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Utility of assessing CD3 (+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia
After allogeneic hematopoietic stem‐cell transplantation (alloHSCT), the chimerism assay is used to monitor cell engraftment and quantify the respective proportions of donor/recipient cells in blood or bone‐marrow samples. Here, we aimed to better assess the utility of determining CD3(+) cell chimer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303291/ https://www.ncbi.nlm.nih.gov/pubmed/35064642 http://dx.doi.org/10.1111/tan.14557 |
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author | Bendjelloul, Mehdi Usureau, Cédric Etancelin, Pascaline Saidak, Zuzana Lebon, Delphine Garçon, Loïc Marolleau, Jean‐Pierre Desoutter, Judith Guillaume, Nicolas |
author_facet | Bendjelloul, Mehdi Usureau, Cédric Etancelin, Pascaline Saidak, Zuzana Lebon, Delphine Garçon, Loïc Marolleau, Jean‐Pierre Desoutter, Judith Guillaume, Nicolas |
author_sort | Bendjelloul, Mehdi |
collection | PubMed |
description | After allogeneic hematopoietic stem‐cell transplantation (alloHSCT), the chimerism assay is used to monitor cell engraftment and quantify the respective proportions of donor/recipient cells in blood or bone‐marrow samples. Here, we aimed to better assess the utility of determining CD3(+) cell chimerism within the first 6 months post alloHSCT. One hundred and thirty five patients diagnosed with acute myeloid leukemia were enrolled in this study. We observed significantly lower overall survival and relapse free survival for patients without full donor chimerism (<95%, <98%, <99%) in whole blood at Day 30, as well as at Day 90 after alloHSCT, than for patients with full donor chimerism. This outcome was not observed when assessing selected CD3(+) cells. However, at Day 90, patients with discordant whole blood versus selected CD3(+) cell chimerism showed both significantly lower overall survival and relapse free survival, giving an interest to assess selected cells chimerism. |
format | Online Article Text |
id | pubmed-9303291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-93032912022-07-22 Utility of assessing CD3 (+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia Bendjelloul, Mehdi Usureau, Cédric Etancelin, Pascaline Saidak, Zuzana Lebon, Delphine Garçon, Loïc Marolleau, Jean‐Pierre Desoutter, Judith Guillaume, Nicolas HLA Original Articles After allogeneic hematopoietic stem‐cell transplantation (alloHSCT), the chimerism assay is used to monitor cell engraftment and quantify the respective proportions of donor/recipient cells in blood or bone‐marrow samples. Here, we aimed to better assess the utility of determining CD3(+) cell chimerism within the first 6 months post alloHSCT. One hundred and thirty five patients diagnosed with acute myeloid leukemia were enrolled in this study. We observed significantly lower overall survival and relapse free survival for patients without full donor chimerism (<95%, <98%, <99%) in whole blood at Day 30, as well as at Day 90 after alloHSCT, than for patients with full donor chimerism. This outcome was not observed when assessing selected CD3(+) cells. However, at Day 90, patients with discordant whole blood versus selected CD3(+) cell chimerism showed both significantly lower overall survival and relapse free survival, giving an interest to assess selected cells chimerism. Blackwell Publishing Ltd 2022-01-30 2022-07 /pmc/articles/PMC9303291/ /pubmed/35064642 http://dx.doi.org/10.1111/tan.14557 Text en © 2022 The Authors. HLA: Immune Response Genetics published by John Wiley & Sons Ltd. 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 | Original Articles Bendjelloul, Mehdi Usureau, Cédric Etancelin, Pascaline Saidak, Zuzana Lebon, Delphine Garçon, Loïc Marolleau, Jean‐Pierre Desoutter, Judith Guillaume, Nicolas Utility of assessing CD3 (+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
title | Utility of assessing CD3
(+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
title_full | Utility of assessing CD3
(+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
title_fullStr | Utility of assessing CD3
(+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
title_full_unstemmed | Utility of assessing CD3
(+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
title_short | Utility of assessing CD3
(+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
title_sort | utility of assessing cd3
(+) cell chimerism within the first months after allogeneic hematopoietic stem‐cell transplantation for acute myeloid leukemia |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303291/ https://www.ncbi.nlm.nih.gov/pubmed/35064642 http://dx.doi.org/10.1111/tan.14557 |
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