The study of the relationship of indicators of immune status and serum ferritin in patients with thalassemia.
DOI:
https://doi.org/10.61841/aa2mq652Keywords:
hemosiderosis, hemolysis, humoral immunity, immunoglobulin, cellular immunity, ferritinAbstract
Data on increased susceptibility to infections with thalassemia have generated interest in studying the immune status of patients with beta-thalassemia. The state of cellular and humoral immunity and the amount of iron-containing ferritin protein were studied in 200 patients, girls and boys with various forms of thalassemia. The indicators of humoral immunity, immunoglobulins A, M, G, as well as some indicators of cellular immunity CD3+, CD4+, CD8+, CD16+ were determined. Determination of immunoglobulins A, M, G was carried out by enzyme-linked immunosorbent assay on an apparatus of Human GmbH (Germany). Indicators of humoral immunity show a decrease in immunoglobulin A, but immunoglobulins M and G are elevated. Normally, ferritin is -10-120 ng / ml, and according to the results of our study, the content of serum ferritin is -1513.1 ng / ml, this indicator is 12.6 times higher, which indicates a risk of developing hemosiderosis of internal organs.
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References
1. Asadov Ch.D., Ragimov A.A. Immunological disorders in beta-thalassemia (literature review). Bulletin of the blood service of Russia, 2011. No. 1. Page37-42.
2. Volkova S.A., Borovkov N.N. The basics of clinical hematology: a training manual, 2013.400 p.
3. Krasilnikova M.V., Lokhmatova M.E., Smetanina N.S. Hematology / Oncology and Immunopathology at the pediatrician, 2009; 1: 43-6.
4. Decree of the President of the Republic of Uzbekistan dated September 7, 2019 No. PP4440 “On measures to further improve medical and social care for children with rare (orphanic) and other genetic diseases”.
5. Sisla B. Guide to laboratory hematology / trans. from English under the general. ed. A.I. Vorobyov. M .: Practical medicine, 2011.352 s.: Ill.
6. Bazi, Ali & Shahramian, Iraj & Yaghoobi, Hajar & Naderi, Majid & Azizi, Hakim. (2017). The Role of Immune System in Thalassemia Major: A Narrative Review. Journal of Pediatrics Review. In Press. 10.5812/jpr.14508.
7. Kountouras D, et al, Liver disease in adult transfusion-dependent beta-thalassaemic patients: investigating the role of iron overload and chronic HCV infection. PG - 420-7. Liver Int. 2013 Mar;33(3):420-7. doi: 10.1111/liv.12095.
8. Azarkeivan A et. al, Correlation between Heart, Liver and Pancreas Hemosiderosis Measured by MRI T2* among Thalassemia Major Patients from Iran.Arch Iran Med. 2016 Feb;19(2):96-100. doi: 0161902/AIM.006.
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