Akar Rüçhan, Durdu Serkan, Arat Mutlu, Eren Neyyir Tuncay, Arslan Öder, Çorapçıoğlu Tümer, Sancak Tanzer, Uzun Burcu, Kİr Metin, İlhan Osman, Özyurda Ümit
Turk J Haematol. 2004 Mar 5;21(1):13-21.
Bone marrow implantation into ischaemic limbs could enhance angiogenesis by supplying endothelialprogeniter cells and angiogenic cytokinesot factors. We investigated efficacy and safety of autologousimplantation of bonemarrow-mononuclearcells (BMMC)in patients with ischaemic limbs due to Buerger's disease. We commence daciinical study to test cell therapy with autologous BMMC in patients with ischaemic limbs at the University of Ankara School of Medicine. In order for the patients to qualify for BMMC implantation, they should have critical limb ischaemia define das ischaemic rest painin a limb with or without non healing ulcers, should not respond to previous iloprost infusions and smoking cessation six months prior to evaluation and should not be candidates for nonsurgicalor surgical revascularisation. Primaryend points were safety andfeasibility of the treatmentand total healing of the most importantlesion. Secondary endpoints were total relief of rest pain without the need for analgesies,change in peak walkingtime (PWT)at 12 weeks, improvements in ankle-brachial pressure index(ABI), transcutaneous oxygen saturation using pulse oximetry(SaO2),angiographic evidence of newcollatera lvesselformation, tissue perfusion in the affected extremity using Thallium perfusions cintigraphyW. hilepatients(meanage46.7: !: 10.3years)were undergeneraal naesthesiaw, eharvested bonemarrow(519: t 45.5mUfromtheposteridilriacspineA. fterredbloodcell(RBCd) epletiaannd volumereduction using a continuous flow cell separator,we achieved 91% RBC depletian and concentrated /~MMC to a final volume and concentration of 51.5: t io.1 mLand7.04: t 1.9 x ioe7/mL total nucleated cells, respectively W.eimplantedBMMC (mean12.16: t 4.3 x ioe8) within three hours after marrow aspiration by intramuscular injection into the gastrocnemiusmuscle of ischaemic legs. Isotonic saline were injected into the other extremityin as similar fashion as control. 13 Unilateral intramuscular administration of BMMC was not associated with any complications. The primary efficacy end point, total healing of the most importantlesion, was achieved in three patients. All patients were followed up for at least four weeks. The secondary measures; change in PWT(LlPWT)at 12 weeks, total relief of rest pain without the need of analgesics improved in three patjents. These improvements were sustained for 24 weeks in the first two patients. Digital subtraction angiographic studies before and 3 months after the BMMC implantation showed the presence of a new vascular collateral network across the affected arteries in three patients. Preliminary results of the presentedstudy are promising. Thus, bone marrow maybe a potential source of cells for Buerger'spatients with end-stage Iimbischaemia refractory to other medical treatment modalities.
将骨髓植入缺血肢体可通过提供内皮祖细胞和血管生成细胞因子来促进血管生成。我们研究了自体骨髓单个核细胞(BMMC)植入治疗血栓闭塞性脉管炎所致缺血肢体患者的疗效和安全性。我们在安卡拉大学医学院开展了一项临床研究,以测试自体BMMC对缺血肢体患者的细胞治疗效果。为使患者符合BMMC植入条件,他们应患有严重肢体缺血,定义为肢体出现缺血性静息痛,伴有或不伴有不愈合溃疡,对先前的伊洛前列素输注无反应,且在评估前6个月已戒烟,并且不应是非手术或手术血管重建的候选者。主要终点是治疗的安全性和可行性以及最重要病变的完全愈合。次要终点是无需使用镇痛药即可完全缓解静息痛、12周时峰值步行时间(PWT)的变化、踝肱压力指数(ABI)的改善、使用脉搏血氧饱和度仪测定的经皮氧饱和度(SaO2)、新侧支血管形成的血管造影证据、使用铊灌注闪烁扫描法测定的患侧肢体组织灌注。在全身麻醉下,我们从后髂嵴采集骨髓(519±45.5 mL)。使用连续流动细胞分离器去除红细胞(RBC)并减少体积后,我们实现了91%的RBC去除,并将BMMC浓缩至最终体积和浓度分别为51.5±10.1 mL和7.04±1.9×10⁷/mL的总有核细胞。我们在骨髓抽吸后三小时内,通过肌肉注射将BMMC(平均12.16±4.3×10⁸)注入缺血腿部的腓肠肌。以类似方式向另一肢体注射等渗盐水作为对照。13例患者单侧肌肉注射BMMC均未出现任何并发症。三名患者实现了主要疗效终点,即最重要病变的完全愈合。所有患者均随访至少四周。次要指标方面,三名患者12周时PWT的变化(ΔPWT)、无需使用镇痛药即可完全缓解静息痛情况有所改善。前两名患者的这些改善持续了24周。BMMC植入前和植入后3个月的数字减影血管造影研究显示,三名患者的患侧动脉出现了新的血管侧支网络。本研究的初步结果很有前景。因此,对于其他治疗方式难治的终末期肢体缺血的血栓闭塞性脉管炎患者,骨髓可能是细胞的潜在来源。