Sigler Matthias, Klötzer Julia, Quentin Thomas, Paul Thomas, Möller Oliver
Department of Pediatric Cardiology and Intensive Care Medicine, University Medical Center, Georg August University Göttingen, Robert Koch Strasse 40, D 37075, Göttingen, Germany.
Mol Cell Pediatr. 2015 Dec;2(1):10. doi: 10.1186/s40348-015-0021-7. Epub 2015 Nov 5.
Stent implantation into the tracheo-bronchial system may be life-saving in selected pediatric patients with otherwise intractable stenosis of the upper airways. Following implantation, significant tissue proliferation may occur, requiring re-interventions. We sought to evaluate the effect of immunosuppressive coating of the stents on the extent of tissue proliferation in an animal model.
Bare metal and sirolimus-coated stents (Bx Sonic and Cypher Select, Johnson & Johnson, Cordis) were implanted into non-stenotic lower airways of New Zealand white rabbits (weight 3.1 to 4.8 kg). Three stents with sirolimus coating and six bare metal stents could be analyzed by means of histology and immunohistochemistry 12 months after implantation.
On a macroscopic evaluation, all stents were partially covered with a considerable amount of whitish tissue. Histologically, these proliferations contained fiber-rich connective tissue and some fibromuscular cells without significant differences between both stent types. The superficial tissue layer was formed by typical respiratory epithelium and polygonal cells. Abundant lymphocyte infiltrations and moderate granulocyte infiltrations were found in both groups correspondingly, whereas foreign-body reaction was more pronounced around sirolimus-eluting stents.
After stent implantation in the tracheo-bronchial system of rabbits, we found tissue reactions comparable to those seen after stent implantation into the vascular system. There was no difference between coated and uncoated stents with regard to quality and quantity of tissue proliferation. We found, however, a significantly different inflammatory reaction with a more pronounced foreign-body reaction in sirolimus-coated stents. In our small series, drug-eluting stents did not exhibit any benefit over bare metal stents in an experimental setting.
对于某些患有上气道顽固性狭窄的儿科患者,气管支气管系统支架植入术可能挽救生命。植入后,可能会发生显著的组织增生,需要再次干预。我们试图在动物模型中评估支架的免疫抑制涂层对组织增生程度的影响。
将裸金属支架和西罗莫司涂层支架(Bx Sonic和Cypher Select,强生公司,科迪斯)植入新西兰白兔(体重3.1至4.8千克)的非狭窄下气道。植入12个月后,可通过组织学和免疫组织化学分析3个西罗莫司涂层支架和6个裸金属支架。
宏观评估显示,所有支架均部分覆盖有大量白色组织。组织学上,这些增生包含富含纤维的结缔组织和一些纤维肌细胞,两种支架类型之间无显著差异。表层组织由典型的呼吸道上皮和多边形细胞形成。两组均相应地发现大量淋巴细胞浸润和中度粒细胞浸润,而西罗莫司洗脱支架周围的异物反应更明显。
在兔气管支气管系统植入支架后,我们发现组织反应与血管系统植入支架后所见的反应相当。涂层支架和未涂层支架在组织增生的质量和数量方面没有差异。然而,我们发现西罗莫司涂层支架的炎症反应明显不同,异物反应更明显。在我们的小样本研究中,在实验环境中,药物洗脱支架并未显示出优于裸金属支架的任何优势。