One, two, three steps toward cell therapy for stroke - PubMed (original) (raw)

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One, two, three steps toward cell therapy for stroke

Theo Diamandis et al. Stroke. 2015 Feb.

Abstract

Many clinical trials have failed despite positive laboratory findings. Stroke clinical trials are no exception, with tissue plasminogen activator (tPA) still the only effective drug for stroke with limited therapeutic window. In order to enhance the successful outcome of novel therapies in the clinic, initiatives for translational research guidelines have been pursued. In particular, the advancement of stem cell therapy for stroke from the laboratory to the clinic has now been guided by a set of recommendations called Stem cell Therapeutics as an Emerging Paradigm for Stroke or STEPS. We review here the major criteria for preclinical studies of stem cells arising from the three STEPS meetings in an effort to further emphasize the need for careful and rigorous assessment of the safety, efficacy, and mechanism of action associated with stem cell therapy for stroke. Learning from our previous mistakes and identifying gaps in knowledge will likely prevent stem cell therapy from becoming yet another statistic of failed clinical trial in stroke.

Keywords: standards; stem cells; stroke; therapy.

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Conflict of interest statement

Disclosures: The authors declare no competing interests.

Figures

Figure 1

Figure 1

Both intravenous and stereotaxic intracerebral routes of stem cell delivery are being tested in FDA-approved limited clinical trials for acute and chronic stroke patients, respectively. Preclinical data that led to these clinical trials were partially collected under STEPS guidelines. These preclinical studies used rat models of stroke, and some cases non-human primates to assess cell delivery routes and dosage.

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References

    1. Tajiri N, Dailey T, Metcalf C, Mosley YI, Lau T, Staples M, et al. In vivo animal stroke models: a rationale for rodent and non-human primate models. Transl Stroke Res. 2013;4:308–321. - PMC - PubMed
    1. Hess DC, Borlongan CV. Cell-based therapy in ischemic stroke. Expert Rev Neurother. 2008;8:1193–1201. - PMC - PubMed
    1. The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group. Tissue plasminogen activator for acute ischemic stroke. N Engl J Med. 1995;333:1581–1587. - PubMed
    1. Borlongan CV, Glover LE, Tajiri N, Kaneko Y, Freeman TB. The great migration of bone marrow-derived stem cells toward the ischemic brain: therapeutic implications for stroke and other neurological disorders. Prog Neurobiol. 2011;95:213–228. - PMC - PubMed
    1. Tan Tanny SP, Busija L, Liew D, Teo S, Davis SM, Yan B. Cost-effectiveness of thrombolysis within 4.5 hours of acute ischemic stroke: experience from Australian stroke center. Stroke. 2013;44:2269–2274. - PubMed

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