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Heart Failure

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Cover of 'Heart Failure'

Table of Contents

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    Book Overview
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    Chapter 13 Direct Myosin Activation by Omecamtiv Mecarbil for Heart Failure with Reduced Ejection Fraction
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    Chapter 23 Mesenchymal Stem Cell Therapy for the Treatment of Heart Failure Caused by Ischemic or Non-ischemic Cardiomyopathy: Immunosuppression and Its Implications
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    Chapter 24 Heart Failure Guidelines on Pharmacotherapy
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    Chapter 25 Role of Hyperkalemia in Heart Failure and the Therapeutic Use of Potassium Binders
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    Chapter 27 Comorbidities in Heart Failure
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    Chapter 28 Vasopressin and Vasopressin Antagonists in Heart Failure
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    Chapter 30 Iron Deficiency Treatment in Patients with Heart Failure
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    Chapter 31 Cardiac Myosin Activation with Gene Therapy Produces Sustained Inotropic Effects and May Treat Heart Failure with Reduced Ejection Fraction
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    Chapter 55 Ivabradine.
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    Chapter 56 Wnt Signaling in Cardiac Remodeling and Heart Failure
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    Chapter 74 Epidemiology of Heart Failure
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    Chapter 75 Clinical Trial Design, Endpoints, and Regulatory Requirements
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    Chapter 76 Steroidal and Novel Non-steroidal Mineralocorticoid Receptor Antagonists in Heart Failure and Cardiorenal Diseases: Comparison at Bench and Bedside
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    Chapter 77 Sacubitril/Valsartan (LCZ696) in Heart Failure
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    Chapter 80 Platelet-Derived Growth Factor in Heart Failure
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    Chapter 81 Gene Therapy in Heart Failure
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    Chapter 82 Cardiac Phosphodiesterases and Their Modulation for Treating Heart Disease
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    Chapter 83 Partial Adenosine A1 Agonist in Heart Failure
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    Chapter 86 Biomarkers of Heart Failure with Preserved and Reduced Ejection Fraction
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    Chapter 88 New and Emerging Therapies and Targets: Beta-3 Agonists
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    Chapter 99 Noncoding RNAs in Heart Failure
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    Chapter 100 Novel sGC Stimulators and sGC Activators for the Treatment of Heart Failure
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    Chapter 101 The Three-Decade Long Journey in Heart Failure Drug Development
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    Chapter 123 Mitochondrial Therapies in Heart Failure
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    Chapter 126 Anticoagulation Therapy and NOACs in Heart Failure
Attention for Chapter 23: Mesenchymal Stem Cell Therapy for the Treatment of Heart Failure Caused by Ischemic or Non-ischemic Cardiomyopathy: Immunosuppression and Its Implications
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Chapter title
Mesenchymal Stem Cell Therapy for the Treatment of Heart Failure Caused by Ischemic or Non-ischemic Cardiomyopathy: Immunosuppression and Its Implications
Chapter number 23
Book title
Heart Failure
Published in
Handbook of experimental pharmacology, January 2017
DOI 10.1007/164_2017_23
Pubmed ID
Book ISBNs
978-3-31-959658-7, 978-3-31-959659-4
Authors

Michael J. Lipinski, Dror Luger, Stephen E. Epstein

Abstract

HF patients with signs and symptoms of worsening heart failure (HF), despite optimal medical therapy, have a poor prognosis. The pathways contributing to HF are multiple, probably accounting, in part, for current treatment approaches not being more effective. Stem cells, particularly mesenchymal stem cells (MSCs), have a broad range of activities, making them particularly interesting candidates for a new HF therapeutic. This review presents an overview of the studies examining the efficacy of stem cell studies administered to HF patients, focusing mainly on MSCs. It examines the issues surrounding autologous vs. allogenic stem cells, the results of different routes of administration, and implications deriving from the belief that for stem cells to be effective, they must engraft in the myocardium and exert local effects. Since intravenous administration of stem cells leads to sparse cardiac engraftment, stem cell delivery strategies have uniformly involved catheter-based delivery systems. This becomes problematic in a disease that will almost certainly require delivery of the therapeutic throughout the course of the disease. Importantly, it appears that a critical contributing cause of the progressive cardiac dysfunction experienced by HF patients is the existence of a persistent inflammatory response. Since MSCs exert potent anti-inflammatory effects through paracrine mechanisms, it is possible that intravenous delivery of MSCs may be therapeutically effective. If this concept is valid, it could lead to a transformational change in stem cell delivery strategies.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 12 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 12 100%

Demographic breakdown

Readers by professional status Count As %
Professor 2 17%
Student > Master 2 17%
Student > Postgraduate 2 17%
Student > Doctoral Student 1 8%
Student > Ph. D. Student 1 8%
Other 3 25%
Unknown 1 8%
Readers by discipline Count As %
Medicine and Dentistry 8 67%
Social Sciences 1 8%
Pharmacology, Toxicology and Pharmaceutical Science 1 8%
Unknown 2 17%