THE INFLUENCE OF IL-7 AND IL-15 ON T-REGULATORY CELLS OF DONORS AND PATIENTS WITH RHEUMATOID ARTHRITIS IN VITRO
- Authors: Shevyrev D.V.1, Kozlov V.A.1, Omelchenko V.O.2
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Affiliations:
- Federal State Budgetary Scientific Institution Research Institute of Fundamental and Clinical Immunology
- Research Institute of Clinical and Experimental Lymphology – a branch of the Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
- Issue: Vol 22, No 2-1 (2019)
- Pages: 653-656
- Section: ORIGINAL ARTICLES
- Submitted: 26.05.2020
- Accepted: 26.05.2020
- Published: 15.04.2019
- URL: https://rusimmun.ru/jour/article/view/251
- DOI: https://doi.org/10.31857/S102872210007004-9
- ID: 251
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Abstract
The aim of this study was to assess the infl uence of homeostatic factors IL-7 and IL-15, that induced homeostatic proliferation (HP), on the phenotypic characteristics of T-regulatory cells (Treg) from healthy donors and patients with rheumatoid arthritis (RA) in vitro. Analysis of Treg phenotype was performed by fl ow cytometry, using Foxp3, CD127, CD4 and CD25. Isolated from the blood cells were cultured with and without stimulation during 7 days. IL-7, IL-15 and anti-CD3 antibodies supplemented IL-2 were chosen as activators. Purifi ed Treg cells were labeled with CFSE dye to assess proliferation. We estimated that HP factors eff ectively maintain the number and phenotype (CD25+FoxP3+) of Treg in vitro. Also, in patients group we showed an increasing of CD4+CD25+FoxP3+ cells under all stimulation condition that may indicate the induction of Treg from conventional T cells. Herewith under IL-7 and IL-15 Treg cells from RA patients had a low proliferative activity than Treg from donors. The reduced proliferative activity of Treg in the group of RA-patients under IL-7 and IL-15 perhaps make a signifi - cant contribution to the development of the disease due to the delay of Treg pool reconstitution in the lymphopenia conditions on the initial stage. Furthermore, increased induction of CD4+CD25+FoxP3+ cells in PBMC cultures in patients group associated with pathogenesis of RA, since induced Treg have transient and unstable expression of FoxP3.
About the authors
D. V. Shevyrev
Federal State Budgetary Scientific Institution Research Institute of Fundamental and Clinical Immunology
Author for correspondence.
Email: dr.daniil25@mail.ru
PhD student, laboratory of clinical immunopathology,
Novosibirsk
Russian FederationV. A. Kozlov
Federal State Budgetary Scientific Institution Research Institute of Fundamental and Clinical Immunology
Email: fake@neicon.ru
Full Member of the Russian Academy of Sciences, doctor of medical sciences, professor,
Novosibirsk
Russian FederationV. O. Omelchenko
Research Institute of Clinical and Experimental Lymphology – a branch of the Institute of Cytologyand Genetics of the Siberian Branch of the Russian Academy of Sciences
Email: fake@neicon.ru
junior researcher, laboratory of connective tissue pathology,
Novosibirsk
Russian FederationReferences
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