Liver metastases are relatively resistant to checkpoint blockade immunotherapy. The hepatic tissue has distinctive features including high numbers of NK cells. It was therefore important to conduct in-depth single-cell analysis of NK cells in colorectal cancer liver metastases (CRLMs) with an effort to dissect their diversity and to identify candidate therapeutic targets. By combining unbiased single-cell transcriptomic with multiparametric flow cytometry analysis, we identified an abundant level of chemokines, and targetable immune checkpoints, including CXCR4 and the IL-1 receptor family member IL-1R8. CXCR4 pharmacological blocking and an anti-IL-1R8 mAb enhanced the effector function of CRLM NK cells. Targeting the diversity of liver NK cells and their distinct immune checkpoint repertoires is key to optimize the current immune therapy protocols in CRLM.
Tissue-specific antitumor NK cell subsets identified in colorectal cancer liver metastases express candidate therapeutic targets / J. Mikulak, D. Supino, P. Marzano, S. Terzoli, R. Carriero, V. Cazzetta, R. Piazza, E. Bruni, P. Kunderfranco, A. Donato, S.N. Mapelli, R. Garuti, S. Carnevale, F. Scavello, E. Magrini, J. Zeleznjak, C. Peano, M. Donadon, G. Costa, G. Torzilli, A. Mantovani, C. Garlanda, D. Mavilio. - In: THE JOURNAL OF CLINICAL INVESTIGATION. - ISSN 1558-8238. - 135:24(2025 Dec 15), pp. e190778.1-e190778.19. [10.1172/JCI190778]
Tissue-specific antitumor NK cell subsets identified in colorectal cancer liver metastases express candidate therapeutic targets
J. MikulakCo-primo
;P. MarzanoSecondo
;V. Cazzetta;M. Donadon;G. Costa;G. Torzilli;A. Mantovani;D. Mavilio
Ultimo
2025
Abstract
Liver metastases are relatively resistant to checkpoint blockade immunotherapy. The hepatic tissue has distinctive features including high numbers of NK cells. It was therefore important to conduct in-depth single-cell analysis of NK cells in colorectal cancer liver metastases (CRLMs) with an effort to dissect their diversity and to identify candidate therapeutic targets. By combining unbiased single-cell transcriptomic with multiparametric flow cytometry analysis, we identified an abundant level of chemokines, and targetable immune checkpoints, including CXCR4 and the IL-1 receptor family member IL-1R8. CXCR4 pharmacological blocking and an anti-IL-1R8 mAb enhanced the effector function of CRLM NK cells. Targeting the diversity of liver NK cells and their distinct immune checkpoint repertoires is key to optimize the current immune therapy protocols in CRLM.| File | Dimensione | Formato | |
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