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Tumor-infiltrating dendritic cell states are conserved across solid human cancers

Dendritic cells (DCs) contribute a small fraction of the tumor microenvironment but are emerging as an essential antitumor component based on their ability to foster T cell immunity and immunotherapy responses. Here, we discuss our expanding view of DC heterogeneity in human tumors, as revealed with...

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Autores principales: Gerhard, Genevieve M., Bill, Ruben, Messemaker, Marius, Klein, Allon M., Pittet, Mikael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754678/
https://www.ncbi.nlm.nih.gov/pubmed/33601412
http://dx.doi.org/10.1084/jem.20200264
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author Gerhard, Genevieve M.
Bill, Ruben
Messemaker, Marius
Klein, Allon M.
Pittet, Mikael J.
author_facet Gerhard, Genevieve M.
Bill, Ruben
Messemaker, Marius
Klein, Allon M.
Pittet, Mikael J.
author_sort Gerhard, Genevieve M.
collection PubMed
description Dendritic cells (DCs) contribute a small fraction of the tumor microenvironment but are emerging as an essential antitumor component based on their ability to foster T cell immunity and immunotherapy responses. Here, we discuss our expanding view of DC heterogeneity in human tumors, as revealed with meta-analysis of single-cell transcriptome profiling studies. We further examine tumor-infiltrating DC states that are conserved across patients, cancer types, and species and consider the fundamental and clinical relevance of these findings. Finally, we provide an outlook on research opportunities to further explore mechanisms governing tumor-infiltrating DC behavior and functions.
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spelling pubmed-77546782021-07-04 Tumor-infiltrating dendritic cell states are conserved across solid human cancers Gerhard, Genevieve M. Bill, Ruben Messemaker, Marius Klein, Allon M. Pittet, Mikael J. J Exp Med Review Dendritic cells (DCs) contribute a small fraction of the tumor microenvironment but are emerging as an essential antitumor component based on their ability to foster T cell immunity and immunotherapy responses. Here, we discuss our expanding view of DC heterogeneity in human tumors, as revealed with meta-analysis of single-cell transcriptome profiling studies. We further examine tumor-infiltrating DC states that are conserved across patients, cancer types, and species and consider the fundamental and clinical relevance of these findings. Finally, we provide an outlook on research opportunities to further explore mechanisms governing tumor-infiltrating DC behavior and functions. Rockefeller University Press 2020-12-18 /pmc/articles/PMC7754678/ /pubmed/33601412 http://dx.doi.org/10.1084/jem.20200264 Text en © 2020 Gerhard 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 Review
Gerhard, Genevieve M.
Bill, Ruben
Messemaker, Marius
Klein, Allon M.
Pittet, Mikael J.
Tumor-infiltrating dendritic cell states are conserved across solid human cancers
title Tumor-infiltrating dendritic cell states are conserved across solid human cancers
title_full Tumor-infiltrating dendritic cell states are conserved across solid human cancers
title_fullStr Tumor-infiltrating dendritic cell states are conserved across solid human cancers
title_full_unstemmed Tumor-infiltrating dendritic cell states are conserved across solid human cancers
title_short Tumor-infiltrating dendritic cell states are conserved across solid human cancers
title_sort tumor-infiltrating dendritic cell states are conserved across solid human cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754678/
https://www.ncbi.nlm.nih.gov/pubmed/33601412
http://dx.doi.org/10.1084/jem.20200264
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