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(Circulation. 2003;108:2127.)
© 2003 American Heart Association, Inc.

Basic Science Reports

Noninvasive Imaging of Transgene Expression by Use of Positron Emission Tomography in a Pig Model of Myocardial Gene Transfer

Frank M. Bengel, MD; Martina Anton, PhD; Thomas Richter, MD; Marcus V. Simoes, MD; Roland Haubner, PhD; Julia Henke, DVM; Wolf Erhardt, DVM; Sybille Reder, BSc; Terry Lehner, BSc; Wolfgang Brandau, PhD; Peter Boekstegers, MD; Stephan G. Nekolla, PhD; Bernd Gansbacher, MD; Markus Schwaiger, MD

From the Nuklearmedizinische Klinik und Poliklinik (F.M.B., M.V.S., R.H., S.R., T.L., S.G.N., M.S.), Institut für Experimentelle Onkologie und Therapieforschung (M.A., J.H., W.E., B.G.), and Institut für Pathologie und Pathologische Anatomie, Technische Universität München (T.R.); the Nuklearmedizinische Klinik der Universität Essen (W.B.); and the Medizinische Klinik I der Ludwig-Maximilians-Universität München (P.B.), Germany.

Correspondence to Frank M. Bengel, MD, Nuklearmedizinische Klinik und Poliklinik, Technische Universität München, Klinikum rechts der Isar, Ismaninger Straße 22, 81675 München, Germany. E-mail frank.bengel{at}lrz.tum.de

Received February 7, 2003; de novo received April 23, 2003; revision received June 12, 2003; accepted June 13, 2003.

Background— Radionuclide imaging of reporter gene expression may be useful for noninvasive monitoring of clinical cardiac gene therapy. Experience until now, however, has been limited to small animals.

Methods and Results— To evaluate feasibility in a clinically applicable setting, pigs were studied by conventional positron emission tomography (PET) 2 days after regional intramyocardial injection of control adenovirus or adenovirus carrying herpesviral thymidine kinase reporter gene (HSV1-tk). Myocardial blood flow was quantified by use of [¹³N]ammonia. Subsequently, kinetics of the reporter substrate [¹²⁴I]-2'-fluoro-2'-deoxy-5-iodo-1-ß-D-arabino-furanosyluracil (FIAU) were assessed over a period of 2 hours. Areas infected with adenovirus expressing HSV1-tk showed significantly elevated FIAU retention during the first 30 minutes after injection. At later times, washout was observed, and retention was not different from that in areas infected with control virus or remote myocardium. Early in vivo FIAU uptake correlated with ex vivo images, autoradiography, and immunohistochemistry for reporter gene product after euthanasia. After intramyocardial injection of both adenoviruses, myocardial blood flow was mildly elevated compared with that in remote areas, consistent with histological signs of regional inflammation.

Conclusions— In vivo quantification of regional myocardial transgene expression is feasible with clinical PET methodology, the radioiodinated reporter probe FIAU, and the HSV1-tk reporter gene. Radioactivity efflux after specific initial uptake was not observed previously in tumor studies, suggesting that tissue-specific differences in nucleoside metabolism influence reporter probe kinetics. By coregistering reporter gene expression with additional biological parameters such as myocardial blood flow, PET allows for noninvasive characterization of the success of cardiac gene transfer along with its functional correlates.

Key Words: imaging • gene therapy • radioisotopes • genes

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