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Characterization of Potential Mechan...

Iqbal, Farwah.

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Characterization of Potential Mechanisms That Render the Combination of First Trimester Umbilical Cord-derived Perivascular Cells (FTM HUCPVC) and Endothelial Progenitor Cells (EPC) a Promising Cellular Therapeutic Strategy Following Ischemic Cardiac Injury.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Characterization of Potential Mechanisms That Render the Combination of First Trimester Umbilical Cord-derived Perivascular Cells (FTM HUCPVC) and Endothelial Progenitor Cells (EPC) a Promising Cellular Therapeutic Strategy Following Ischemic Cardiac Injury./
作者:	Iqbal, Farwah.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2019,
面頁冊數:	354 p.
附註:	Source: Dissertations Abstracts International, Volume: 81-06, Section: B.
Contained By:	Dissertations Abstracts International81-06B.
標題:	Therapy. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=22622786
ISBN:	9781392840665

Characterization of Potential Mechanisms That Render the Combination of First Trimester Umbilical Cord-derived Perivascular Cells (FTM HUCPVC) and Endothelial Progenitor Cells (EPC) a Promising Cellular Therapeutic Strategy Following Ischemic Cardiac Injury.
Iqbal, Farwah.

Characterization of Potential Mechanisms That Render the Combination of First Trimester Umbilical Cord-derived Perivascular Cells (FTM HUCPVC) and Endothelial Progenitor Cells (EPC) a Promising Cellular Therapeutic Strategy Following Ischemic Cardiac Injury. - Ann Arbor : ProQuest Dissertations & Theses, 2019 - 354 p.

Source: Dissertations Abstracts International, Volume: 81-06, Section: B.

Thesis (Ph.D.)--University of Toronto (Canada), 2019.

This item must not be sold to any third party vendors.

Heart disease is the main cause of mortality worldwide. The available treatments are limited, high risk and often inefficient. Cell-based therapies are being developed to provide an efficient and safe option to improve quality of life, prevent future mortality and the need for heart transplantation. Aged and ill individuals often have impaired endogenous regenerative cells. Instead, healthy, young cells can be delivered into the damaged heart to decrease inflammation, restore blood flow, preserve the myocardium and increase cardiac output. Pre-clinically and clinically tested therapeutic cell types achieved some of these goals, but no single-cell type seems to be versatile enough, to heal the heart on its own. Herein, I propose the combined use of two regenerative cell types as a treatment after myocardial infarction (MI). The first cell type is the endothelial progenitor cell (EPC), which are the origin of new blood vessels, second is the first trimester human umbilical cord-derived perivascular cell (FTM HUCPVC). FTM HUCPVC can support developing blood vessels, control inflammation and release growth factors. We hypothesized that combined administration of these cells can achieve clinically significant healing in a damaged heart. We previously found that FTM HUCPVC have greater regenerative potential following cardiac injury compared to term HUCPVC and bone marrow-derived mesenchymal stem cells. Optimal cell ratios were determined by a mouse model of subcutaneous angiogenesis and an immunocompromised rat model of MI. The combination of FTM HUCPVC and EPC significantly improved vasculogenesis compared to single cell-type treatments partly through the platelet-derived growth factor beta (PDGF-B) signalling cascade. Both FTM HUCPVC and EPC in combination support perivascular niches in the myocardium by homing to vascular structures and secreting pro-angiogenic factors. The resultant cardiac perfusion is likely required for cardiac muscle preservation, scar tissue reduction, and ultimately the improved cardiac function. To our knowledge, this study is the first to show significant structural and functional cardiac improvements following combination cell therapy compared to single cell-type therapies.Currently our group is working on large animal studies to test this novel therapeutic approach as we plan for a phase I clinical trial to provide a novel treatment option for patients following MI.

ISBN: 9781392840665Subjects--Topical Terms:

3343697
Therapy.
Subjects--Index Terms:

Angiogenesis

Characterization of Potential Mechanisms That Render the Combination of First Trimester Umbilical Cord-derived Perivascular Cells (FTM HUCPVC) and Endothelial Progenitor Cells (EPC) a Promising Cellular Therapeutic Strategy Following Ischemic Cardiac Injury.
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