.1241
来源: SCIE
【 摘 要 】

Background. Chronic thromboembolic pulmonary hypertension (CTEPH) is a disorder characterized by pulmonary arterial hypertension as a consequence of organized thrombotic material in the central pulmonary arteries. Incomplete resolution of acute pulmonary emboli is believed to be pathogenically important; however, the mechanism for poor thrombus dissolution remains to be explained. We undertook this study to assess the major determinants of plasma fibrinolysis in patients with CTEPH (n=32). Methods and Results. Immunological and functional levels of tissue-type plasminogen activator (t-PA) and type 1 plasminogen activator inhibitor (PAI-1) were quantified in platelet-poor plasma (PPP) from patients with CTEPH as well as age-matched controls. Although basal PPP t-PA antigen levels (CTEPH mean, 29.5 ng/ml; control mean, 2.7 ng/ml) and PAI-1 antigen levels (CTEPH mean, 55.8 ng/ml; control mean, 21.0 ng/ml) were higher in the CTEPH group, no between-group differences were detected in the enzymatic activities of these two molecules. The CTEPH group demonstrated a greater rise in t-PA antigen (CTEPH mean rise, 53.0 ng/ml; control mean rise, 5.6 ng/ml) and PA activity (CTEPH mean rise, 10.5 IU/ml; control mean rise, 1.2 IU/ml) than controls in response to an experimentally induced venous occlusion. Immunoprecipitation and fibrin autography of PPP from two patients with markedly elevated basal t-PA antigen levels demonstrate that the t-PA antigen was present in PPP primarily in complex with PAI-1. Conclusions. Although abnormalities of the fibrinolytic system were detected, neither a high resting plasma PAI-1 activity nor a blunted response of t-PA to venous occlusion can be invoked as an etiology for CTEPH.

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