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What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination

The process of tumorigenesis leaves a series of indelible genetic changes in tumor cells, that when expressed, have the potential to be tumor-specific immune targets. Neoantigen vaccines that capitalize on this potential immunogenicity have shown efficacy in preclinical models and have now entered c...

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Detalles Bibliográficos
Autores principales: Redwood, Alec J., Dick, Ian M., Creaney, Jenette, Robinson, Bruce W. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855878/
https://www.ncbi.nlm.nih.gov/pubmed/35186441
http://dx.doi.org/10.1080/2162402X.2022.2038403
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author Redwood, Alec J.
Dick, Ian M.
Creaney, Jenette
Robinson, Bruce W. S.
author_facet Redwood, Alec J.
Dick, Ian M.
Creaney, Jenette
Robinson, Bruce W. S.
author_sort Redwood, Alec J.
collection PubMed
description The process of tumorigenesis leaves a series of indelible genetic changes in tumor cells, that when expressed, have the potential to be tumor-specific immune targets. Neoantigen vaccines that capitalize on this potential immunogenicity have shown efficacy in preclinical models and have now entered clinical trials. Here we discuss the status of personalized neoantigen vaccines and the current major challenges to this nascent field. In particular, we focus on the types of antigens that can be targeted by vaccination and on the role that preexisting immunosuppression, and in particular T-cell exhaustion, will play in the development of effective cancer vaccines.
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spelling pubmed-88558782022-02-19 What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination Redwood, Alec J. Dick, Ian M. Creaney, Jenette Robinson, Bruce W. S. Oncoimmunology Review The process of tumorigenesis leaves a series of indelible genetic changes in tumor cells, that when expressed, have the potential to be tumor-specific immune targets. Neoantigen vaccines that capitalize on this potential immunogenicity have shown efficacy in preclinical models and have now entered clinical trials. Here we discuss the status of personalized neoantigen vaccines and the current major challenges to this nascent field. In particular, we focus on the types of antigens that can be targeted by vaccination and on the role that preexisting immunosuppression, and in particular T-cell exhaustion, will play in the development of effective cancer vaccines. Taylor & Francis 2022-02-13 /pmc/articles/PMC8855878/ /pubmed/35186441 http://dx.doi.org/10.1080/2162402X.2022.2038403 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Redwood, Alec J.
Dick, Ian M.
Creaney, Jenette
Robinson, Bruce W. S.
What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination
title What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination
title_full What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination
title_fullStr What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination
title_full_unstemmed What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination
title_short What’s next in cancer immunotherapy? - The promise and challenges of neoantigen vaccination
title_sort what’s next in cancer immunotherapy? - the promise and challenges of neoantigen vaccination
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855878/
https://www.ncbi.nlm.nih.gov/pubmed/35186441
http://dx.doi.org/10.1080/2162402X.2022.2038403
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