2009
DOI: 10.1177/1545968309335978
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The Neural Stem Cell Line CTX0E03 Promotes Behavioral Recovery and Endogenous Neurogenesis After Experimental Stroke in a Dose-Dependent Fashion

Abstract: . This study found that the implantation of CTX0E03 human neural stem cells in rats after MCAO stroke promoted significant behavioral recovery depending on cell dose. The authors propose a paracrine trophic mechanism, which is triggered early after CTX0E03 cell implantation, and which in turn targets restoration of neurogenesis in the SVZ of MCAO rats.

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Cited by 135 publications
(130 citation statements)
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“…The FDA recently granted approval to initiate a Phase I safety evaluation for MultiStem infusion at day 2 following ischemic stroke. That clinical study as well as the evaluation of bone marrow mononuclear cells (Savitz 2009) or gene modified neuronal stem cells (Stroemer et al 2009) will comprise an important translational dataset to resolve this important unmet clinical need.…”
Section: Discussionmentioning
confidence: 99%
“…The FDA recently granted approval to initiate a Phase I safety evaluation for MultiStem infusion at day 2 following ischemic stroke. That clinical study as well as the evaluation of bone marrow mononuclear cells (Savitz 2009) or gene modified neuronal stem cells (Stroemer et al 2009) will comprise an important translational dataset to resolve this important unmet clinical need.…”
Section: Discussionmentioning
confidence: 99%
“…Preclinical stroke model data reported dose dependent improvements in sensorimotor recovery over 12 weeks post-implantation when delivered 3-5 weeks after middle cerebral artery occlusive stroke in the rat. 46 In PISCES 1, eleven male patients underwent implantation a median of 22 months after stroke. No cell-related safety issues were observed, with serious adverse events being related either to the neurosurgical procedure or to long-term consequences of stroke comorbidities.…”
Section: Late Subacute or Chronic Strokementioning
confidence: 99%
“…Cell therapy for stroke has tested several types of transplantable cells in the laboratory, with a few reaching clinical trials, such as fetal cells, NT2N cells, CTX0E3, embryonic stem cells, neural stem/progenitor cells, umbilical cord blood, amnion, adipose, and induced pluripotent stem cells [67][68][69][70][71][72]. Compared to these other stem cells, MSCs have established a solid safety profile in other disease indications, providing the basis for on-going clinical trials to explore MSCs and their cell subpopulations [73,74].…”
Section: Mscs Their Mechanism Of Action and Safety Profilementioning
confidence: 99%