References
1. Mezger M., Nording H., Sauter R., et al. Platelets and immune responses during thrombo inflammation. Front Immunol. 2019; 10: 1731. DOI: https://www.doi.org/10.3389/fimmu.2019.01731
2. Gerrits A.J., Frelinger A.L. 3rd, Michelson A.D. Whole blood analysis of leukocyte-platelet aggregates. Curr. Protoc. Cytom. 2016; 78: 6.15.1–10. DOI: https://www.doi.org/10.1002/cpcy.8
3. Xu X.R., Zhang D., Oswald B.E., Carrim N., Wang X., Hou Y., Zhang Q., Lavalle C., McKeown T., Marshall A.H., Ni H. Platelets are versatile cells: New discoveries in hemostasis, thrombosis, immune responses, tumor metastasis and beyond. Crit Rev Clin Lab Sci. 2016; 53(6): 409–30. DOI: https://www.doi.org/10.1080/10408363.2016.1200008
4. Sviridova S.P., Somonova O.V., Kashiya S.R., Obukhova O.A., Sotnikov A.V. The role of platelets in inflammation and immunity. Issledovaniya i praktika v medicine. 2018; 5(3): 40-52. DOI: https://www.doi.org/10.17709/2409-2231-2018-5-3-4 (in Russian)
5. Ali R.A., Wuescher L.M., Worth R.G. Platelets: essential components of the immune system. Curr. Trends Immunol. 2015; 16: 65–78. PMID: 27818580; PMCID: PMC5096834.
6. Nurden A.T. The biology of the platelet with special reference to inflammation, wound healing and immunity. Front. Biosci. (Landmark Ed.). 2018; 23: 726–51. DOI: https://www.doi.org/10.2741/4613
7. Łukasik Z.M., Makowski M., Makowska J.S. From blood coagulation to innate and adaptive immunity: the role of platelets in the physiology and pathology of autoimmune disorders. Rheumatol. Int. 2018; 38 (6): 959–74. DOI: https://www.doi.org/10.1007/s00296-018-4001-9
8. Lam F.W., Vijayan K.V., Rumbaut R.E. Platelets and their interactions with other immune cells. Compr. Physiol. 2015; 5 (3): 1265–80. DOI: https://www.doi.org/:10.1002/cphy.c140074
9. Hottz E.D., Azevedo-Quintanilha I.G., Palhinha L., et al. Platelet activation and platelet-monocyte aggregate formation trigger tissue factor expression in patients with severe COVID-19. Blood. 2020; 136 (11): 1330–41. DOI: https://www.doi.org/10.1182/blood.2020007252
10. Lisco A., Wong C.S., Price S., et al. Paradoxical CD4 lymphopenia in autoimmune lymphoproliferative syndrome (ALPS). Front. Immunol. 2019; 10: 1193. DOI: https://www.doi.org/10.3389/fimmu.2019.01193
11. Bohner P., Chevalier M.F., Cesson V., et al. Double positive CD4+CD8+ T cells are enriched in urological cancers and favor T helper-2 polarization. Front. Immunol. 2019; 10: 622. DOI: https://www.doi.org/10.3389/fimmu.2019.00622
12. Vitkovsky Yu.A., Kuznik B.I., Solpov A.V. The phenomenon of lymphocyte-platelet rosette formation. Immunologiya. 1999; (4): 35–7. (in Russian)
13. Solpov A., Shenkman B., Vitkovsky Y., Brill G., Koltakov A., Farzam N., Varon D., Bank I., Savion N. Platelets enhance CD4+ lymphocyte adhesion to extracellular matrix under flow conditions: role of platelet aggregation, integrins, and non-integrin receptors. Thromb. Haemost. 2006; 95 (5): 815–21. PMID: 16676073.
14. Vitkovsky Yu.A., Kuznik B.I., Solpov A.V. Pathogenetic significance of lymphocyte-platelet adhesion. Meditsinskaya immunologiya. 2006; 8 (5–6): 745–53. (in Russian)
15. Diacovo T.G., Roth S.J., Morita C.T., Rosat J.P., Brenner M.B., Springer T.A. Interactions of human alpha/beta and gamma/delta T lymphocyte subsets in shear flow with E-selectin and P-selectin. J Exp Med. 1996; 183 (3): 1193–203. DOI: https://www.doi.org/10.1084/jem.183. 3.1193
16. Kuznik B.I., Batozhargalova B.Ts., Vitkovsky Yu.A. The state of immunity and lymphocyte-platelet adhesion in children with chronic deforming bronchitis. Meditsinskaya immunologiya. 2008; 10 (6): 583–8. (in Russian)
17. Dolina A.B., Kuznik B.I., Rosenberg V.Ya., Vishnyakova T.M., Vitkovsky Yu.A. Influence of thymalin on the state of immunity and lymphocytic-platelet adhesion in children with secondary infective endocarditis. Medical immunology. 2010; 12 (4-5): 381–6. DOI: https://doi.org/10.15789/1563-0625-2010-4-5-381-386 (in Russian)
18. Vignesh P., Rawat A., Shandilya J.K., Singh Sachdeva M.U., Ahluwalia J., Singh S. Monocyte platelet aggregates in children with Kawasaki disease – a preliminary study from a tertiary care centre in North-West India. Pediatr. Rheumatol. Online J. 2021; 19 (1): 25. DOI: https://www.doi.org/10.1186/s12969-021-00515-3
19. Khaydukov S., Baydun L., Zurochka A., Totolyan A. Methods. Meditsinskaya immunologiya. 2012; 14 (3): 255–68. DOI: https://doi.org/10.15789/1563-0625-2012-3-255-268 (in Russian)
20. Finsterbusch M., Schrottmaier W.C., Kral-Pointner J.B., Salzmann M., Assinger A. Measuring and interpreting platelet-leukocyte aggregates. Platelets. 2018; 29 (7): 677–85. DOI: https://www.doi.org/:10.1080/09537104.2018.1430358
21. Kuznik B.I., Vitkovsky Yu.A., Solpov A.V. Adhesive molecules and leukocyte-platelet interactions. Vestnik gematologii. 2006; 2 (2): 42–55. (in Russian)
22. Zamora C., Cantó E., Nieto J.C., Bardina J., Diaz-Torné C., Moya P., Magallares B., Ortiz M.A., Julià G., Juarez C., Llobet J.M., Vidal S. Binding of platelets to lymphocytes: a potential anti-inflammatory therapy in rheumatoid arthritis. J. Immunol. 2017; 198 (8): 3099–108. DOI: https://www.doi.org/10.4049/jimmunol.1601708
23. Tan S., Zhang J., Sun Y., Gistera A., Sheng Z., Malmström R.E., Hou M., Peng J., Ma C., Liao W., Li N. Platelets enhance CD4+ central memory T cell responses via platelet factor 4-dependent mitochondrial biogenesis and cell proliferation. Platelets. 2021; Jun 17: 1–11. DOI: https://www.doi.org/10.1080/09537104.2021.1936479
24. Solpova O.A. Participation of TCRαβ- and γδ-T-lymphocytes, P-selectin in the formation of cell-platelet coaggregates. Zabaykal’skiy meditsinskiy vestnik. 2016; (2): 71–9. (in Russian)
25. Koupenova M., Clancy L., Corkrey H.A., Freedman J.E. Circulating platelets as mediators of immunity, inflammation, and thrombosis. Circ. Res. 2018; 122 (2): 337–51. DOI: https://www.doi.org/10.1161/CIRCRESAHA.117.310795
26. Herken K., Glauner M., Robert S.C., et al. Age-dependent control of collagen-dependent platelet responses by thrombospondin-1-comparative analysis of platelets from neonates, children, adolescents, and adults. Int. J. Mol. Sci. 2021; 22 (9): 4883. DOI: https://www.doi.org/10.3390/ijms22094883
27. Gaertner F., Massberg S. Patrolling the vascular borders: platelets in immunity to infection and cancer. Nat. Rev. Immunol. 2019; 19 (12): 747–60. DOI: https://www.doi.org/10.1038/s41577-019-0202-z
28. Suprun E.N. The state of the immune system at different age periods. Allergologiya i immunologiya v pediatrii. 2013; (35): 31–6. (in Russian)
29. Gusel’nikova V.V., Polevshchikov A.V. Thymus mast cells: at the crossroads of three roads. Immunologiya. 2021; 42 (4): 327–36. DOI: https://doi.org/10.33029/0206-4952-2021-42-4-327-336 (in Russian)
30. Thomas R., Wang W., Su D.M. Contributions of age-related thymic involution to immunosenescence and inflammaging. Immun. Ageing. 2020; 17: 2. DOI: https://doi.org/10.1186/s12979-020-0173-8
31. Zhirkov A.A., Alekseeva L.A., Zheleznikova G.F., Skripchenko N.V., Monakhova N.E., Bessonova T.V. Major and minor subpopulations of blood and cerebrospinal fluid lymphocytes in children with meningitis. Infektsiya i immunitet. 2021; 11 (1): 111–22. (in Russian)
32. Shenkman B., Brill G., Solpov A., Vitkovsky Y., Kuznik B., Koltakov A., Kotev-Emeth S., Savion N., Bank I. CD4+ lymphocytes require platelets for adhesion to immobilized fibronectin in flow: role of beta(1) (CD29)-, beta(2) (CD18)-related integrins and non-integrin receptors. Cell. Immunol. 2006; 242 (1): 52–9. DOI: https://doi.org/10.1016/j.cellimm.2006.09.005
33. Yip C., Ignjatovic V., Attard C., Monagle P., Linden M.D. First report of elevated monocyte-platelet aggregates in healthy children. PLoS One. 2013; 8 (6): e67416. DOI: https://www.doi.org/10.1371/journal.pone.0067416
34. Kim J., Bae J.S. Tumor-associated macrophages and neutrophils in tumor microenvironment. Mediators Inflamm. 2016; 2016: 6058147. DOI: https://doi.org/10.1155/2016/6058147
35. Starskaya I.S., Polevshchikov A.V. Morphological aspects of thymus atrophy under stress. Immunologiya. 2013; 34 (5): 271–7. (in Russian)
36. Lerkvaleekul B., Apiwattanakul N., Klinmalai C., Hongeng S.,Vilaiyuk S. Age-related changes in lymphocyte subpopulations in healthy Thai children. J. Clin. Lab. Anal. 2020; 34 (5): e23156. DOI: https://www.doi.org/10.1002/jcla.23156