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Interleukin-10-regulated tumour tolerance in non-small cell lung cancer
BACKGROUND: Lung cancer is the most life-threatening cancer type worldwide. Treatment options include surgery, radio- and chemotherapy, as well as the use of immunomodulatory antibodies. Interleukin (IL)-10 is an immunosuppressive cytokine involved in tumour immune escape. METHODS: Immunohistochemis...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729436/ https://www.ncbi.nlm.nih.gov/pubmed/29016555 http://dx.doi.org/10.1038/bjc.2017.336 |
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author | Vahl, Julius Malte Friedrich, Juliane Mittler, Susanne Trump, Sonja Heim, Lisanne Kachler, Katerina Balabko, Liubov Fuhrich, Nicole Geppert, Carol-Immanuel Trufa, Denis Iulian Sopel, Nina Rieker, Ralf Sirbu, Horia Finotto, Susetta |
author_facet | Vahl, Julius Malte Friedrich, Juliane Mittler, Susanne Trump, Sonja Heim, Lisanne Kachler, Katerina Balabko, Liubov Fuhrich, Nicole Geppert, Carol-Immanuel Trufa, Denis Iulian Sopel, Nina Rieker, Ralf Sirbu, Horia Finotto, Susetta |
author_sort | Vahl, Julius Malte |
collection | PubMed |
description | BACKGROUND: Lung cancer is the most life-threatening cancer type worldwide. Treatment options include surgery, radio- and chemotherapy, as well as the use of immunomodulatory antibodies. Interleukin (IL)-10 is an immunosuppressive cytokine involved in tumour immune escape. METHODS: Immunohistochemistry (IHC) on human lung surgery tissue as well as human tumour cell line cultures, FACS analysis, real-time PCR and experimental lung cancer. RESULTS: Here we discovered a positive correlation between IL-10 and IL-10 receptor (IL-10R) expression in the lung with tumour diameter in patients with lung cancer (non-small cell lung cancer), the most life-threatening cancer type worldwide. IL-10 and IL-10R were found induced in cells surrounding the lung tumour cells, and IL-10R was mainly expressed on the surface of Foxp-3(+) T-regulatory lymphocytes infiltrating the tumour of these patients where its expression inversely correlated with programmed cell death 1. These findings were confirmed in translational studies. In a human lung adenocarcinoma cell line, IL-10R was found induced under metabolic restrictions present during tumour growth, whereby IL-10 inhibited PDL1 and tumour cell apoptosis. CONCLUSIONS: These new findings suggest that IL-10 counteracts IFN-γ effects on PD1/PDL1 pathway, resulting in possible resistance of the tumour to anti-PD1/PDL1 immunotherapy. |
format | Online Article Text |
id | pubmed-5729436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57294362018-11-21 Interleukin-10-regulated tumour tolerance in non-small cell lung cancer Vahl, Julius Malte Friedrich, Juliane Mittler, Susanne Trump, Sonja Heim, Lisanne Kachler, Katerina Balabko, Liubov Fuhrich, Nicole Geppert, Carol-Immanuel Trufa, Denis Iulian Sopel, Nina Rieker, Ralf Sirbu, Horia Finotto, Susetta Br J Cancer Translational Therapeutics BACKGROUND: Lung cancer is the most life-threatening cancer type worldwide. Treatment options include surgery, radio- and chemotherapy, as well as the use of immunomodulatory antibodies. Interleukin (IL)-10 is an immunosuppressive cytokine involved in tumour immune escape. METHODS: Immunohistochemistry (IHC) on human lung surgery tissue as well as human tumour cell line cultures, FACS analysis, real-time PCR and experimental lung cancer. RESULTS: Here we discovered a positive correlation between IL-10 and IL-10 receptor (IL-10R) expression in the lung with tumour diameter in patients with lung cancer (non-small cell lung cancer), the most life-threatening cancer type worldwide. IL-10 and IL-10R were found induced in cells surrounding the lung tumour cells, and IL-10R was mainly expressed on the surface of Foxp-3(+) T-regulatory lymphocytes infiltrating the tumour of these patients where its expression inversely correlated with programmed cell death 1. These findings were confirmed in translational studies. In a human lung adenocarcinoma cell line, IL-10R was found induced under metabolic restrictions present during tumour growth, whereby IL-10 inhibited PDL1 and tumour cell apoptosis. CONCLUSIONS: These new findings suggest that IL-10 counteracts IFN-γ effects on PD1/PDL1 pathway, resulting in possible resistance of the tumour to anti-PD1/PDL1 immunotherapy. Nature Publishing Group 2017-11-21 2017-10-10 /pmc/articles/PMC5729436/ /pubmed/29016555 http://dx.doi.org/10.1038/bjc.2017.336 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Translational Therapeutics Vahl, Julius Malte Friedrich, Juliane Mittler, Susanne Trump, Sonja Heim, Lisanne Kachler, Katerina Balabko, Liubov Fuhrich, Nicole Geppert, Carol-Immanuel Trufa, Denis Iulian Sopel, Nina Rieker, Ralf Sirbu, Horia Finotto, Susetta Interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
title | Interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
title_full | Interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
title_fullStr | Interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
title_full_unstemmed | Interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
title_short | Interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
title_sort | interleukin-10-regulated tumour tolerance in non-small cell lung cancer |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729436/ https://www.ncbi.nlm.nih.gov/pubmed/29016555 http://dx.doi.org/10.1038/bjc.2017.336 |
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