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Update on cell therapy for stroke

Ischaemic stroke remains a leading cause of death and disability. Current stroke treatment options aim to minimise the damage from a pending stroke during the acute stroke period using intravenous thrombolytics and endovascular thrombectomy; however, there are no currently approved treatment options...

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Autores principales: Kenmuir, Cynthia L, Wechsler, Lawrence R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600013/
https://www.ncbi.nlm.nih.gov/pubmed/28959493
http://dx.doi.org/10.1136/svn-2017-000070
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author Kenmuir, Cynthia L
Wechsler, Lawrence R
author_facet Kenmuir, Cynthia L
Wechsler, Lawrence R
author_sort Kenmuir, Cynthia L
collection PubMed
description Ischaemic stroke remains a leading cause of death and disability. Current stroke treatment options aim to minimise the damage from a pending stroke during the acute stroke period using intravenous thrombolytics and endovascular thrombectomy; however, there are no currently approved treatment options for reversing neurological damage once a stroke is completed. Preclinical studies suggest that cell therapy may be safe and effective in improving functional outcomes. Several recent clinical trials have reported safety and some improvement in outcomes following cell therapy administration in ischaemic stroke, which are reviewed. Cell therapy may provide a promising new treatment for stroke reducing stroke-related disability. Further investigation is needed to determine specific effects of cell therapy and to optimise cell delivery methods, cell dosing, type of cells used, timing of delivery, infarct size and location of infarct that are likely to benefit from cell therapy.
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spelling pubmed-56000132017-09-28 Update on cell therapy for stroke Kenmuir, Cynthia L Wechsler, Lawrence R Stroke Vasc Neurol Review Ischaemic stroke remains a leading cause of death and disability. Current stroke treatment options aim to minimise the damage from a pending stroke during the acute stroke period using intravenous thrombolytics and endovascular thrombectomy; however, there are no currently approved treatment options for reversing neurological damage once a stroke is completed. Preclinical studies suggest that cell therapy may be safe and effective in improving functional outcomes. Several recent clinical trials have reported safety and some improvement in outcomes following cell therapy administration in ischaemic stroke, which are reviewed. Cell therapy may provide a promising new treatment for stroke reducing stroke-related disability. Further investigation is needed to determine specific effects of cell therapy and to optimise cell delivery methods, cell dosing, type of cells used, timing of delivery, infarct size and location of infarct that are likely to benefit from cell therapy. BMJ Publishing Group 2017-05-22 /pmc/articles/PMC5600013/ /pubmed/28959493 http://dx.doi.org/10.1136/svn-2017-000070 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Review
Kenmuir, Cynthia L
Wechsler, Lawrence R
Update on cell therapy for stroke
title Update on cell therapy for stroke
title_full Update on cell therapy for stroke
title_fullStr Update on cell therapy for stroke
title_full_unstemmed Update on cell therapy for stroke
title_short Update on cell therapy for stroke
title_sort update on cell therapy for stroke
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600013/
https://www.ncbi.nlm.nih.gov/pubmed/28959493
http://dx.doi.org/10.1136/svn-2017-000070
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