DOI: https://dx.doi.org/10.18565/epidem.2022.12.1.115-20
Rakityanskaya I.A., Ryabova T.S., Kalashnikova A.A.
1) City Polyclinic One Hundred and Twelve, Saint Petersburg, Russia; 2) S.M. Kirov Military Medical Academy, Saint Petersburg, Russia; 3) A.M. Nikiforov All-Russian Center of Emergency and Radiation Medicine, Ministry of the Russian Federation for Civil Defense, Emergencies and Elimination of Consequences of Natural Disasters (EMERCOM of Russia, Saint Petersburg, Russia
1. Kandarian F., Sunga G.M., Arango-Saenz D., Rossetti M. A flow cytometry-based cytotoxicity assay for the assessment of human NK cell activity. J Vis Exp. 2017; 2017 (126): 56191. doi: https://doi.org/10.3791/56191 2. Mandal A., Viswanathan C. Natural killer cells: In health and disease. Hematol. Oncol. Stem. Cell Ther. 2015; 8(2): 47–55 3. George L.C., Rowe M., Fox C.P. Epstein-barr virus and the pathogenesis of T and NK lymphoma: A mystery unsolved. Curr. Hematol. Malig. Rep. 2012; (7): 276–84. doi: 10.1007/s11899-012-0136-z. 4. van Erp E.A., van Kampen M.R. , van Kasteren P.B. , de Witе J. Viral Infection of Human Natural Killer Cells. Viruses 2019; 11(3): 243. doi: 10.3390/v11030243 5. Schuster I.S., Coudert J.D., Andoniou C.E., Degli-Esposti M.A. «Natural Regulators»: NK Cells as Modulators of T Cell Immunity. Front. Immunol. 2016; (7): 235. doi: 10.3389/fimmu.2016.00235 6. Stabile H., Fionda C., Gismondi A., Santoni A. Role of distinct natural killer cell subsets in anticancer response. Front Immunol. 2017; (8): 293. DOI: 10.3389/fimmu.2017.00293 7. Zhang Y., Huang B. The development and diversity of ILCs, NK cells and their relevance in health and diseases. Adv. Exp. Med. Biol. 2017; 1024: 225–44. doi: 10.1007/978-981-10-5987-2_11 8. Abel A.M., Chao Yang M., Thakar S., Malarkannan S. Natural Killer Cells Development, Maturation, and Clinical Utilization. Front Immunol. 2018; (9): 1869. doi: 10.3389/fimmu.2018.01869 9. Björkström N.K., 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(19): 3853–64. doi: 10.3389/fimmu.2017.00293 10. Handgretinger R., Lang P., André M.C. Exploitation of natural killer cells for the treatment of acute leukemia. Blood 2016; 127(26): 3341–9. doi: 10.1182/blood-2015-12-629055. 11. Kuczer M., Czarniewska А., Majewska A., Różanowska M., Rosiński G., Lisowski M. Novel analogs of alloferon: Synthesis, conformational studies, pro-apoptotic and antiviral activity. Bioorg. Chem. 2016; 66: 12–20. doi: 10.1016/j.bioorg.2016.03.002 12. Angus K.L., Griffiths G.M. Cell polarisation and the immunological synapse. Curr. Opin. Cell Biol. 2013; 25(1): 85–91. doi: 10.1016/j.ceb.2012.08.013 13. Dongfang L., Jose A M., Xufeng S.W., Hammer J.A. 3rd, Long E.O. Two modes of lytic granule fusion during degranulation by natural killer cells. Immunol. Cell. Biol. 2011; 89(6): 728–38. doi: 10.1038/icb.2010.167 14. Kiesgen S., Messinger J.C., Chintala N.K., Tano Z, Adusumilli P.S. Comparative analysis of assays to measure CAR T-cell-mediated cytotoxicity. Nat. Protoc. 2021; 16(3): 1331–42. doi: 10.1038/s41596-020-00467-0 15. Lee N., Bae S., Kim H. et al. Inhibition of lytic reactivation of Kaposi’s sarcoma-associated herpesvirus by alloferon. Antivir. Ther. 2011; 16(1): 17–26. doi: 10.3851/IMP1709 16. Thomas D., Michou V., TegosV., Patargias T., Moustakarias T., Kanakas N. et al. The effect of valacyclovir treatment on natural killer cells of infertile women. Am. J. Reprod. Immunol. 2004; 51(3): 248–55.DOI: 10.1111/j.1600-0897.2004.00152.x 17. Kuczer M., Majewska A., Zahorska R. New alloferon analogues: synthesis and antiviral properties. Chem. Biol. Drug Des. 2013; 81(2): 302–9. doi: 10.1111/cbdd.12020 18. Chernysh S., Kim S.I., Bekker G., Pleskach V.A., Filatova N.A., Anikin V.B. et al. Antiviral and antitumor peptides from insects. Proc. Nat. Acad. Sci. USA. 2002; 99(20): 12628–32. doi: [10.1073/pnas.192301899] 19. Черныш С.И. Аллокины (цитокиноподобные пептиды насекомых) как модуляторы иммунного ответа человека и других млекопитающих. Российский иммунологический журнал 2004; 9(1): 36. Chernysh S.I. [Alloquins (cytokine-like peptides of insects) as modulators of the immune response of humans and other mammals]. Russian Journal of Immunology 2004; 9(1): 36. (In Russ.).
Professor Irina A. Rakitуanskaya, MD, Clinical Immunologist; Immunology Consultant, City Outpatient Unit of Allergology, Immunology, and Clinical Transfusiology, City Polyclinic One Hundred and Twelve, Saint Petersburg, Russia; tat-akyla@inbox.ru; https://orcid.org/0000-0003-2524-4602
Tatiana S. Rуabova, MD, Nephrologist; Associate Professor, Department of Nephrology and Efferent Therapy, S.M. Kirov Military Medical Academy; Consulting Cardiologist, Outpatient Unit of Allergology, Immunology, and Clinical Transfusiology, City Polyclinic One Hundred and Twelve, St. Petersburg, Russia; tita74@ mail.ru; https://orcid.org/0000-0001-9543-9646
Anastasia A. Kalashnikova, Cand Biol. Sci., Senior Researcher, Laboratory of Clinical Immunology, A.M. Nikiforov All-Russian Center of Emergency and Radiation Medicine, Russian Ministry for Civil Defense, Emergencies and Elimination of Consequences of Natural Disasters EMERCOM of Russia, St. Petersburg, Russia; petkova_nas@mail.ru; https://orcid.org /0000-0002-5338-0866