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Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits
Incurable neuroretinal degeneration diseases cause severe vision loss and blindness in millions of patients worldwide. In previous studies, we demonstrated that transplanting human bone marrow stromal cells (hBMSCs) in the extravascular spaces of the choroid (EVSC) of the Royal College of Surgeon ra...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494107/ https://www.ncbi.nlm.nih.gov/pubmed/28698719 http://dx.doi.org/10.1155/2017/4061975 |
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author | Tzameret, Adi Kalish, Sapir E. Sher, Ifat Twito, Lea Meir, Amilia Levy, Itay Margel, Shlomo Moroz, Iris Rosner, Mordechai Treves, Avraham J. Nagler, Arnon Belkin, Michael Rotenstreich, Ygal |
author_facet | Tzameret, Adi Kalish, Sapir E. Sher, Ifat Twito, Lea Meir, Amilia Levy, Itay Margel, Shlomo Moroz, Iris Rosner, Mordechai Treves, Avraham J. Nagler, Arnon Belkin, Michael Rotenstreich, Ygal |
author_sort | Tzameret, Adi |
collection | PubMed |
description | Incurable neuroretinal degeneration diseases cause severe vision loss and blindness in millions of patients worldwide. In previous studies, we demonstrated that transplanting human bone marrow stromal cells (hBMSCs) in the extravascular spaces of the choroid (EVSC) of the Royal College of Surgeon rats ameliorated retinal degeneration for up to 5 months. Assessing the safety of hBMSC treatment and graft survival in a large animal is a crucial step before initiating clinical trials. Here, we transplanted hBMSCs into the EVSC compartment of New Zealand White rabbits. No immunosuppressants were used. Transplanted cells were spread across the EVSC covering over 80 percent of the subretinal surface. No cells were detected in the sclera. Cells were retained in the EVSC compartment 10 weeks following transplantation. Spectral domain optical coherence tomography (SD-OCT) and histopathology analysis demonstrated no choroidal hemorrhages, retinal detachment, inflammation, or any untoward pathological reactions in any of transplanted eyes or in the control noninjected contralateral eyes. No reduction in retinal function was recorded by electroretinogram up to 10 weeks following transplantation. This study demonstrates the feasibility and safety of transplanting hBMSCs in the EVSC compartment in a large eye model of rabbits. |
format | Online Article Text |
id | pubmed-5494107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54941072017-07-11 Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits Tzameret, Adi Kalish, Sapir E. Sher, Ifat Twito, Lea Meir, Amilia Levy, Itay Margel, Shlomo Moroz, Iris Rosner, Mordechai Treves, Avraham J. Nagler, Arnon Belkin, Michael Rotenstreich, Ygal Stem Cells Int Research Article Incurable neuroretinal degeneration diseases cause severe vision loss and blindness in millions of patients worldwide. In previous studies, we demonstrated that transplanting human bone marrow stromal cells (hBMSCs) in the extravascular spaces of the choroid (EVSC) of the Royal College of Surgeon rats ameliorated retinal degeneration for up to 5 months. Assessing the safety of hBMSC treatment and graft survival in a large animal is a crucial step before initiating clinical trials. Here, we transplanted hBMSCs into the EVSC compartment of New Zealand White rabbits. No immunosuppressants were used. Transplanted cells were spread across the EVSC covering over 80 percent of the subretinal surface. No cells were detected in the sclera. Cells were retained in the EVSC compartment 10 weeks following transplantation. Spectral domain optical coherence tomography (SD-OCT) and histopathology analysis demonstrated no choroidal hemorrhages, retinal detachment, inflammation, or any untoward pathological reactions in any of transplanted eyes or in the control noninjected contralateral eyes. No reduction in retinal function was recorded by electroretinogram up to 10 weeks following transplantation. This study demonstrates the feasibility and safety of transplanting hBMSCs in the EVSC compartment in a large eye model of rabbits. Hindawi 2017 2017-06-18 /pmc/articles/PMC5494107/ /pubmed/28698719 http://dx.doi.org/10.1155/2017/4061975 Text en Copyright © 2017 Adi Tzameret et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tzameret, Adi Kalish, Sapir E. Sher, Ifat Twito, Lea Meir, Amilia Levy, Itay Margel, Shlomo Moroz, Iris Rosner, Mordechai Treves, Avraham J. Nagler, Arnon Belkin, Michael Rotenstreich, Ygal Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits |
title | Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits |
title_full | Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits |
title_fullStr | Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits |
title_full_unstemmed | Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits |
title_short | Long-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits |
title_sort | long-term safety of transplanting human bone marrow stromal cells into the extravascular spaces of the choroid of rabbits |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494107/ https://www.ncbi.nlm.nih.gov/pubmed/28698719 http://dx.doi.org/10.1155/2017/4061975 |
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