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Improvement of Intrapleural Fibrinol...
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De Vera, Christian Jordan.
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Improvement of Intrapleural Fibrinolytic Therapy in a Streptococcus pneumoniae-Induced Advanced Empyema Rabbit Model.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Improvement of Intrapleural Fibrinolytic Therapy in a Streptococcus pneumoniae-Induced Advanced Empyema Rabbit Model./
作者:
De Vera, Christian Jordan.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2020,
面頁冊數:
85 p.
附註:
Source: Masters Abstracts International, Volume: 82-01.
Contained By:
Masters Abstracts International82-01.
標題:
Translation studies. -
電子資源:
https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28024108
ISBN:
9798662411326
Improvement of Intrapleural Fibrinolytic Therapy in a Streptococcus pneumoniae-Induced Advanced Empyema Rabbit Model.
De Vera, Christian Jordan.
Improvement of Intrapleural Fibrinolytic Therapy in a Streptococcus pneumoniae-Induced Advanced Empyema Rabbit Model.
- Ann Arbor : ProQuest Dissertations & Theses, 2020 - 85 p.
Source: Masters Abstracts International, Volume: 82-01.
Thesis (M.S.)--The University of Texas Health Science Center at Tyler, 2020.
This item is not available from ProQuest Dissertations & Theses.
Empyema is clinically defined as the accumulation of pus in the pleural cavity, as a complication of severe pneumonia. Intrapleural Fibrinolytic Therapy (IPFT) is a low invasive and more economical option for treating empyema. IPFT with single chain (sc) urokinase (uPA) and tissue (tPA) plasminogen activators of advanced Streptococcus pneumoniae-induced empyema in rabbits was studied in order to understand molecular mechanisms of fibrinolysis. The results demonstrate that: (1) the rabbit model recapitulates human empyema, where advanced stage becomes more resistant to IPFT; (2) slow fibrinolysis may require higher bolus doses or multiple injections of plasminogen activators; (3) elevated plasminogen activator inhibitor-1 (PAI-1) remains a molecular target susceptible for IPFT with sctPA and Docking Site Peptide (DSP); (4) Nb42, a nanobody, which interferes with exosite interactions, could be used together with DSP to increase efficacy of PAI-1 targeting. This thesis contributes to a foundation for finding successful treatment for advanced empyema.
ISBN: 9798662411326Subjects--Topical Terms:
3310485
Translation studies.
Subjects--Index Terms:
Biochemistry
Improvement of Intrapleural Fibrinolytic Therapy in a Streptococcus pneumoniae-Induced Advanced Empyema Rabbit Model.
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Empyema is clinically defined as the accumulation of pus in the pleural cavity, as a complication of severe pneumonia. Intrapleural Fibrinolytic Therapy (IPFT) is a low invasive and more economical option for treating empyema. IPFT with single chain (sc) urokinase (uPA) and tissue (tPA) plasminogen activators of advanced Streptococcus pneumoniae-induced empyema in rabbits was studied in order to understand molecular mechanisms of fibrinolysis. The results demonstrate that: (1) the rabbit model recapitulates human empyema, where advanced stage becomes more resistant to IPFT; (2) slow fibrinolysis may require higher bolus doses or multiple injections of plasminogen activators; (3) elevated plasminogen activator inhibitor-1 (PAI-1) remains a molecular target susceptible for IPFT with sctPA and Docking Site Peptide (DSP); (4) Nb42, a nanobody, which interferes with exosite interactions, could be used together with DSP to increase efficacy of PAI-1 targeting. This thesis contributes to a foundation for finding successful treatment for advanced empyema.
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