Level of reactive oxygen species production in peripheral blood monocytes in patients with Graves’ disease after radioiodine therapy
https://doi.org/10.14341/probl13444
Abstract
BACKGROUND: Autoimmune diseases such as Graves’ disease are complex pathologies that often require intensive and long-term treatment. However, the mechanisms contributing to the development and maintenance of this pathology are still not fully understood. Understanding the role of the innate immune response, especially in the context of monocytes, in the development of Graves’ disease remains a poorly understood aspect.
AIM: To study the level of ROS production in monocytes in patients with Graves’ disease after RAI to identify the level of activation of the macrophage-monocyte system.
MATERIALS AND METHODS: The hormonal status and monocyte activity were analyzed before and 1, 3 and 6 months after RAI. The level of ROS was determined using spontaneous and luminol- and luceginin-derived chemiluminescence.
RESULTS: The study included 48 patients with Graves’ disease, aged from 18 to 65 years. In patients with Graves’ disease, a decrease in the intensity of free radical processes in monocytes was detected compared to the control group. These changes were observed both before and after RAI. It has been shown that changes in ROS production are independent of thyroid function and antibody levels. The changes indicate the potential immunosuppressive effects of radionuclide treatment and its effect on monocyte NADPH oxidase activity. A decrease in the production of secondary ROS in monocytes was also noted, which may indicate a decrease in the activation of monocytes during antigenic stimulation and inhibition of autoimmune processes.
CONCLUSION: Reduced metabolic activity of monocytes and low levels of ROS synthesis correlate with inhibition of the autoimmune process and decreased activation of the macrophage-monocyte system. The study confirms the importance of the role of monocytes in the ROS production system and their influence on the autoimmune process in Graves’ disease. These results may have clinical significance and contribute to the development of new immunotropic strategies for the treatment of this disease.
About the Authors
D. V. FominaRussian Federation
Daria V. Fomina
660022, Krasnoyarsk, Partizana Zheleznyka str., 1
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи
S. A. Dogadin
Russian Federation
Sergey A. Dogadin, MD, PhD, Professor
Krasnoyarsk
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи
A. A. Savchenko
Russian Federation
Andrei A. Savchenko, MD, PhD, Professor
Krasnoyarsk
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи
I. I. Gvozdev
Russian Federation
Ivan I. Gvozdev
Krasnoyarsk
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи
References
1. Davies TF, Andersen S, Latif R, et al. Graves’ disease. Nat Rev Dis Primers. 2020;6(1):52. doi: https://doi.org/10.1038/s41572-020-0184-y
2. Lichiardopol C, Moţa M. The thyroid and autoimmunity. Rom J Intern Med. 2009;47(3):207-15
3. Nurieva RI, Chung Y, Hwang D, et al. Generation of T follicular helper cells is mediated by interleukin-21 but independent of T helper 1, 2, or 17 cell lineages. Immunity. 2008;29(1):138-49. doi: https://doi.org/10.1016/j.immuni.2008.05.009
4. Zhu C, Ma J, Liu Y et al. Increased frequency of follicular helper T cells in patients with autoimmune thyroid disease. J Clin Endocrinol Metab. 2012;97(3):943-50. doi: https://doi.org/10.1210/jc.2011-2003
5. Ożańska A, Szymczak D, Rybka J. Pattern of human monocyte subpopulations in health and disease. Scand J Immunol. 2020;92(1):e12883. doi: https://doi.org/10.1111/sji.12883
6. Sedeek M, Nasrallah R, Touyz RM, Hébert RL. NADPH oxidases, reactive oxygen species, and the kidney: friend and foe. J Am Soc Nephrol. 2013;24(10):1512-8. doi: https://doi.org/10.1681/ASN.2012111112
7. Mseddi M, Ben Mansour R, Gargouri B, et al. Proteins oxidation and autoantibodies’ reactivity against hydrogen peroxide and malondialdehyde -oxidized thyroid antigens in patients’ plasmas with Graves’ disease and Hashimoto Thyroiditis. Chem Biol Interact. 2017;272:145-152. doi: https://doi.org/10.1016/j.cbi.2017.04.013
8. Troshina EA, Sviridenko NYu, Vanushko VE, et al. Russian Association of Endocrinologists clinical practice guidelines for thyrotoxicosis diagnosis and treatment. Clinical and experimental thyroidology. 2014;10(3):8-19. (In Russ.) doi: https://doi.org/10.14341/ket201438-19
9. Diana T, Daiber A, Oelze M, et al. Stimulatory TSHReceptor Antibodies and Oxidative Stress in Graves Disease. J Clin Endocrinol Metab. 2018;103(10):3668-3677. doi: https://doi.org/10.1210/jc.2018-00509
10. Dogadin SA, Dudina MA, Savchenko AA, et al. The respiratory explosion activity of neutrophils in blood from patients with Graves’ disease manifestation. Problems of Endocrinology. 2017;63(1):4-8. (in Russ.) doi: https://doi.org/10.14341/probl20176314-8
11. Ma WT, Chang C, Gershwin ME, Lian ZX. J Autoimmun. 2017;83:95- 112. doi: https://doi.org/10.1016/j.jaut.2017.07.003.
12. Chen X, Wang Y, Qi Y, et al. Expansion of inflammatory monocytes in periphery and infiltrated into thyroid tissue in Graves’ disease. Sci Rep. 2021;11(1):13443. doi: https://doi.org/10.1038/s41598-021-92737-4
13. González A, Calleja A, Santiago E, et al. Correlation of activated monocytes or B cells with T lymphocyte subsets in patients with Graves’ disease. Int J Mol Med. 1998;1(1):95-103
14. López-Moratalla N, Calleja A, González A, et al. Inducible nitric oxide synthase in monocytes from patients with Graves’ disease. Biochem Biophys Res Commun. 1996;226(3):723-9. doi: https://doi.org/10.1006/bbrc.1996.1420
15. Pautz A, Art J, Hahn S, et al. Regulation of the expression of inducible nitric oxide synthase. Nitric Oxide. 2010;23(2):75-93. doi: https://doi.org/10.1016/j.niox.2010.04.007
16. Van der Weerd K, Van Hagen PM, Schrijver B, et al. The peripheral blood compartment in patients with Graves’ disease: activated T lymphocytes and increased transitional and pre-naive mature B lymphocytes. Clin Exp Immunol. 2013;174(2):256-64. doi: https://doi.org/10.1111/cei.12183
Supplementary files
Review
For citations:
Fomina D.V., Dogadin S.A., Savchenko A.A., Gvozdev I.I. Level of reactive oxygen species production in peripheral blood monocytes in patients with Graves’ disease after radioiodine therapy. Problems of Endocrinology. 2025;71(2):14-21. (In Russ.) https://doi.org/10.14341/probl13444

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0).