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Grandmaternal cells in cord blood
BACKGROUND: During pregnancy a feto-maternal exchange of cells through the placenta conducts to maternal microchimerism (Mc) in the child and fetal Mc in the mother. Because of this bidirectional traffic of cells, pregnant women have also acquired maternal cells in utero from their mother and could...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720789/ https://www.ncbi.nlm.nih.gov/pubmed/34844192 http://dx.doi.org/10.1016/j.ebiom.2021.103721 |
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author | Karlmark, Karlin R. Haddad, Marina El Donato, Xavier-Côme Martin, Gabriel V. Bretelle, Florence Lesavre, Nathalie Cocallemen, Jean-François Martin, Marielle Picard, Christophe Albentosa, Tiffany Roudier, Jean Desbriere, Raoul Lambert, Nathalie C. |
author_facet | Karlmark, Karlin R. Haddad, Marina El Donato, Xavier-Côme Martin, Gabriel V. Bretelle, Florence Lesavre, Nathalie Cocallemen, Jean-François Martin, Marielle Picard, Christophe Albentosa, Tiffany Roudier, Jean Desbriere, Raoul Lambert, Nathalie C. |
author_sort | Karlmark, Karlin R. |
collection | PubMed |
description | BACKGROUND: During pregnancy a feto-maternal exchange of cells through the placenta conducts to maternal microchimerism (Mc) in the child and fetal Mc in the mother. Because of this bidirectional traffic of cells, pregnant women have also acquired maternal cells in utero from their mother and could transfer grandmaternal (GdM) cells to their child through the maternal bloodstream during pregnancy. Thus, cord blood (CB) samples could theoretically carry GdMMc. Nevertheless this has never been demonstrated. METHODS: Using Human Leukocyte Antigen (HLA)-specific quantitative PCR assays on three-generation families, we were able to test 28 CB samples from healthy primigravid women for GdMMc in whole blood (WB) and isolated cells (PBMC, T, B, granulocytes, stem cells). FINDINGS: Five CB samples (18%) had GdMMc which could not be confounded with maternal source, with quantities 100 fold lower than maternal Mc in WB and PBMC. Risk of aneuploidies and/or related invasive prenatal procedures significantly correlated with the presence of GdMMc in CB (p=0.024). Significantly decreased HLA compatibility was observed in three-generation families from CB samples carrying GdMMc (p=0.019). INTERPRETATION: Transgenerational transfer of cells could have implications in immunology and evolution. Further analyses will be necessary to evaluate whether GdMMc in CB is a passive or immunologically active transfer and whether invasive prenatal procedures could trigger GdMMc. FUNDING: Provence-Alpes-Côte d'Azur APEX grant # 2012_06549E, 2012_11786F and 2014_03978) and the Foundation for Medical Research (FRM Grant #ING20140129045). |
format | Online Article Text |
id | pubmed-8720789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87207892022-01-07 Grandmaternal cells in cord blood Karlmark, Karlin R. Haddad, Marina El Donato, Xavier-Côme Martin, Gabriel V. Bretelle, Florence Lesavre, Nathalie Cocallemen, Jean-François Martin, Marielle Picard, Christophe Albentosa, Tiffany Roudier, Jean Desbriere, Raoul Lambert, Nathalie C. EBioMedicine Research Paper BACKGROUND: During pregnancy a feto-maternal exchange of cells through the placenta conducts to maternal microchimerism (Mc) in the child and fetal Mc in the mother. Because of this bidirectional traffic of cells, pregnant women have also acquired maternal cells in utero from their mother and could transfer grandmaternal (GdM) cells to their child through the maternal bloodstream during pregnancy. Thus, cord blood (CB) samples could theoretically carry GdMMc. Nevertheless this has never been demonstrated. METHODS: Using Human Leukocyte Antigen (HLA)-specific quantitative PCR assays on three-generation families, we were able to test 28 CB samples from healthy primigravid women for GdMMc in whole blood (WB) and isolated cells (PBMC, T, B, granulocytes, stem cells). FINDINGS: Five CB samples (18%) had GdMMc which could not be confounded with maternal source, with quantities 100 fold lower than maternal Mc in WB and PBMC. Risk of aneuploidies and/or related invasive prenatal procedures significantly correlated with the presence of GdMMc in CB (p=0.024). Significantly decreased HLA compatibility was observed in three-generation families from CB samples carrying GdMMc (p=0.019). INTERPRETATION: Transgenerational transfer of cells could have implications in immunology and evolution. Further analyses will be necessary to evaluate whether GdMMc in CB is a passive or immunologically active transfer and whether invasive prenatal procedures could trigger GdMMc. FUNDING: Provence-Alpes-Côte d'Azur APEX grant # 2012_06549E, 2012_11786F and 2014_03978) and the Foundation for Medical Research (FRM Grant #ING20140129045). Elsevier 2021-11-26 /pmc/articles/PMC8720789/ /pubmed/34844192 http://dx.doi.org/10.1016/j.ebiom.2021.103721 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Karlmark, Karlin R. Haddad, Marina El Donato, Xavier-Côme Martin, Gabriel V. Bretelle, Florence Lesavre, Nathalie Cocallemen, Jean-François Martin, Marielle Picard, Christophe Albentosa, Tiffany Roudier, Jean Desbriere, Raoul Lambert, Nathalie C. Grandmaternal cells in cord blood |
title | Grandmaternal cells in cord blood |
title_full | Grandmaternal cells in cord blood |
title_fullStr | Grandmaternal cells in cord blood |
title_full_unstemmed | Grandmaternal cells in cord blood |
title_short | Grandmaternal cells in cord blood |
title_sort | grandmaternal cells in cord blood |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720789/ https://www.ncbi.nlm.nih.gov/pubmed/34844192 http://dx.doi.org/10.1016/j.ebiom.2021.103721 |
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