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Macrophage-Mediated Subversion of Anti-Tumour Immunity

Despite the incredible clinical benefits obtained by the use of immune checkpoint blockers (ICBs), resistance is still common for many types of cancer. Central for ICBs to work is activation and infiltration of cytotoxic CD8(+) T cells following tumour-antigen recognition. However, it is now accepte...

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Detalles Bibliográficos
Autores principales: Quaranta, Valeria, Schmid, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678757/
https://www.ncbi.nlm.nih.gov/pubmed/31331034
http://dx.doi.org/10.3390/cells8070747
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author Quaranta, Valeria
Schmid, Michael C.
author_facet Quaranta, Valeria
Schmid, Michael C.
author_sort Quaranta, Valeria
collection PubMed
description Despite the incredible clinical benefits obtained by the use of immune checkpoint blockers (ICBs), resistance is still common for many types of cancer. Central for ICBs to work is activation and infiltration of cytotoxic CD8(+) T cells following tumour-antigen recognition. However, it is now accepted that even in the case of immunogenic tumours, the effector functions of CD8(+) T cells are highly compromised by the presence of an immunosuppressive tumour microenvironment (TME) at the tumour site. Tumour-associated macrophages (TAMs) are among the most abundant non-malignant stromal cell types within the TME and they are crucial drivers of tumour progression, metastasis and resistance to therapy. TAMs are able to regulate either directly or indirectly various aspects of tumour immunity, including T cell recruitment and functions. In this review we discuss the mechanisms by which TAMs subvert CD8(+) T cell immune surveillance and how their targeting in combination with ICBs represents a very powerful therapeutic strategy.
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spelling pubmed-66787572019-08-19 Macrophage-Mediated Subversion of Anti-Tumour Immunity Quaranta, Valeria Schmid, Michael C. Cells Review Despite the incredible clinical benefits obtained by the use of immune checkpoint blockers (ICBs), resistance is still common for many types of cancer. Central for ICBs to work is activation and infiltration of cytotoxic CD8(+) T cells following tumour-antigen recognition. However, it is now accepted that even in the case of immunogenic tumours, the effector functions of CD8(+) T cells are highly compromised by the presence of an immunosuppressive tumour microenvironment (TME) at the tumour site. Tumour-associated macrophages (TAMs) are among the most abundant non-malignant stromal cell types within the TME and they are crucial drivers of tumour progression, metastasis and resistance to therapy. TAMs are able to regulate either directly or indirectly various aspects of tumour immunity, including T cell recruitment and functions. In this review we discuss the mechanisms by which TAMs subvert CD8(+) T cell immune surveillance and how their targeting in combination with ICBs represents a very powerful therapeutic strategy. MDPI 2019-07-19 /pmc/articles/PMC6678757/ /pubmed/31331034 http://dx.doi.org/10.3390/cells8070747 Text en © 2019 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
Quaranta, Valeria
Schmid, Michael C.
Macrophage-Mediated Subversion of Anti-Tumour Immunity
title Macrophage-Mediated Subversion of Anti-Tumour Immunity
title_full Macrophage-Mediated Subversion of Anti-Tumour Immunity
title_fullStr Macrophage-Mediated Subversion of Anti-Tumour Immunity
title_full_unstemmed Macrophage-Mediated Subversion of Anti-Tumour Immunity
title_short Macrophage-Mediated Subversion of Anti-Tumour Immunity
title_sort macrophage-mediated subversion of anti-tumour immunity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678757/
https://www.ncbi.nlm.nih.gov/pubmed/31331034
http://dx.doi.org/10.3390/cells8070747
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