Biological Therapies for Cardiac Arrhythmias Can Genes and Cells Replace Drugs and Devices?

被引:78
作者
Cho, Hee Cheol [1 ]
Marban, Eduardo [1 ]
机构
[1] Cedars Sinai Heart Inst, Los Angeles, CA 90048 USA
关键词
bradycardia; tachycardia; gene therapy; cell therapy; MESENCHYMAL STEM-CELLS; IN-VIVO; INTRACELLULAR CALCIUM; ATRIAL-FIBRILLATION; CHANNEL EXPRESSION; MEDICAL PROGRESS; PURKINJE NEURONS; SINOATRIAL NODE; PACEMAKER; HEART;
D O I
10.1161/CIRCRESAHA.109.212936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac rhythm disorders reflect failures of impulse generation and/or conduction. With the exception of ablation methods that yield selective endocardial destruction, present therapies are nonspecific and/or palliative. Progress in understanding the underlying biology opens up prospects for new alternatives. This article reviews the present state of the art in gene- and cell-based therapies to correct cardiac rhythm disturbances. We begin with the rationale for such approaches, briefly discuss efforts to address aspects of tachyarrhythmia, and review advances in creating a biological pacemaker to cure bradyarrhythmia. Insights gained bring the field closer to a paradigm shift away from devices and drugs, and toward biologics, in the treatment of rhythm disorders. ( Circ Res. 2010; 106: 674-685.)
引用
收藏
页码:674 / 685
页数:12
相关论文
共 100 条
[91]   Mesenchymal stem cells in health and disease [J].
Uccelli, Antonio ;
Moretta, Lorenzo ;
Pistoia, Vito .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (09) :726-736
[92]   Cardiac gap junctions and connexins: their role in atrial fibrillation and potential as therapeutic targets [J].
van der Velden, HMW ;
Jongsma, HJ .
CARDIOVASCULAR RESEARCH, 2002, 54 (02) :270-279
[93]   Endogenous channels in HEK cells and potential roles in HCN ionic current measurements [J].
Varghese, A ;
TenBroek, EM ;
Coles, J ;
Sigg, DC .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2006, 90 (1-3) :26-37
[94]   Gene therapy in heart failure [J].
Vinge, Leif Erik ;
Raake, Philip W. ;
Koch, Walter J. .
CIRCULATION RESEARCH, 2008, 102 (12) :1458-1470
[95]   Effect of d-sotalol on mortality in patients with left ventricular dysfunction after recent and remote myocardial infarction [J].
Waldo, AL ;
Camm, AJ ;
deRuyter, H ;
Friedman, PL ;
MacNeil, DJ ;
Pauls, JF ;
Pitt, B ;
Pratt, CM ;
Schwartz, PJ ;
Veltri, EP .
LANCET, 1996, 348 (9019) :7-12
[96]   Stable reprogrammed heterokaryons form spontaneously in Purkinje neurons after bone marrow transplant [J].
Weimann, JM ;
Johansson, CB ;
Trejo, A ;
Blau, HM .
NATURE CELL BIOLOGY, 2003, 5 (11) :959-966
[97]   State of the art:: Catheter ablation of atrial fibrillation [J].
Wright, Matthew ;
Haissaguerre, Michel ;
Knecht, Sebastien ;
Matsuo, Seiichiro ;
O'Neill, Mark D. ;
Nault, Isabelle ;
Lellouche, Nicolas ;
Hocini, Meleze ;
Sacher, Frederic ;
Jais, Pierre .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2008, 19 (06) :583-592
[98]   Characterization and enrichment of cardiomyocytes derived from human embryonic stem cells [J].
Xu, CH ;
Police, S ;
Rao, N ;
Carpenter, MK .
CIRCULATION RESEARCH, 2002, 91 (06) :501-508
[99]   Functional integration of electrically active cardiac derivatives from genetically engineered human embryonic stem cells with quiescent recipient ventricular cardiomyocytes -: Insights into the development of cell-based pacemakers [J].
Xue, T ;
Cho, HC ;
Akar, FG ;
Tsang, SY ;
Jones, SP ;
Marbán, E ;
Tomaselli, GF ;
Li, RA .
CIRCULATION, 2005, 111 (01) :11-20
[100]   Functional Cardiomyocytes Derived From Human Induced Pluripotent Stem Cells [J].
Zhang, Jianhua ;
Wilson, Gisela F. ;
Soerens, Andrew G. ;
Koonce, Chad H. ;
Yu, Junying ;
Palecek, Sean P. ;
Thomson, James A. ;
Kamp, Timothy J. .
CIRCULATION RESEARCH, 2009, 104 (04) :E30-E41