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Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation
The gut microbiota is now recognized as a key parameter affecting the host’s anti-cancer immunosurveillance and ability to respond to immunotherapy. Therefore, optimal modulation for preventive and therapeutic purposes is very appealing. Diet is one of the most potent modulators of microbiota, and t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981629/ https://www.ncbi.nlm.nih.gov/pubmed/36875124 http://dx.doi.org/10.3389/fimmu.2023.1104224 |
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author | Boucher, Emilie Plazy, Caroline Richard, Mathias L. Suau, Antonia Mangin, Irène Cornet, Muriel Aldebert, Delphine Toussaint, Bertrand Hannani, Dalil |
author_facet | Boucher, Emilie Plazy, Caroline Richard, Mathias L. Suau, Antonia Mangin, Irène Cornet, Muriel Aldebert, Delphine Toussaint, Bertrand Hannani, Dalil |
author_sort | Boucher, Emilie |
collection | PubMed |
description | The gut microbiota is now recognized as a key parameter affecting the host’s anti-cancer immunosurveillance and ability to respond to immunotherapy. Therefore, optimal modulation for preventive and therapeutic purposes is very appealing. Diet is one of the most potent modulators of microbiota, and thus nutritional intervention could be exploited to improve host anti-cancer immunity. Here, we show that an inulin-enriched diet, a prebiotic known to promote immunostimulatory bacteria, triggers an enhanced Th1-polarized CD4(+) and CD8(+) αβ T cell-mediated anti-tumor response and attenuates tumor growth in three preclinical tumor-bearing mouse models. We highlighted that the inulin-mediated anti-tumor effect relies on the activation of both intestinal and tumor-infiltrating ɣδ T cells that are indispensable for αβ T cell activation and subsequent tumor growth control, in a microbiota-dependent manner. Overall, our data identified these cells as a critical immune subset, mandatory for inulin-mediated anti-tumor immunity in vivo, further supporting and rationalizing the use of such prebiotic approaches, as well as the development of immunotherapies targeting ɣδ T cells in cancer prevention and immunotherapy. |
format | Online Article Text |
id | pubmed-9981629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99816292023-03-04 Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation Boucher, Emilie Plazy, Caroline Richard, Mathias L. Suau, Antonia Mangin, Irène Cornet, Muriel Aldebert, Delphine Toussaint, Bertrand Hannani, Dalil Front Immunol Immunology The gut microbiota is now recognized as a key parameter affecting the host’s anti-cancer immunosurveillance and ability to respond to immunotherapy. Therefore, optimal modulation for preventive and therapeutic purposes is very appealing. Diet is one of the most potent modulators of microbiota, and thus nutritional intervention could be exploited to improve host anti-cancer immunity. Here, we show that an inulin-enriched diet, a prebiotic known to promote immunostimulatory bacteria, triggers an enhanced Th1-polarized CD4(+) and CD8(+) αβ T cell-mediated anti-tumor response and attenuates tumor growth in three preclinical tumor-bearing mouse models. We highlighted that the inulin-mediated anti-tumor effect relies on the activation of both intestinal and tumor-infiltrating ɣδ T cells that are indispensable for αβ T cell activation and subsequent tumor growth control, in a microbiota-dependent manner. Overall, our data identified these cells as a critical immune subset, mandatory for inulin-mediated anti-tumor immunity in vivo, further supporting and rationalizing the use of such prebiotic approaches, as well as the development of immunotherapies targeting ɣδ T cells in cancer prevention and immunotherapy. Frontiers Media S.A. 2023-02-17 /pmc/articles/PMC9981629/ /pubmed/36875124 http://dx.doi.org/10.3389/fimmu.2023.1104224 Text en Copyright © 2023 Boucher, Plazy, Richard, Suau, Mangin, Cornet, Aldebert, Toussaint and Hannani https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Boucher, Emilie Plazy, Caroline Richard, Mathias L. Suau, Antonia Mangin, Irène Cornet, Muriel Aldebert, Delphine Toussaint, Bertrand Hannani, Dalil Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation |
title | Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation |
title_full | Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation |
title_fullStr | Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation |
title_full_unstemmed | Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation |
title_short | Inulin prebiotic reinforces host cancer immunosurveillance via ɣδ T cell activation |
title_sort | inulin prebiotic reinforces host cancer immunosurveillance via ɣδ t cell activation |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981629/ https://www.ncbi.nlm.nih.gov/pubmed/36875124 http://dx.doi.org/10.3389/fimmu.2023.1104224 |
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