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Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma
Lenvatinib was expected to enhance the effect of immune checkpoint inhibitors (ICIs) for unresectable HCC; however, their combination therapy failed to show the synergy in the phase III clinical trial. METHODS: To elucidate lenvatinib-induced molecular modulation, we performed bulk RNA-sequencing an...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351952/ https://www.ncbi.nlm.nih.gov/pubmed/37471053 http://dx.doi.org/10.1097/HC9.0000000000000209 |
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author | Yamada, Tomoharu Fujiwara, Naoto Kubota, Naoto Matsushita, Yuki Nakatsuka, Takuma Kurosaki, Shigeyuki Minami, Tatsuya Tateishi, Ryosuke Ichida, Akihiko Arita, Junichi Hasegawa, Kiyoshi Koike, Kazuhiko Fujishiro, Mitsuhiro Nakagawa, Hayato |
author_facet | Yamada, Tomoharu Fujiwara, Naoto Kubota, Naoto Matsushita, Yuki Nakatsuka, Takuma Kurosaki, Shigeyuki Minami, Tatsuya Tateishi, Ryosuke Ichida, Akihiko Arita, Junichi Hasegawa, Kiyoshi Koike, Kazuhiko Fujishiro, Mitsuhiro Nakagawa, Hayato |
author_sort | Yamada, Tomoharu |
collection | PubMed |
description | Lenvatinib was expected to enhance the effect of immune checkpoint inhibitors (ICIs) for unresectable HCC; however, their combination therapy failed to show the synergy in the phase III clinical trial. METHODS: To elucidate lenvatinib-induced molecular modulation, we performed bulk RNA-sequencing and digital spatial profiling of 5 surgically resected human HCC specimens after lenvatinib treatment and 10 matched controls without any preceding therapy. FINDINGS: Besides its direct antitumor effects, lenvatinib recruited cytotoxic GZMK+CD8 T cells in intratumor stroma by CXCL9 from tumor-associated macrophages, suggesting that lenvatinib-treated HCC is in the so-called excluded condition that can diminish ICI efficacy. |
format | Online Article Text |
id | pubmed-10351952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-103519522023-07-18 Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma Yamada, Tomoharu Fujiwara, Naoto Kubota, Naoto Matsushita, Yuki Nakatsuka, Takuma Kurosaki, Shigeyuki Minami, Tatsuya Tateishi, Ryosuke Ichida, Akihiko Arita, Junichi Hasegawa, Kiyoshi Koike, Kazuhiko Fujishiro, Mitsuhiro Nakagawa, Hayato Hepatol Commun Research Letter Lenvatinib was expected to enhance the effect of immune checkpoint inhibitors (ICIs) for unresectable HCC; however, their combination therapy failed to show the synergy in the phase III clinical trial. METHODS: To elucidate lenvatinib-induced molecular modulation, we performed bulk RNA-sequencing and digital spatial profiling of 5 surgically resected human HCC specimens after lenvatinib treatment and 10 matched controls without any preceding therapy. FINDINGS: Besides its direct antitumor effects, lenvatinib recruited cytotoxic GZMK+CD8 T cells in intratumor stroma by CXCL9 from tumor-associated macrophages, suggesting that lenvatinib-treated HCC is in the so-called excluded condition that can diminish ICI efficacy. Lippincott Williams & Wilkins 2023-07-17 /pmc/articles/PMC10351952/ /pubmed/37471053 http://dx.doi.org/10.1097/HC9.0000000000000209 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/) (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Letter Yamada, Tomoharu Fujiwara, Naoto Kubota, Naoto Matsushita, Yuki Nakatsuka, Takuma Kurosaki, Shigeyuki Minami, Tatsuya Tateishi, Ryosuke Ichida, Akihiko Arita, Junichi Hasegawa, Kiyoshi Koike, Kazuhiko Fujishiro, Mitsuhiro Nakagawa, Hayato Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma |
title | Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma |
title_full | Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma |
title_fullStr | Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma |
title_full_unstemmed | Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma |
title_short | Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma |
title_sort | lenvatinib recruits cytotoxic gzmk+cd8 t cells in hepatocellular carcinoma |
topic | Research Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351952/ https://www.ncbi.nlm.nih.gov/pubmed/37471053 http://dx.doi.org/10.1097/HC9.0000000000000209 |
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