Open Access
| Issue |
Med Sci (Paris)
Volume 42, Number 5, Mai 2026
|
|
|---|---|---|
| Page(s) | 451 - 458 | |
| Section | M/S Revues | |
| DOI | https://doi.org/10.1051/medsci/2026080 | |
| Published online | 29 mai 2026 | |
- Herberman RB, Nunn ME, Holden HT, et al. Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. II. Characterization of effector cells. Int J Cancer 1975 ; 16 : 230–9. [Google Scholar]
- Kiessling R, Klein E, Pross H, et al. Natural killer cells in the mouse. II. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Characteristics of the killer cell. Eur J Immunol 1975 ; 5 : 117–21. [Google Scholar]
- Kiessling R, Klein E, Wigzell H. Natural killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype. Eur J Immunol 1975 ; 5 : 112–7. [Google Scholar]
- Melsen JE, Themeli M, Ostaijen-Ten Dam MM. Protocol for isolation, stimulation and functional profiling of primary and IPSC-derived human NK cells. Bio Protoc 2020 ; 10 : 3845. [Google Scholar]
- Vivier E, Artis D, Colonna M, et al. Innate lymphoid cells: 10 years on. Cell 2018 ; 174 : 1054–66. [Google Scholar]
- Lanier LL, Le AM, Civin CI, et al. The relationship of CD16 (Leu-11) and Leu-19 (NKH-1) antigen expression on human peripheral blood NK cells and cytotoxic T lymphocytes. J Immunol 1986 ; 136 : 4480–6. [Google Scholar]
- Juelke K, Killig M, Luetke-Eversloh M. CD62L expression identifies a unique subset of polyfunctional CD56dim NK cells. Blood 2010 ; 116 : 1299–307. [Google Scholar]
- Lopez-Vergès S, Milush JM, Pandey S, et al. CD57 defines a functionally distinct population of mature NK cells in the human CD56dimCD16+ NK-cell subset. Blood 2010 ; 116 : 3865–74. [Google Scholar]
- Luetke-Eversloh M, Killig M, Romagnani C. Signatures of human NK cell development and terminal differentiation. Front Immunol 2013 ; 4 : 499. [Google Scholar]
- Yu J, Mao HC, Wei M. CD94 surface density identifies a functional intermediary between the CD56bright and CD56dim human NK-cell subsets. Blood 2010 ; 115 : 274–81. [Google Scholar]
- Bjorkstrom NK, Riese P, Heuts F. Expression patterns of NKG2A, KIR, and CD57 define a process of CD56dim NK-cell differentiation uncoupled from NK-cell education. Blood 2010 ; 116 : 3853–64. [Google Scholar]
- Hammer Q, Ruckert T, Borst EM. Peptide-specific recognition of human cytomegalovirus strains controls adaptive natural killer cells. Nat Immunol 2018 ; 19 : 453–63. [Google Scholar]
- Guma M, Angulo A, Vilches C. Imprint of human cytomegalovirus infection on the NK cell receptor repertoire. Blood 2004 ; 104 : 3664–71. [Google Scholar]
- Ruckert T, Romagnani C. Extrinsic and intrinsic drivers of natural killer cell clonality. Immunol Rev 2024 ; 323 : 80–106. [Google Scholar]
- Narni-Mancinelli E, Ugolini S, Vivier E. Les cellules natural killer: adaptation et mémoire dans le système immunitaire inné. Med Sci (Paris) 2013 ; 29 : 389–95. [Google Scholar]
- Schlums H, Cichocki F, Tesi B. Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector function. Immunity 2015 ; 42 : 443–56. [Google Scholar]
- Sojka DK, Plougastel-Douglas B, Yang L, et al. Tissue-resident natural killer (NK) cells are cell lineages distinct from thymic and conventional splenic NK cells. Elife 2014 ; 3 : e01659. [Google Scholar]
- Bjorkstrom NK, Ljunggren HG, Michaelsson J. Emerging insights into natural killer cells in human peripheral tissues. Nat Rev Immunol 2016 ; 16 : 310–20. [Google Scholar]
- Freud AG, Mundy-Bosse BL, Yu J, et al. The broad spectrum of human natural killer cell diversity. Immunity 2017 ; 47 : 820–33. [Google Scholar]
- Gao Y, Souza-Fonseca-Guimaraes F, Bald T, et al. Tumor immunoevasion by the conversion of effector NK cells into type 1 innate lymphoid cells. Nat Immunol 2017 ; 18 : 1004–15. [Google Scholar]
- Romagnani C, Juelke K, Falco M. CD56brightCD16-killer Ig-like receptor-NK cells display longer telomeres and acquire features of CD56dim NK cells upon activation. J Immunol 2007 ; 178 : 4947–55. [Google Scholar]
- Chretien A-S, Devillier R, Granjeaud S, et al. High-dimensional mass cytometry analysis of NK cell alterations in AML identifies a subgroup with adverse clinical outcome. Proc Natl Acad Sci USA 2021 ; 118 : e2020459118. [Google Scholar]
- Horowitz A, Strauss-Albee DM, Leipold M. Genetic and environmental determinants of human NK cell diversity revealed by mass cytometry. Sci Transl Med 2013 ; 5 : 208ra145. [Google Scholar]
- Coënon L, Geindreau M, Ghiringhelli F, et al. Natural killer cells at the frontline in the fight against cancer. Cell Death Dis 2024 ; 15 : 614. [Google Scholar]
- Paul S, Lal G. The molecular mechanism of natural killer cells function and its importance in cancer immunotherapy. Front Immunol 2017 ; 8 : 1124. [Google Scholar]
- Böttcher JP, Bonavita E, Chakravarty P, et al. NK cells stimulate recruitment of cDC1 into the tumor microenvironment promoting cancer immune control. Cell 2018 ; 172 : 1022–1037.e14. [Google Scholar]
- Allen F, Bobanga ID, Rauhe P, et al. CCL3 augments tumor rejection and enhances CD8+T cell infiltration through NK and CD103+ dendritic cell recruitment via IFNγ. Oncoimmunology 2018 ; 7 : e1393598. [Google Scholar]
- Lopez-Soto A, Gonzalez S, Smyth MJ, et al. Control of metastasis by NK cells. Cancer Cell 2017 ; 32 : 135–54. [Google Scholar]
- Huergo-Zapico L, Acebes-Huerta A, Lopez-Soto A. Molecular bases for the regulation of NKG2D ligands in cancer. Front Immunol 2014 ; 5 : 106. [Google Scholar]
- Okumura G, Iguchi-Manaka A, Murata R, et al. Tumor-derived soluble CD155 inhibits DNAM-1–mediated antitumor activity of natural killer cells. J Exp Med 2020 ; 217 : e20191290. [Google Scholar]
- Merino AM, Kim H, Miller JS, et al. Unraveling exhaustion in adaptive and conventional NK cells. J Leukoc Biol 2020 ; 108 : 1361–8. [Google Scholar]
- Platonova S, Cherfils-Vicini J, Damotte D. Profound coordinated alterations of intratumoral NK cell phenotype and function in lung carcinoma. Cancer Res 2011 ; 71 : 5412–22. [Google Scholar]
- Sun C, Xu J, Huang Q. High NKG2A expression contributes to NK cell exhaustion and predicts a poor prognosis of patients with liver cancer. Oncoimmunology 2017 ; 6 : e1264562. [Google Scholar]
- Cornen S, Andre P, Gauthier L. Les cellules natural killer : des cibles prometteuses dans la thérapie contre le cancer. Med Sci (Paris 2019 ; 35 : 990–2. [Google Scholar]
- Vijayan D, Young A, Teng MWL, et al. Targeting immunosuppressive adenosine in cancer. Nat Rev Cancer 2017 ; 17 : 709–24. [Google Scholar]
- Holt D, Ma X, Kundu N, et al. Prostaglandin E(2) (PGE (2)) suppresses natural killer cell function primarily through the PGE(2) receptor EP4. Cancer Immunol Immunother 2011 ; 60 : 1577–86. [Google Scholar]
- Rautela J, Dagley LF, Oliveira CC. Therapeutic blockade of activin-A improves NK cell function and antitumor immunity. Sci Signal 2019 ; 12 : eaat7527. [Google Scholar]
- Ma S, Caligiuri MA, Yu J. Harnessing natural killer cells for lung cancer therapy. Cancer Res 2023 ; 83 : 3327–39. [Google Scholar]
- Trzonkowski P, Szmit E, Mysliwska J. CD4+CD25+ T regulatory cells inhibit cytotoxic activity of T CD8+ and NK lymphocytes in the direct cell-to-cell interaction. Clin Immunol 2004 ; 112 : 258–67. [Google Scholar]
- Park MD, Reyes-Torres I, LeBerichel J. TREM2 macrophages drive NK cell paucity and dysfunction in lung cancer. Nat Immunol 2023 ; 24 : 792–801. [Google Scholar]
- Wherry EJ, Kurachi M. Molecular and cellular insights into T cell exhaustion. Nat Rev Immunol 2015 ; 15 : 486–99. [Google Scholar]
- Pouxvielh K, Marotel M, Drouillard A, et al. Tumor-induced natural killer cell dysfunction is a rapid and reversible process uncoupled from the expression of immune checkpoints. Sci Adv 2024 ; 10 : eadn0164. [Google Scholar]
- Rebuffet L, Melsen JE, Escalière B, et al. High-dimensional single-cell analysis of human natural killer cell heterogeneity. Nat Immunol 2024 ; 25 : 1474–88. [Google Scholar]
- Hao Y, Hao S, Andersen-Nissen E, et al. Integrated analysis of multimodal single-cell data. Cell 2021 ; 184 : 3573–3587.e29. [Google Scholar]
- Ding Y, Lavaert M, Grassmann S, et al. Distinct developmental pathways generate functionally distinct populations of natural killer cells. Nat Immunol 2024 ; 25 : 1183–92. [Google Scholar]
- Tang F, Li J, Qi L, et al. A pan-cancer single-cell panorama of human natural killer cells. Cell 2023 ; 186 : 4235–4251.e20. [Google Scholar]
- Netskar H, Pfefferle A, Goodridge JP, et al. Pan-cancer profiling of tumor-infiltrating natural killer cells through transcriptional reference mapping. Nat Immunol 2024 ; 25 : 1445–59. [Google Scholar]
- Serger C, Rebuffet L, Sandholzer MT, et al. Integrated single cell analysis identifies CD39+ tumor-associated NK cells with cytotoxic potential in lung cancer. 2025. [Google Scholar]
- Duhen T, Duhen R, Montler R. Co-expression of CD39 and CD103 identifies tumor-reactive CD8 T cells in human solid tumors. Nat Commun 2018 ; 9 : 2724. [Google Scholar]
- Cayatte M, Picant V, Vétizou M, et al. Bringing natural killer cells to the clinic: Opportunities beyond cancer. J Exp Med 2026 ; 223 : e20250612. [Google Scholar]
- Bernard PL, Laletin V, Pastor S, et al. Une piste en immunothérapie du cancer : cibler la signalisation des cellules NK. Med Sci (Paris) 2020 ; 36 : 50–5. [Google Scholar]
- Romee R, Rosario M, Berrien-Elliott MM, et al. Cytokine-induced memory-like natural killer cells exhibit enhanced responses against myeloid leukemia. Sci Transl Med 2016 ; 8 : 357ra123. [Google Scholar]
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