Jørgensen Lars Nannestad
Copenhagen Wound Healing Center, Bispebjerg Hospital University of Copenhagen, Denmark.
APMIS Suppl. 2003(115):1-56.
Wound healing encompasses coagulation, inflammation, angiogenesis, fibroplasia, contraction, epithelialisation and remodeling. A granulation tissue is produced following incision of tissue such as skin, abdominal wall or the gastrointestinal tract, and the strength of the wound is determined primarily by the collagen content early in the healing course. Few models are available to study wound healing in man. The percutaneous insertion of expanded poly-tetrafluoroethylene tubes (ePTFE) into the subcutaneous tissue has been an established model for 20 years. The procedure is performed using a local anesthesia. The model has a diameter of 2.5 mm, a length of 5-10 cm and a pore size of 90-120 microns which is substantially more than that of vascular grafts. The polymer accumulates granulation tissue, the architecture of which resembles that of a normal surgical wound. Previous studies on the use of the ePTFE model in wound healing research are summarized in detail. Histological and immunohistochemical analyses of the granulation tissue deposited in the model were undertaken. The content of amino acids following hydrolysis of the granulation tissue was determined applying spectrophotometric or HPLC assays. Collagen amounts accumulated in the model are expressed as hydroxyproline per length of ePTFE or per total protein. Following a study in rats we examined 85 healthy volunteers and 158 surgical patients in the studies. Higher contents of hydroxyproline were found 10 days after implantation as compared to 5 days with considerable inter-person variation. Regarding median values there was a 25% difference between two measurements performed on two distinct ePTFE tubes from the same person, and a 12% difference between values obtained from two different pieces of the same ePTFE. Higher accumulation levels of hydroxyproline did not result in higher variability. Deposition of proline in the model correlated closely to total protein content. The ePTFE and a modified PVA model were compared in surgical patients. No reproducible measurements of hydroxyproline deposition were obtained with the PVA model as opposed to the ePTFE model. It is concluded that the modified PVA model is inadequate for determination of collagen deposition in subcutaneous granulation tissue. We found no correlation between collagen deposition levels obtained with placement of the ePTFE model in the subcutaneous tissue of the arm and in an uncomplicated surgical wound of the groin in the same patient, respectively. Significantly higher collagen deposition levels in the model were found in the surgical wound. Conversely, there was a significant correlation between protein deposition levels obtained at the two sites. Patients undergoing minor surgery (groin hernia repair) did not differ from healthy non-traumatized volunteers as regards deposition of collagen in subcutaneous tissue of the arm, whereas patients subjected to major general surgery demonstrated a significant decline during the postoperative phase compared to a preoperative evaluation. This decline was enhanced in patients who had infectious complications. Non-smoking volunteers were found to specifically accumulate more collagen (median value 82%) than smokers matched for age and gender. Irrespective of the smoking status women accumulated significantly more collagen in the model than men. These findings were re-tested in a prospective series leading to the same conclusion. Matrix metalloproteinases (MMP-2 and MMP-9) were determined in wound fluid obtained from the subcutaneous cavities of herniotomy wounds 24 and 48 h after operation. A significant and inverse correlation was demonstrated between MMP-9 after 24 h and accumulation levels of collagen in the ePTFE tube 10 days after implantation in the wound. Finally, it was demonstrated that local application of granulocyte-macrophage colony-stimulating factor into the ePTFE model during implantation specifically and dose-dependently reduced the number of fibroblasts and deposition of collagen. The doses chosen for the experiments resulted in both a local and a systemic effect. It is concluded that the minimally invasive ePTFE model, despite a certain level of variability, presently provides one of the best possibilities of evaluation of the wound healing potential in both volunteers and patients under various conditions. We found the model convenient for the assessment of both matrix deposition during wound healing and the influence of several factors including demographic characteristics, trauma, tobacco smoking, drugs and tissue degrading components of the wound.
伤口愈合包括凝血、炎症、血管生成、纤维增生、收缩、上皮化和重塑。在诸如皮肤、腹壁或胃肠道等组织切开后会形成肉芽组织,伤口的强度在愈合过程早期主要由胶原蛋白含量决定。用于研究人类伤口愈合的模型很少。将膨体聚四氟乙烯管(ePTFE)经皮插入皮下组织作为一种成熟的模型已使用了20年。该操作采用局部麻醉。该模型直径为2.5毫米,长度为5 - 10厘米,孔径为90 - 120微米,远大于血管移植物的孔径。这种聚合物会积聚肉芽组织,其结构类似于正常手术伤口的结构。此前关于ePTFE模型在伤口愈合研究中的应用的研究已详细总结。对模型中沉积的肉芽组织进行了组织学和免疫组织化学分析。采用分光光度法或高效液相色谱法测定肉芽组织水解后的氨基酸含量。模型中积累的胶原蛋白量以每单位长度ePTFE或每总蛋白中的羟脯氨酸表示。在对大鼠进行研究后,我们在研究中检查了85名健康志愿者和158名手术患者。与植入后5天相比,植入后10天发现羟脯氨酸含量更高,且个体间差异较大。就中位数而言,对同一个人的两根不同ePTFE管进行的两次测量之间存在25%的差异,从同一段ePTFE的不同部位获得的值之间存在12%的差异。较高的羟脯氨酸积累水平并未导致更高的变异性。模型中脯氨酸的沉积与总蛋白含量密切相关。在手术患者中对ePTFE模型和改良聚乙烯醇(PVA)模型进行了比较。与ePTFE模型不同,PVA模型未获得可重复的羟脯氨酸沉积测量值。结论是改良的PVA模型不足以测定皮下肉芽组织中的胶原蛋白沉积。我们发现,将ePTFE模型分别置于同一患者手臂的皮下组织和腹股沟的无并发症手术伤口中,所获得的胶原蛋白沉积水平之间没有相关性。在手术伤口中发现模型中的胶原蛋白沉积水平明显更高。相反,在这两个部位获得的蛋白质沉积水平之间存在显著相关性。接受小手术(腹股沟疝修补术)的患者在手臂皮下组织中的胶原蛋白沉积与健康未受创伤的志愿者没有差异,而接受大手术的患者与术前评估相比,术后阶段胶原蛋白沉积显著下降。有感染并发症的患者这种下降更为明显。发现不吸烟的志愿者比年龄和性别匹配的吸烟者特异性地积累更多胶原蛋白(中位数为82%)。无论吸烟状况如何,女性在模型中积累的胶原蛋白都明显多于男性。这些发现在前瞻性系列研究中得到了再次验证,得出了相同的结论。在手术后24小时和48小时从疝修补术伤口的皮下腔隙获取的伤口液中测定基质金属蛋白酶(MMP - 2和MMP - 9)。结果表明,术后24小时的MMP - 9与伤口植入后10天ePTFE管中的胶原蛋白积累水平之间存在显著的负相关。最后,结果表明在植入过程中向ePTFE模型局部应用粒细胞 - 巨噬细胞集落刺激因子可特异性且剂量依赖性地减少成纤维细胞数量和胶原蛋白沉积。实验中选择的剂量产生了局部和全身效应。结论是,尽管存在一定程度的变异性,但微创ePTFE模型目前为评估不同条件下志愿者和患者的伤口愈合潜力提供了最佳可能性之一。我们发现该模型便于评估伤口愈合过程中的基质沉积以及包括人口统计学特征、创伤、吸烟、药物和伤口组织降解成分等多种因素的影响。