Schlegel Philipp, Huditz Regina, Meinhardt Eric, Rapti Kleopatra, Geis Nicolas, Most Patrick, Katus Hugo A, Müller Oliver J, Bekeredjian Raffi, Raake Philip W
1 Department of Internal Medicine III, Cardiology, Heidelberg University Hospital , University of Heidelberg, Heidelberg, Germany .
2 Department of Medicine, Center for Translational Medicine, Thomas Jefferson University , Philadelphia, Pennsylvania.
Hum Gene Ther Methods. 2016 Apr;27(2):71-8. doi: 10.1089/hgtb.2015.120.
Cardiac gene therapy is a promising approach for treating heart diseases. Although clinical studies are ongoing, effective and targeted transgene delivery is still a major obstacle. We sought to improve and direct transgene expression in myocardium by ultrasound-targeted microbubble destruction (UTMD). In pigs, adeno-associated virus-derived (AAV) vectors harboring the luciferase reporter gene were delivered via retroinfusion into the anterior interventricular coronary vein (AIV). AAV vectors were either loaded to lipid microbubbles before injection or injected unmodified. Upon injection of AAV/microbubble solution, UTMD was performed. After 4 weeks, reporter gene expression levels in the anterior wall (target area), in the posterior wall (control area), and in noncardiac organs were analyzed. Retroinfusion of AAV-luciferase vectors loaded to lipid microbubbles led to a significant increase in transgene expression, with an increase in UTMD targeted areas of the anterior wall. Moreover, off-target expression was reduced in comparison to control animals, receiving AAV-luciferase without microbubbles. Besides an increase in overall target area transgene expression, UTMD alters the spatial expression of the luciferase transgene, focusing expression to ultrasound-targeted left ventricular wall. These data suggest UTMD as a promising approach for directing AAV to specific cardiac segments.
心脏基因治疗是一种治疗心脏病的有前景的方法。尽管临床研究正在进行,但有效且靶向性的转基因递送仍然是一个主要障碍。我们试图通过超声靶向微泡破坏(UTMD)来改善和指导心肌中的转基因表达。在猪中,携带荧光素酶报告基因的腺相关病毒(AAV)载体通过逆向灌注被递送至前室间冠状静脉(AIV)。AAV载体在注射前要么加载到脂质微泡上,要么未经修饰直接注射。在注射AAV/微泡溶液后,进行UTMD。4周后,分析前壁(靶区域)、后壁(对照区域)和非心脏器官中的报告基因表达水平。将加载到脂质微泡上的AAV-荧光素酶载体逆向灌注导致转基因表达显著增加,前壁UTMD靶向区域的表达增加。此外,与接受无微泡的AAV-荧光素酶的对照动物相比,脱靶表达减少。除了整体靶区域转基因表达增加外,UTMD还改变了荧光素酶转基因的空间表达,使表达集中在超声靶向的左心室壁上。这些数据表明UTMD是一种将AAV导向特定心脏节段的有前景的方法。