Defining the success of cardiac gene therapy: how can nuclear imaging contribute?

被引:18
作者
Avril, N
Bengel, FM
机构
[1] Tech Univ Munich, Nukl Med Klin, Klinikum Rechts Isar, D-81675 Munich, Germany
[2] Univ Pittsburgh, Med Ctr, Div Nucl Med, Pittsburgh, PA 15260 USA
关键词
gene therapy; myocardium; reporter gene; positron emission tomography; nuclear cardiology;
D O I
10.1007/s00259-002-1100-2
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Gene therapy is a promising modality for the treatment of various cardiovascular diseases such as ischaemia, heart failure, restenosis after revascularisation, hypertension and hyperlipidaemia. An increasing number of approaches are moving from experimental and preclinical validation to clinical application, and several multi-centre trials are currently underway. Despite the rapid progress in cardiac gene therapy, many basic tools and principles remain under development. Questions with regard to the optimal method for gene delivery in a given situation remain open, as do questions concerning therapeutic efficacy and the time course and maunitude of gene expression in target and remote areas. Nuclear imaging provides valuable tools to address these open issues non-invasively. Functional effects of molecular therapy at the tissue level can be identified using, tracers of blood flow, metabolism, innervation or cell death. The use of reporter genes and radiolabelled reporter probes allows for non-invasive assessment of location, magnitude and persistence of transgene expression in the heart and the whole body. Co-expression of a reporter gene will allow for indirect imaging of the expression of a therapeutic gene of choice, and linkage of measures of transgene expression to downstream functional effects will enhance the understanding of basic mechanisms of cardiac gene therapy. Hence, nuclear imaging offers great potential to facilitate and refine the determination of therapeutic effects in preclinical and clinical cardiovascular gene therapy.
引用
收藏
页码:757 / 771
页数:15
相关论文
共 103 条
[1]   Restoration of beta-adrenergic signaling in failing cardiac ventricular myocytes via adenoviral-mediated gene transfer [J].
Akhter, SA ;
Skaer, CA ;
Kypson, AP ;
McDonald, PH ;
Peppel, KC ;
Glower, DD ;
Lefkowitz, RJ ;
Koch, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (22) :12100-12105
[2]   Synthesis and preliminary evaluation of 9-(4-[18F]-fluoro-3-hydroxymethylbutyl)guanine ([18F]FHBG):: A new potential imaging agent for viral infection and gene therapy using PET [J].
Alauddin, MM ;
Conti, PS .
NUCLEAR MEDICINE AND BIOLOGY, 1998, 25 (03) :175-180
[3]   Synthesis of 9-[(3-[F-18]-fluoro-1-hydroxy-2-propoxy)methyl]guanine ([F-18]-FHPG): A potential imaging agent of viral infection and gene therapy using PET [J].
Alauddin, MM ;
Conti, PS ;
Mazza, SM ;
Hamzeh, FM ;
Lever, JR .
NUCLEAR MEDICINE AND BIOLOGY, 1996, 23 (06) :787-792
[4]   Gene therapy and heart transplantation [J].
Ardehali, A ;
Reddy, R ;
Laks, H .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2000, 9 (05) :1021-1027
[5]  
BARR E, 1994, GENE THER, V1, P51
[6]   The effects of β1-blockade on oxidative metabolism and the metabolic cost of ventricular work in patients with left ventricular dysfunction -: A double-blind, placebo-controlled, positron-emission tomography study [J].
Beanlands, RSB ;
Nahmias, C ;
Gordon, E ;
Coates, G ;
deKemp, R ;
deKemp, R ;
Firnau, G ;
Fallen, E .
CIRCULATION, 2000, 102 (17) :2070-2075
[7]   Uptake of radiolabeled 2′-fluoro-2′-deoxy-5-iodo-1-β-D-arabinofuranosyluracil in cardiac cells after adenoviral transfer of the herpesvirus thymidine kinase gene -: The cellular basis for cardiac gene imaging [J].
Bengel, FM ;
Anton, M ;
Avril, N ;
Brill, T ;
Nguyen, N ;
Haubner, R ;
Gleiter, E ;
Gansbacher, B ;
Schwaiger, M .
CIRCULATION, 2000, 102 (09) :948-950
[8]   Nuclear medicine studies of the heart [J].
Bengel, FM ;
Schwaiger, M .
EUROPEAN RADIOLOGY, 1998, 8 (09) :1698-1706
[9]  
Bengel FM, 2002, CIRCULATION, V106, P331
[10]   Non-invasive estimation of myocardial efficiency using positron emission tomography and carbon-11 acetate - comparison between the normal and failing human heart [J].
Bengel, FM ;
Permanetter, B ;
Ungerer, M ;
Nekolla, S ;
Schwaiger, M .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 2000, 27 (03) :319-326