Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.761131
Title: The use of autologous adult stem cells in the treatment of multiple sclerosis : evidence for pathophysiological roles of sub-populations and clinical monitoring of cells and treatment effects
Author: Witherick, Jonathan
ISNI:       0000 0004 7432 792X
Awarding Body: University of Bristol
Current Institution: University of Bristol
Date of Award: 2018
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Abstract:
Despite significant advances in the efficacy of immunotherapies that target increasingly specific inflammatory elements critical to the development of the disease, there remains a significant therapeutic shortfall for sufferers of Multiple Sclerosis (MS). The pathophysiological disconnect between inflammation and the neurodegeneration that ultimately underlines disability is well described and continues to limit the success of increasingly potent immunosuppression. Neuroprotection, immunomodulation and cell replacement, all demonstrable properties of adult multipotent mesenchymal stem cells (MSCs) offer further therapeutic potential that may help to address both the inflammatory disease component and the neuronal loss that underscores disability. Much work has been done over the last decade and more to elucidate these properties with the accumulation of a critical body of evidence enabling translation to clinical trials including in Bristol. Animal models of inflammatory neurological pathology have yielded many clues to the mode of activity of MSCs. Detailed knowledge of their pathophysiological role in man however is lacking. This thesis was principally directed towards supporting and refining the imminent translational study. The aim of this work was twofold; to identify stem cell populations with proven advantageous properties in the bloodstream and in the brains of individuals with MS and interrogation of Neurophysiological outcome measures as a surrogate for disability measures. Stem cells of the bone marrow niche were identified in patients undergoing clinical relapse, as well as in those taking commonly prescribed disease modifying therapies. Whilst MSCs were readily identified in bone marrow samples, they were not detectable in peripheral blood at current technological thresholds. Cells expressing markers commonly expressed by MSCs were also identified in postmortem brain tissue from individuals with active MS, suggesting possible central nervous system infiltration. Finally evoked potential-based composite scores were demonstrated to correlate with clinical disability scoring methods both in crosssectional and to a lesser extent longitudinal analysis.
Supervisor: Scolding, Neil ; Wilkins, Alastair Sponsor: Not available
Qualification Name: Thesis (M.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.761131  DOI: Not available
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