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Gut microbiome immaturity and childhood acute lymphoblastic leukaemia

Acute lymphoblastic leukaemia (ALL) is the most common cancer of childhood. Here, we map emerging evidence suggesting that children with ALL at the time of diagnosis may have a delayed maturation of the gut microbiome compared with healthy children. This finding may be associated with early-life epi...

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Autores principales: Peppas, Ioannis, Ford, Anthony M., Furness, Caroline L., Greaves, Mel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243253/
https://www.ncbi.nlm.nih.gov/pubmed/37280427
http://dx.doi.org/10.1038/s41568-023-00584-4
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author Peppas, Ioannis
Ford, Anthony M.
Furness, Caroline L.
Greaves, Mel F.
author_facet Peppas, Ioannis
Ford, Anthony M.
Furness, Caroline L.
Greaves, Mel F.
author_sort Peppas, Ioannis
collection PubMed
description Acute lymphoblastic leukaemia (ALL) is the most common cancer of childhood. Here, we map emerging evidence suggesting that children with ALL at the time of diagnosis may have a delayed maturation of the gut microbiome compared with healthy children. This finding may be associated with early-life epidemiological factors previously identified as risk indicators for childhood ALL, including caesarean section birth, diminished breast feeding and paucity of social contacts. The consistently observed deficiency in short-chain fatty-acid-producing bacterial taxa in children with ALL has the potential to promote dysregulated immune responses and to, ultimately, increase the risk of transformation of preleukaemic clones in response to common infectious triggers. These data endorse the concept that a microbiome deficit in early life may contribute to the development of the major subtypes of childhood ALL and encourage the notion of risk-reducing microbiome-targeted intervention in the future.
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spelling pubmed-102432532023-06-07 Gut microbiome immaturity and childhood acute lymphoblastic leukaemia Peppas, Ioannis Ford, Anthony M. Furness, Caroline L. Greaves, Mel F. Nat Rev Cancer Perspective Acute lymphoblastic leukaemia (ALL) is the most common cancer of childhood. Here, we map emerging evidence suggesting that children with ALL at the time of diagnosis may have a delayed maturation of the gut microbiome compared with healthy children. This finding may be associated with early-life epidemiological factors previously identified as risk indicators for childhood ALL, including caesarean section birth, diminished breast feeding and paucity of social contacts. The consistently observed deficiency in short-chain fatty-acid-producing bacterial taxa in children with ALL has the potential to promote dysregulated immune responses and to, ultimately, increase the risk of transformation of preleukaemic clones in response to common infectious triggers. These data endorse the concept that a microbiome deficit in early life may contribute to the development of the major subtypes of childhood ALL and encourage the notion of risk-reducing microbiome-targeted intervention in the future. Nature Publishing Group UK 2023-06-06 /pmc/articles/PMC10243253/ /pubmed/37280427 http://dx.doi.org/10.1038/s41568-023-00584-4 Text en © Springer Nature Limited 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Perspective
Peppas, Ioannis
Ford, Anthony M.
Furness, Caroline L.
Greaves, Mel F.
Gut microbiome immaturity and childhood acute lymphoblastic leukaemia
title Gut microbiome immaturity and childhood acute lymphoblastic leukaemia
title_full Gut microbiome immaturity and childhood acute lymphoblastic leukaemia
title_fullStr Gut microbiome immaturity and childhood acute lymphoblastic leukaemia
title_full_unstemmed Gut microbiome immaturity and childhood acute lymphoblastic leukaemia
title_short Gut microbiome immaturity and childhood acute lymphoblastic leukaemia
title_sort gut microbiome immaturity and childhood acute lymphoblastic leukaemia
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243253/
https://www.ncbi.nlm.nih.gov/pubmed/37280427
http://dx.doi.org/10.1038/s41568-023-00584-4
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