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TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma
Antibodies against programmed cell death-1 (PD-1) have considerably changed the treatment for melanoma. However, many patients do not display therapeutic response or eventually relapse. Moreover, patients treated with anti-PD-1 develop immune-related adverse events that can be cured with anti-tumor...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741628/ https://www.ncbi.nlm.nih.gov/pubmed/29273790 http://dx.doi.org/10.1038/s41467-017-02358-7 |
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author | Bertrand, Florie Montfort, Anne Marcheteau, Elie Imbert, Caroline Gilhodes, Julia Filleron, Thomas Rochaix, Philippe Andrieu-Abadie, Nathalie Levade, Thierry Meyer, Nicolas Colacios, Céline Ségui, Bruno |
author_facet | Bertrand, Florie Montfort, Anne Marcheteau, Elie Imbert, Caroline Gilhodes, Julia Filleron, Thomas Rochaix, Philippe Andrieu-Abadie, Nathalie Levade, Thierry Meyer, Nicolas Colacios, Céline Ségui, Bruno |
author_sort | Bertrand, Florie |
collection | PubMed |
description | Antibodies against programmed cell death-1 (PD-1) have considerably changed the treatment for melanoma. However, many patients do not display therapeutic response or eventually relapse. Moreover, patients treated with anti-PD-1 develop immune-related adverse events that can be cured with anti-tumor necrosis factor α (TNF) antibodies. Whether anti-TNF antibodies affect the anti-cancer immune response remains unknown. Our recent work has highlighted that TNFR1-dependent TNF signalling impairs the accumulation of CD8+ tumor-infiltrating T lymphocytes (CD8+ TILs) in mouse melanoma. Herein, our results indicate that TNF or TNFR1 blockade synergizes with anti-PD-1 on anti-cancer immune responses towards solid cancers. Mechanistically, TNF blockade prevents anti-PD-1-induced TIL cell death as well as PD-L1 and TIM-3 expression. TNF expression positively correlates with expression of PD-L1 and TIM-3 in human melanoma specimens. This study provides a strong rationale to develop a combination therapy based on the use of anti-PD-1 and anti-TNF in cancer patients. |
format | Online Article Text |
id | pubmed-5741628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57416282017-12-29 TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma Bertrand, Florie Montfort, Anne Marcheteau, Elie Imbert, Caroline Gilhodes, Julia Filleron, Thomas Rochaix, Philippe Andrieu-Abadie, Nathalie Levade, Thierry Meyer, Nicolas Colacios, Céline Ségui, Bruno Nat Commun Article Antibodies against programmed cell death-1 (PD-1) have considerably changed the treatment for melanoma. However, many patients do not display therapeutic response or eventually relapse. Moreover, patients treated with anti-PD-1 develop immune-related adverse events that can be cured with anti-tumor necrosis factor α (TNF) antibodies. Whether anti-TNF antibodies affect the anti-cancer immune response remains unknown. Our recent work has highlighted that TNFR1-dependent TNF signalling impairs the accumulation of CD8+ tumor-infiltrating T lymphocytes (CD8+ TILs) in mouse melanoma. Herein, our results indicate that TNF or TNFR1 blockade synergizes with anti-PD-1 on anti-cancer immune responses towards solid cancers. Mechanistically, TNF blockade prevents anti-PD-1-induced TIL cell death as well as PD-L1 and TIM-3 expression. TNF expression positively correlates with expression of PD-L1 and TIM-3 in human melanoma specimens. This study provides a strong rationale to develop a combination therapy based on the use of anti-PD-1 and anti-TNF in cancer patients. Nature Publishing Group UK 2017-12-22 /pmc/articles/PMC5741628/ /pubmed/29273790 http://dx.doi.org/10.1038/s41467-017-02358-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bertrand, Florie Montfort, Anne Marcheteau, Elie Imbert, Caroline Gilhodes, Julia Filleron, Thomas Rochaix, Philippe Andrieu-Abadie, Nathalie Levade, Thierry Meyer, Nicolas Colacios, Céline Ségui, Bruno TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma |
title | TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma |
title_full | TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma |
title_fullStr | TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma |
title_full_unstemmed | TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma |
title_short | TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma |
title_sort | tnfα blockade overcomes resistance to anti-pd-1 in experimental melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741628/ https://www.ncbi.nlm.nih.gov/pubmed/29273790 http://dx.doi.org/10.1038/s41467-017-02358-7 |
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