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Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke

This study was conducted to evaluate the safety and efficacy of human peripheral blood CD34 positive (CD34(+)) cells transplanted into a murine chronic stroke model to obtain pre-clinical proof of concept, prior to clinical testing. Granulocyte colony stimulating factor (G-CSF) mobilized human CD34(...

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Autores principales: Ogawa, Yuko, Okinaka, Yuka, Kikuchi-Taura, Akie, Saino, Orie, Tani-Yokoyama, Ayumi, Masuda, Satoru, Komatsu-Horii, Miki, Ikemoto, Yoshihiko, Kawamoto, Atsuhiko, Fukushima, Masanori, Taguchi, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963182/
https://www.ncbi.nlm.nih.gov/pubmed/35360717
http://dx.doi.org/10.3389/fmed.2022.681316
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author Ogawa, Yuko
Okinaka, Yuka
Kikuchi-Taura, Akie
Saino, Orie
Tani-Yokoyama, Ayumi
Masuda, Satoru
Komatsu-Horii, Miki
Ikemoto, Yoshihiko
Kawamoto, Atsuhiko
Fukushima, Masanori
Taguchi, Akihiko
author_facet Ogawa, Yuko
Okinaka, Yuka
Kikuchi-Taura, Akie
Saino, Orie
Tani-Yokoyama, Ayumi
Masuda, Satoru
Komatsu-Horii, Miki
Ikemoto, Yoshihiko
Kawamoto, Atsuhiko
Fukushima, Masanori
Taguchi, Akihiko
author_sort Ogawa, Yuko
collection PubMed
description This study was conducted to evaluate the safety and efficacy of human peripheral blood CD34 positive (CD34(+)) cells transplanted into a murine chronic stroke model to obtain pre-clinical proof of concept, prior to clinical testing. Granulocyte colony stimulating factor (G-CSF) mobilized human CD34(+) cells [1 × 10(4) cells in 50 μl phosphate-buffered saline (PBS)] were intravenously (iv) or intra-carotid arterially (ia) transplanted 4 weeks after the induction of stroke (chronic stage), and neurological function was evaluated. In this study, severe combined immune deficiency (SCID) mice were used to prevent excessive immune response after cell therapy. Two weeks post cell therapy, the ia CD34(+) cells group demonstrated a significant improvement in neurological functions compared to the PBS control. The therapeutic effect was maintained 8 weeks after the treatment. Even after a single administration, ia transplantation of CD34(+) cells had a significant therapeutic effect on chronic stroke. Based on the result of this pre-clinical proof of concept study, a future clinical trial of autologous peripheral blood CD34(+) cells administration in the intra-carotid artery for chronic stroke patients is planned.
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spelling pubmed-89631822022-03-30 Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke Ogawa, Yuko Okinaka, Yuka Kikuchi-Taura, Akie Saino, Orie Tani-Yokoyama, Ayumi Masuda, Satoru Komatsu-Horii, Miki Ikemoto, Yoshihiko Kawamoto, Atsuhiko Fukushima, Masanori Taguchi, Akihiko Front Med (Lausanne) Medicine This study was conducted to evaluate the safety and efficacy of human peripheral blood CD34 positive (CD34(+)) cells transplanted into a murine chronic stroke model to obtain pre-clinical proof of concept, prior to clinical testing. Granulocyte colony stimulating factor (G-CSF) mobilized human CD34(+) cells [1 × 10(4) cells in 50 μl phosphate-buffered saline (PBS)] were intravenously (iv) or intra-carotid arterially (ia) transplanted 4 weeks after the induction of stroke (chronic stage), and neurological function was evaluated. In this study, severe combined immune deficiency (SCID) mice were used to prevent excessive immune response after cell therapy. Two weeks post cell therapy, the ia CD34(+) cells group demonstrated a significant improvement in neurological functions compared to the PBS control. The therapeutic effect was maintained 8 weeks after the treatment. Even after a single administration, ia transplantation of CD34(+) cells had a significant therapeutic effect on chronic stroke. Based on the result of this pre-clinical proof of concept study, a future clinical trial of autologous peripheral blood CD34(+) cells administration in the intra-carotid artery for chronic stroke patients is planned. Frontiers Media S.A. 2022-03-11 /pmc/articles/PMC8963182/ /pubmed/35360717 http://dx.doi.org/10.3389/fmed.2022.681316 Text en Copyright © 2022 Ogawa, Okinaka, Kikuchi-Taura, Saino, Tani-Yokoyama, Masuda, Komatsu-Horii, Ikemoto, Kawamoto, Fukushima and Taguchi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Ogawa, Yuko
Okinaka, Yuka
Kikuchi-Taura, Akie
Saino, Orie
Tani-Yokoyama, Ayumi
Masuda, Satoru
Komatsu-Horii, Miki
Ikemoto, Yoshihiko
Kawamoto, Atsuhiko
Fukushima, Masanori
Taguchi, Akihiko
Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke
title Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke
title_full Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke
title_fullStr Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke
title_full_unstemmed Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke
title_short Pre-Clinical Proof of Concept: Intra-Carotid Injection of Autologous CD34-Positive Cells for Chronic Ischemic Stroke
title_sort pre-clinical proof of concept: intra-carotid injection of autologous cd34-positive cells for chronic ischemic stroke
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963182/
https://www.ncbi.nlm.nih.gov/pubmed/35360717
http://dx.doi.org/10.3389/fmed.2022.681316
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