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Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition
How bacterial strains within a complex human microbiota collectively shape intestinal T cell homeostasis is not well understood. Methods that quickly identify effector strains or species that drive specific mucosal T cell phenotypes are needed to define general principles for how the microbiota modu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041165/ https://www.ncbi.nlm.nih.gov/pubmed/36917674 http://dx.doi.org/10.1073/pnas.2215914120 |
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author | Spindler, Matthew P. Mogno, Ilaria Suri, Prerna Britton, Graham J. Faith, Jeremiah J. |
author_facet | Spindler, Matthew P. Mogno, Ilaria Suri, Prerna Britton, Graham J. Faith, Jeremiah J. |
author_sort | Spindler, Matthew P. |
collection | PubMed |
description | How bacterial strains within a complex human microbiota collectively shape intestinal T cell homeostasis is not well understood. Methods that quickly identify effector strains or species that drive specific mucosal T cell phenotypes are needed to define general principles for how the microbiota modulates host immunity. We colonize germ-free mice with defined communities of cultured strains and profile antigen-specific responses directed toward individual strains ex vivo. We find that lamina propria T cells are specific to bacterial strains at the species level and can discriminate between strains of the same species. Ex vivo restimulations consistently identify the strains within complex communities that induce Th17 responses in vivo, providing the potential to shape baseline immune tone via community composition. Using an adoptive transfer model of colitis, we find that lamina propria T cells respond to different bacterial strains in conditions of inflammation versus homeostasis. Collectively, our approach represents a unique method for efficiently predicting the relative impact of individual bacterial strains within a complex community and for parsing microbiota-dependent phenotypes into component fractions. |
format | Online Article Text |
id | pubmed-10041165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-100411652023-09-14 Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition Spindler, Matthew P. Mogno, Ilaria Suri, Prerna Britton, Graham J. Faith, Jeremiah J. Proc Natl Acad Sci U S A Biological Sciences How bacterial strains within a complex human microbiota collectively shape intestinal T cell homeostasis is not well understood. Methods that quickly identify effector strains or species that drive specific mucosal T cell phenotypes are needed to define general principles for how the microbiota modulates host immunity. We colonize germ-free mice with defined communities of cultured strains and profile antigen-specific responses directed toward individual strains ex vivo. We find that lamina propria T cells are specific to bacterial strains at the species level and can discriminate between strains of the same species. Ex vivo restimulations consistently identify the strains within complex communities that induce Th17 responses in vivo, providing the potential to shape baseline immune tone via community composition. Using an adoptive transfer model of colitis, we find that lamina propria T cells respond to different bacterial strains in conditions of inflammation versus homeostasis. Collectively, our approach represents a unique method for efficiently predicting the relative impact of individual bacterial strains within a complex community and for parsing microbiota-dependent phenotypes into component fractions. National Academy of Sciences 2023-03-14 2023-03-21 /pmc/articles/PMC10041165/ /pubmed/36917674 http://dx.doi.org/10.1073/pnas.2215914120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Spindler, Matthew P. Mogno, Ilaria Suri, Prerna Britton, Graham J. Faith, Jeremiah J. Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition |
title | Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition |
title_full | Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition |
title_fullStr | Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition |
title_full_unstemmed | Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition |
title_short | Species-specific CD4(+) T cells enable prediction of mucosal immune phenotypes from microbiota composition |
title_sort | species-specific cd4(+) t cells enable prediction of mucosal immune phenotypes from microbiota composition |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041165/ https://www.ncbi.nlm.nih.gov/pubmed/36917674 http://dx.doi.org/10.1073/pnas.2215914120 |
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