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Understanding adverse events of immunotherapy: A mechanistic perspective

The treatment of many cancers has been revolutionized by immune checkpoint blockade (ICB) as a standard-of-care therapeutic. Despite many successes, a large proportion of patients treated with ICB agents experience immune-related adverse events (irAEs) in the form of clinical autoimmunity, ranging f...

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Detalles Bibliográficos
Autores principales: Burke, Kelly P., Grebinoski, Stephanie, Sharpe, Arlene H., Vignali, Dario A.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754677/
https://www.ncbi.nlm.nih.gov/pubmed/33601411
http://dx.doi.org/10.1084/jem.20192179
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author Burke, Kelly P.
Grebinoski, Stephanie
Sharpe, Arlene H.
Vignali, Dario A.A.
author_facet Burke, Kelly P.
Grebinoski, Stephanie
Sharpe, Arlene H.
Vignali, Dario A.A.
author_sort Burke, Kelly P.
collection PubMed
description The treatment of many cancers has been revolutionized by immune checkpoint blockade (ICB) as a standard-of-care therapeutic. Despite many successes, a large proportion of patients treated with ICB agents experience immune-related adverse events (irAEs) in the form of clinical autoimmunity, ranging from mild to life threatening, that can limit cancer treatment. A mechanistic understanding of these irAEs is required to better treat or prevent irAEs and to predict those patients who are susceptible to irAEs. We propose several mechanisms that may contribute to the generation of irAEs: (1) preexisting susceptibility to autoimmunity, (2) aberrant presentation of “self” by the tumor, and (3) loss of tolerance driven by the tumor or tissue microenvironment.
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spelling pubmed-77546772021-07-04 Understanding adverse events of immunotherapy: A mechanistic perspective Burke, Kelly P. Grebinoski, Stephanie Sharpe, Arlene H. Vignali, Dario A.A. J Exp Med Perspective The treatment of many cancers has been revolutionized by immune checkpoint blockade (ICB) as a standard-of-care therapeutic. Despite many successes, a large proportion of patients treated with ICB agents experience immune-related adverse events (irAEs) in the form of clinical autoimmunity, ranging from mild to life threatening, that can limit cancer treatment. A mechanistic understanding of these irAEs is required to better treat or prevent irAEs and to predict those patients who are susceptible to irAEs. We propose several mechanisms that may contribute to the generation of irAEs: (1) preexisting susceptibility to autoimmunity, (2) aberrant presentation of “self” by the tumor, and (3) loss of tolerance driven by the tumor or tissue microenvironment. Rockefeller University Press 2020-12-18 /pmc/articles/PMC7754677/ /pubmed/33601411 http://dx.doi.org/10.1084/jem.20192179 Text en © 2020 Burke et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Perspective
Burke, Kelly P.
Grebinoski, Stephanie
Sharpe, Arlene H.
Vignali, Dario A.A.
Understanding adverse events of immunotherapy: A mechanistic perspective
title Understanding adverse events of immunotherapy: A mechanistic perspective
title_full Understanding adverse events of immunotherapy: A mechanistic perspective
title_fullStr Understanding adverse events of immunotherapy: A mechanistic perspective
title_full_unstemmed Understanding adverse events of immunotherapy: A mechanistic perspective
title_short Understanding adverse events of immunotherapy: A mechanistic perspective
title_sort understanding adverse events of immunotherapy: a mechanistic perspective
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754677/
https://www.ncbi.nlm.nih.gov/pubmed/33601411
http://dx.doi.org/10.1084/jem.20192179
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