The dark side of the force - constraints and complications of cell therapies for stroke

被引:122
作者
Boltze, Johannes [1 ,2 ]
Arnold, Antje [3 ,4 ]
Walczak, Piotr [3 ,4 ]
Jolkkonen, Jukka [5 ]
Cui, Lili [5 ]
Wagner, Daniel-Christoph [1 ]
机构
[1] Fraunhofer Inst Cell Therapy & Immunol, Dept Cell Therapy, D-04103 Leipzig, Germany
[2] Univ Leipzig, Translat Ctr Regenerat Med, D-04109 Leipzig, Germany
[3] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div MR Res, Baltimore, MD USA
[4] Johns Hopkins Univ, Inst Cell Engn, Baltimore, MD USA
[5] Univ Eastern Finland, Inst Clin Med, Dept Neurol, Kuopio, Finland
关键词
ischemic stroke; cell therapy; cell transplantation; translational research; clinical trial; side effect; complication; safety; MESENCHYMAL STEM-CELLS; MARROW MONONUCLEAR-CELLS; COLONY-STIMULATING FACTOR; NEURAL PRECURSOR CELLS; CORD BLOOD-CELLS; CEREBRAL-ARTERY OCCLUSION; VERSUS-HOST-DISEASE; TOLL-LIKE RECEPTORS; BONE-MARROW; STROMAL CELLS;
D O I
10.3389/fneur.2015.00155
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cell therapies are increasingly recognized as a promising option to augment the limited therapeutic arsenal available to fight ischemic stroke. During the last two decades, cumulating preclinical evidence has indicated a substantial efficacy for most cell treatment paradigms and first clinical trials are currently underway to assess safety and feasibility in patients. However, the strong and still unmet demand for novel stroke treatment options and exciting findings reported from experimental studies may have drawn our attention away from potential side effects related to cell therapies and the ways by which they are commonly applied. This review summarizes common and less frequent adverse events that have been discovered in preclinical and clinical investigations assessing cell therapies for stroke. Such adverse events range from immunological and neoplastic complications over seizures to cell clotting and cell-induced embolism. It also describes potential complications of clinically applicable administration procedures, detrimental interactions between therapeutic cells, and the pathophysiological environment that they are placed into, as well as problems related to cell manufacturing. Virtually each therapeutic intervention comes at a certain risk for complications. Side effects do therefore not generally compromise the value of cell treatments for stroke, but underestimating such complications might severely limit therapeutic safety and efficacy of cell treatment protocols currently under development. On the other hand, a better understanding will provide opportunities to further improve existing therapeutic strategies and might help to define those circumstances, under which an optimal effect can be realized. Hence, the review eventually discusses strategies and recommendations allowing us to prevent or at least balance potential complications in order to ensure the maximum therapeutic benefit at minimum risk for stroke patients.
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页数:21
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共 195 条
[1]   Human pancreatic islet-derived progenitor cell engraftment in immunocompetent mice [J].
Abraham, EJ ;
Kodama, S ;
Lin, JC ;
Ubeda, M ;
Faustman, DL ;
Hebener, JF .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (03) :817-830
[2]   Allorecognition Pathways in Transplant Rejection and Tolerance [J].
Ali, Jason M. ;
Bolton, Eleanor M. ;
Bradley, J. Andrew ;
Pettigrew, Gavin J. .
TRANSPLANTATION, 2013, 96 (08) :681-688
[3]   Donor-Derived Brain Tumor Following Neural Stem Cell Transplantation in an Ataxia Telangiectasia Patient [J].
Amariglio, Ninette ;
Hirshberg, Abraham ;
Scheithauer, Bernd W. ;
Cohen, Yoram ;
Loewenthal, Ron ;
Trakhtenbrot, Luba ;
Paz, Nurit ;
Koren-Michowitz, Maya ;
Waldman, Dalia ;
Leider-Trejo, Leonor ;
Toren, Amos ;
Constantini, Shlomi ;
Rechavi, Gideon .
PLOS MEDICINE, 2009, 6 (02) :221-231
[4]   Human neural stem cells enhance structural plasticity and axonal transport in the ischaemic brain [J].
Andres, Robert H. ;
Horie, Nobutaka ;
Slikker, William ;
Keren-Gill, Hadar ;
Zhan, Ke ;
Sun, Guohua ;
Manley, Nathan C. ;
Pereira, Marta P. ;
Sheikh, Lamiya A. ;
McMillan, Erin L. ;
Schaar, Bruce T. ;
Svendsen, Clive N. ;
Bliss, Tonya M. ;
Steinberg, Gary K. .
BRAIN, 2011, 134 :1777-1789
[5]   Macrophage-Associated Mesenchymal Stem Cells Assume an Activated, Migratory, Pro-Inflammatory Phenotype with Increased IL-6 and CXCL10 Secretion [J].
Anton, Kevin ;
Banerjee, Debabrata ;
Glod, John .
PLOS ONE, 2012, 7 (04)
[6]   Negligible immunogenicity of terminally differentiated cells derived from induced pluripotent or embryonic stem cells [J].
Araki, Ryoko ;
Uda, Masahiro ;
Hoki, Yuko ;
Sunayama, Misato ;
Nakamura, Miki ;
Ando, Shunsuke ;
Sugiura, Mayumi ;
Ideno, Hisashi ;
Shimada, Akemi ;
Nifuji, Akira ;
Abe, Masumi .
NATURE, 2013, 494 (7435) :100-104
[7]   Predictive factors of early seizures after acute cerebrovascular disease [J].
Arboix, A ;
GarciaEroles, L ;
Massons, JB ;
Oliveres, M ;
Comes, E .
STROKE, 1997, 28 (08) :1590-1594
[8]   Adult human dental pulp stem cells differentiate toward functionally active neurons under appropriate environmental cues [J].
Arthur, Agnes ;
Rychkov, Grigori ;
Shi, Songtao ;
Koblar, Simon Andrea ;
Gronthos, Stan .
STEM CELLS, 2008, 26 (07) :1787-1795
[9]   High White Blood Cell Concentration in the Peripheral Blood Stem Cell Product Can Induce Seizures during Infusion of Autologous Peripheral Blood Stem Cells [J].
Bachier, Carlos ;
Potter, Josh ;
Potter, Grant ;
Sugay, Rominna ;
Shaughnessy, Paul ;
Chan, Kawah ;
Jude, Veronica ;
Madden, Renee ;
LeMaistre, Charles F. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2012, 18 (07) :1055-1060
[10]   Delayed post-ischaemic neuroprotection following systemic neural stem cell transplantation involves multiple mechanisms [J].
Bacigaluppi, Marco ;
Pluchino, Stefano ;
Jametti, Luca Peruzzotti ;
Kilic, Ertugrul ;
Kilic, Uelkan ;
Salani, Giuliana ;
Brambilla, Elena ;
West, Mark J. ;
Comi, Giancarlo ;
Martino, Gianvito ;
Hermann, Dirk M. .
BRAIN, 2009, 132 :2239-2251