Cargando…
Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study
Persistent cytopenia in the post-hematopoietic cell transplantation (HCT) setting can occur despite adequate engraftment of donor cells. PLX-R18, a placental-derived mesenchymal-like cell product, is expanded ex vivo in a 3-dimensional environment. PLX-R18 cells secrete a large array of hematopoieti...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622312/ https://www.ncbi.nlm.nih.gov/pubmed/37553467 http://dx.doi.org/10.1038/s41409-023-02068-3 |
_version_ | 1785130508396527616 |
---|---|
author | McGuirk, Joseph P. Metheny, Leland Pineiro, Luis Litzow, Mark Rowley, Scott D. Avni, Batia Tamari, Roni Lazarus, Hillard M. Rowe, Jacob M. Sheleg, Michal Rothenstein, Daniel Halevy, Nitsan Zuckerman, Tsila |
author_facet | McGuirk, Joseph P. Metheny, Leland Pineiro, Luis Litzow, Mark Rowley, Scott D. Avni, Batia Tamari, Roni Lazarus, Hillard M. Rowe, Jacob M. Sheleg, Michal Rothenstein, Daniel Halevy, Nitsan Zuckerman, Tsila |
author_sort | McGuirk, Joseph P. |
collection | PubMed |
description | Persistent cytopenia in the post-hematopoietic cell transplantation (HCT) setting can occur despite adequate engraftment of donor cells. PLX-R18, a placental-derived mesenchymal-like cell product, is expanded ex vivo in a 3-dimensional environment. PLX-R18 cells secrete a large array of hematopoietic factors, which promote regeneration, maturation, and differentiation of hematopoietic cells and stimulate their migration to peripheral blood. This phase 1, first-in-human study (NCT03002519), included 21 patients with incomplete hematopoietic recovery post-HCT. Patients were treated with escalating doses of PLX-R18: 3 patients received 1 million cells/kg, 6 received 2 million cells/kg, and 12 received 4 million cells/kg via multiple intramuscular injections. While patients received only two administrations of cells during the first week, peripheral blood counts continued to increase for months, peaking at 6 months for hemoglobin (Hb, p = 0.002), lymphocytes (p = 0.008), and neutrophils (ANC, p = 0.063), and at 9 months for platelets (p < 0.001) and was maintained until 12 months for all but ANC. The need for platelet transfusions was reduced from 5.09 units/month at baseline to 0.55 at month 12 (p = 0.05). Likewise, red blood cell transfusions decreased from 2.91 units/month at baseline to 0 at month 12 (p = 0.0005). PLX-R18 was safe and well tolerated and shows promise in improving incomplete hematopoietic recovery post-HCT. |
format | Online Article Text |
id | pubmed-10622312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106223122023-11-04 Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study McGuirk, Joseph P. Metheny, Leland Pineiro, Luis Litzow, Mark Rowley, Scott D. Avni, Batia Tamari, Roni Lazarus, Hillard M. Rowe, Jacob M. Sheleg, Michal Rothenstein, Daniel Halevy, Nitsan Zuckerman, Tsila Bone Marrow Transplant Article Persistent cytopenia in the post-hematopoietic cell transplantation (HCT) setting can occur despite adequate engraftment of donor cells. PLX-R18, a placental-derived mesenchymal-like cell product, is expanded ex vivo in a 3-dimensional environment. PLX-R18 cells secrete a large array of hematopoietic factors, which promote regeneration, maturation, and differentiation of hematopoietic cells and stimulate their migration to peripheral blood. This phase 1, first-in-human study (NCT03002519), included 21 patients with incomplete hematopoietic recovery post-HCT. Patients were treated with escalating doses of PLX-R18: 3 patients received 1 million cells/kg, 6 received 2 million cells/kg, and 12 received 4 million cells/kg via multiple intramuscular injections. While patients received only two administrations of cells during the first week, peripheral blood counts continued to increase for months, peaking at 6 months for hemoglobin (Hb, p = 0.002), lymphocytes (p = 0.008), and neutrophils (ANC, p = 0.063), and at 9 months for platelets (p < 0.001) and was maintained until 12 months for all but ANC. The need for platelet transfusions was reduced from 5.09 units/month at baseline to 0.55 at month 12 (p = 0.05). Likewise, red blood cell transfusions decreased from 2.91 units/month at baseline to 0 at month 12 (p = 0.0005). PLX-R18 was safe and well tolerated and shows promise in improving incomplete hematopoietic recovery post-HCT. Nature Publishing Group UK 2023-08-08 2023 /pmc/articles/PMC10622312/ /pubmed/37553467 http://dx.doi.org/10.1038/s41409-023-02068-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article McGuirk, Joseph P. Metheny, Leland Pineiro, Luis Litzow, Mark Rowley, Scott D. Avni, Batia Tamari, Roni Lazarus, Hillard M. Rowe, Jacob M. Sheleg, Michal Rothenstein, Daniel Halevy, Nitsan Zuckerman, Tsila Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study |
title | Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study |
title_full | Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study |
title_fullStr | Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study |
title_full_unstemmed | Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study |
title_short | Placental expanded mesenchymal-like cells (PLX-R18) for poor graft function after hematopoietic cell transplantation: A phase I study |
title_sort | placental expanded mesenchymal-like cells (plx-r18) for poor graft function after hematopoietic cell transplantation: a phase i study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622312/ https://www.ncbi.nlm.nih.gov/pubmed/37553467 http://dx.doi.org/10.1038/s41409-023-02068-3 |
work_keys_str_mv | AT mcguirkjosephp placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT methenyleland placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT pineiroluis placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT litzowmark placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT rowleyscottd placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT avnibatia placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT tamarironi placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT lazarushillardm placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT rowejacobm placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT shelegmichal placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT rothensteindaniel placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT halevynitsan placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy AT zuckermantsila placentalexpandedmesenchymallikecellsplxr18forpoorgraftfunctionafterhematopoieticcelltransplantationaphaseistudy |