Acknowledgement
This research was supported by the National Research Foundation of Korea (NRF), funded by the Korea Government (MSIT) (Grant Nos. RS-2023-00242443, RS-2024-00345126, and RS-2025-00519514), a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health and Welfare, Korea (Grant No. KH129441), and the Future Medicine 2030 Project of the Samsung Medical Center (Grant No. SMO1250091).
References
- Vivier E, Artis D, Colonna M, Diefenbach A, Di Santo JP, Eberl G, et al. Innate lymphoid cells: 10 years on. Cell 2018;174:1054-66. https://doi.org/10.1016/j.cell.2018.07.017
- Fauriat C, Long EO, Ljunggren HG, Bryceson YT. Regulation of human NK-cell cytokine and chemokine production by target cell recognition. Blood 2010;115:2167-76. https://doi.org/10.1182/blood-2009-08-238469
- Rebuffet L, Melsen JE, Escalière B, Basurto-Lozada D, Bhandoola A, Björkström NK, et al. High-dimensional single-cell analysis of human natural killer cell heterogeneity. Nat Immunol 2024;25:1474-88.
- Henter JI, Horne A, Aricó M, Egeler RM, Filipovich AH, Imashuku S, et al. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 2007;48:124-31. https://doi.org/10.1002/pbc.v48:2
- Zoref-Lorenz A, Murakami J, Hofstetter L, Iyer S, Alotaibi AS, Mohamed SF, et al. An improved index for diagnosis and mortality prediction in malignancy-associated hemophagocytic lymphohistiocytosis. Blood 2022;139:1098-110.
- Kucuksezer UC, Aktas Cetin E, Esen F, Tahrali I, Akdeniz N, Gelmez MY, et al. The role of natural killer cells in autoimmune diseases. Front Immunol 2021;12:622306. https://doi.org/10.3389/fimmu.2021.622306
- Coënon L, Geindreau M, Ghiringhelli F, Villalba M, Bruchard M. Natural killer cells at the frontline in the fight against cancer. Cell Death Dis 2024;15:614.
- Björkström NK, Strunz B, Ljunggren HG. Natural killer cells in antiviral immunity. Nat Rev Immunol 2022;22:112-23. https://doi.org/10.1038/s41577-021-00558-3
- Freud AG, Mundy-Bosse BL, Yu J, Caligiuri MA. The broad spectrum of human natural killer cell diversity. Immunity 2017;47:820-33. https://doi.org/10.1016/j.immuni.2017.10.008
- Bernardini G, Gismondi A, Santoni A. Chemokines and NK cells: Regulators of development, trafficking and functions. Immunol Lett 2012;145:39-46. https://doi.org/10.1016/j.imlet.2012.04.014
- Xie M, Li Y, Meng YZ, Xu P, Yang YG, Dong S, et al. Uterine natural killer cells: A rising star in human pregnancy regulation. Front Immunol 2022;13:918550. https://doi.org/10.3389/fimmu.2022.918550
- Peng H and Sun R. Liver-resident NK cells and their potential functions. Cell Mol Immunol 2017;14:890-4. https://doi.org/10.1038/cmi.2017.72
- Liu S, Dhar P, Wu JD. NK cell plasticity in cancer. J Clin Med 2019;8:1492. https://doi.org/10.3390/jcm8091492
- Albini A and Noonan DM. Decidual-like NK cell polarization: From cancer killing to cancer nurturing. Cancer Discov 2021;11:28-33. https://doi.org/10.1158/2159-8290.CD-20-0796
- Parisi L, Bassani B, Tremolati M, Gini E, Farronato G, Bruno A. Natural killer cells in the orchestration of chronic inflammatory diseases. J Immunol Res 2017;2017:4218254. https://doi.org/10.1155/2017/4218254
- Tognarelli S, Jacobs B, Staiger N, Ullrich E. Flow cytometry-based assay for the monitoring of NK cell functions. J Vis Exp 2016;116:54615.
- Pegram HJ, Andrews DM, Smyth MJ, Darcy PK, Kershaw MH. Activating and inhibitory receptors of natural killer cells. Immunol Cell Biol 2011;89:216-24. https://doi.org/10.1038/icb.2010.78
- Borrego F, Robertson MJ, Ritz J, Peña J, Solana R. CD69 is a stimulatory receptor for natural killer cell and its cytotoxic effect is blocked by CD94 inhibitory receptor. Immunology 1999;97:159-65. https://doi.org/10.1046/j.1365-2567.1999.00738.x
- Gu Y, Bi Y, Huang Z, Liao C, Li X, Hu H, et al. CD69 expression is negatively associated with T-cell immunity and predicts antiviral therapy response in chronic hepatitis B. Ann Lab Med 2025;45:185-98. https://doi.org/10.3343/alm.2024.0178
- Christensen EB, Schaefer M, Barnkob MB, Nielsen C, Barington T. OMIP-115: High-dimensional phenotypic characterization of human natural killer cells for therapeutic use. Cytometry A 2025;107:372-7. https://doi.org/10.1002/cyto.a.v107.6
- Shin KH, Choi HW, Lim J, Kang ES. Reference values for extended lymphocyte subsets in Korean children: a multicenter study using the EuroFlow PIDOT panel. Ann Lab Med 2026;46:297-308. https://doi.org/10.3343/alm.2025.0241
- Kay AW, Strauss-Albee DM, Blish CA. Application of mass cytometry (CyTOF) for functional and phenotypic analysis of natural killer cells. Methods Mol Biol 2016;1441:13-26. https://doi.org/10.1007/978-1-4939-3684-7
- Elsner L and Dressel R. 51Cr-release to monitor NK cell cytotoxicity. Methods Enzymol 2020;631:497-512. https://doi.org/10.1016/bs.mie.2019.05.037
- Lichtenfels R, Biddison WE, Schulz H, Vogt AB, Martin R. CARE-LASS (calcein-release-assay), an improved fluorescence-based test system to measure cytotoxic T lymphocyte activity. J Immunol Methods 1994;172:227-39. https://doi.org/10.1016/0022-1759(94)90110-4
- Neri S, Mariani E, Meneghetti A, Cattini L, Facchini A. Calcein-acetyoxymethyl cytotoxicity assay: Standardization of a method allowing additional analyses on recovered effector cells and supernatants. Clin Diagn Lab Immunol 2001;8:1131-5. https://doi.org/10.1128/CDLI.8.6.1131-1135.2001
- Jang YY, Cho D, Kim SK, Shin DJ, Park MH, Lee JJ, et al. An improved flow cytometry-based natural killer cytotoxicity assay involving calcein AM staining of effector cells. Ann Clin Lab Sci 2012;42:42-9.
- Weyermann J, Lochmann D, Zimmer A. A practical note on the use of cytotoxicity assays. Int J Pharm 2005;288:369-76. https://doi.org/10.1016/j.ijpharm.2004.09.018
- Tanito K, Oshiro Y, Tagawa H, Kishlmura A, Mori T, Katayama Y. Comparative evaluation of natural killer cell-mediated cell killing assay based on the leakage of an endogenous enzyme or a pre-loaded fluorophore. Anal Sci 2021;37:1571-5. https://doi.org/10.2116/analsci.21P117
- Cho MH, Niles A, Huang R, Inglese J, Austin CP, Riss T, et al. A bioluminescent cytotoxicity assay for assessment of membrane integrity using a proteolytic biomarker. Toxicol In Vitro 2008;22:1099-106. https://doi.org/10.1016/j.tiv.2008.02.013
- Alshehade SA, Almoustafa HA, Alshawsh MA, Chik Z. Flow cytometrybased quantitative analysis of cellular protein expression in apoptosis subpopulations: A protocol. Heliyon 2024;10:e33665.
- Zimmermann SY, Esser R, Rohrbach E, Klingebiel T, Koehl U. A novel four-colour flow cytometric assay to determine natural killer cell or T-cell-mediated cellular cytotoxicity against leukaemic cells in peripheral or bone marrow specimens containing greater than 20% of normal cells. J Immunol Methods 2005;296:63-76. https://doi.org/10.1016/j.jim.2004.10.014
- Veluchamy JP, Delso-Vallejo M, Kok N, Bohme F, Seggewiss-Bernhardt R, van der Vliet HJ, et al. Standardized and flexible eight colour flow cytometry panels harmonized between different laboratories to study human NK cell phenotype and function. Sci Rep 2017;7:43873. https://doi.org/10.1038/srep43873
- Ryu J, Choi J, Kim M, Cho YU, Hwang SH, Jang S, et al. Suitability of EDTA-anticoagulated blood for natural killer cell activity testing using flow cytometry. Ann Lab Med 2023;43:307-9. https://doi.org/10.3343/alm.2023.43.3.307
- Kim J, Phan MT, Kweon S, Yu H, Park J, Kim KH, et al. A flow cytometry-based whole blood natural killer cell cytotoxicity assay using overnight cytokine activation. Front Immunol 2020;11:1851. https://doi.org/10.3389/fimmu.2020.01851
- Krzewski K and Coligan JE. Human NK cell lytic granules and regulation of their exocytosis. Front Immunol 2012;3:335. https://doi.org/10.3389/fimmu.2012.00335
- Krzewski K, Gil-Krzewska A, Nguyen V, Peruzzi G, Coligan JE. LAMP1/CD107a is required for efficient perforin delivery to lytic granules and NK-cell cytotoxicity. Blood 2013;121:4672-83. https://doi.org/10.1182/blood-2012-08-453738
- Alter G, Malenfant JM, Altfeld M. CD107a as a functional marker for the identification of natural killer cell activity. J Immunol Methods 2004;294:15-22. https://doi.org/10.1016/j.jim.2004.08.008
- Kalyuzhny AE. Handbook of ELISPOT. Methods in Molecular Biology. 2005;302:323. https://doi.org/10.1385/1592599036
- Chiswick EL, Duffy E, Japp B, Remick D. Detection and quantification of cytokines and other biomarkers. Methods Mol Biol 2012;844:15-30. https://doi.org/10.1007/978-1-61779-527-5
- Long EO, Kim HS, Liu D, Peterson ME, Rajagopalan S. Controlling natural killer cell responses: Integration of signals for activation and inhibition. Annu Rev Immunol 2013;31:227-58. https://doi.org/10.1146/immunol.2013.31.issue-1
- Lee SB, Cha J, Kim IK, Yoon JC, Lee HJ, Park SW, et al. A high-throughput assay of NK cell activity in whole blood and its clinical application. Biochem Biophys Res Commun 2014;445:584-90. https://doi.org/10.1016/j.bbrc.2014.02.040
- Nederby L, Jakobsen A, Hokland M, Hansen TF. Quantification of NK cell activity using whole blood: Methodological aspects of a new test. J Immunol Methods 2018;458:21-5. https://doi.org/10.1016/j.jim.2018.04.002
- Choi SI, Lee SH, Park JY, Kim KA, Lee EJ, Lee SY, et al. Clinical utility of a novel natural killer cell activity assay for diagnosing non-small cell lung cancer: A prospective pilot study. Onco Targets Ther 2019;12:1661-9. https://doi.org/10.2147/OTT
- Gunesch JT, Angelo LS, Mahapatra S, Deering RP, Kowalko JE, Sleiman P, et al. Genome-wide analyses and functional profiling of human NK cell lines. Mol Immunol 2019;115:64-75. https://doi.org/10.1016/j.molimm.2018.07.015
- Mitsunaga F and Nakamura S. A sensitive and simple method to assess NK cell activity by RT-qPCR for granzyme B using spleen and blood. J Biosci Med 2021;9:27-38. https://doi.org/10.4236/jbm.2021.93004
- Nishimura Y, Kumagai-Takei N, Lee S, Matsuzaki H, Yoshiotme K, Otsuki T. A new method to determine natural killer cell activity without target cells. In: Aribi M, ed. Natural killer cells. Rijeka: IntechOpen, 2017.
- Liu Z, Lavis LD, Betzig E. Imaging live-cell dynamics and structure at the single-molecule level. Mol Cell 2015;58:644-59. https://doi.org/10.1016/j.molcel.2015.02.033
- Choi PJ and Mitchison TJ. Imaging burst kinetics and spatial coordination during serial killing by single natural killer cells. Proc Natl Acad Sci U S A 2013;110:6488-93. https://doi.org/10.1073/pnas.1221312110
- Martinez AL, Shannon MJ, Eisman SE, Hegewisch-Solloa E, Asif AN, Ebrahim TAM, et al. Quantifying human natural killer cell migration by imaging and image analysis. Methods Mol Biol 2022;2463:129-51. https://doi.org/10.1007/978-1-0716-2160-8
- Tran T, Galdina V, Urquidi O, Reis Galvão D, Rieben R, Adachi TBM, et al. Assessment of NK cytotoxicity and interactions with porcine endothelial cells by live-cell imaging in 2D static and 3D microfluidic systems. Sci Rep 2024;14:24199.
- Shin HS, Park J, Lee SY, Yun HG, Kim B, Kim J, et al. Integrative magneto-microfluidic separation of immune cells facilitates clinical functional assays. Small 2023;19:e2302809. https://doi.org/10.1002/smll.v19.43
- Park J, Shin Y, Kim JM, Kweon S, Song AY, Baek Y, et al. Multifunctional microparticles with stimulation and sensing capabilities for facile NK cell activity assay. ACS Sens 2021;6:693-7. https://doi.org/10.1021/acssensors.0c02138
- Sztajnbok F, Fonseca AR, Campos LR, Lino K, Rodrigues MCF, Silva RM, et al. Hemophagocytic lymphohistiocytosis and macrophage activation syndrome: two rare sides of the same devastating coin. Adv Rheumatol 2024;64:28. https://doi.org/10.1186/s42358-024-00370-2
- Risma K and Jordan MB. Hemophagocytic lymphohistiocytosis: updates and evolving concepts. Curr Opin Pediatr 2012;24:9-15. https://doi.org/10.1097/MOP.0b013e32834ec9c1
- Zhang J, Sun Y, Shi X, Zhang R, Wang Y, Xiao J, et al. Genotype characteristics and immunological indicator evaluation of 311 hemophagocytic lymphohistiocytosis cases in China. Orphanet J Rare Dis 2020;15:112. https://doi.org/10.1186/s13023-020-01390-z
- Ramos-Casals M, Brito-Zerón P, López-Guillermo A, Khamashta MA, Bosch X. Adult haemophagocytic syndrome. Lancet 2014;383:1503-16. https://doi.org/10.1016/S0140-6736(13)61048-X
- Filipovich AH. Hemophagocytic lymphohistiocytosis (HLH) and related disorders. Hematology Am Soc Hematol Educ Program 2009:127-31.
- Chiang SCC, Bleesing JJ, Marsh RA. Current flow cytometric assays for the screening and diagnosis of primary HLH. Front Immunol 2019;10:1740. https://doi.org/10.3389/fimmu.2019.01740
- Chung HJ, Park CJ, Lim JH, Jang S, Chi HS, Im HJ, et al. Establishment of a reference interval for natural killer cell activity through flow cytometry and its clinical application in the diagnosis of hemophagocytic lymphohistiocytosis. Int J Lab Hematol 2010;32:239-47. https://doi.org/10.1111/clh.2010.32.issue-2
- Oh EJ, Yoon JH, Park KH, Bae HJ, Yun SJ, Min GJ, et al. Natural-killer cell cytotoxicity as a diagnostic and prognostic marker for adult patients with secondary hemophagocytic lymphohistiocytosis: A prospective phase II observational study. Ther Adv Hematol 2021;12:20406207211020544. https://doi.org/10.1177/20406207211020544
- Hayden A, Lin M, Park S, Pudek M, Schneider M, Jordan MB, et al. Soluble interleukin-2 receptor is a sensitive diagnostic test in adult HLH. Blood Adv 2017;1:2529-34. https://doi.org/10.1182/bloodadvances.2017012310
- Yoon SE, Eun Y, Huh K, Chung CR, Yoo IY, Cho J, et al. A comprehensive analysis of adult patients with secondary hemophagocytic lymphohistiocytosis: A prospective cohort study. Ann Hematol 2020;99:2095-104. https://doi.org/10.1007/s00277-020-04083-6
- Henter JI, Sieni E, Eriksson J, Bergsten E, Hed Myrberg I, Canna SW, et al. Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited. Blood 2024;144:2308-18. https://doi.org/10.1182/blood.2024025077
- Kiessling R, Klein E, Pross H, Wigzell H. "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. https://doi.org/10.1002/eji.v5:2
- Nersesian S, Schwartz SL, Grantham SR, MacLean LK, Lee SN, Pugh-Toole M, et al. NK cell infiltration is associated with improved overall survival in solid cancers: A systematic review and meta-analysis. Transl Oncol 2021;14:100930. https://doi.org/10.1016/j.tranon.2020.100930
- Mamessier E, Pradel LC, Thibult ML, Drevet C, Zouine A, Jacquemier J, et al. Peripheral blood NK cells from breast cancer patients are tumor-induced composite subsets. J Immunol 2013;190:2424-36. https://doi.org/10.4049/jimmunol.1200140
- Stegmann KA, Robertson F, Hansi N, Gill U, Pallant C, Christophides T, et al. CXCR6 marks a novel subset of T-betloEomeshi natural killer cells residing in human liver. Sci Rep 2016;6:26157. https://doi.org/10.1038/srep26157
- Lee J, Park KH, Ryu JH, Bae HJ, Choi A, Lee H, et al. Natural killer cell activity for IFN-gamma production as a supportive diagnostic marker for gastric cancer. Oncotarget 2017;8:70431-40. https://doi.org/10.18632/oncotarget.v8i41
- Furue H, Matsuo K, Kumimoto H, Hiraki A, Suzuki T, Yatabe Y, et al. Decreased risk of colorectal cancer with the high natural killer cell activity NKG2D genotype in Japanese. Carcinogenesis 2008;29:316-20. https://doi.org/10.1093/carcin/bgm260
- Xu Y, Xu Q, Ni S, Liu F, Cai G, Wu F, et al. Decrease in natural killer cell associated gene expression as a major characteristic of the immune status in the bloodstream of colorectal cancer patients. Cancer Biol Ther 2011;11:188-95. https://doi.org/10.4161/cbt.11.2.13670
- Han B, Mao FY, Zhao YL, Lv YP, Teng YS, Duan M, et al. Altered NKp30, NKp46, NKG2D, and DNAM-1 expression on circulating NK cells is associated with tumor progression in human gastric cancer. J Immunol Res 2018;2018:6248590. https://doi.org/10.1155/2018/6248590
- Sun C, Xu J, Huang Q, Huang M, Wen H, Zhang C, et al. High NKG2A expression contributes to NK cell exhaustion and predicts a poor prognosis of patients with liver cancer. Oncoimmunology 2016;6:e1264562. https://doi.org/10.1080/2162402X.2016.1264562
- Gulubova M, Manolova I, Kyurkchiev D, Julianov A, Altunkova I. Decrease in intrahepatic CD56+ lymphocytes in gastric and colorectal cancer patients with liver metastases. APMIS 2009;117:870-9. https://doi.org/10.1111/apm.2009.117.issue-12
- Sun JR, Kong CF, Ye YX, Wang Q, Qu XK, Jia LQ, et al. Integrated analysis of single-cell and bulk RNA-sequencing reveals a novel signature based on NK cell marker genes to predict prognosis and immunotherapy response in gastric cancer. Sci Rep 2024;14:7648.
- Yang Y, She S, Ren L, Zhao B, Chen D, Chen H. Prognosis and therapeutic benefits prediction based on NK cell marker genes through single-cell RNA-seq with integrated bulk RNA-seq analysis for hepatocellular carcinoma. Front Oncol 2023;13:1208165. https://doi.org/10.3389/fonc.2023.1208165
- Björkström NK, Lindgren T, Stoltz M, Fauriat C, Braun M, Evander M, et al. Rapid expansion and long-term persistence of elevated NK cell numbers in humans infected with hantavirus. J Exp Med 2011;208:13-21. https://doi.org/10.1084/jem.20100762
- Ebbo M, Gérard L, Carpentier S, Vély F, Cypowyj S, Farnarier C, et al. Low circulating natural killer cell counts are associated with severe disease in patients with common variable immunodeficiency. EBioMedicine 2016;6:222-30. https://doi.org/10.1016/j.ebiom.2016.02.025
- Knapp S, Warshow U, Ho KM, Hegazy D, Little AM, Fowell A, et al. A polymorphism in IL28B distinguishes exposed, uninfected individuals from spontaneous resolvers of HCV infection. Gastroenterology 2011;141:320-5.e1-2. https://doi.org/10.1053/j.gastro.2011.04.005
- Alter G, Jost S, Rihn S, Reyor LL, Nolan BE, Ghebremichael M, et al. Reduced frequencies of NKp30+NKp46+, CD161+, and NKG2D+ NK cells in acute HCV infection may predict viral clearance. J Hepatol 2011;55:278-88. https://doi.org/10.1016/j.jhep.2010.11.030
- Dessouki O, Kamiya Y, Nagahama H, Tanaka M, Suzu S, Sasaki Y, et al. Chronic hepatitis C viral infection reduces NK cell frequency and suppresses cytokine secretion: Reversion by anti-viral treatment. Biochem Biophys Res Commun 2010;393:331-7. https://doi.org/10.1016/j.bbrc.2010.02.008
- Krämer B, Knoll R, Bonaguro L, ToVinh M, Raabe J, Astaburuaga-García R et al. Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19. Immunity 2021;54:2650-69.e14. https://doi.org/10.1016/j.immuni.2021.09.002
- Li M, Guo W, Dong Y, Wang X, Dai D, Liu X, et al. Elevated exhaustion levels of NK and CD8+ T cells as indicators for progression and prognosis of COVID-19 disease. Front Immunol 2020;11:580237. https://doi.org/10.3389/fimmu.2020.580237
- Nishio A, Bolte FJ, Takeda K, Park N, Yu ZX, Park H, et al. Clearance of pegylated interferon by Kupffer cells limits NK cell activation and therapy response of patients with HBV infection. Sci Transl Med 2021;13:eaba6322. https://doi.org/10.1126/scitranslmed.aba6322
- Liu M, Liang S, Zhang C. NK cells in autoimmune diseases: Protective or pathogenic? Front Immunol 2021;12:624687. https://doi.org/10.3389/fimmu.2021.624687
- Lünemann A, Lünemann JD, Münz C. Regulatory NK-Cell functions in inflammation and autoimmunity. Mol Med 2009;15:352-8. https://doi.org/10.2119/molmed.2009.00035
- Hervier B, Beziat V, Haroche J, Mathian A, Lebon P, Ghillani-Dalbin P, et al. Phenotype and function of natural killer cells in systemic lupus erythematosus: Excess interferon-γ production in patients with active disease. Arthritis Rheum 2011;63:1698-706. https://doi.org/10.1002/art.30313
- Yoon Kim D and Kwon Lee J. Type 1 and 2 diabetes are associated with reduced natural killer cell cytotoxicity. Cell Immunol 2022;379:104578. https://doi.org/10.1016/j.cellimm.2022.104578
- Liu M, Liu J, Zhang X, Xiao Y, Jiang G, Huang X. Activation status of CD56dim natural killer cells is associated with disease activity of patients with systemic lupus erythematosus. Clin Rheumatol 2021;40:1103-12. https://doi.org/10.1007/s10067-020-05306-x
- Chalan P, Bijzet J, Kroesen BJ, Boots AM, Brouwer E. Altered natural killer cell subsets in seropositive arthralgia and early rheumatoid arthritis are associated with autoantibody status. J Rheumatol 2016;43:1008-16. https://doi.org/10.3899/jrheum.150644
- Mimpen M, Muris AH, Rolf L, Gerlach O, Kuhle J, Hupperts R, et al. Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis. Eur J Neurol 2021;28:901-9. https://doi.org/10.1111/ene.v28.3
- Zhang X and Wei H. Role of decidual natural killer cells in human pregnancy and related pregnancy complications. Front Immunol 2021;12:728291. https://doi.org/10.3389/fimmu.2021.728291
- Nakimuli A, Chazara O, Hiby SE, Farrell L, Tukwasibwe S, Jayaraman J, et al. A KIR B centromeric region present in Africans but not Europeans protects pregnant women from pre-eclampsia. Proc Natl Acad Sci U S A 2015;112:845-50. https://doi.org/10.1073/pnas.1413453112
- Quenby S, Nik H, Innes B, Lash G, Turner M, Drury J, et al. Uterine natural killer cells and angiogenesis in recurrent reproductive failure. Hum Reprod 2009;24:45-54.
- Bagkou Dimakou D, Tamblyn J, Lissauer D, Richter A. Evaluation of peripheral NK tests offered to women with recurrent pregnancy loss and a search for novel candidate biomarkers. J Reprod Immunol 2025;169:104522. https://doi.org/10.1016/j.jri.2025.104522
- Von Woon E, Greer O, Shah N, Nikolaou D, Johnson M, Male V. Number and function of uterine natural killer cells in recurrent miscarriage and implantation failure: A systematic review and meta-analysis. Hum Reprod Update 2022;28:548-82. https://doi.org/10.1093/humupd/dmac006
- Angelo LS, Banerjee PP, Monaco-Shawver L, Rosen JB, Makedonas G, Forbes LR et al. Practical NK cell phenotyping and variability in healthy adults. Immunol Res 2015;62:341-56. https://doi.org/10.1007/s12026-015-8664-y
- Practice Committee of the American Society for Reproductive Medicine. Evaluation and treatment of recurrent pregnancy loss: A committee opinion. Fertil Steril 2012;98:1103-11. https://doi.org/10.1016/j.fertnstert.2012.06.048
- National Evidence-Based Healthcare Collaborating Agency. NK cell activity tests. https://scholarworks.bwise.kr/neca/bitstream/2023. sw.neca/260/1/NR23-001-15.pdf, updated on Nov 2025.
- Jung YS, Kwon MJ, Park DI, Sohn CI, Park JH. Association between natural killer cell activity and the risk of colorectal neoplasia. J Gastroenterol Hepatol 2018;33:831-6. https://doi.org/10.1111/jgh.2018.33.issue-4
- Lee YK, Suh E, Oh H, Haam JH, Kim YS. Decreased natural killer cell activity as a potential predictor of hypertensive incidence. Front Immunol 2024;15:1376421.
- Jung YS, Park JH, Park DI, Sohn CI, Lee JM, Kim TI. Physical inactivity and unhealthy metabolic status are associated with decreased natural killer cell activity. Yonsei Med J 2018;59:554-62. https://doi.org/10.3349/ymj.2018.59.4.554
- Brolinson PG and Elliott D. Exercise and the immune system. Clin Sports Med 2007;26:311-9. https://doi.org/10.1016/j.csm.2007.04.011
- Jo H, Jo Y, Koh SK, Lee M, Kim J, Kweon SH, et al. Optimization of natural killer cell expansion with K562-mbIL-18/-21 feeder cells and assurance of feeder cell-free products. Ann Lab Med 2026;46:180-9. https://doi.org/10.3343/alm.2025.0168
- Park JD, Shin HE, An YS, Jang HS, Park J, Kim SN, et al. Advancing natural killer cell therapy: genetic engineering strategies for enhanced cancer immunotherapy. Ann Lab Med 2025;45:145-59. https://doi.org/10.3343/alm.2024.0380