Kwiatkowski Tomasz, Zbierska-Rubinkiewicz Katarzyna, Krzywoń Jerzy W, Szkółka Łukasz, Kuczmik Wacław, Majka Marcin, Maga Paweł, Drelicharz Łukasz, Musiałek Piotr, Trystuła Mariusz
Department of Vascular Surgery and Endovascular Interventions, John Paul II Hospital, Krakow, Poland.
Depratment of Vascular Surgery, University Hospital, Krakow, Poland.
Postepy Kardiol Interwencyjnej. 2022 Dec;18(4):340-349. doi: 10.5114/aic.2022.120962. Epub 2022 Nov 7.
Critical limb ischemia - an advanced stage of lower extremity arterial disease with presence of rest pain and/or ischemic ulcers - remains an important cause of major amputations and disability in developed societies. Novel treatment strategies are urgently needed to prevent (or delay) amputations in particular for patients in whom effective revascularization is no longer feasible for anatomic and/or technical reasons (no-option critical limb ischemia - N-O CLI). Cellular therapies have been gaining the growing attention of researchers and clinicians in the last two decades. Several cell types have been used in pre-clinical and clinical studies, and a number of mechanisms have been proposed to contribute to vascular reparation and regeneration in N-O CLI. Although early trials suggested clinical improvement with use of cell-based therapies in N-O CLI, meta-analyses that included randomized controlled trials have not provided definitive conclusions. Fundamental limitations have involved poorly defined cell lines/populations, limited numbers of study participants and limited follow-up periods, and enrolling patients "too sick to benefit" (such as those in Rutherford class 6). Recent advances include standardized "unlimited" sources of therapeutic cells and better understanding of mechanisms that may contribute to vascular reparation and regeneration. Furthermore, based on recent pre-clinical and clinical studies, cell-free preparations (such as microvesicle-based) are being increasingly developed along with advanced therapy medical products consisting of engineered cells and pro-angiogenic factors.
严重肢体缺血——下肢动脉疾病的晚期阶段,伴有静息痛和/或缺血性溃疡——仍然是发达社会中主要截肢和残疾的重要原因。迫切需要新的治疗策略来预防(或延迟)截肢,特别是对于那些由于解剖和/或技术原因无法进行有效血运重建的患者(无选择严重肢体缺血——N-O CLI)。在过去二十年中,细胞疗法越来越受到研究人员和临床医生的关注。几种细胞类型已用于临床前和临床研究,并提出了一些机制来促进N-O CLI中的血管修复和再生。尽管早期试验表明在N-O CLI中使用基于细胞的疗法可改善临床症状,但纳入随机对照试验的荟萃分析尚未得出明确结论。基本局限性包括细胞系/群体定义不明确、研究参与者数量有限和随访期有限,以及纳入“病情过重无法受益”的患者(如卢瑟福6级患者)。最近的进展包括标准化的“无限”治疗细胞来源,以及对可能有助于血管修复和再生的机制有了更好的理解。此外,基于最近的临床前和临床研究,无细胞制剂(如基于微泡的制剂)以及由工程细胞和促血管生成因子组成的先进治疗医疗产品正在越来越多地得到开发。