Detiger Suzanne E L, Helder Marco N, Smit Theodoor H, Hoogendoorn Roel J W
Department of Orthopaedic Surgery, VU University Medical Center, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands,
Eur Spine J. 2015 Sep;24(9):1992-2000. doi: 10.1007/s00586-015-3803-7. Epub 2015 Feb 15.
Stromal vascular fraction (SVF), an adipose tissue-derived heterogeneous cell mixture containing, among others, multipotent adipose stromal cells (ASCs) and erythrocytes, has proved beneficial for a wide range of applications in regenerative medicine. We sought to establish intervertebral disc (IVD) regeneration by injecting SVF intradiscally during a one-step surgical procedure in an enzymatically (Chondroitinase ABC; cABC) induced goat model of disc degeneration. Unexpectedly, we observed a severe inflammatory response that has not been described before, including massive lymphocyte infiltration, neovascularisation and endplate destruction. A second study investigated two main suspects for these adverse effects: cABC and erythrocytes within SVF. The same destructive response was observed in healthy goat discs injected with SVF, thereby eliminating cABC as a cause. Density gradient removal of erythrocytes and ASCs purified by culturing did not lead to adverse effects. Following these observations, we incorporated an extra washing step in the SVF harvesting protocol. In a third study, we applied this protocol in a one-step procedure to a goat herniation model, in which no adverse responses were observed either. However, upon intradiscal injection of an identically processed SVF mixture into our goat IVD degeneration model during a fourth study, the adverse effects surprisingly occurred again. Despite our quest for the responsible agent, we eventually could not identify the mechanism through which the observed destructive responses occurred. Although we cannot exclude that the adverse effects are species-dependent or model-specific, we advertise caution with the clinical application of autologous SVF injections into the IVD until the responsible agent(s) are identified.
基质血管成分(SVF)是一种源自脂肪组织的异质细胞混合物,其中包括多能脂肪基质细胞(ASC)和红细胞等,已被证明在再生医学的广泛应用中具有益处。我们试图通过在酶促(软骨素酶ABC;cABC)诱导的山羊椎间盘退变模型的一步手术过程中向椎间盘内注射SVF来建立椎间盘(IVD)再生。出乎意料的是,我们观察到了一种以前未描述过的严重炎症反应,包括大量淋巴细胞浸润、新生血管形成和终板破坏。第二项研究调查了这些不良反应的两个主要可疑因素:cABC和SVF中的红细胞。在注射了SVF的健康山羊椎间盘中观察到了相同的破坏反应,从而排除了cABC作为病因。通过密度梯度去除红细胞以及通过培养纯化的ASC并未导致不良反应。基于这些观察结果,我们在SVF采集方案中增加了一个额外的洗涤步骤。在第三项研究中,我们在一步手术中对山羊椎间盘突出模型应用了该方案,在该模型中也未观察到不良反应。然而,在第四项研究中,当将经过相同处理的SVF混合物注射到我们的山羊IVD退变模型的椎间盘内时,不良反应令人惊讶地再次出现。尽管我们一直在寻找责任因素,但最终我们无法确定所观察到的破坏反应发生的机制。虽然我们不能排除不良反应是物种依赖性或模型特异性的,但在确定责任因素之前,我们建议在将自体SVF注射到IVD的临床应用中要谨慎。