Huemer Georg M, Shafighi Maziar, Meirer Romed, Debagge Paul, Piza-Katzer Hildegunde, Gurunluoglu Raffi
Department of Plastic and Reconstructive Surgery, Ludwig-Boltzmann Institute for Quality Control in Plastic Surgery, Leopold-Franzens University, Anichstrasse 35, A-1060 Innsbruck, Austria.
J Surg Res. 2004 Sep;121(1):101-7. doi: 10.1016/j.jss.2004.02.012.
Gene therapy has been recently introduced as a novel approach to treat ischemic tissues by using the angiogenic potential of certain growth factors. We investigated the effect of adenovirus-mediated gene therapy with transforming growth factor-beta (TGF-beta) delivered into the subdermal space to treat ischemically challenged epigastric skin flaps in a rat model.
A pilot study was conducted in a group of 5 animals pretreated with Ad-GFP and expression of green fluorescent protein in the skin flap sections was demonstrated under fluorescence microscopy at 2, 4, and 7 days after the treatment, indicating a successful transfection of the skin flaps following subdermal gene therapy. Next, 30 male Sprague Dawley rats were divided into 3 groups of 10 rats each. An epigastric skin flap model, based solely on the right inferior epigastric vessels, was used as the model in this study. Rats received subdermal injections of adenovirus encoding TGF-beta (Ad-TGF-beta) or green fluorescent protein (Ad-GFP) as treatment control. The third group (n = 10) received saline and served as a control group. A flap measuring 8 x 8 cm was outlined on the abdominal skin extending from the xiphoid process proximally and the pubic region distally, to the anterior axillary lines bilaterally. Just prior to flap elevation, the injections were given subdermally in the left upper corner of the flap. The flap was then sutured back to its bed. Flap viability was evaluated seven days after the initial operation. Digital images of the epigastric flaps were taken and areas of necrotic zones relative to total flap surface area were measured and expressed as percentages by using a software program.
There was a significant increase in mean percent surviving area between the Ad-TGF-beta group and the two other control groups (P < 0.05). (Ad-TGF-beta: 90.3 +/- 4.0% versus Ad-GFP: 82.2 +/- 8.7% and saline group: 82.6 +/- 4.3%.)
In this study, the authors were able to demonstrate that adenovirus-mediated gene therapy using TGF-beta ameliorated ischemic necrosis in an epigastric skin flap model, as confirmed by significant reduction in the necrotic zones of the flap. The results of this study raise the possibility of using adenovirus-mediated TGF-beta gene therapy to promote perfusion in random portion of skin flaps, especially in high-risk patients.
基因治疗作为一种新方法,近来已被用于通过利用某些生长因子的血管生成潜力来治疗缺血组织。我们研究了将腺病毒介导的转化生长因子-β(TGF-β)基因治疗导入皮下空间,对大鼠模型中受缺血挑战的腹壁皮瓣进行治疗的效果。
对一组5只预先接受Ad-GFP治疗的动物进行了一项初步研究,并在治疗后第2、4和7天通过荧光显微镜观察皮瓣切片中绿色荧光蛋白的表达,表明皮下基因治疗后皮瓣成功转染。接下来,将30只雄性Sprague Dawley大鼠分为3组,每组10只。本研究采用仅基于右下腹壁血管的腹壁皮瓣模型。大鼠接受皮下注射编码TGF-β的腺病毒(Ad-TGF-β)或绿色荧光蛋白(Ad-GFP)作为治疗对照。第三组(n = 10)接受生理盐水注射作为对照组。在腹部皮肤上划出一个8×8 cm的皮瓣,其近端起自剑突,远端至耻骨区域,两侧至腋前线。在掀起皮瓣之前,在皮瓣左上角皮下进行注射。然后将皮瓣缝合回原位。在初次手术后7天评估皮瓣活力。拍摄腹壁皮瓣的数字图像,并使用软件程序测量坏死区域相对于皮瓣总面积的面积,并以百分比表示。
Ad-TGF-β组与其他两个对照组之间的平均存活面积百分比有显著增加(P < 0.05)。(Ad-TGF-β组:90.3±4.0%,Ad-GFP组:82.2±8.7%,生理盐水组:82.6±4.3%。)
在本研究中,作者能够证明,腺病毒介导的使用TGF-β的基因治疗改善了腹壁皮瓣模型中的缺血性坏死,皮瓣坏死区域显著减少证实了这一点。本研究结果增加了使用腺病毒介导的TGF-β基因治疗促进随意型皮瓣灌注的可能性,尤其是在高危患者中。