Circadian tumor infiltration and function of CD8+ T cells dictate immunotherapy efficacy.

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Název: Circadian tumor infiltration and function of CD8+ T cells dictate immunotherapy efficacy.
Autoři: Wang, C., Zeng, Q., Gül, Z.M., Wang, S., Pick, R., Cheng, P., Bill, R., Wu, Y., Naulaerts, S., Barnoud, C., Hsueh, P.C., Moller, S.H., Cenerenti, M., Sun, M., Su, Z., Jemelin, S., Petrenko, V., Dibner, C., Hugues, S., Jandus, C., Li, Z., Michielin, O., Ho, P.C., Garg, A.D., Simonetta, F., Pittet, M.J., Scheiermann, C.
Zdroj: Cell, vol. 187, no. 11, pp. 2690-2702.e17
Rok vydání: 2024
Sbírka: Université de Lausanne (UNIL): Serval - Serveur académique lausannois
Témata: Animals, Humans, Mice, CD8-Positive T-Lymphocytes/immunology, Cell Line, Tumor, Circadian Clocks, Circadian Rhythm, Endothelial Cells/immunology, Immune Checkpoint Inhibitors/therapeutic use, Immune Checkpoint Inhibitors/pharmacology, Immunotherapy/methods, Lymphocytes, Tumor-Infiltrating/immunology, Melanoma/immunology, Melanoma/therapy, Melanoma/pathology, Inbred C57BL, Tumor Microenvironment/immunology, BMAL1, CAR T therapy, PD-1, chronotherapy, circadian, immune checkpoint blockade, immunology, melanoma, tumor-infiltrating leukocyte
Popis: The quality and quantity of tumor-infiltrating lymphocytes, particularly CD8 + T cells, are important parameters for the control of tumor growth and response to immunotherapy. Here, we show in murine and human cancers that these parameters exhibit circadian oscillations, driven by both the endogenous circadian clock of leukocytes and rhythmic leukocyte infiltration, which depends on the circadian clock of endothelial cells in the tumor microenvironment. To harness these rhythms therapeutically, we demonstrate that efficacy of chimeric antigen receptor T cell therapy and immune checkpoint blockade can be improved by adjusting the time of treatment during the day. Furthermore, time-of-day-dependent T cell signatures in murine tumor models predict overall survival in patients with melanoma and correlate with response to anti-PD-1 therapy. Our data demonstrate the functional significance of circadian dynamics in the tumor microenvironment and suggest the importance of leveraging these features for improving future clinical trial design and patient care.
Druh dokumentu: article in journal/newspaper
Popis souboru: application/pdf
Jazyk: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/38723627; info:eu-repo/semantics/altIdentifier/eissn/1097-4172; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_BEDDA80F90135; https://serval.unil.ch/notice/serval:BIB_BEDDA80F9013; https://serval.unil.ch/resource/serval:BIB_BEDDA80F9013.P001/REF.pdf
DOI: 10.1016/j.cell.2024.04.015
Dostupnost: https://serval.unil.ch/notice/serval:BIB_BEDDA80F9013
https://doi.org/10.1016/j.cell.2024.04.015
https://serval.unil.ch/resource/serval:BIB_BEDDA80F9013.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_BEDDA80F90135
Rights: info:eu-repo/semantics/openAccess ; CC BY 4.0 ; https://creativecommons.org/licenses/by/4.0/
Přístupové číslo: edsbas.935E0E3C
Databáze: BASE
Popis
Abstrakt:The quality and quantity of tumor-infiltrating lymphocytes, particularly CD8 <sup>+</sup> T cells, are important parameters for the control of tumor growth and response to immunotherapy. Here, we show in murine and human cancers that these parameters exhibit circadian oscillations, driven by both the endogenous circadian clock of leukocytes and rhythmic leukocyte infiltration, which depends on the circadian clock of endothelial cells in the tumor microenvironment. To harness these rhythms therapeutically, we demonstrate that efficacy of chimeric antigen receptor T cell therapy and immune checkpoint blockade can be improved by adjusting the time of treatment during the day. Furthermore, time-of-day-dependent T cell signatures in murine tumor models predict overall survival in patients with melanoma and correlate with response to anti-PD-1 therapy. Our data demonstrate the functional significance of circadian dynamics in the tumor microenvironment and suggest the importance of leveraging these features for improving future clinical trial design and patient care.
DOI:10.1016/j.cell.2024.04.015