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Microbiome influencers of checkpoint blockade–associated toxicity

Immunotherapy has greatly improved cancer outcomes, yet variability in response and off-target tissue damage can occur with these treatments, including immune checkpoint inhibitors (ICIs). Multiple lines of evidence indicate the host microbiome influences ICI response and risk of immune-related adve...

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Autores principales: Wang, Yinghong, Jenq, Robert R., Wargo, Jennifer A., Watowich, Stephanie S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836236/
https://www.ncbi.nlm.nih.gov/pubmed/36622383
http://dx.doi.org/10.1084/jem.20220948
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author Wang, Yinghong
Jenq, Robert R.
Wargo, Jennifer A.
Watowich, Stephanie S.
author_facet Wang, Yinghong
Jenq, Robert R.
Wargo, Jennifer A.
Watowich, Stephanie S.
author_sort Wang, Yinghong
collection PubMed
description Immunotherapy has greatly improved cancer outcomes, yet variability in response and off-target tissue damage can occur with these treatments, including immune checkpoint inhibitors (ICIs). Multiple lines of evidence indicate the host microbiome influences ICI response and risk of immune-related adverse events (irAEs). As the microbiome is modifiable, these advances indicate the potential to manipulate microbiome components to increase ICI success. We discuss microbiome features associated with ICI response, with focus on bacterial taxa and potential immune mechanisms involved in irAEs, and the overall goal of driving novel approaches to manipulate the microbiome to improve ICI efficacy while avoiding irAE risk.
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spelling pubmed-98362362023-01-13 Microbiome influencers of checkpoint blockade–associated toxicity Wang, Yinghong Jenq, Robert R. Wargo, Jennifer A. Watowich, Stephanie S. J Exp Med Review Immunotherapy has greatly improved cancer outcomes, yet variability in response and off-target tissue damage can occur with these treatments, including immune checkpoint inhibitors (ICIs). Multiple lines of evidence indicate the host microbiome influences ICI response and risk of immune-related adverse events (irAEs). As the microbiome is modifiable, these advances indicate the potential to manipulate microbiome components to increase ICI success. We discuss microbiome features associated with ICI response, with focus on bacterial taxa and potential immune mechanisms involved in irAEs, and the overall goal of driving novel approaches to manipulate the microbiome to improve ICI efficacy while avoiding irAE risk. Rockefeller University Press 2023-01-09 /pmc/articles/PMC9836236/ /pubmed/36622383 http://dx.doi.org/10.1084/jem.20220948 Text en © 2023 Wang et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Yinghong
Jenq, Robert R.
Wargo, Jennifer A.
Watowich, Stephanie S.
Microbiome influencers of checkpoint blockade–associated toxicity
title Microbiome influencers of checkpoint blockade–associated toxicity
title_full Microbiome influencers of checkpoint blockade–associated toxicity
title_fullStr Microbiome influencers of checkpoint blockade–associated toxicity
title_full_unstemmed Microbiome influencers of checkpoint blockade–associated toxicity
title_short Microbiome influencers of checkpoint blockade–associated toxicity
title_sort microbiome influencers of checkpoint blockade–associated toxicity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836236/
https://www.ncbi.nlm.nih.gov/pubmed/36622383
http://dx.doi.org/10.1084/jem.20220948
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