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Vertically transferred maternal immune cells promote neonatal immunity against early life infections

During mammalian pregnancy, immune cells are vertically transferred from mother to fetus. The functional role of these maternal microchimeric cells (MMc) in the offspring is mostly unknown. Here we show a mouse model in which MMc numbers are either normal or low, which enables functional assessment...

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Autores principales: Stelzer, Ina Annelies, Urbschat, Christopher, Schepanski, Steven, Thiele, Kristin, Triviai, Ioanna, Wieczorek, Agnes, Alawi, Malik, Ohnezeit, Denise, Kottlau, Julian, Huang, Jiabin, Fischer, Nicole, Mittrücker, Hans-Willi, Solano, Maria Emilia, Fehse, Boris, Diemert, Anke, Stahl, Felix R., Arck, Petra Clara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8338998/
https://www.ncbi.nlm.nih.gov/pubmed/34349112
http://dx.doi.org/10.1038/s41467-021-24719-z
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author Stelzer, Ina Annelies
Urbschat, Christopher
Schepanski, Steven
Thiele, Kristin
Triviai, Ioanna
Wieczorek, Agnes
Alawi, Malik
Ohnezeit, Denise
Kottlau, Julian
Huang, Jiabin
Fischer, Nicole
Mittrücker, Hans-Willi
Solano, Maria Emilia
Fehse, Boris
Diemert, Anke
Stahl, Felix R.
Arck, Petra Clara
author_facet Stelzer, Ina Annelies
Urbschat, Christopher
Schepanski, Steven
Thiele, Kristin
Triviai, Ioanna
Wieczorek, Agnes
Alawi, Malik
Ohnezeit, Denise
Kottlau, Julian
Huang, Jiabin
Fischer, Nicole
Mittrücker, Hans-Willi
Solano, Maria Emilia
Fehse, Boris
Diemert, Anke
Stahl, Felix R.
Arck, Petra Clara
author_sort Stelzer, Ina Annelies
collection PubMed
description During mammalian pregnancy, immune cells are vertically transferred from mother to fetus. The functional role of these maternal microchimeric cells (MMc) in the offspring is mostly unknown. Here we show a mouse model in which MMc numbers are either normal or low, which enables functional assessment of MMc. We report a functional role of MMc in promoting fetal immune development. MMc induces preferential differentiation of hematopoietic stem cells in fetal bone marrow towards monocytes within the myeloid compartment. Neonatal mice with higher numbers of MMc and monocytes show enhanced resilience against cytomegalovirus infection. Similarly, higher numbers of MMc in human cord blood are linked to a lower number of respiratory infections during the first year of life. Our data highlight the importance of MMc in promoting fetal immune development, potentially averting the threats caused by early life exposure to pathogens.
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spelling pubmed-83389982021-08-12 Vertically transferred maternal immune cells promote neonatal immunity against early life infections Stelzer, Ina Annelies Urbschat, Christopher Schepanski, Steven Thiele, Kristin Triviai, Ioanna Wieczorek, Agnes Alawi, Malik Ohnezeit, Denise Kottlau, Julian Huang, Jiabin Fischer, Nicole Mittrücker, Hans-Willi Solano, Maria Emilia Fehse, Boris Diemert, Anke Stahl, Felix R. Arck, Petra Clara Nat Commun Article During mammalian pregnancy, immune cells are vertically transferred from mother to fetus. The functional role of these maternal microchimeric cells (MMc) in the offspring is mostly unknown. Here we show a mouse model in which MMc numbers are either normal or low, which enables functional assessment of MMc. We report a functional role of MMc in promoting fetal immune development. MMc induces preferential differentiation of hematopoietic stem cells in fetal bone marrow towards monocytes within the myeloid compartment. Neonatal mice with higher numbers of MMc and monocytes show enhanced resilience against cytomegalovirus infection. Similarly, higher numbers of MMc in human cord blood are linked to a lower number of respiratory infections during the first year of life. Our data highlight the importance of MMc in promoting fetal immune development, potentially averting the threats caused by early life exposure to pathogens. Nature Publishing Group UK 2021-08-04 /pmc/articles/PMC8338998/ /pubmed/34349112 http://dx.doi.org/10.1038/s41467-021-24719-z Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Stelzer, Ina Annelies
Urbschat, Christopher
Schepanski, Steven
Thiele, Kristin
Triviai, Ioanna
Wieczorek, Agnes
Alawi, Malik
Ohnezeit, Denise
Kottlau, Julian
Huang, Jiabin
Fischer, Nicole
Mittrücker, Hans-Willi
Solano, Maria Emilia
Fehse, Boris
Diemert, Anke
Stahl, Felix R.
Arck, Petra Clara
Vertically transferred maternal immune cells promote neonatal immunity against early life infections
title Vertically transferred maternal immune cells promote neonatal immunity against early life infections
title_full Vertically transferred maternal immune cells promote neonatal immunity against early life infections
title_fullStr Vertically transferred maternal immune cells promote neonatal immunity against early life infections
title_full_unstemmed Vertically transferred maternal immune cells promote neonatal immunity against early life infections
title_short Vertically transferred maternal immune cells promote neonatal immunity against early life infections
title_sort vertically transferred maternal immune cells promote neonatal immunity against early life infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8338998/
https://www.ncbi.nlm.nih.gov/pubmed/34349112
http://dx.doi.org/10.1038/s41467-021-24719-z
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