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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/21260


    Title: 血漿溶解性尿激?型纖溶?原活化因子受體與社區型肺炎嚴重程度的探討
    Ping-Kun Tsai
    Authors: 蔡秉昆
    Tsai, Ping-Kun
    Contributors: 中山醫學大學:醫學院醫學研究所;楊順發(Shun-Fa Yang)
    Keywords: 社區型肺炎;溶解性尿激?型血纖維蛋白溶解?原活化因子受體;脂多醣;肺炎嚴重程度指數
    community-acquired pneumonia;suPAR;LPS;pneumonia severity index
    Date: 2020-07-01
    Issue Date: 2021-01-15T02:04:45Z (UTC)
    Abstract: 尿激?型血纖維蛋白溶解?原活化因子受體 (urokinase-type plasminogen activator receptor, uPAR) 可調解各種細胞活性,並參與蛋白水解、血管生成和發炎。在這項研究中其目的為探討溶解性uPAR  (soluble PAR, suPAR)程度與社區型肺炎 (community-acquired pneumonia, CAP) 嚴重程度之間的關聯性。我們首先利用酵素免疫分析法 (Enzyme-linked immunosorbent assay; ELISA) 進行測量67位健康對照組和75位CAP患者其血漿中suPAR的濃度。我們的結果顯示,與對照組相比,CAP患者血漿中suPAR濃度有顯著升高,而抗生素治療可有效降低suPAR的濃度。基於肺炎嚴重程度指數 (pneumonia severity index, PSI)評分,血漿suPAR濃度與CAP嚴重程度具關聯性。此外,我們利用細胞實驗觀察到,在脂多醣 (lipopolysaccharide, LPS)的刺激下會顯著增加uPAR在RAW 264.7巨噬細胞中的表現。總結以上,血漿中的suPAR濃度可能在CAP嚴重程度的臨床評估扮演重要的角色。而這些發現對於CAP治療可能會提供更多新資訊。
    The urokinase-type plasminogen activator receptor (uPAR) mediates various cellular activities and is involved in proteolysis, angiogenesis, and inflammation. The objective of this study was to investigate the association between soluble uPAR (suPAR) levels and community-acquired pneumonia (CAP) severity. A commercial enzyme-linked immunosorbent assay (ELISA) was performed to measure the plasma suPAR levels in 67 healthy controls and 75 patients with CAP. Our results revealed that plasma suPAR levels were significantly elevated in patients with CAP compared with the controls, and antibiotic treatment was effective in reducing suPAR levels. The plasma suPAR levels were correlated with the severity of CAP based on the pneumonia severity index (PSI) scores. Furthermore, in cell lines model, lipopolysaccharide (LPS)-stimulation significantly increased uPAR expression in RAW264.7 macrophages. In conclusion, plasma suPAR levels may play a role in the clinical assessment of CAP severity; these findings may provide information on new targets for treatment of CAP.
    URI: http://ir.csmu.edu.tw:8080/ir/handle/310902500/21260
    Appears in Collections:[Institute of Medicine] Electronic Theses of Dissertations
    [Institute of Medicine] Electronic Theses of Dissertations

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