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Sibling umbilical cord blood infusion is safe in young children with cerebral palsy
Preclinical and early phase clinical studies suggest that an appropriately dosed umbilical cord blood (CB) infusion has the potential to help improve motor function in young children with cerebral palsy (CP). As many children with CP do not have their own CB available, use of allogeneic cells would...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380440/ https://www.ncbi.nlm.nih.gov/pubmed/34085782 http://dx.doi.org/10.1002/sctm.20-0470 |
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author | Sun, Jessica M. Case, Laura E. Mikati, Mohamad A. M. Jasien, Joan McLaughlin, Colleen Waters‐Pick, Barbara Worley, Gordon Troy, Jesse Kurtzberg, Joanne |
author_facet | Sun, Jessica M. Case, Laura E. Mikati, Mohamad A. M. Jasien, Joan McLaughlin, Colleen Waters‐Pick, Barbara Worley, Gordon Troy, Jesse Kurtzberg, Joanne |
author_sort | Sun, Jessica M. |
collection | PubMed |
description | Preclinical and early phase clinical studies suggest that an appropriately dosed umbilical cord blood (CB) infusion has the potential to help improve motor function in young children with cerebral palsy (CP). As many children with CP do not have their own CB available, use of allogeneic cells would extend access to this potentially beneficial therapy to more children. In this phase I, open‐label study, 15 children, aged 1 to 6 years, with moderate to severe spastic CP were treated with a single intravenous infusion of allogeneic human leukocyte antigen (HLA) matched or partially matched sibling CB with a cell dose of ≥2.5 × 10(7) cells/kg based on the pre‐cryopreservation count (median infused cell dose, 3.3 × 10(7); range, 1.8‐5.2 × 10(7)). There were a total of 49 adverse events (AEs) over a 2‐year time period, but there were no AEs related to the CB infusions. Specifically, there were no acute infusion reactions and no antibody formation against platelets, red blood cells, or donor‐specific HLA antigens. Donor cells were not detected in peripheral blood 6 months later. Six months after infusion, participants were assessed for response and experienced a mean ± SD increase of 4.7 ± 2.5 points on the Gross Motor Function Measure‐66 and 1 ± 2.9 points on the Peabody Gross Motor Quotient. Appropriately dosed, allogeneic partially or fully HLA‐matched sibling CB infusion is well tolerated and potentially beneficial in young children with CP. |
format | Online Article Text |
id | pubmed-8380440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83804402021-08-27 Sibling umbilical cord blood infusion is safe in young children with cerebral palsy Sun, Jessica M. Case, Laura E. Mikati, Mohamad A. M. Jasien, Joan McLaughlin, Colleen Waters‐Pick, Barbara Worley, Gordon Troy, Jesse Kurtzberg, Joanne Stem Cells Transl Med Human Clinical Articles Preclinical and early phase clinical studies suggest that an appropriately dosed umbilical cord blood (CB) infusion has the potential to help improve motor function in young children with cerebral palsy (CP). As many children with CP do not have their own CB available, use of allogeneic cells would extend access to this potentially beneficial therapy to more children. In this phase I, open‐label study, 15 children, aged 1 to 6 years, with moderate to severe spastic CP were treated with a single intravenous infusion of allogeneic human leukocyte antigen (HLA) matched or partially matched sibling CB with a cell dose of ≥2.5 × 10(7) cells/kg based on the pre‐cryopreservation count (median infused cell dose, 3.3 × 10(7); range, 1.8‐5.2 × 10(7)). There were a total of 49 adverse events (AEs) over a 2‐year time period, but there were no AEs related to the CB infusions. Specifically, there were no acute infusion reactions and no antibody formation against platelets, red blood cells, or donor‐specific HLA antigens. Donor cells were not detected in peripheral blood 6 months later. Six months after infusion, participants were assessed for response and experienced a mean ± SD increase of 4.7 ± 2.5 points on the Gross Motor Function Measure‐66 and 1 ± 2.9 points on the Peabody Gross Motor Quotient. Appropriately dosed, allogeneic partially or fully HLA‐matched sibling CB infusion is well tolerated and potentially beneficial in young children with CP. John Wiley & Sons, Inc. 2021-06-04 /pmc/articles/PMC8380440/ /pubmed/34085782 http://dx.doi.org/10.1002/sctm.20-0470 Text en © 2021 The Authors. stem cells translational medicine published by Wiley Periodicals LLC on behalf of AlphaMed Press. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Human Clinical Articles Sun, Jessica M. Case, Laura E. Mikati, Mohamad A. M. Jasien, Joan McLaughlin, Colleen Waters‐Pick, Barbara Worley, Gordon Troy, Jesse Kurtzberg, Joanne Sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
title | Sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
title_full | Sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
title_fullStr | Sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
title_full_unstemmed | Sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
title_short | Sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
title_sort | sibling umbilical cord blood infusion is safe in young children with cerebral palsy |
topic | Human Clinical Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380440/ https://www.ncbi.nlm.nih.gov/pubmed/34085782 http://dx.doi.org/10.1002/sctm.20-0470 |
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