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      Mobilisation of Hematopoietic CD34 + Precursor Cells in Patients with Acute Stroke Is Safe - Results of an Open-Labeled Non Randomized Phase I/II Trial

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          Abstract

          Background

          Regenerative strategies in the treatment of acute stroke may have great potential. Hematopoietic growth factors mobilize hematopoietic stem cells and may convey neuroprotective effects. We examined the safety, potential functional and structural changes, and CD34 + cell–mobilization characteristics of G-CSF treatment in patients with acute ischemic stroke.

          Methods and Results

          Three cohorts of patients (8, 6, and 6 patients per cohort) were treated subcutaneously with 2.5, 5, or 10 µg/kg body weight rhG-CSF for 5 consecutive days within 12 hrs of onset of acute stroke. Standard treatment included IV thrombolysis. Safety monitoring consisted of obtaining standardized clinical assessment scores, monitoring of CD34 + stem cells, blood chemistry, serial neuroradiology, and neuropsychology. Voxel-guided morphometry (VGM) enabled an assessment of changes in the patients' structural parenchyma. 20 patients (mean age 55 yrs) were enrolled in this study, 5 of whom received routine thrombolytic therapy with r-tPA. G-CSF treatment was discontinued in 4 patients because of unrelated adverse events. Mobilization of CD34 + cells was observed with no concomitant changes in blood chemistry, except for an increase in the leukocyte count up to 75,500/µl. Neuroradiological and neuropsychological follow-up studies did not disclose any specific G-CSF toxicity. VGM findings indicated substantial atrophy of related hemispheres, a substantial increase in the CSF space, and a localized increase in parenchyma within the ischemic area in 2 patients.

          Conclusions

          We demonstrate a good safety profile for daily administration of G-CSF when begun within 12 hours after onset of ischemic stroke and, in part in combination with routine IV thrombolysis. Additional analyses using VGM and a battery of neuropsychological tests indicated a positive functional and potentially structural effect of G-CSF treatment in some of our patients.

          Trial Registration

          German Clinical Trial Register DRKS 00000723

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          Most cited references47

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          Turning blood into brain: cells bearing neuronal antigens generated in vivo from bone marrow.

          Bone marrow stem cells give rise to a variety of hematopoietic lineages and repopulate the blood throughout adult life. We show that, in a strain of mice incapable of developing cells of the myeloid and lymphoid lineages, transplanted adult bone marrow cells migrated into the brain and differentiated into cells that expressed neuron-specific antigens. These findings raise the possibility that bone marrow-derived cells may provide an alternative source of neurons in patients with neurodegenerative diseases or central nervous system injury.
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            From marrow to brain: expression of neuronal phenotypes in adult mice.

            After intravascular delivery of genetically marked adult mouse bone marrow into lethally irradiated normal adult hosts, donor-derived cells expressing neuronal proteins (neuronal phenotypes) developed in the central nervous system. Flow cytometry revealed a population of donor-derived cells in the brain with characteristics distinct from bone marrow. Confocal microscopy of individual cells showed that hundreds of marrow-derived cells in brain sections expressed gene products typical of neurons (NeuN, 200-kilodalton neurofilament, and class III beta-tubulin) and were able to activate the transcription factor cAMP response element-binding protein (CREB). The generation of neuronal phenotypes in the adult brain 1 to 6 months after an adult bone marrow transplant demonstrates a remarkable plasticity of adult tissues with potential clinical applications.
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              The hematopoietic factor G-CSF is a neuronal ligand that counteracts programmed cell death and drives neurogenesis.

              G-CSF is a potent hematopoietic factor that enhances survival and drives differentiation of myeloid lineage cells, resulting in the generation of neutrophilic granulocytes. Here, we show that G-CSF passes the intact blood-brain barrier and reduces infarct volume in 2 different rat models of acute stroke. G-CSF displays strong anti-apoptotic activity in mature neurons and activates multiple cell survival pathways. Both G-CSF and its receptor are widely expressed by neurons in the CNS, and their expression is induced by ischemia, which suggests an autocrine protective signaling mechanism. Surprisingly, the G-CSF receptor was also expressed by adult neural stem cells, and G-CSF induced neuronal differentiation in vitro. G-CSF markedly improved long-term behavioral outcome after cortical ischemia, while stimulating neural progenitor response in vivo, providing a link to functional recovery. Thus, G-CSF is an endogenous ligand in the CNS that has a dual activity beneficial both in counteracting acute neuronal degeneration and contributing to long-term plasticity after cerebral ischemia. We therefore propose G-CSF as a potential new drug for stroke and neurodegenerative diseases.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                26 August 2011
                : 6
                : 8
                : e23099
                Affiliations
                [1 ]Department of Neurology, University of Regensburg, Bezirksklinikum Regensburg, Regensburg, Germany
                [2 ]Neurological Therapy Center and St. Marien Hospital, Köln, Germany
                [3 ]Department of Neurology, University Medical Centre, Düsseldorf, Germany
                [4 ]Institute of Neuroradiology, Regensburg University Medical Centre, District Medical Centre Regensburg, Regensburg, Germany
                [5 ]Department of Hemato-Oncology, Regensburg University Medical Centre, Regensburg, Germany
                [6 ]Department of Clinical Chemistry, Regensburg University Medical Centre, Regensburg, Germany
                [7 ]St. Mauritius Therapy Clinic, Meerbusch, Germany
                Julius-Maximilians-Universität Würzburg, Germany
                Author notes

                Conceived and designed the experiments: SB SS MK GS JW UB. Performed the experiments: SB SS MK FS GS RL BH EO. Analyzed the data: SB SS MK FS GS UB TS AD. Contributed reagents/materials/analysis tools: MK BH EO TS AD. Wrote the paper: SB SS FS RL UB.

                Article
                PONE-D-11-04568
                10.1371/journal.pone.0023099
                3162562
                21887230
                8d59d758-8b99-4004-9192-c4c24c524846
                Boy et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 8 March 2011
                : 7 July 2011
                Page count
                Pages: 10
                Categories
                Research Article
                Medicine
                Cardiovascular
                Stroke
                Clinical Research Design
                Clinical Trials
                Critical Care and Emergency Medicine
                Drugs and Devices
                Clinical Pharmacology
                Drug Interactions
                Neuropharmacology
                Neurology
                Cerebrovascular Diseases
                Ischemic Stroke
                Cognitive Neurology
                Neuroimaging
                Neuropharmacology
                Physiotherapy and Rehabilitation
                Radiology
                Diagnostic Radiology
                Magnetic Resonance Imaging

                Uncategorized
                Uncategorized

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