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Catheter-based myocardial gene transfer utilizing nonfluoroscopic electromechanical left ventricular mapping
Journal of the American College of Cardiology © 1999 by the American College of Cardiology Published by Elsevier Science Inc.
Vol. 34, No. 1, 1999 ISSN 0735-1097/99/$20.00 PII S0735-1097(99)00143-6
EXPERIMENTAL STUDY
Catheter-Based Myocardial Gene Transfer Utilizing Nonfluoroscopic Electromechanical Left Ventricular Mapping Peter R. Vale, MD, Douglas W. Losordo, MD, FACC, Tengiz Tkebuchava, MD, Donghui Chen, MD, Charles E. Milliken, MA, Jeffrey M. Isner, MD, FACC Boston, Massachusetts OBJECTIVES
This study investigated the feasibility and safety of percutaneous, catheter-based myocardial gene transfer.
BACKGROUND Direct myocardial gene transfer has, to date, required direct injection via an open thoracotomy. METHODS
Electroanatomical mapping was performed to establish the site of left ventricular (LV) gene transfer. A steerable, deformable 7F catheter with a 27G needle, which can be advanced 3 to 5 mm beyond its distal tip, was then directed to previously acquired map sites, the needle was advanced, and injections were made into the LV myocardium.
RESULTS
In two pigs in which methylene blue dye was injected, discretely stained LV sites were observed at necropsy in each pig, corresponding to the injection sites indicated prospectively by the endocardial map. In six pigs in which the injection catheter was used to deliver plasmid using cytomegalovirus promoter/enhancer, encoding nuclear-specific LacZ gene (pCMVnlsLacZ) (50 mg/ml) to a single LV myocardial region, peak beta-galactosidase activity after five days (relative light units [RLU], mean 135,333 6 28,239, range 5 31,508 to 192,748) was documented in the target area of myocardial injection in each pig. Percutaneous gene transfer of pCMV-nlsLacZ (50 mg/ml) was also performed in two pigs with an ameroid constrictor applied to the left circumflex coronary artery; in each pig, peak beta-galactosidase activity after five days (214,851 and 23,140 RLU) was documented at the injection site. All pigs survived until sacrifice, and no complications were observed with either the mapping or the injection procedures.
CONCLUSIONS Percutaneous myocardial gene transfer can be successfully achieved in normal and ischemic myocardium without significant morbidity or mortality. These findings establish the potential for minimally invasive cardiovascular gene transfer. (J Am Coll Cardiol 1999;34:246 –54) © 1999 by the American College of Cardiology
From the time of the initial description of direct gene transfer to the artery wall by Nabel et al. (1), gene therapy has been proposed or investigated for a number of cardiovascular applications including prevention of restenosis, treatment of congestive heart failure and therapeutic angiogenesis (2). Each of these potential applications requires consideration of the appropriate gene, vector and delivery technique. To date, successful transfection with a variety of genes, using both viral and nonviral vectors, has been accomplished by intravascular gene transfer (3,4), direct From the Division of Cardiovascular Research, St. Elizabeth’s Medical Center, and Tufts University School of Medicine, Boston, Massachusetts. This study was supported in part by NIH grants HL-53354, HL-57516 and HL-60911 (Dr. Isner), a grant from the E.L. Weigand Foundation, Reno, Nevada, and the Peter Lewis Educational Foundation. Dr. Vale is the recipient of a travelling fellowship from the St. Vincent’s Clinic Foundation, Sydney, Australia. Manuscript received October 5, 1998; revised manuscript received February 2, 1999, accepted March 15, 1999.
transcutaneous intramuscular injection (5–9), transcutaneous pericardial injection (10), and direct intramyocardial injection (11–13). Although intravascular, pericardial, and intramuscular gene transfer have all been performed using minimally invasive delivery techniques, intramyocardial gene transfer has to date required an operative thoracotomy. Such an approach clearly implies additional morbidity and limits the feasibility of repeat administrations. Successful execution of percutaneous, catheter-based myocardial gene transfer has not been previously reported. Accordingly, we sought to investigate the safety and feasibility of a novel delivery catheter for percutaneous myocardial gene transfer. To determine whether the delivery catheter could be used in a site-specific manner, myocardial gene transfer was integrated with a previously described catheter mapping technology (14). The results of this preliminary study indeed establish that percutaneous
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Abbreviations and Acronyms LV 5 left ventricle LCx 5 left circumflex coronary artery pCMV-nlsLacZ 5 plasmid using cytomegalovirus promoter/enhancer, encoding nuclear-specific LacZ gene RLU 5 relative light units VEGF 5 vascular endothelial growth factor
myocardial gene transfer can be successfully achieved in normal and ischemic myocardium in a relatively site-specific fashion without significant morbidity or mortality. These findings thus establish the potential to replace currently used operative approaches with a minimally invasive technique for applications of cardiovascular gene therapy designed to target myocardial function.
METHODS Electromechanical left ventricular mapping. The NOGA system (Biosense, Johnson & Johnson) is designed to acquire, analyze, and display electroanatomical maps of the human heart. The maps are constructed by combining and integrating information from intracardiac electrograms acquired at multiple endocardial locations. Catheters designed for use with the NOGA system are equipped with an electromagnetic sensor, which provides real-time location of the catheter. As the catheter is moved along the endocardium, local endocardial electrograms, together with the catheter tip location, are reported simultaneously. The system then uses this information to construct a threedimensional (3D) electroanatomical map that constitutes a geometrical representation of the left ventricle (LV). The NOGA system analyzes both global and local parameters that characterize mechanical, dynamic, and electrical LV function. Functional analysis is based on local shortening as an index of local mechanical function, whereas measurement of local intracardiac signals determines viability based upon preserved electrical function. The combination of these data permits assessment of electromechanical coupling (15). NOGA components. The mapping and navigation system consists of a locator pad, a reference catheter, a mapping catheter and a processing unit with a graphics computer (Silicon Graphics, Mountain View, California). A similar system, CARTO (Biosense), has been previously described in detail (14,16). The locator pad consists of a triangular arrangement of three magnetic coils, which generate an ultra-low intensity magnetic field (0.02 G to 0.5 G). The pad attaches to the undersurface of the catheterization table. The reference catheter (Cordis-Webster, Baldwin Park, California) is taped directly to the skin overlying the anterior or posterior chest wall within the frame of reference
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created by the three coils of the locator pad. It is used to detect small changes in intracardiac position due to respiration or movement of the subject. These small changes are analyzed by the computer to correct spatial information generated by the mapping catheter. The mapping catheter (Cordis-Webster) is a 7F fused tip catheter with a miniature passive magnetic field sensor embedded within its distal tip. On the basis of the strength of the magnetic field emitted from the locator pad coils, this sensor maps the distance from each coil; these distances determine the radii of theoretical spheres around each coil. The intersection of these three spheres determines the location and orientation of the sensor in 6 degrees of freedom (x, y, z, roll, pitch and yaw), which thus indicates the position and rotation of the distal catheter segment. The accuracy of the sensor position in this low magnetic field is 0.8 mm and 5 degrees (14,16). Unipolar or bipolar signals (timing related to a reference signal) are also obtained from the distal tip of the catheter, allowing generation of activation times in relation to the position of the catheter in the heart. Mapping procedure. The mapping procedure has been previously described in detail (14,16). Briefly, the reference catheter was placed within the field of reference. The mapping catheter was introduced via a femoral arteriotomy and advanced to the LV. Three points (high septum, high lateral wall, and apex) were obtained with fluoroscopic guidance to generate the initial 3D image of the LV. The location of the mapping catheter was gated to a reliable point in the cardiac cycle (recorded relative to the location of the fixed reference catheter at that time) and its location was continuously shown on the screen of the mapping computer. An icon of the mapping catheter is displayed superimposed on the 3D map, thus enabling catheter manipulation in relation to the 3D map. At each site, three parameters are calculated to determine the stability of endocardial contact with the catheter tip: location, cycle length (CL) and local activation time (LAT). Location is a measure of how stable the tip location is between beats. The CL indicates the difference between the current CL and the median CL of the last 100 acquired points. The LAT is calculated as the interval between a reliable point on the body-surface electrocardiogram (ECG) and the steepest negative intrinsic deflection from the mapping-catheter unipolar recording, as determined from the intracardiac electrogram. This electrophysiologic information is color-coded (red being the shortest LAT and purple being the longest) and superimposed on the 3D chamber geometry. The reconstruction was updated in real time with the acquisition of each new site. Validation of both intracardiac signal recording and location accuracy, both in vitro and in vivo, and correlation between electromechanical characteristics and pathology, have been previously established (14 –16). In addition, early reports suggest
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Figure 1. (A) The endocardial surface following dissection through the left lateral free wall following injections with methylene blue. Left ventricle with papillary muscles, left atrium and mitral valve apparatus are displayed. Lateral wall and septum are labeled. Methylene blue injection sites (arrows) are demonstrated at the apex, septum, and posterolateral wall. (B) Corresponding NOGA™ map (left anterior oblique [LAO] projection) with injection sites indicated by red hexagons. LA 5 left arm; RA 5 right arm.
that LV mapping may allow the detection of on-line myocardial viability (17). Injection catheter. The injection catheter (CordisWebster) is a modified 7F mapping catheter, the distal tip of which incorporates a 27G needle that can be protruded 3 to 5 mm. The injection catheter was manipulated to acquire
stable points within the target region based on the parameters described above and superimposed upon the previously acquired 3D electroanatomic map. Once a stable point was attained, the needle was advanced 4 to 5 mm into the myocardium; the intracardiac electrogram detected transient myocardial injury or premature ventricular contractions as
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Figure 2. Endocardial mapping and injection of normal male swine (RAO projection). NOGA maximum voltage and linear log shortening maps show injection sites into nonischemic myocardium. Note the coupling of normal mechanical function with normal electrical activity. Injections in this case were localized to the left ventricular apex. LA 5 left arm; RA 5 right arm.
evidence of needle penetration into the myocardium. Injectate was delivered according to one of three protocols as outlined below. Each injection consisted of 1 ml of solution (total volume 5 6 ml/animal) delivered from a 1-ml syringe. The lumen was prefilled with 0.1 ml of sterile saline prior to entry into the circulation, and following each injection the lumen was again flushed with 0.1 ml of sterile saline. Following completion of the injection, the needle was retracted and the catheter was moved to another endocardial site. Animal studies. A total of 10 swine weighing 30 to 50 kg each were studied under protocols approved by the Animal Care and Use Committee of the St. Elizabeth’s Medical Center. All procedures were performed under anesthesia using a combination of intramuscular (IM) ketamine (15 mg/kg), acepromazine (0.2 mg/kg), and atropine (0.05 mg/kg). All animals received inhalation ventilation with 2% isofluorane to ensure adequate anesthesia throughout the experiment, and supplemental oxygen @ 3 l/min. Before introduction of the mapping catheter, all pigs received intravenous (IV) cefazolin 500 mg (Kefzol, Eli Lilly, Indianapolis, Indiana), heparin 5,000 IU, bretylium tosylate (50 mg/kg), and lidocaine (0.5 mg/kg). Levodromaron (2 mg subcutaneous [s.c.]) was given for analgesia at the beginning of the procedure with supplemental doses as required; on completion of each procedure, animals received an additional injection of levodromaron. A further dose of lidocaine (0.5 mg/kg IV) was given before the injection procedure. Following the mapping and injection procedures, the arteriotomy was closed and the pig was allowed to recover (except in Protocol 1 in which the animals were immediately sacrificed). Animals were observed during recovery until fully conscious, returned to housing 24 h later, and given cefazolin 2 3 500 mg s.c. daily for three to five days. At the end of the study period, the animals were returned to the
laboratory, sacrificed with euthanasia solution (sodium pentobarbital), and the heart excised for macroscopic and microscopic evaluation. PROTOCOL 1. Two healthy and nonischemic pigs each received six 1-ml injections of methylene blue dye. Injections were made in three LV myocardial regions in each pig. Immediately postoperatively, each animal was sacrificed and the heart removed. Both the success and the accuracy of myocardial injections were assessed by correlating the number and location of apparent injection sites on the in vivo 3D electroanatomical map with those identified at necropsy. The extent of myocardial staining was measured to identify the spread of dye from the injection site.
To determine the feasibility of using the injection catheter to perform gene transfer, six healthy, nonischemic pigs each received six injections of 1 ml of a reporter gene (see below) to a single area of LV myocardium. These pigs were sacrificed three to five days later and tissue obtained for quantitative analysis of gene expression.
PROTOCOL 2.
PROTOCOL 3. Under general anesthesia administered via an endotracheal tube, ischemia was induced in two pigs by placing an ameroid constrictor around the proximal left circumflex (LCx) artery as previously described (13,18,19). Three weeks later, selective coronary angiography was performed to determine the maturity of the constrictor, and endocardial mapping was used to identify the area of ischemic myocardium (as evidenced by uncoupling of mechanical function and electrical activity). Each pig received six injections of 1.0 ml of LacZ (50 mg/ml) to a single LV area. Pigs were sacrificed after three to five days and tissue obtained for macroscopic and microscopic evaluation.
Gene expression. Naked plasmid deoxyribonucleic acid (DNA) encoding for nuclear-specific beta-galactosidase transcriptionally regulated by the CMV promoter/enhancer
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Figure 3. Quantitative beta-galactosidase assays of catheter-based single-site left ventricular (LV) injections in normal swine (pigs 3 to 8). Note the focal distribution of peak activity. A 5 anterior wall, L 5 lateral wall, P 5 posterior wall, S 5 septum. Numbers refer to the harvested tissue specimens, 1 being closest to the apex, and 4 being adjacent to the LV outflow tract and mitral valve ring.
(pCMV-nlsLacZ) was used as a reporter gene to evaluate percutaneous myocardial gene transfer. Gene expression was evaluated with a chemoiluminescence assay (20) (GalactoLight, Tropix, Bedford, Massachusetts) designed to measure beta-galactosidase activity. Before measuring betagalactosidase activity, tissue homogenates were pretreated with Chelex 100 to inactivate a natural inhibitor of the enzyme (21).
RESULTS Mapping procedure. During the mapping procedure, heart rate (premapping 5 118 6 8/min vs. postmapping 5 120 6 10/min), systolic blood pressure (BP, 92 6 3 vs. 87 6 4 mm Hg) and O2 saturation (98 6 0.5 vs. 99 6 0.4%) remained stable. Mapping was associated with transient ventricular ectopic activity but no sustained ventricular
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arrhythmias. No other complications were associated with the mapping procedure. Activation (electroanatomic) maps of the LV during sinus rhythm were created in all pigs. All maps were completed in ,20 min. The mean number of points acquired per map was 93 6 6 (45 to 127). The site of earliest activation was in each case at the superior part of the septum (red/orange); the latest site of activation was on the left lateral wall close to the mitral valve apparatus (purple). Before injection, electromechanic interrogation was performed, consisting of maximum voltage (electrical activity) and linear log shortening (mechanical function) maps. Electrically viable tissue produced maximum unipolar voltage .10 mV, and mechanically functional myocardium produced linear log shortening .5%. In all nonischemic pigs, both mechanical function and electrical activity were within normal limits. In the two pigs with an ameroid constrictor, evidence of myocardial ischemia was detected in the lateral wall as evidenced by electromechanical uncoupling (high electrical voltage but low linear log shortening). Percutaneous LV gene transfer. Percutaneous catheterbased myocardial injections caused no significant changes in heart rate (preinjection 5 120 6 10/min vs. postinjection 5 128 6 11/min), systolic BP (87 6 3 vs. 89 6 4 mm Hg), or O2 saturation (99 6 0.4 vs. 98 6 0.7%). Transient unifocal ventricular ectopic activity was observed at the time the needle was extended into the myocardium. In all pigs, sporadic premature ventricular contractions occurred during injection. No episodes of sustained ventricular (or atrial) arrhythmias occurred. No sustained injury pattern was observed during the injections as recorded by the endocardial electrogram. Likewise, the surface ECG showed no evidence of myocardial infarction in any pig. All pigs survived until sacrifice; complications, including pericardial effusion or cardiac tamponade, were not observed in any animals. Six discrete sites of methylene blue staining, located in three LV myocardial areas (anteroapical [n 5 2], septum [n 5 2] and posterolateral wall [n 5 2]), were identified at necropsy in each heart; these sites corresponded to the injection sites indicated prospectively in vivo on the endocardial map (Fig. 1). Myocardial staining was 5.2 6 1.7 mm in depth and 6.4 6 0.7 mm in width. No epicardial staining was demonstrated. In addition, X-gal staining produced no evidence of nuclear-specific beta-galactosidase activity in the myocardium at these sites (Table 1); these two hearts thus constituted negative controls (because no gene transfer was performed in either case) for Protocol 2 below.
PROTOCOL 1.
PROTOCOL 2. The injection catheter was used to deliver pCMV-nlsLacZ (50 mg/ml) to a single LV myocardial region (Fig. 2) in six pigs (apex [n 5 2], septum [n 5 2], posterolateral wall [n 5 1] and the anterior wall [n 5 1]). In each of the six pigs, peak beta-galactosidase activity after
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Figure 4. Fluoroscopic image (anteroposterior projection) of the injection catheter in the left ventricle angled toward the lateral wall. (Distal tip of injection catheter appears to point toward ameroid constrictor.)
five days (relative light units [RLU], mean 5 135,333 6 28,239, [31,508 to 192,748]) was documented in the target area of myocardial injection (Table 1; Fig. 3). Adjacent myocardial areas demonstrated low-level activity, and areas remote from the injection sites had negligible activity. Thus, percutaneous LV myocardial gene transfer was directed in a relatively localized fashion to those sites indicated by preinjection electroanatomical mapping. PROTOCOL 3. Percutaneous gene transfer of pCMVnlsLacZ (50 mg/ml) was also performed in two pigs in which an ameroid constrictor had applied to the left circumflex coronary artery (Fig. 4). Myocardial ischemia was demonstrated in the lateral wall of both pigs (Fig. 5). In each of these two pigs, peak beta-galactosidase activity after five days (214,851 and 23,140 RLU) was documented in the target area of myocardial injection (Table 1; Fig. 6). As in the nonischemic hearts, beta-galactosidase activity was markedly diminished in tissue sections retrieved from adjacent myocardium and was negligible at remote sites.
DISCUSSION Although intra-arterial delivery was used to establish the precedent for cardiovascular gene transfer (1) and has been subsequently exploited to accomplish gene transfer successfully in a variety of animal models (2) as well as patients (3), this route of administration has several inherent limitations for myocardial gene transfer. In the case of naked DNA (i.e., DNA unassociated with viral or other adjunctive vectors), cellular uptake is virtually nil when the transgene is directly injected into the coronary artery lumen, presumably due to prompt degradation by circulating nucleases. Gene transfer performed to the coronary arterial wall itself requires access to a satisfactory donor site; in patients with chronic myocardial ischemia—particularly those patients whose anatomy is not amenable to angioplasty or bypass
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Figure 5. Catheter-based myocardial injections into ischemic swine left ventricle (LV). NOGA™ electrical (maximum unipolar voltage) and mechanical (linear log shortening) maps of the swine LV are shown. Note area of ischemia in the lateral wall—normal electrical activity (blue/green) coupled with poor mechanical function (red). Images A and B represent anteroposterior projections demonstrating six injection sites (red hexagons) in an area of normal myocardial (apex) remote from the ischemic zone. Images C and D depict LAO projections of indicated injection sites in the ischemic lateral LV free wall. LA 5 left arm; RA 5 right arm.
Figure 6. Quantitative beta-galactosidase assays of catheter-based single-site LV injections in swine models of chronic myocardial ischemia (pigs 9 and 10). Injections into myocardium remote from the ischemic zone are distinguished from injections made into the ischemic lateral wall. A 5 anterior wall, L 5 lateral wall, P 5 posterior wall, S 5 septum. Numbers refer to the harvested tissue specimens, 1 being closest to the apex, and 4 being adjacent to the LV outflow tract and mitral valve ring.
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Table 1. Results of Mapping and Injection Procedures Beta-galactosidase Activity (RLU) Pig
Ischemia
1 2 3 4 5 6 7 8 9 10
None None None None None None None None Lateral Lateral
Rx dose
Site 3 no.
Arrhythmias
Total
Peak
Peak/Total (%)
Methylene blue Methylene blue LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg
32 apex/32 lateral/32 septum 32 apex/32 lateral/32 septum Apex 36 Post 36 Apex 36 Septum 36 Anterior 36 Septum 36 Posterior 36 Lateral 36
None None None None None None None None None None
0 0 214,843 182,502 210,409 82,826 59,537 115,960 59,249 365,232
0 0 192,748 149,900 140,991 57,694 31,508 69,357 23,140 214,851
90 82 67 69 53 60 39 59
surgery— diffuse distribution of neointimal thickening or extensive calcific deposits (22) may limit gene transfer to the smooth muscle cells of the arterial media (20). Ischemic muscle as a target for naked DNA. Ischemic muscle represents an alternative target for gene transfer. Striated (5– 8) and cardiac (11,12,23) muscle have been shown to take up and express naked plasmid DNA as well as transgenes incorporated into viral vectors (9,13). Moreover, previous studies (6,24) have shown that the transfection efficiency of intramuscular (IM) gene transfer is augmented more than fivefold when the injected muscle is ischemic. This finding may be the result of the skeletal muscle regeneration, including stem cell (myoblast) proliferation. Vitadello et al. (25) reported an 80-fold increase in chloramphenicol acetyltransferase (CAT) activity following transfection of regenerating versus control muscle. Consistent with this concept, Danko et al. (26) found that bupivacaine, which produces myonecrosis followed by satellite cell (muscle stem cell) proliferation and myotube formation one to three days later, may be used to enhance the expression of naked DNA injected IM into striated muscles. Therapeutic angiogenesis as a model for myocardial gene therapy. We have previously exploited these features of skeletal and cardiac muscle to perform gene transfer of naked DNA encoding for angiogenic growth factors. Preclinical animal studies from our laboratory established that IM gene transfer could be utilized to accomplish successful therapeutic angiogenesis in animals with hindlimb ischemia (6). Subsequently, Phase 1 clinical studies from our institution have established that IM gene transfer of naked DNA encoding for vascular endothelial growth factor (VEGF) may be utilized to accomplish safe and successful therapeutic angiogenesis in patients with critical limb ischemia (7). The notion that this concept could be extrapolated to the treatment of chronic myocardial ischemia was implied by experiments performed in both our laboratory (19) and in others’ (13,27,28) in which recombinant human VEGF was administered to a porcine animal model of chronic myocar-
dial ischemia. This same animal model has been utilized to demonstrate that therapeutic angiogenesis can also be successfully achieved by direct myocardial administration of VEGF, as naked DNA (29) or using an adenoviral vector (13). Preliminary results utilizing this approach as sole therapy (no bypass) for patients with chronic myocardial ischemia suggest that direct injection of VEGF into cardiac myocytes improves collateral blood flow and markedly reduces the frequency of and threshold for myocardial ischemia (30,31). Percutaneous myocardial gene transfer. To date, all of the aforementioned work involving myocardial gene transfer has been achieved via a mini-thoracotomy used for less invasive coronary artery bypass surgery. Although this approach has clearly reduced the length of hospital stay and morbidity associated with conventional bypass surgery, it nevertheless requires general anesthesia and is not easily repeatable. The capability to perform myocardial gene transfer percutaneously could thus further reduce the morbidity and facilitate repeat use of myocardial gene transfer. The experiments described in this report suggest that percutaneous myocardial gene transfer is indeed feasible and can be safely performed in normal and ischemic myocardium of swine (Table 1). Injection of methylene blue was successfully achieved at 6/6 (100%) sites in two pigs. The extent of transmural distribution was limited to the LV wall, as evidenced by the absence of epicardial staining. Maximum gene expression was localized to the injection site in all pigs, ischemic as well as normal, injected with pCMVnlsLacZ. Myocardium adjacent to the target sites of injection demonstrated low-level beta-galactosidase activity, indicating limited distribution following gene transfer. All remote noninjected areas of myocardium were essentially devoid of beta-galactosidase activity. Role of adjunctive electromechanical mapping. Although the mapping capabilities of the NOGA system utilized in this study were useful for demonstrating that gene expression could be directed to specific LV sites, it must be acknowledged that these findings do not establish
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that LV endocardial mapping is required for percutaneous myocardial gene transfer. Electroanatomic mapping clearly may be advantageous both for avoiding gene transfer to sites of myocardial scar and for relocating with accuracy the tip of the injection catheter to areas of myocardial ischemia (or hibernating myocardium) where gene transfer may be potentially optimized (6,32). Theoretically, adjunctive mapping could be employed in a serial fashion to gauge the success of certain gene therapy strategies (e.g., therapeutic angiogenesis). These potential advantages, however, will require further documentation and assessment of physiologic improvement following delivery of a nonreporter gene to establish the value of adjunctive mapping. Reprint requests and correspondence: Dr. Jeffrey M. Isner, St. Elizabeth’s Medical Center, 736 Cambridge Street, Boston, Massachusetts 02135. E-mail: [email protected].
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JACC Vol. 34, No. 1, 1999 July 1999:246–54 13. Mack CA, Patel SR, Schwarz EA, et al. Biologic bypass with the use of adenovirus-mediated gene transfer of the complementary deoxyribonucleic acid for vascular endothelial growth factor 121 improves myocardial perfusion and function in the ischemic porcine heart. J Thorac Cardiovasc Surg 1998;115:168 –76. 14. Gepstein L, Hayam G, Ben-Haim SA. A novel method for nonfluoroscopic catheter-based electroanatomical mapping of the heart: in vitro and in vivo accuracy results. Circulation 1997;95:1611–22. 15. Gepstein L, Goldin A, Lessick J, et al. Electromechanical characterization of chronic myocardial infarction in the canine coronary occlusion model. Circulation 1998;98:2055– 64. 16. Ben-Haim SA, Osadchy D, Schuster I, Gepstein L, Hayam G, Josephson ME. Nonfluoroscopic, in vivo navigation and mapping technology. Nat Med 1996;2:1393–5. 17. Kornowski R, Hong MK, Leon MB. Comparison between left ventricular electromechanical mapping and radionuclide perfusion imaging for detection of myocardial viability. Circulation 1998;98: 1837– 41. 18. White FC, Carroll SM, Magnet A, Bloor CM. Coronary collateral development in swine after coronary artery occlusion. Circ Res 1992;71:1490 –1500. 19. Hariawala M, Horowitz JR, Esakof D, et al. VEGF improves myocardial blood flow but produces EDRF-mediated hypotension in porcine hearts. J Surg Res 1996;63:77– 82. 20. Feldman LJ, Steg PG, Zheng LP, et al. Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbit. J Clin Invest 1995;95:2662–71. 21. Oswald H, Heinemann F, Nikol S, Salmons B, Gunzburg WH. Removal of an inhibitor of marker enzyme activity in artery extracts by chelating agents. Biotechniques 1997;22:78 – 81. 22. Dietz W, Tobis JA, Isner JM. Failure of angiography to accurately depict the extent of coronary arterial narrowing in three fatal cases of percutaneous transluminal coronary angioplasty. J Am Coll Cardiol 1992;19:1261–70. 23. Acsadi G, Jiao S, Jani A, et al. Direct gene transfer and expression into rat heart in vivo. The New Biologist 1991;3:71– 81. 24. Takeshita S, Isshiki T, Sato T. Increased expression of direct gene transfer into skeletal muscles observed after acute ischemic injury in rats. Lab Invest 1996;74:1061– 65. 25. Vitadello M, Schiaffino M, Picard A, Scarpa M, Schiaffino S. Gene transfer in regenerating muscle. Human Gene Ther 1994;5:11–18. 26. Danko I, Fritz JD, Jiao S, Hogan K, Latendresse JS, Wolff JA. Pharmacological enhancement of in vivo foreign gene expression in muscle. Gene Therapy 1994;1:114 –21. 27. Pearlman JD, Hibberd MG, Chuang ML, et al. Magnetic resonance mapping demonstrates benefits of VEGF-induced myocardial angiogenesis. Nat Med 1995;1:1085–9. 28. Banai S, Jaklitsch MT, Shou M, et al. Angiogenic-induced enhancement of collateral blood flow to ischemic myocardium by vascular endothelial growth factor in dogs. Circulation 1994;89:2183–9. 29. Tio RA, Lebherz C, Scheuermann TH, Jr, Tkebuchava T, Magner M, Symes J. Intramyocardial injection with naked DNA encoding for VEGF causes local and systemic production of VEGF, and improves collateral flow to ischemic myocardial tissue [abstr]. Circulation 1998;98:I-526. 30. Vale PR, Losordo DW, Symes JF, Isner JM. Gene therapy for myocardial angiogenesis [abstr]. Circulation 1998;98:I-322. 31. Losordo DW, Vale PR, Symes J, et al. Gene therapy for myocardial angiogenesis: initial clinical results with direct myocardial injection of phVEGF165 as sole therapy for myocardial ischemia. Circulation 1998;98:2800 – 4. 32. Wijns W, Vatner SF, Camici PG. Hibernating myocardium. N Engl J Med 1998;3:173– 81.
Vol. 34, No. 1, 1999 ISSN 0735-1097/99/$20.00 PII S0735-1097(99)00143-6
EXPERIMENTAL STUDY
Catheter-Based Myocardial Gene Transfer Utilizing Nonfluoroscopic Electromechanical Left Ventricular Mapping Peter R. Vale, MD, Douglas W. Losordo, MD, FACC, Tengiz Tkebuchava, MD, Donghui Chen, MD, Charles E. Milliken, MA, Jeffrey M. Isner, MD, FACC Boston, Massachusetts OBJECTIVES
This study investigated the feasibility and safety of percutaneous, catheter-based myocardial gene transfer.
BACKGROUND Direct myocardial gene transfer has, to date, required direct injection via an open thoracotomy. METHODS
Electroanatomical mapping was performed to establish the site of left ventricular (LV) gene transfer. A steerable, deformable 7F catheter with a 27G needle, which can be advanced 3 to 5 mm beyond its distal tip, was then directed to previously acquired map sites, the needle was advanced, and injections were made into the LV myocardium.
RESULTS
In two pigs in which methylene blue dye was injected, discretely stained LV sites were observed at necropsy in each pig, corresponding to the injection sites indicated prospectively by the endocardial map. In six pigs in which the injection catheter was used to deliver plasmid using cytomegalovirus promoter/enhancer, encoding nuclear-specific LacZ gene (pCMVnlsLacZ) (50 mg/ml) to a single LV myocardial region, peak beta-galactosidase activity after five days (relative light units [RLU], mean 135,333 6 28,239, range 5 31,508 to 192,748) was documented in the target area of myocardial injection in each pig. Percutaneous gene transfer of pCMV-nlsLacZ (50 mg/ml) was also performed in two pigs with an ameroid constrictor applied to the left circumflex coronary artery; in each pig, peak beta-galactosidase activity after five days (214,851 and 23,140 RLU) was documented at the injection site. All pigs survived until sacrifice, and no complications were observed with either the mapping or the injection procedures.
CONCLUSIONS Percutaneous myocardial gene transfer can be successfully achieved in normal and ischemic myocardium without significant morbidity or mortality. These findings establish the potential for minimally invasive cardiovascular gene transfer. (J Am Coll Cardiol 1999;34:246 –54) © 1999 by the American College of Cardiology
From the time of the initial description of direct gene transfer to the artery wall by Nabel et al. (1), gene therapy has been proposed or investigated for a number of cardiovascular applications including prevention of restenosis, treatment of congestive heart failure and therapeutic angiogenesis (2). Each of these potential applications requires consideration of the appropriate gene, vector and delivery technique. To date, successful transfection with a variety of genes, using both viral and nonviral vectors, has been accomplished by intravascular gene transfer (3,4), direct From the Division of Cardiovascular Research, St. Elizabeth’s Medical Center, and Tufts University School of Medicine, Boston, Massachusetts. This study was supported in part by NIH grants HL-53354, HL-57516 and HL-60911 (Dr. Isner), a grant from the E.L. Weigand Foundation, Reno, Nevada, and the Peter Lewis Educational Foundation. Dr. Vale is the recipient of a travelling fellowship from the St. Vincent’s Clinic Foundation, Sydney, Australia. Manuscript received October 5, 1998; revised manuscript received February 2, 1999, accepted March 15, 1999.
transcutaneous intramuscular injection (5–9), transcutaneous pericardial injection (10), and direct intramyocardial injection (11–13). Although intravascular, pericardial, and intramuscular gene transfer have all been performed using minimally invasive delivery techniques, intramyocardial gene transfer has to date required an operative thoracotomy. Such an approach clearly implies additional morbidity and limits the feasibility of repeat administrations. Successful execution of percutaneous, catheter-based myocardial gene transfer has not been previously reported. Accordingly, we sought to investigate the safety and feasibility of a novel delivery catheter for percutaneous myocardial gene transfer. To determine whether the delivery catheter could be used in a site-specific manner, myocardial gene transfer was integrated with a previously described catheter mapping technology (14). The results of this preliminary study indeed establish that percutaneous
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Abbreviations and Acronyms LV 5 left ventricle LCx 5 left circumflex coronary artery pCMV-nlsLacZ 5 plasmid using cytomegalovirus promoter/enhancer, encoding nuclear-specific LacZ gene RLU 5 relative light units VEGF 5 vascular endothelial growth factor
myocardial gene transfer can be successfully achieved in normal and ischemic myocardium in a relatively site-specific fashion without significant morbidity or mortality. These findings thus establish the potential to replace currently used operative approaches with a minimally invasive technique for applications of cardiovascular gene therapy designed to target myocardial function.
METHODS Electromechanical left ventricular mapping. The NOGA system (Biosense, Johnson & Johnson) is designed to acquire, analyze, and display electroanatomical maps of the human heart. The maps are constructed by combining and integrating information from intracardiac electrograms acquired at multiple endocardial locations. Catheters designed for use with the NOGA system are equipped with an electromagnetic sensor, which provides real-time location of the catheter. As the catheter is moved along the endocardium, local endocardial electrograms, together with the catheter tip location, are reported simultaneously. The system then uses this information to construct a threedimensional (3D) electroanatomical map that constitutes a geometrical representation of the left ventricle (LV). The NOGA system analyzes both global and local parameters that characterize mechanical, dynamic, and electrical LV function. Functional analysis is based on local shortening as an index of local mechanical function, whereas measurement of local intracardiac signals determines viability based upon preserved electrical function. The combination of these data permits assessment of electromechanical coupling (15). NOGA components. The mapping and navigation system consists of a locator pad, a reference catheter, a mapping catheter and a processing unit with a graphics computer (Silicon Graphics, Mountain View, California). A similar system, CARTO (Biosense), has been previously described in detail (14,16). The locator pad consists of a triangular arrangement of three magnetic coils, which generate an ultra-low intensity magnetic field (0.02 G to 0.5 G). The pad attaches to the undersurface of the catheterization table. The reference catheter (Cordis-Webster, Baldwin Park, California) is taped directly to the skin overlying the anterior or posterior chest wall within the frame of reference
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created by the three coils of the locator pad. It is used to detect small changes in intracardiac position due to respiration or movement of the subject. These small changes are analyzed by the computer to correct spatial information generated by the mapping catheter. The mapping catheter (Cordis-Webster) is a 7F fused tip catheter with a miniature passive magnetic field sensor embedded within its distal tip. On the basis of the strength of the magnetic field emitted from the locator pad coils, this sensor maps the distance from each coil; these distances determine the radii of theoretical spheres around each coil. The intersection of these three spheres determines the location and orientation of the sensor in 6 degrees of freedom (x, y, z, roll, pitch and yaw), which thus indicates the position and rotation of the distal catheter segment. The accuracy of the sensor position in this low magnetic field is 0.8 mm and 5 degrees (14,16). Unipolar or bipolar signals (timing related to a reference signal) are also obtained from the distal tip of the catheter, allowing generation of activation times in relation to the position of the catheter in the heart. Mapping procedure. The mapping procedure has been previously described in detail (14,16). Briefly, the reference catheter was placed within the field of reference. The mapping catheter was introduced via a femoral arteriotomy and advanced to the LV. Three points (high septum, high lateral wall, and apex) were obtained with fluoroscopic guidance to generate the initial 3D image of the LV. The location of the mapping catheter was gated to a reliable point in the cardiac cycle (recorded relative to the location of the fixed reference catheter at that time) and its location was continuously shown on the screen of the mapping computer. An icon of the mapping catheter is displayed superimposed on the 3D map, thus enabling catheter manipulation in relation to the 3D map. At each site, three parameters are calculated to determine the stability of endocardial contact with the catheter tip: location, cycle length (CL) and local activation time (LAT). Location is a measure of how stable the tip location is between beats. The CL indicates the difference between the current CL and the median CL of the last 100 acquired points. The LAT is calculated as the interval between a reliable point on the body-surface electrocardiogram (ECG) and the steepest negative intrinsic deflection from the mapping-catheter unipolar recording, as determined from the intracardiac electrogram. This electrophysiologic information is color-coded (red being the shortest LAT and purple being the longest) and superimposed on the 3D chamber geometry. The reconstruction was updated in real time with the acquisition of each new site. Validation of both intracardiac signal recording and location accuracy, both in vitro and in vivo, and correlation between electromechanical characteristics and pathology, have been previously established (14 –16). In addition, early reports suggest
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Figure 1. (A) The endocardial surface following dissection through the left lateral free wall following injections with methylene blue. Left ventricle with papillary muscles, left atrium and mitral valve apparatus are displayed. Lateral wall and septum are labeled. Methylene blue injection sites (arrows) are demonstrated at the apex, septum, and posterolateral wall. (B) Corresponding NOGA™ map (left anterior oblique [LAO] projection) with injection sites indicated by red hexagons. LA 5 left arm; RA 5 right arm.
that LV mapping may allow the detection of on-line myocardial viability (17). Injection catheter. The injection catheter (CordisWebster) is a modified 7F mapping catheter, the distal tip of which incorporates a 27G needle that can be protruded 3 to 5 mm. The injection catheter was manipulated to acquire
stable points within the target region based on the parameters described above and superimposed upon the previously acquired 3D electroanatomic map. Once a stable point was attained, the needle was advanced 4 to 5 mm into the myocardium; the intracardiac electrogram detected transient myocardial injury or premature ventricular contractions as
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Figure 2. Endocardial mapping and injection of normal male swine (RAO projection). NOGA maximum voltage and linear log shortening maps show injection sites into nonischemic myocardium. Note the coupling of normal mechanical function with normal electrical activity. Injections in this case were localized to the left ventricular apex. LA 5 left arm; RA 5 right arm.
evidence of needle penetration into the myocardium. Injectate was delivered according to one of three protocols as outlined below. Each injection consisted of 1 ml of solution (total volume 5 6 ml/animal) delivered from a 1-ml syringe. The lumen was prefilled with 0.1 ml of sterile saline prior to entry into the circulation, and following each injection the lumen was again flushed with 0.1 ml of sterile saline. Following completion of the injection, the needle was retracted and the catheter was moved to another endocardial site. Animal studies. A total of 10 swine weighing 30 to 50 kg each were studied under protocols approved by the Animal Care and Use Committee of the St. Elizabeth’s Medical Center. All procedures were performed under anesthesia using a combination of intramuscular (IM) ketamine (15 mg/kg), acepromazine (0.2 mg/kg), and atropine (0.05 mg/kg). All animals received inhalation ventilation with 2% isofluorane to ensure adequate anesthesia throughout the experiment, and supplemental oxygen @ 3 l/min. Before introduction of the mapping catheter, all pigs received intravenous (IV) cefazolin 500 mg (Kefzol, Eli Lilly, Indianapolis, Indiana), heparin 5,000 IU, bretylium tosylate (50 mg/kg), and lidocaine (0.5 mg/kg). Levodromaron (2 mg subcutaneous [s.c.]) was given for analgesia at the beginning of the procedure with supplemental doses as required; on completion of each procedure, animals received an additional injection of levodromaron. A further dose of lidocaine (0.5 mg/kg IV) was given before the injection procedure. Following the mapping and injection procedures, the arteriotomy was closed and the pig was allowed to recover (except in Protocol 1 in which the animals were immediately sacrificed). Animals were observed during recovery until fully conscious, returned to housing 24 h later, and given cefazolin 2 3 500 mg s.c. daily for three to five days. At the end of the study period, the animals were returned to the
laboratory, sacrificed with euthanasia solution (sodium pentobarbital), and the heart excised for macroscopic and microscopic evaluation. PROTOCOL 1. Two healthy and nonischemic pigs each received six 1-ml injections of methylene blue dye. Injections were made in three LV myocardial regions in each pig. Immediately postoperatively, each animal was sacrificed and the heart removed. Both the success and the accuracy of myocardial injections were assessed by correlating the number and location of apparent injection sites on the in vivo 3D electroanatomical map with those identified at necropsy. The extent of myocardial staining was measured to identify the spread of dye from the injection site.
To determine the feasibility of using the injection catheter to perform gene transfer, six healthy, nonischemic pigs each received six injections of 1 ml of a reporter gene (see below) to a single area of LV myocardium. These pigs were sacrificed three to five days later and tissue obtained for quantitative analysis of gene expression.
PROTOCOL 2.
PROTOCOL 3. Under general anesthesia administered via an endotracheal tube, ischemia was induced in two pigs by placing an ameroid constrictor around the proximal left circumflex (LCx) artery as previously described (13,18,19). Three weeks later, selective coronary angiography was performed to determine the maturity of the constrictor, and endocardial mapping was used to identify the area of ischemic myocardium (as evidenced by uncoupling of mechanical function and electrical activity). Each pig received six injections of 1.0 ml of LacZ (50 mg/ml) to a single LV area. Pigs were sacrificed after three to five days and tissue obtained for macroscopic and microscopic evaluation.
Gene expression. Naked plasmid deoxyribonucleic acid (DNA) encoding for nuclear-specific beta-galactosidase transcriptionally regulated by the CMV promoter/enhancer
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Figure 3. Quantitative beta-galactosidase assays of catheter-based single-site left ventricular (LV) injections in normal swine (pigs 3 to 8). Note the focal distribution of peak activity. A 5 anterior wall, L 5 lateral wall, P 5 posterior wall, S 5 septum. Numbers refer to the harvested tissue specimens, 1 being closest to the apex, and 4 being adjacent to the LV outflow tract and mitral valve ring.
(pCMV-nlsLacZ) was used as a reporter gene to evaluate percutaneous myocardial gene transfer. Gene expression was evaluated with a chemoiluminescence assay (20) (GalactoLight, Tropix, Bedford, Massachusetts) designed to measure beta-galactosidase activity. Before measuring betagalactosidase activity, tissue homogenates were pretreated with Chelex 100 to inactivate a natural inhibitor of the enzyme (21).
RESULTS Mapping procedure. During the mapping procedure, heart rate (premapping 5 118 6 8/min vs. postmapping 5 120 6 10/min), systolic blood pressure (BP, 92 6 3 vs. 87 6 4 mm Hg) and O2 saturation (98 6 0.5 vs. 99 6 0.4%) remained stable. Mapping was associated with transient ventricular ectopic activity but no sustained ventricular
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arrhythmias. No other complications were associated with the mapping procedure. Activation (electroanatomic) maps of the LV during sinus rhythm were created in all pigs. All maps were completed in ,20 min. The mean number of points acquired per map was 93 6 6 (45 to 127). The site of earliest activation was in each case at the superior part of the septum (red/orange); the latest site of activation was on the left lateral wall close to the mitral valve apparatus (purple). Before injection, electromechanic interrogation was performed, consisting of maximum voltage (electrical activity) and linear log shortening (mechanical function) maps. Electrically viable tissue produced maximum unipolar voltage .10 mV, and mechanically functional myocardium produced linear log shortening .5%. In all nonischemic pigs, both mechanical function and electrical activity were within normal limits. In the two pigs with an ameroid constrictor, evidence of myocardial ischemia was detected in the lateral wall as evidenced by electromechanical uncoupling (high electrical voltage but low linear log shortening). Percutaneous LV gene transfer. Percutaneous catheterbased myocardial injections caused no significant changes in heart rate (preinjection 5 120 6 10/min vs. postinjection 5 128 6 11/min), systolic BP (87 6 3 vs. 89 6 4 mm Hg), or O2 saturation (99 6 0.4 vs. 98 6 0.7%). Transient unifocal ventricular ectopic activity was observed at the time the needle was extended into the myocardium. In all pigs, sporadic premature ventricular contractions occurred during injection. No episodes of sustained ventricular (or atrial) arrhythmias occurred. No sustained injury pattern was observed during the injections as recorded by the endocardial electrogram. Likewise, the surface ECG showed no evidence of myocardial infarction in any pig. All pigs survived until sacrifice; complications, including pericardial effusion or cardiac tamponade, were not observed in any animals. Six discrete sites of methylene blue staining, located in three LV myocardial areas (anteroapical [n 5 2], septum [n 5 2] and posterolateral wall [n 5 2]), were identified at necropsy in each heart; these sites corresponded to the injection sites indicated prospectively in vivo on the endocardial map (Fig. 1). Myocardial staining was 5.2 6 1.7 mm in depth and 6.4 6 0.7 mm in width. No epicardial staining was demonstrated. In addition, X-gal staining produced no evidence of nuclear-specific beta-galactosidase activity in the myocardium at these sites (Table 1); these two hearts thus constituted negative controls (because no gene transfer was performed in either case) for Protocol 2 below.
PROTOCOL 1.
PROTOCOL 2. The injection catheter was used to deliver pCMV-nlsLacZ (50 mg/ml) to a single LV myocardial region (Fig. 2) in six pigs (apex [n 5 2], septum [n 5 2], posterolateral wall [n 5 1] and the anterior wall [n 5 1]). In each of the six pigs, peak beta-galactosidase activity after
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Figure 4. Fluoroscopic image (anteroposterior projection) of the injection catheter in the left ventricle angled toward the lateral wall. (Distal tip of injection catheter appears to point toward ameroid constrictor.)
five days (relative light units [RLU], mean 5 135,333 6 28,239, [31,508 to 192,748]) was documented in the target area of myocardial injection (Table 1; Fig. 3). Adjacent myocardial areas demonstrated low-level activity, and areas remote from the injection sites had negligible activity. Thus, percutaneous LV myocardial gene transfer was directed in a relatively localized fashion to those sites indicated by preinjection electroanatomical mapping. PROTOCOL 3. Percutaneous gene transfer of pCMVnlsLacZ (50 mg/ml) was also performed in two pigs in which an ameroid constrictor had applied to the left circumflex coronary artery (Fig. 4). Myocardial ischemia was demonstrated in the lateral wall of both pigs (Fig. 5). In each of these two pigs, peak beta-galactosidase activity after five days (214,851 and 23,140 RLU) was documented in the target area of myocardial injection (Table 1; Fig. 6). As in the nonischemic hearts, beta-galactosidase activity was markedly diminished in tissue sections retrieved from adjacent myocardium and was negligible at remote sites.
DISCUSSION Although intra-arterial delivery was used to establish the precedent for cardiovascular gene transfer (1) and has been subsequently exploited to accomplish gene transfer successfully in a variety of animal models (2) as well as patients (3), this route of administration has several inherent limitations for myocardial gene transfer. In the case of naked DNA (i.e., DNA unassociated with viral or other adjunctive vectors), cellular uptake is virtually nil when the transgene is directly injected into the coronary artery lumen, presumably due to prompt degradation by circulating nucleases. Gene transfer performed to the coronary arterial wall itself requires access to a satisfactory donor site; in patients with chronic myocardial ischemia—particularly those patients whose anatomy is not amenable to angioplasty or bypass
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Figure 5. Catheter-based myocardial injections into ischemic swine left ventricle (LV). NOGA™ electrical (maximum unipolar voltage) and mechanical (linear log shortening) maps of the swine LV are shown. Note area of ischemia in the lateral wall—normal electrical activity (blue/green) coupled with poor mechanical function (red). Images A and B represent anteroposterior projections demonstrating six injection sites (red hexagons) in an area of normal myocardial (apex) remote from the ischemic zone. Images C and D depict LAO projections of indicated injection sites in the ischemic lateral LV free wall. LA 5 left arm; RA 5 right arm.
Figure 6. Quantitative beta-galactosidase assays of catheter-based single-site LV injections in swine models of chronic myocardial ischemia (pigs 9 and 10). Injections into myocardium remote from the ischemic zone are distinguished from injections made into the ischemic lateral wall. A 5 anterior wall, L 5 lateral wall, P 5 posterior wall, S 5 septum. Numbers refer to the harvested tissue specimens, 1 being closest to the apex, and 4 being adjacent to the LV outflow tract and mitral valve ring.
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Table 1. Results of Mapping and Injection Procedures Beta-galactosidase Activity (RLU) Pig
Ischemia
1 2 3 4 5 6 7 8 9 10
None None None None None None None None Lateral Lateral
Rx dose
Site 3 no.
Arrhythmias
Total
Peak
Peak/Total (%)
Methylene blue Methylene blue LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg LacZ 50 mg
32 apex/32 lateral/32 septum 32 apex/32 lateral/32 septum Apex 36 Post 36 Apex 36 Septum 36 Anterior 36 Septum 36 Posterior 36 Lateral 36
None None None None None None None None None None
0 0 214,843 182,502 210,409 82,826 59,537 115,960 59,249 365,232
0 0 192,748 149,900 140,991 57,694 31,508 69,357 23,140 214,851
90 82 67 69 53 60 39 59
surgery— diffuse distribution of neointimal thickening or extensive calcific deposits (22) may limit gene transfer to the smooth muscle cells of the arterial media (20). Ischemic muscle as a target for naked DNA. Ischemic muscle represents an alternative target for gene transfer. Striated (5– 8) and cardiac (11,12,23) muscle have been shown to take up and express naked plasmid DNA as well as transgenes incorporated into viral vectors (9,13). Moreover, previous studies (6,24) have shown that the transfection efficiency of intramuscular (IM) gene transfer is augmented more than fivefold when the injected muscle is ischemic. This finding may be the result of the skeletal muscle regeneration, including stem cell (myoblast) proliferation. Vitadello et al. (25) reported an 80-fold increase in chloramphenicol acetyltransferase (CAT) activity following transfection of regenerating versus control muscle. Consistent with this concept, Danko et al. (26) found that bupivacaine, which produces myonecrosis followed by satellite cell (muscle stem cell) proliferation and myotube formation one to three days later, may be used to enhance the expression of naked DNA injected IM into striated muscles. Therapeutic angiogenesis as a model for myocardial gene therapy. We have previously exploited these features of skeletal and cardiac muscle to perform gene transfer of naked DNA encoding for angiogenic growth factors. Preclinical animal studies from our laboratory established that IM gene transfer could be utilized to accomplish successful therapeutic angiogenesis in animals with hindlimb ischemia (6). Subsequently, Phase 1 clinical studies from our institution have established that IM gene transfer of naked DNA encoding for vascular endothelial growth factor (VEGF) may be utilized to accomplish safe and successful therapeutic angiogenesis in patients with critical limb ischemia (7). The notion that this concept could be extrapolated to the treatment of chronic myocardial ischemia was implied by experiments performed in both our laboratory (19) and in others’ (13,27,28) in which recombinant human VEGF was administered to a porcine animal model of chronic myocar-
dial ischemia. This same animal model has been utilized to demonstrate that therapeutic angiogenesis can also be successfully achieved by direct myocardial administration of VEGF, as naked DNA (29) or using an adenoviral vector (13). Preliminary results utilizing this approach as sole therapy (no bypass) for patients with chronic myocardial ischemia suggest that direct injection of VEGF into cardiac myocytes improves collateral blood flow and markedly reduces the frequency of and threshold for myocardial ischemia (30,31). Percutaneous myocardial gene transfer. To date, all of the aforementioned work involving myocardial gene transfer has been achieved via a mini-thoracotomy used for less invasive coronary artery bypass surgery. Although this approach has clearly reduced the length of hospital stay and morbidity associated with conventional bypass surgery, it nevertheless requires general anesthesia and is not easily repeatable. The capability to perform myocardial gene transfer percutaneously could thus further reduce the morbidity and facilitate repeat use of myocardial gene transfer. The experiments described in this report suggest that percutaneous myocardial gene transfer is indeed feasible and can be safely performed in normal and ischemic myocardium of swine (Table 1). Injection of methylene blue was successfully achieved at 6/6 (100%) sites in two pigs. The extent of transmural distribution was limited to the LV wall, as evidenced by the absence of epicardial staining. Maximum gene expression was localized to the injection site in all pigs, ischemic as well as normal, injected with pCMVnlsLacZ. Myocardium adjacent to the target sites of injection demonstrated low-level beta-galactosidase activity, indicating limited distribution following gene transfer. All remote noninjected areas of myocardium were essentially devoid of beta-galactosidase activity. Role of adjunctive electromechanical mapping. Although the mapping capabilities of the NOGA system utilized in this study were useful for demonstrating that gene expression could be directed to specific LV sites, it must be acknowledged that these findings do not establish
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that LV endocardial mapping is required for percutaneous myocardial gene transfer. Electroanatomic mapping clearly may be advantageous both for avoiding gene transfer to sites of myocardial scar and for relocating with accuracy the tip of the injection catheter to areas of myocardial ischemia (or hibernating myocardium) where gene transfer may be potentially optimized (6,32). Theoretically, adjunctive mapping could be employed in a serial fashion to gauge the success of certain gene therapy strategies (e.g., therapeutic angiogenesis). These potential advantages, however, will require further documentation and assessment of physiologic improvement following delivery of a nonreporter gene to establish the value of adjunctive mapping. Reprint requests and correspondence: Dr. Jeffrey M. Isner, St. Elizabeth’s Medical Center, 736 Cambridge Street, Boston, Massachusetts 02135. E-mail: [email protected].
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