Emerging hurdles in stem cell therapy for peripheral vascular disease

被引:59
作者
Aranguren, Xabier L. [1 ]
Verfaillie, Catherine M. [2 ]
Luttun, Aernout [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Mol & Vasc Biol, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Stamcel Inst, B-3000 Louvain, Belgium
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2009年 / 87卷 / 01期
基金
欧洲研究理事会;
关键词
Vascular disease; Stem cells; Clinical research; Regeneration; Ischemia; Endothelium; ENDOTHELIAL PROGENITOR CELLS; MARROW-MONONUCLEAR-CELLS; UMBILICAL-CORD BLOOD; SEVERE ARTERIOSCLEROSIS OBLITERANS; ARTERIAL OCCLUSIVE DISEASE; COLONY-STIMULATING FACTOR; FIBROBLAST-GROWTH-FACTOR; CRITICAL LIMB ISCHEMIA; BONE-MARROW; AUTOLOGOUS TRANSPLANTATION;
D O I
10.1007/s00109-008-0394-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Peripheral vascular disease (PVD) is a growing medical problem in Western societies and presents itself mainly in two different clinical forms. Intermittent claudication is an early moderate manifestation, while patients with critical limb ischemia suffer from severe muscle tissue loss or ulcers and are at high risk for limb amputation. Unfortunately, many patients cannot be helped with currently available surgical or endovascular revascularization procedures because of the complex anatomy of the vascular occlusion and/or the presence of other risk factors. Noninvasive stem cell therapy has been proposed as an alternative for such patients. Although pioneering clinical experience with stem cell-related therapy seems promising, it is too early for general clinical use of this technique, since many questions remain unanswered. Indeed, while questions about safety, dose, and administration route/timing/frequency are the first ones to be addressed when designing a stem cell-based clinical approach, there is accumulating evidence from recent (pre-)clinical studies that other issues may also be at stake. For instance, the choice of stem cells to be used and its precise mechanism of action, the need/possibility for concurrent tissue regeneration in case of irreversible tissue loss, the differentiation degree and specific vascular identity of the transplanted cells, and the long-term survival of engrafted cells in the absence of a normal supportive tissue environment should be well considered. Here, rather than presenting a comprehensive and extensive overview on the current literature on stem/progenitor cells and revascularization, we highlight some of the outstanding issues emerging from the recent (pre-)clinical literature that may codetermine the successful application of stem cells in a wide range of PVD patients in the future.
引用
收藏
页码:3 / 16
页数:14
相关论文
共 108 条
[1]   Repeated thermal therapy up-regulates endothelial nitric oxide synthase and augments angiogenesis in a mouse model of hindlimb ischemia [J].
Akasaki, Y ;
Miyata, M ;
Eto, H ;
Shirasawa, T ;
Hamada, N ;
Ikeda, Y ;
Biro, S ;
Otsuji, Y ;
Tei, C .
CIRCULATION JOURNAL, 2006, 70 (04) :463-470
[2]  
Aranguren XL, 2008, J CLIN INVEST, V118, P505, DOI [10.1172/JC131153, 10.1172/JCI31153]
[3]   In vitro and in vivo arterial differentiation of human multipotent adult progenitor cells [J].
Aranguren, Xabier L. ;
Luttun, Aernout ;
Clavel, Carlos ;
Moreno, Cristina ;
Abizanda, Gloria ;
Barajas, Miguel A. ;
Pelacho, Beatriz ;
Uriz, Maialen ;
Arana, Miriam ;
Echavarri, Ana ;
Soriano, Mario ;
Andreu, Enrique J. ;
Merino, Juana ;
Garcia-Verdugo, Jose Manuel ;
Verfaillie, Catherine M. ;
Prosper, Felipe .
BLOOD, 2007, 109 (06) :2634-2642
[4]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[5]   Hyperbaric oxygen induces basic fibroblast growth factor and hepatocyte growth factor expression, and enhances blood perfusion and muscle regeneration in mouse ischemic hind limbs [J].
Asano, Tetsuichi ;
Kaneko, Eiji ;
Shinozaki, Shohei ;
Imai, Yutaka ;
Shibayama, Masaharu ;
Chiba, Tsuyoshi ;
Ai, Masumi ;
Kawakami, Akio ;
Asaoka, Hiroshi ;
Nakayama, Toru ;
Mano, Yoshihiro ;
Shimokado, Kentaro .
CIRCULATION JOURNAL, 2007, 71 (03) :405-411
[6]   Differential healing activities of CD34+ and CD14+ endothelial cell progenitors [J].
Awad, O ;
Dedkov, EI ;
Jiao, CH ;
Bloomer, S ;
Tomanek, RJ ;
Schatteman, GC .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (04) :758-764
[7]   Myeloid lineage progenitors give rise to vascular endothelium [J].
Bailey, Alexis S. ;
Willenbring, Holger ;
Jiang, Shuguang ;
Anderson, Daniel A. ;
Schroeder, David A. ;
Wong, Melissa H. ;
Grompe, Markus ;
Fleming, William H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (35) :13156-13161
[8]   Transplantation of autologous mononuclear bone marrow stem cells in patients with peripheral arterial disease (The TAM-PAD study) [J].
Bartsch, T. ;
Brehm, M. ;
Zeus, T. ;
Koegler, G. ;
Wernet, P. ;
Strauer, B. E. .
CLINICAL RESEARCH IN CARDIOLOGY, 2007, 96 (12) :891-899
[9]  
Bartsch T, 2006, MED KLIN, V101, P195
[10]   Novel treatment of therapy-refractory limb ischemia by intra-arterial and intra-muscular transplantation of autologous adult bone marrow stem cells [J].
Bartsch, T ;
Falke, T ;
Brehm, M ;
Zeus, T ;
Kögler, G ;
Wernet, P ;
Strauer, BE .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2006, 131 (03) :79-83