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Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy

Immune checkpoint inhibitors (ICI) targeting cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4) and programmed death 1 (PD-1) proteins transformed the management of advanced cancers. Many tumor-intrinsic factors modulate immunological and clinical responses to such therapies, but ample evidence al...

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Detalles Bibliográficos
Autores principales: Davar, Diwakar, Zarour, Hassane M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561605/
https://www.ncbi.nlm.nih.gov/pubmed/35748749
http://dx.doi.org/10.1158/1078-0432.CCR-21-1129
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author Davar, Diwakar
Zarour, Hassane M.
author_facet Davar, Diwakar
Zarour, Hassane M.
author_sort Davar, Diwakar
collection PubMed
description Immune checkpoint inhibitors (ICI) targeting cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4) and programmed death 1 (PD-1) proteins transformed the management of advanced cancers. Many tumor-intrinsic factors modulate immunological and clinical responses to such therapies, but ample evidence also implicates the gut microbiome in responses. The gut microbiome, comprising the bacteria, archaea, fungi, and viruses that live in the human digestive tract, is an established determinant of host immunity, but its impact on response to ICI therapy in mice and humans with cancer has only recently been appreciated. Therapeutic interventions to optimize microbiota composition to improve immunotherapy outcomes show promise in mice and humans with cancer. In this review, we discuss the rationale for gut microbiome–based cancer therapies, the results from early-phase clinical trials, and possible future developments.
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spelling pubmed-95616052023-01-05 Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy Davar, Diwakar Zarour, Hassane M. Clin Cancer Res Reviews Immune checkpoint inhibitors (ICI) targeting cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4) and programmed death 1 (PD-1) proteins transformed the management of advanced cancers. Many tumor-intrinsic factors modulate immunological and clinical responses to such therapies, but ample evidence also implicates the gut microbiome in responses. The gut microbiome, comprising the bacteria, archaea, fungi, and viruses that live in the human digestive tract, is an established determinant of host immunity, but its impact on response to ICI therapy in mice and humans with cancer has only recently been appreciated. Therapeutic interventions to optimize microbiota composition to improve immunotherapy outcomes show promise in mice and humans with cancer. In this review, we discuss the rationale for gut microbiome–based cancer therapies, the results from early-phase clinical trials, and possible future developments. American Association for Cancer Research 2022-10-14 2022-06-24 /pmc/articles/PMC9561605/ /pubmed/35748749 http://dx.doi.org/10.1158/1078-0432.CCR-21-1129 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
spellingShingle Reviews
Davar, Diwakar
Zarour, Hassane M.
Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
title Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
title_full Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
title_fullStr Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
title_full_unstemmed Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
title_short Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
title_sort facts and hopes for gut microbiota interventions in cancer immunotherapy
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561605/
https://www.ncbi.nlm.nih.gov/pubmed/35748749
http://dx.doi.org/10.1158/1078-0432.CCR-21-1129
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