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Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy

The use of dendritic cells (DCs) to generate effective anti-tumor T cell immunity has garnered much attention over the last thirty-plus years. Despite this, limited clinical benefit has been demonstrated thus far. There has been a revival of interest in DC-based treatment strategies following the re...

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Detalles Bibliográficos
Autores principales: Audsley, Katherine M., McDonnell, Alison M., Waithman, Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140519/
https://www.ncbi.nlm.nih.gov/pubmed/32121071
http://dx.doi.org/10.3390/cells9030565
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author Audsley, Katherine M.
McDonnell, Alison M.
Waithman, Jason
author_facet Audsley, Katherine M.
McDonnell, Alison M.
Waithman, Jason
author_sort Audsley, Katherine M.
collection PubMed
description The use of dendritic cells (DCs) to generate effective anti-tumor T cell immunity has garnered much attention over the last thirty-plus years. Despite this, limited clinical benefit has been demonstrated thus far. There has been a revival of interest in DC-based treatment strategies following the remarkable patient responses observed with novel checkpoint blockade therapies, due to the potential for synergistic treatment. Cross-presenting DCs are recognized for their ability to prime CD8(+) T cell responses to directly induce tumor death. Consequently, they are an attractive target for next-generation DC-based strategies. In this review, we define the universal classification system for cross-presenting DCs, and the vital role of this subset in mediating anti-tumor immunity. Furthermore, we will detail methods of targeting these DCs both ex vivo and in vivo to boost their function and drive effective anti-tumor responses.
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spelling pubmed-71405192020-04-13 Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy Audsley, Katherine M. McDonnell, Alison M. Waithman, Jason Cells Review The use of dendritic cells (DCs) to generate effective anti-tumor T cell immunity has garnered much attention over the last thirty-plus years. Despite this, limited clinical benefit has been demonstrated thus far. There has been a revival of interest in DC-based treatment strategies following the remarkable patient responses observed with novel checkpoint blockade therapies, due to the potential for synergistic treatment. Cross-presenting DCs are recognized for their ability to prime CD8(+) T cell responses to directly induce tumor death. Consequently, they are an attractive target for next-generation DC-based strategies. In this review, we define the universal classification system for cross-presenting DCs, and the vital role of this subset in mediating anti-tumor immunity. Furthermore, we will detail methods of targeting these DCs both ex vivo and in vivo to boost their function and drive effective anti-tumor responses. MDPI 2020-02-28 /pmc/articles/PMC7140519/ /pubmed/32121071 http://dx.doi.org/10.3390/cells9030565 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Audsley, Katherine M.
McDonnell, Alison M.
Waithman, Jason
Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy
title Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy
title_full Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy
title_fullStr Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy
title_full_unstemmed Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy
title_short Cross-Presenting XCR1(+) Dendritic Cells as Targets for Cancer Immunotherapy
title_sort cross-presenting xcr1(+) dendritic cells as targets for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140519/
https://www.ncbi.nlm.nih.gov/pubmed/32121071
http://dx.doi.org/10.3390/cells9030565
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