The content of platelet coaggregates with αβ-, γδ-Т-lymphocytes and their some minor subpopulations in the blood of healthy children

Abstract

Introduction. Platelets are able to enter into contact adhesive interactions with almost all blood cells. The formation of coaggregates of platelets and leukocytes in the bloodstream plays a certain role in the physiological processes of cell migration, and the degree of their interaction changes in pathology. In the literature, information on the adhesive interaction of platelets with leukocytes, and especially with lymphocytes and their subpopulations in the blood of healthy children is scarce.

The aim of the study – to research the relative and absolute content of coaggregates of platelets with lymphocytes, T-lymphocytes, αβ- and γδ-T-lymphocytes, their minor subpopulations – double negative and double positive T-lymphocytes (DNT and DPT cells) in the peripheral blood of healthy children of different age, as well as an assessment of the correlation between the studied parameters and the age of children.

Material and methods. The objects of the study were venous blood samples from 83 healthy children (boys and girls) aged from 7 months to 14 years. Monoclonal antibodies conjugated with various fluorochromes were used to detect lymphocyte-platelet coaggregates. Determination of the studied parameters was carried out using flow cytometry.

Results. The relative content and absolute amount of lymphocyte-platelet coaggregates in healthy children of different age groups have been investigated. A decrease in the absolute number of platelet coaggregates with T-lymphocytes, namely, with αβ-T-lymphocytes in the blood of older children, was established. At the same time, there was an increase in the relative content of the total pool of leukocyte-platelet coaggregates and coaggregates (platelets) with double negative T cells in older children compared with younger children.

Conclusion. The content of lymphocyte-platelet coaggregates depends on age. The absolute number of coaggregates of platelets with T-lymphocytes, αβ-T-lymphocytes decreases with age, and the content of coaggregates with γδ-T-lymphocytes remains unchanged. At the same time, there was an increase in the relative content of the total pool of leukocyte-platelet coaggregates and coaggregates (platelets) with double negative T cells in older children.

Keywords:lymphocyte-platelet adhesion; lymphocyte-platelet coaggregates

For citation: Bogomyagkova E.N., Solpov A.V., Vitkovsky Yu.A., Tereshkov P.P. The content of platelet coaggregates with αβ-, γδ-Т-lymphocytes and their some minor subpopulations in the blood of healthy children. Immunologiya. 2022; 43 (1): 78–88. DOI: https://doi.org/10.33029/0206-4952-2021-42-6-78-88 (in Russian)

Funding. The study had no sponsor support.

Conflict of interests. Authors declare no conflict of interests.

Authors’ contributions. Research concept and design – Bogomyagkova E.N., Solpov A.V.; collection and processing of material – Bogomyagkova E.N., Tereshkov P.P.; text writing – Bogomyagkova E.N., Solpov A.V., Vitkovsky Yu.A.

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

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