Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers
Recent clinical trials combining MEK inhibitors with anti-PD-L1 in solid tumours show moderate responses. Here, the authors demonstrate that the combination of MEK inhibition and PD-L1 blockade in KRAS mutant lung cancer models leads to a transient tumour regressions and resistance due to increased...
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Nature Portfolio
2021
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oai:doaj.org-article:c550e9da14dd40faac0c52202ab9def22021-12-02T16:57:12ZTh17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers10.1038/s41467-021-22875-w2041-1723https://doaj.org/article/c550e9da14dd40faac0c52202ab9def22021-05-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-22875-whttps://doaj.org/toc/2041-1723Recent clinical trials combining MEK inhibitors with anti-PD-L1 in solid tumours show moderate responses. Here, the authors demonstrate that the combination of MEK inhibition and PD-L1 blockade in KRAS mutant lung cancer models leads to a transient tumour regressions and resistance due to increased infiltration of Th17 cells and that the triple therapy targeting MEK, PD-L1 and IL-17 produced better in vivo responses.David H. PengB. Leticia RodriguezLixia DiaoPierre-Olivier GaudreauAparna PadhyeJessica M. KonenJoshua K. OchiengCaleb A. ClassJared J. FradetteLaura GibsonLimo ChenJing WangLauren A. ByersDon. L. GibbonsNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-15 (2021) |
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Science Q David H. Peng B. Leticia Rodriguez Lixia Diao Pierre-Olivier Gaudreau Aparna Padhye Jessica M. Konen Joshua K. Ochieng Caleb A. Class Jared J. Fradette Laura Gibson Limo Chen Jing Wang Lauren A. Byers Don. L. Gibbons Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers |
description |
Recent clinical trials combining MEK inhibitors with anti-PD-L1 in solid tumours show moderate responses. Here, the authors demonstrate that the combination of MEK inhibition and PD-L1 blockade in KRAS mutant lung cancer models leads to a transient tumour regressions and resistance due to increased infiltration of Th17 cells and that the triple therapy targeting MEK, PD-L1 and IL-17 produced better in vivo responses. |
format |
article |
author |
David H. Peng B. Leticia Rodriguez Lixia Diao Pierre-Olivier Gaudreau Aparna Padhye Jessica M. Konen Joshua K. Ochieng Caleb A. Class Jared J. Fradette Laura Gibson Limo Chen Jing Wang Lauren A. Byers Don. L. Gibbons |
author_facet |
David H. Peng B. Leticia Rodriguez Lixia Diao Pierre-Olivier Gaudreau Aparna Padhye Jessica M. Konen Joshua K. Ochieng Caleb A. Class Jared J. Fradette Laura Gibson Limo Chen Jing Wang Lauren A. Byers Don. L. Gibbons |
author_sort |
David H. Peng |
title |
Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers |
title_short |
Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers |
title_full |
Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers |
title_fullStr |
Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers |
title_full_unstemmed |
Th17 cells contribute to combination MEK inhibitor and anti-PD-L1 therapy resistance in KRAS/p53 mutant lung cancers |
title_sort |
th17 cells contribute to combination mek inhibitor and anti-pd-l1 therapy resistance in kras/p53 mutant lung cancers |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/c550e9da14dd40faac0c52202ab9def2 |
work_keys_str_mv |
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