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Trial watch: Toll-like receptor ligands in cancer therapy

Accumulating evidence indicates that Toll-like receptor (TLR) agonists proficiently (re)instore cancer immunosurveillance as immunological adjuvants. So far, three TLR agonists have been approved by regulatory agencies for use in oncological applications. Additionally, these immunotherapeutics have...

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Autores principales: Le Naour, Julie, Kroemer, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980677/
https://www.ncbi.nlm.nih.gov/pubmed/36875550
http://dx.doi.org/10.1080/2162402X.2023.2180237
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author Le Naour, Julie
Kroemer, Guido
author_facet Le Naour, Julie
Kroemer, Guido
author_sort Le Naour, Julie
collection PubMed
description Accumulating evidence indicates that Toll-like receptor (TLR) agonists proficiently (re)instore cancer immunosurveillance as immunological adjuvants. So far, three TLR agonists have been approved by regulatory agencies for use in oncological applications. Additionally, these immunotherapeutics have been extensively investigated over the past few years. Multiple clinical trials are currently evaluating the combination of TLR agonists with chemotherapy, radiotherapy, or different immunotherapies. Moreover, antibodies targeting tumor-enriched surface proteins that have been conjugated to TLR agonists are being developed to stimulate anticancer immune responses specifically within the tumor microenvironment. Solid preclinical and translational results support the favorable immune-activating effects of TLR agonists. Here, we summarize recent preclinical and clinical advances in the development of TLR agonists for anticancer immunotherapy.
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spelling pubmed-99806772023-03-03 Trial watch: Toll-like receptor ligands in cancer therapy Le Naour, Julie Kroemer, Guido Oncoimmunology Trial Watch Accumulating evidence indicates that Toll-like receptor (TLR) agonists proficiently (re)instore cancer immunosurveillance as immunological adjuvants. So far, three TLR agonists have been approved by regulatory agencies for use in oncological applications. Additionally, these immunotherapeutics have been extensively investigated over the past few years. Multiple clinical trials are currently evaluating the combination of TLR agonists with chemotherapy, radiotherapy, or different immunotherapies. Moreover, antibodies targeting tumor-enriched surface proteins that have been conjugated to TLR agonists are being developed to stimulate anticancer immune responses specifically within the tumor microenvironment. Solid preclinical and translational results support the favorable immune-activating effects of TLR agonists. Here, we summarize recent preclinical and clinical advances in the development of TLR agonists for anticancer immunotherapy. Taylor & Francis 2023-02-17 /pmc/articles/PMC9980677/ /pubmed/36875550 http://dx.doi.org/10.1080/2162402X.2023.2180237 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.
spellingShingle Trial Watch
Le Naour, Julie
Kroemer, Guido
Trial watch: Toll-like receptor ligands in cancer therapy
title Trial watch: Toll-like receptor ligands in cancer therapy
title_full Trial watch: Toll-like receptor ligands in cancer therapy
title_fullStr Trial watch: Toll-like receptor ligands in cancer therapy
title_full_unstemmed Trial watch: Toll-like receptor ligands in cancer therapy
title_short Trial watch: Toll-like receptor ligands in cancer therapy
title_sort trial watch: toll-like receptor ligands in cancer therapy
topic Trial Watch
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980677/
https://www.ncbi.nlm.nih.gov/pubmed/36875550
http://dx.doi.org/10.1080/2162402X.2023.2180237
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