Lumbar Intraspinal Injection of Neural Stem Cells in Patients with Amyotrophic Lateral Sclerosis: Results of a Phase I Trial in 12 Patients

被引:204
作者
Glass, Jonathan D. [1 ]
Boulis, Nicholas M. [2 ]
Johe, Karl [3 ]
Rutkove, Seward B. [4 ]
Federici, Thais [2 ]
Polak, Meraida [1 ]
Kelly, Crystal [1 ]
Feldman, Eva L. [5 ]
机构
[1] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Neurosurg, Atlanta, GA 30322 USA
[3] Neuralstem Inc, Rockville, MD USA
[4] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Neurol, Boston, MA 02215 USA
[5] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
关键词
Amyotrophic lateral sclerosis; Motor neuron disease; Stem cells; Spinal cord; Clinical trial; SPINAL-CORD; TRANSGENIC RATS; DIFFERENTIATION; GRAFTS; FETAL;
D O I
10.1002/stem.1079
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Advances in stem cell biology have generated intense interest in the prospect of transplanting stem cells into the nervous system for the treatment of neurodegenerative diseases. Here, we report the results of an ongoing phase I trial of intraspinal injections of fetal-derived neural stems cells in patients with amyotrophic lateral sclerosis (ALS). This is a first-in-human clinical trial with the goal of assessing the safety and tolerability of the surgical procedure, the introduction of stem cells into the spinal cord, and the use of immunosuppressant drugs in this patient population. Twelve patients received either five unilateral or five bilateral (10 total) injections into the lumbar spinal cord at a dose of 100,000 cells per injection. All patients tolerated the treatment without any long-term complications related to either the surgical procedure or the implantation of stem cells. Clinical assessments ranging from 6 to 18 months after transplantation demonstrated no evidence of acceleration of disease progression due to the intervention. One patient has shown improvement in his clinical status, although these data must be interpreted with caution since this trial was neither designed nor powered to measure treatment efficacy. These results allow us to report success in achieving the phase I goal of demonstrating safety of this therapeutic approach. Based on these positive results, we can now advance this trial by testing intraspinal injections into the cervical spinal cord, with the goal of protecting motor neuron pools affecting respiratory function, which may prolong life for patients with ALS. STEM CELLS2012;30:11441151
引用
收藏
页码:1144 / 1151
页数:8
相关论文
共 21 条
  • [1] USE OF COMPOSITE SCORES (MEGASCORES) TO MEASURE DEFICIT IN AMYOTROPHIC LATERAL SCLEROSIS
    ANDRES, PL
    FINISON, LJ
    CONLON, T
    THIBODEAU, LM
    MUNSAT, TL
    [J]. NEUROLOGY, 1988, 38 (03) : 405 - 408
  • [2] El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis
    Brooks, BR
    Miller, RG
    Swash, M
    Munsat, TL
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05): : 293 - 299
  • [3] Functional recovery in rats with ischemic paraplegia after spinal grafting of human spinal stem cells
    Cizkova, D.
    Kakinohana, O.
    Kucharova, K.
    Marsala, S.
    Johe, K.
    Hazel, T.
    Hefferan, M. P.
    Marsala, M.
    [J]. NEUROSCIENCE, 2007, 147 (02) : 546 - 560
  • [4] Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model
    Di Giorgio, Francesco Paolo
    Carrasco, Monica A.
    Siao, Michelle C.
    Maniatis, Tom
    Eggan, Kevin
    [J]. NATURE NEUROSCIENCE, 2007, 10 (05) : 608 - 614
  • [5] Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study
    Gil, J.
    Funalot, B.
    Verschueren, A.
    Danel-Brunaud, V.
    Camu, W.
    Vandenberghe, N.
    Desnuelle, C.
    Guy, N.
    Camdessanche, J. P.
    Cintas, P.
    Carluer, L.
    Pittion, S.
    Nicolas, G.
    Corcia, P.
    Fleury, M. -C.
    Maugras, C.
    Besson, G.
    Le Masson, G.
    Couratier, P.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 (11) : 1245 - 1251
  • [6] Characterization of a human fetal spinal cord stem cell line, NSI-566RSC, and its induction to functional motoneurons
    Guo, Xiufang
    Johe, Karl
    Molnar, Peter
    Davis, Hedvika
    Hickman, James
    [J]. JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2010, 4 (03) : 181 - 193
  • [7] Single factors direct the differentiation of stem cells from the fetal and adult central nervous system
    Johe, KK
    Hazel, TG
    Muller, T
    DugichDjordjevic, MM
    McKay, RDG
    [J]. GENES & DEVELOPMENT, 1996, 10 (24) : 3129 - 3140
  • [8] ALSFRS-R score and its ratio: A useful predictor for ALS-progression
    Kollewe, Katja
    Mauss, Ulrike
    Krampfl, Klaus
    Petri, Susanne
    Dengler, Reinhard
    Mohammadi, Bahram
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2008, 275 (1-2) : 69 - 73
  • [9] Amyotrophic lateral sclerosis: a consensus viewpoint on designing and implementing a clinical trial
    Leigh, PN
    Swash, M
    Iwasaki, Y
    Ludolph, A
    Meininger, V
    Miller, RG
    Mitsumoto, H
    Shaw, P
    Tashiro, K
    Van Den Berg, L
    [J]. AMYOTROPHIC LATERAL SCLEROSIS, 2004, 5 (02): : 84 - 98
  • [10] Stem cell technology for the study and treatment of motor neuron diseases
    Lunn, J. Simon
    Sakowski, Stacey A.
    Federici, Thais
    Glass, Jonathan D.
    Boulis, Nicholas M.
    Feldman, Eva L.
    [J]. REGENERATIVE MEDICINE, 2011, 6 (02) : 201 - 213