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Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies
The gut microbiota have long been recognized to play a key role in human health and disease. Currently, several lines of evidence from preclinical to clinical research have gradually established that the gut microbiota can modulate antitumor immunity and affect the efficacy of cancer immunotherapies...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052532/ https://www.ncbi.nlm.nih.gov/pubmed/35488243 http://dx.doi.org/10.1186/s13045-022-01273-9 |
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author | Lu, Yuting Yuan, Xiangliang Wang, Miao He, Zhihao Li, Hongzhong Wang, Ji Li, Qin |
author_facet | Lu, Yuting Yuan, Xiangliang Wang, Miao He, Zhihao Li, Hongzhong Wang, Ji Li, Qin |
author_sort | Lu, Yuting |
collection | PubMed |
description | The gut microbiota have long been recognized to play a key role in human health and disease. Currently, several lines of evidence from preclinical to clinical research have gradually established that the gut microbiota can modulate antitumor immunity and affect the efficacy of cancer immunotherapies, especially immune checkpoint inhibitors (ICIs). Deciphering the underlying mechanisms reveals that the gut microbiota reprogram the immunity of the tumor microenvironment (TME) by engaging innate and/or adaptive immune cells. Notably, one of the primary modes by which the gut microbiota modulate antitumor immunity is by means of metabolites, which are small molecules that could spread from their initial location of the gut and impact local and systemic antitumor immune response to promote ICI efficiency. Mechanistic exploration provides novel insights for developing rational microbiota-based therapeutic strategies by manipulating gut microbiota, such as fecal microbiota transplantation (FMT), probiotics, engineered microbiomes, and specific microbial metabolites, to augment the efficacy of ICI and advance the age utilization of microbiota precision medicine. |
format | Online Article Text |
id | pubmed-9052532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90525322022-04-30 Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies Lu, Yuting Yuan, Xiangliang Wang, Miao He, Zhihao Li, Hongzhong Wang, Ji Li, Qin J Hematol Oncol Review The gut microbiota have long been recognized to play a key role in human health and disease. Currently, several lines of evidence from preclinical to clinical research have gradually established that the gut microbiota can modulate antitumor immunity and affect the efficacy of cancer immunotherapies, especially immune checkpoint inhibitors (ICIs). Deciphering the underlying mechanisms reveals that the gut microbiota reprogram the immunity of the tumor microenvironment (TME) by engaging innate and/or adaptive immune cells. Notably, one of the primary modes by which the gut microbiota modulate antitumor immunity is by means of metabolites, which are small molecules that could spread from their initial location of the gut and impact local and systemic antitumor immune response to promote ICI efficiency. Mechanistic exploration provides novel insights for developing rational microbiota-based therapeutic strategies by manipulating gut microbiota, such as fecal microbiota transplantation (FMT), probiotics, engineered microbiomes, and specific microbial metabolites, to augment the efficacy of ICI and advance the age utilization of microbiota precision medicine. BioMed Central 2022-04-29 /pmc/articles/PMC9052532/ /pubmed/35488243 http://dx.doi.org/10.1186/s13045-022-01273-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Lu, Yuting Yuan, Xiangliang Wang, Miao He, Zhihao Li, Hongzhong Wang, Ji Li, Qin Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
title | Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
title_full | Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
title_fullStr | Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
title_full_unstemmed | Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
title_short | Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
title_sort | gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052532/ https://www.ncbi.nlm.nih.gov/pubmed/35488243 http://dx.doi.org/10.1186/s13045-022-01273-9 |
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