Features of the immune system response in pediatric renal transplant recipients
DOI:
https://doi.org/10.22141/2307-1257.8.4.2019.185120Keywords:
pediatric and adult kidney transplantation, lymphocyte subsets, immunoglobulinsAbstract
Background. We need to take into account patients’ age and their immune system status to improve the results of kidney transplantation. Objective: to study the characteristics of the immune system response to a kidney transplant in pediatric recipients. Materials and methods. We performed a retrospective analysis of the cytometric study of peripheral blood lymphocytes subsets gated on CD45++ with the following antigens: CD3/4/8/45 (T-helper, T-cytotoxic), CD3/DR/19/45 (T-activated, B-cells), CD3/16/56/45 (T-NK- and NK-lymphocytes), CD38/45/19 (activated, total and B-lymphocytes), immunoregulatory index — CD4+/CD8+, and levels of immunoglobulin classes A, M, G in the blood serum in 38 adult and 16 pediatric recipients, who got the first kidney allograft from a living related donor in 2016–2019 at O.O. Shalimov National Institute of Surgery and Transplantology. Immune tests were performed before kidney transplantation, by the end of the first and sixth months after surgery. Results. Children have more pronounced signs of an immune system response to transplant and immunosuppressive therapy than adults. Some of the lymphocyte subsets in children show significantly stronger suppression by the end of the first month after surgery (relative number of CD45++ lymphocytes, relative and absolute number of CD3+19– T-lymphocytes, activated lymphocytes CD38+45+high and B-activated lymphocytes CD38+19+) and in six months (absolute CD45++ lymphocyte count, absolute and relative CD3–19+ B-lymphocyte count, T-activated CD3+DR+). Other lymphocyte subsets, on the contrary, show significantly greater increase in 30 days (absolute and relative CD3–19+ lymphocyte count) and 6 months (relative CD45++ lymphocyte count and T-lymphocytes CD3+19–, relative and absolute count of activated lymphocytes CD38+45+high) after transplantation. Some of the lymphocyte subsets in children recover to preoperative levels faster (relative numbers of CD45++ lymphocytes and T-helper cells CD4+8–). Conclusions. The analysis of the results shows that immune system response to kidney transplant in children and adults is somewhat different and is manifested by multidirectional changes in the absolute and relative number of lymphocyte subsets and immunoglobulin levels, which should be considered when choosing immunosuppressive therapy.
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References
Krystufkova E, Sekerkova A, Striz I, Brabcova I, Gir-manova E, Viklicky O. Regulatory T cells in kidney transplant recipients: the effect of induction immunosuppression thera-py. Nephrol Dial Transplant. 2012 Jun;27(6):2576-82. doi: 10.1093/ndt/gfr693.
Justiz Vaillant AA, Waheed A, Mohseni M. Chronic Transplantation Rejection. Treasure Island (FL): StatPearls Pub-lishing; 2019.
Nairn J, Hodge G, Henning Р. Changes in leukocyte subsets: clinical implications for children with chronic renal failure. Pediatr Nephrol. 2005 Feb;20(2):190-6. doi: 10.1007/s00467-004-1727-2.
Bouts AH, Davin JC, Krediet RT, et al. Children with chronic renal failure have reduced numbers of memory B cells. Clin Exp Immunol. 2004 Sep;137(3):589-94. doi: 10.1111/j.1365-2249.2004.02571.x.
Danovitch GM. Handbook of Kidney Transplantation. Los Angeles: Lippincott Williams & Wilkins; 2012. 496 p. 6. Kurz P, Köhler H, Meuer S, Hütteroth T, Meyer zum Büschenfelde KH. Impaired cellular immune responses in chron-ic renal failure: evidence for a T cell defect. Kidney Int. 1986 Jun;29(6):1209-14. doi: 10.1038/ki.1986.129.
Cendoroglo M, Jaber BL, Balakrishnan VS, Perianaya-gam M, King AJ, Pereira BJ. Neutrophil apoptosis and dysfunc-tion in uremia. J Am Soc Nephrol. 1999 Jan;10(1):93-100.
Fernández-Fresnedo G, Ramos MA, González-Pardo MC, de Francisco AL, López-Hoyos M, Arias M. B lymphopenia in uremia is related to an accelerated in vitro apoptosis and dysregu-lation of Bcl-2. Nephrol Dial Transplant. 2000 Apr;15(4):502-10. doi: 10.1093/ndt/15.4.502.
Zakordonets VP, Zograbian RO, Voroniak OS, Kubashko AV, Baran VYe. Immune system features in pediatric candidates for kidney transplantation. Kidneys. 2017;6(3):144-148. doi: 10.22141/2307-1257.6.3.2017.109029.
Loupy A, Haas M, Solez K, et al. The Banff 2015 Kidney Meeting Report: Current Challenges in Rejection Classification and Prospects for Adopting Molecular Pathology. Am J Trans-plant. 2017 Jan;17(1):28-41. doi: 10.1111/ajt.14107.
Lanh TA, Sesyk M, autors; Leonova VP, editor. Kak opi-syvat' statistiku v meditsine: Annotirovannoe rukovodstvo dlia avtorov, redaktorov i retsenzentov [How to describe statistics in medicine: Annotated Guide for Authors, Editors, and Reviewers]. Moscow: Praktycheskaia medytsyna; 2011. 480 p. (in Russian).
Dunn OJ, Clark VA. Basic Statistics: A Primer for the Biomedical Science. 4thed. New Jersey: Wiley; 2009. 272 p.
Cho MH. Pediatric kidney transplantation is differ-ent from adult kidney transplantation. Korean J Pediatr. 2018 Jul;61(7):205-209. doi: 10.3345/kjp.2018.61.7.205.
Mehrotra A, Heeger PS. B cells and kidney transplanta-tion: beyond antibodies. J Am Soc Nephrol. 2014 Jul;25(7):1373-4. doi: 10.1681/ASN.2014020132.
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Copyright (c) 2019 V.P. Zakordonets, R.O. Zograbyan, A.S. Voroniak, A.V. Kubashko

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