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Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection
Colorectal cancer (CRC) remains a leading cause of cancer-related mortality despite efforts to improve standard interventions. As CRC patients can benefit from immunotherapeutic strategies that incite effector T cell action, cancer vaccines represent a safe and promising therapeutic approach to elic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540654/ https://www.ncbi.nlm.nih.gov/pubmed/37781234 http://dx.doi.org/10.1080/2162402X.2023.2260620 |
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author | Anderson, Trevor S. McCormick, Amanda L. Daugherity, Elizabeth A. Oladejo, Mariam Okpalanwaka, Izuchukwu F. Smith, Savanna L. Appiah, Duke Wood, Laurence M. Lowe, Devin B. |
author_facet | Anderson, Trevor S. McCormick, Amanda L. Daugherity, Elizabeth A. Oladejo, Mariam Okpalanwaka, Izuchukwu F. Smith, Savanna L. Appiah, Duke Wood, Laurence M. Lowe, Devin B. |
author_sort | Anderson, Trevor S. |
collection | PubMed |
description | Colorectal cancer (CRC) remains a leading cause of cancer-related mortality despite efforts to improve standard interventions. As CRC patients can benefit from immunotherapeutic strategies that incite effector T cell action, cancer vaccines represent a safe and promising therapeutic approach to elicit protective and durable immune responses against components of the tumor microenvironment (TME). In this study, we investigate the pre-clinical potential of a Listeria monocytogenes (Lm)-based vaccine targeting the CRC-associated vasculature. CRC survival and progression are reliant on functioning blood vessels to effectively mediate various metabolic processes and oxygenate underlying tissues. We, therefore, advance the strategy of initiating immunity in syngeneic mouse models against the endogenous pericyte antigen RGS5, which is a critical mediator of pathological vascularization. Overall, Lm-based vaccination safely induced potent anti-tumor effects that consisted of recruiting functional Type-1-associated T cells into the TME and reducing tumor blood vessel content. This study underscores the promising clinical potential of targeting RGS5 against vascularized tumors like CRC. |
format | Online Article Text |
id | pubmed-10540654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-105406542023-09-30 Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection Anderson, Trevor S. McCormick, Amanda L. Daugherity, Elizabeth A. Oladejo, Mariam Okpalanwaka, Izuchukwu F. Smith, Savanna L. Appiah, Duke Wood, Laurence M. Lowe, Devin B. Oncoimmunology Original Research Colorectal cancer (CRC) remains a leading cause of cancer-related mortality despite efforts to improve standard interventions. As CRC patients can benefit from immunotherapeutic strategies that incite effector T cell action, cancer vaccines represent a safe and promising therapeutic approach to elicit protective and durable immune responses against components of the tumor microenvironment (TME). In this study, we investigate the pre-clinical potential of a Listeria monocytogenes (Lm)-based vaccine targeting the CRC-associated vasculature. CRC survival and progression are reliant on functioning blood vessels to effectively mediate various metabolic processes and oxygenate underlying tissues. We, therefore, advance the strategy of initiating immunity in syngeneic mouse models against the endogenous pericyte antigen RGS5, which is a critical mediator of pathological vascularization. Overall, Lm-based vaccination safely induced potent anti-tumor effects that consisted of recruiting functional Type-1-associated T cells into the TME and reducing tumor blood vessel content. This study underscores the promising clinical potential of targeting RGS5 against vascularized tumors like CRC. Taylor & Francis 2023-09-28 /pmc/articles/PMC10540654/ /pubmed/37781234 http://dx.doi.org/10.1080/2162402X.2023.2260620 Text en © 2023 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. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Original Research Anderson, Trevor S. McCormick, Amanda L. Daugherity, Elizabeth A. Oladejo, Mariam Okpalanwaka, Izuchukwu F. Smith, Savanna L. Appiah, Duke Wood, Laurence M. Lowe, Devin B. Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection |
title | Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection |
title_full | Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection |
title_fullStr | Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection |
title_full_unstemmed | Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection |
title_short | Listeria-based vaccination against the pericyte antigen RGS5 elicits anti-vascular effects and colon cancer protection |
title_sort | listeria-based vaccination against the pericyte antigen rgs5 elicits anti-vascular effects and colon cancer protection |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540654/ https://www.ncbi.nlm.nih.gov/pubmed/37781234 http://dx.doi.org/10.1080/2162402X.2023.2260620 |
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