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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/2079-701X-2022-16-19-162-166</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-7188</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ШКОЛА ПЕДИАТРА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PEDIATRICIAN SCHOOL</subject></subj-group></article-categories><title-group><article-title>Сравнительная характеристика показателей гуморального иммунитета и их взаимосвязь с хелаторной терапией при талассемии</article-title><trans-title-group xml:lang="en"><trans-title>Comparative characteristics of humoral immunity indicators and their relationship with chelation therapy in thalassemia</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рахманова</surname><given-names>У. У.</given-names></name><name name-style="western" xml:lang="en"><surname>Rakhmanova</surname><given-names>U. U.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рахманова Умида Улугбековна, к.м.н., доцент кафедры военно-полевой терапии и гематологии </p><p>220100, Узбекистан, Хорезмская область, Ургенч, ул. Аль-Хорезмий, д. 28 </p></bio><bio xml:lang="en"><p>Umida U. Rakhmanova, Cand. Sci. (Med.), Associate Professor of the Department of Military Field Therapy and Hematology</p><p>28, Al-Khorezmiy St., Urgench, Khorezm Region, 220100, Uzbekistan </p></bio><email xlink:type="simple">raxmanovaumidahon@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Ургенчский филиал Ташкентской медицинской академии</institution><country>Узбекистан</country></aff><aff xml:lang="en"><institution>Urgench Branch of Tashkent Medical Academy</institution><country>Uzbekistan</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>16</day><month>11</month><year>2022</year></pub-date><volume>0</volume><issue>19</issue><fpage>162</fpage><lpage>166</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рахманова У.У., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Рахманова У.У.</copyright-holder><copyright-holder xml:lang="en">Rakhmanova U.U.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.med-sovet.pro/jour/article/view/7188">https://www.med-sovet.pro/jour/article/view/7188</self-uri><abstract><p>Введение. Данные о повышенной восприимчивости больных талассемией к инфекциям вызывают большой интерес к изучению различных аспектов иммунного статуса больных.Цель. Изучить показатели гуморального звена иммунитета и их взаимосвязь с хелаторной терапией у больных талассемией.Материалы и методы. Настоящее исследование проведено в Республиканском специализированном научно-практическом медицинском центре гематологии с 2015 по 2020 г. Материалом исследования явилась периферическая венозная кровь больных талассемией. При определении иммунологического статуса больных β-талассемией нами были исследованы 74 школьника в возрасте 8–12 лет. Статистическая обработка клинического материала была произведена при помощи статистического пакета прикладных программ «STATISTICA 10.0».Результаты и обсуждение. Результаты изучения содержания сывороточных иммуноглобулинов в крови больных детей показали сниженный синтез IgA (р &lt; 0,001). При этом уровень IgМ был достоверно повышен у больных β-талассемией по сравнению с контролем (р &lt; 0,001), что говорит о наличии острого воспаления в организме. Также результаты наших исследований показали, что наблюдается некоторая тенденция к повышению уровня IgG (11,2 ± 0,41 пг/мл в контроле против 16,13 ± 0,58 пг/мл), наблюдалось достоверное повышение синтеза этого иммуноглобулина (р &lt; 0,001), это позволяет утверждать об аутоиммунном процессе. В группе больных β-талассемией детей уровень С-реактивного белка был в 4 раза выше значений контрольной группы (3,8 ± 0,1 нг/мг в контроле против 15,33 ± 0,17 нг/мг, p &lt; 0,001). Уровень лактоферрина у больных детей был снижен в 4,2 раза по сравнению с данными контрольной группы. Наблюдается дисрегуляция факторов белков острой фазы: С-реактивного белка и лактоферрина. Для β-талассемии характерно резкое повышение уровня провоспалительных цитокинов – уровень IL-6 повышен в 2,9 раза, а уровень IL-18 – в 8,7 раза.Выводы. Выявлена взаимосвязь между показателями иммунного статуса и показателями гемосидероза, имеется достоверная разница во всех изученных показателях, применение хелаторной терапии способствует положительной динамике.</p></abstract><trans-abstract xml:lang="en"><p>Introduction. Data on the increased susceptibility of patients with thalassemia to infections are of great interest to the study of various aspects of the immune status of patients.Aim. The aim of the study was to study the parameters of the humoral immunity and their relationship with chelation therapy in patients with thalassemia.Materials and methods. This study was carried out at the Republican Specialized Scientific and Practical Medical Center for Hematology from 2015 to 2020. The material of the study was the peripheral venous blood of patients with thalassemia. When determining the immunological status of patients with β-thalassemia, we examined 74 schoolchildren, aged 8–12 years. Statistical processing of clinical material was carried out using the statistical package of application programs STATISTICA 10.0.Results and discussion. The results of the study of the content of serum immunoglobulins in the blood of sick children showed a reduced synthesis of IgA (p &lt; 0.001). At the same time, the level of IgM was significantly increased in patients with β-thalassemia, compared with the control (p &lt; 0.001), which indicates the presence of acute inflammation in the body. Also, the results of our studies showed that there is a certain tendency to increase the level of IgG (11.2 ± 0.41 pg/ml in control versus 16.13 ± 0.58 pg/ml), there was a significant increase in the synthesis of this immunoglobulin (p &lt; 0.001), this allows us to state about the autoimmune process. In the group of children with β-thalassemia, the level of C-reactive protein (CRP) was 4 times higher than the values of the control group (3.8 ± 0.1 ng/mg in the control versus 15.33 ± 0.17 ng/mg, p &lt; 0.001). The level of lactoferrin in sick children was reduced by 4.2 times compared with the data of the control group. There is a dysregulation of acute phase protein factors – C-reactive protein and lactoferrin. β-thalassemia is characterized by a sharp increase in the level of pro-inflammatory cytokines – the level of IL-6 is increased by 2.9 times, and the level of IL-18 – by 8.7 times.Conclusion. The relationship between the indicators of the immune status and indicators of hemosiderosis was revealed, there is a significant difference in all the studied indicators, the use of chelation therapy contributes to positive dynamics.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гемотрансфузии</kwd><kwd>гемосидероз</kwd><kwd>лактоферрин</kwd><kwd>пояс талассемии</kwd><kwd>хелаторная терапия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hemotransfusion</kwd><kwd>hemosiderosis</kwd><kwd>lactoferrin</kwd><kwd>thalassemia belt</kwd><kwd>chelation therapy</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Asadov C., Alimirzoeva Z., Hasanova M., Mammadova T., Shirinova A. Clinical News. Application of recombinant erythropoietin in beta-thalassemia intermedia. Georgian Med. 2016;255(6):86–92. Available at: https://pubmed.ncbi.nlm.nih.gov/27441542.</mixed-citation><mixed-citation xml:lang="en">Asadov C., Alimirzoeva Z., Hasanova M., Mammadova T., Shirinova A. Clinical News. Application of recombinant erythropoietin in beta-thalassemia intermedia. Georgian Med. 2016;255(6):86–92. Available at: https://pubmed.ncbi.nlm.nih.gov/27441542.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Abraham A., Sindhuvi Е., Korula A., Fouzia N.A., Srivastava A., George B. et al. Donor Lymphocyte Infusion in Patients with Thalassemia Major Who Have Mixed Chimerism Following Allogeneic Stem Cell Transplant. Biol Blood Marrow Transplant. 2016;22:S19eS481. Available at: https://www.astctjournal.org/article/S1083-8791(15)01232-X/pdf.</mixed-citation><mixed-citation xml:lang="en">Abraham A., Sindhuvi Е., Korula A., Fouzia N.A., Srivastava A., George B. et al. Donor Lymphocyte Infusion in Patients with Thalassemia Major Who Have Mixed Chimerism Following Allogeneic Stem Cell Transplant. Biol Blood Marrow Transplant. 2016;22:S19eS481. Available at: https://www.astctjournal.org/article/S1083-8791(15)01232-X/pdf.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Aleem A., Shakoor Z., Alsaleh K., Algahtani F., Iqbal Z., Al-Momen A. Immunological evaluation of β-thalassemia major patients receiving oral iron chelator deferasirox. J Coll Physicians Surg Pak. 2014;24(7):467–471. Available at: https://pubmed.ncbi.nlm.nih.gov/25052967.</mixed-citation><mixed-citation xml:lang="en">Aleem A., Shakoor Z., Alsaleh K., Algahtani F., Iqbal Z., Al-Momen A. Immunological evaluation of β-thalassemia major patients receiving oral iron chelator deferasirox. J Coll Physicians Surg Pak. 2014;24(7):467–471. Available at: https://pubmed.ncbi.nlm.nih.gov/25052967.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Angelucci E., Santini V., Di Tucci A.A., Quaresmini G., Finelli C., Volpe A. et al. Deferasirox for transfusion-dependent patients with myelodysplastic syndromes: safety, efficacy, and beyond (GIMEMA MDS 0306 Trial). Eur J Haematol. 2014;92(6):527–536. Available at: https://pubmed.ncbi.nlm.nih.gov/24580147.</mixed-citation><mixed-citation xml:lang="en">Angelucci E., Santini V., Di Tucci A.A., Quaresmini G., Finelli C., Volpe A. et al. Deferasirox for transfusion-dependent patients with myelodysplastic syndromes: safety, efficacy, and beyond (GIMEMA MDS 0306 Trial). Eur J Haematol. 2014;92(6):527–536. Available at: https://pubmed.ncbi.nlm.nih.gov/24580147.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Andreani M., Testi M., Gaziev J., Condello R., Bontadini A., Tazzari P.L. et al. Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease. Haematologica. 2011;96(1):128–133. Available at: https://pubmed.ncbi.nlm.nih.gov/20935000.</mixed-citation><mixed-citation xml:lang="en">Andreani M., Testi M., Gaziev J., Condello R., Bontadini A., Tazzari P.L. et al. Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease. Haematologica. 2011;96(1):128–133. Available at: https://pubmed.ncbi.nlm.nih.gov/20935000.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Ansari S., Rashid N., Hanifa A., Siddiqui S., Kaleem B., Naz A. et al. Laboratory diagnosis for thalassemia intermedia: Are we there yet? J Clin Lab Anal. 2019;33(1):e22647. Available at: https://pubmed.ncbi.nlm.nih.gov/30221402.</mixed-citation><mixed-citation xml:lang="en">Ansari S., Rashid N., Hanifa A., Siddiqui S., Kaleem B., Naz A. et al. Laboratory diagnosis for thalassemia intermedia: Are we there yet? J Clin Lab Anal. 2019;33(1):e22647. Available at: https://pubmed.ncbi.nlm.nih.gov/30221402.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Asadov C., Alimirzoeva Z., Mammadova T., Aliyeva G., Gafarova S., Mammadov J. β-Thalassemia intermedia: a comprehensive overview and novel approaches. Int J Hematol. 2018;108(1):5–21. Available at: https://www.researchgate.net/publication/322763987.</mixed-citation><mixed-citation xml:lang="en">Asadov C., Alimirzoeva Z., Mammadova T., Aliyeva G., Gafarova S., Mammadov J. β-Thalassemia intermedia: a comprehensive overview and novel approaches. Int J Hematol. 2018;108(1):5–21. Available at: https://www.researchgate.net/publication/322763987.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Ahluwalia J., Datta U., Marwaha R.K., Sehgal S. Immune functions in splenectomized thalassaemic children. Indian. J Pediatr. 2000;67:871–876. Available at: https://pubmed.ncbi.nlm.nih.gov/11262984.</mixed-citation><mixed-citation xml:lang="en">Ahluwalia J., Datta U., Marwaha R.K., Sehgal S. Immune functions in splenectomized thalassaemic children. Indian. J Pediatr. 2000;67:871–876. Available at: https://pubmed.ncbi.nlm.nih.gov/11262984.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Bollig C., Schell L.K., Rucker G., Allert R., Motschall E., Niemeyer C.M. et al. Deferasirox for managing iron overload in people with thalassemia. Cochrane Database Syst Rev. 2017;2017(8). Available at: https://pubmed.ncbi.nlm.nih.gov/28809446.</mixed-citation><mixed-citation xml:lang="en">Bollig C., Schell L.K., Rucker G., Allert R., Motschall E., Niemeyer C.M. et al. Deferasirox for managing iron overload in people with thalassemia. Cochrane Database Syst Rev. 2017;2017(8). Available at: https://pubmed.ncbi.nlm.nih.gov/28809446.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Bordbar E., Taghipour M., Zucconi B. Reliability of Different RBC Indices and Formulas in Discriminating between β-Thalassemia Minor and other Microcytic Hypochromic Cases. Mediterr. J Hematol Infect Dis. 2015;7(1):e2015022. Available at: https://www.researchgate.net/publication/348430068.</mixed-citation><mixed-citation xml:lang="en">Bordbar E., Taghipour M., Zucconi B. Reliability of Different RBC Indices and Formulas in Discriminating between β-Thalassemia Minor and other Microcytic Hypochromic Cases. Mediterr. J Hematol Infect Dis. 2015;7(1):e2015022. Available at: https://www.researchgate.net/publication/348430068.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Brancaleoni V., Di Pierro E., Motta I., Cappellini M.D. Laboratory diagnosis of thalassemia. Int J Lab Hematol. 2016;38(Suppl. 1):32–40. Available at: https://onlinelibrary.wiley.com/doi/full/10.1111/ijlh.12527.</mixed-citation><mixed-citation xml:lang="en">Brancaleoni V., Di Pierro E., Motta I., Cappellini M.D. Laboratory diagnosis of thalassemia. Int J Lab Hematol. 2016;38(Suppl. 1):32–40. Available at: https://onlinelibrary.wiley.com/doi/full/10.1111/ijlh.12527.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Borgna-Pignatti C., Rugolotto S., De Stefano P., Zhao H., Cappellini M.D., Del Vecchio G.C. et al. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. Haematologica. 2004;89:1187–1193. Available at: https://www.haematologica.org/article/download/3248/11747.</mixed-citation><mixed-citation xml:lang="en">Borgna-Pignatti C., Rugolotto S., De Stefano P., Zhao H., Cappellini M.D., Del Vecchio G.C. et al. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. Haematologica. 2004;89:1187–1193. Available at: https://www.haematologica.org/article/download/3248/11747.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Galanello R., Origa R. Beta-thalassemia. Orphanet J Rare Dis. 2010;5:11. Available at: https://ojrd.biomedcentral.com/articles/10.1186/1750-1172-5-11.</mixed-citation><mixed-citation xml:lang="en">Galanello R., Origa R. Beta-thalassemia. Orphanet J Rare Dis. 2010;5:11. Available at: https://ojrd.biomedcentral.com/articles/10.1186/1750-1172-5-11.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Cantinieaux B., Hariga C., Ferster A., De Maertelaere E., Toppet M., Fondu P. Neutrophil dysfunction in thalassaemia major: The role of iron overload. Eur J Haematol. 1987;39:28–34. Available at: https://www.sciencedirect.com/science/article/abs/pii/S0006497121029268.</mixed-citation><mixed-citation xml:lang="en">Cantinieaux B., Hariga C., Ferster A., De Maertelaere E., Toppet M., Fondu P. Neutrophil dysfunction in thalassaemia major: The role of iron overload. Eur J Haematol. 1987;39:28–34. Available at: https://www.sciencedirect.com/science/article/abs/pii/S0006497121029268.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Ghanavat M., Haybar H., Pezeshki S.M.S., Shahjahani M., Jodat H., Elyasi M., Saki N. Cardiomyopathy in Thalassemia: Quick Review from Cellular Aspects to Diagnosis and Current Treatments. Lab Med. 2020;51(2):143–150. Available at: https://academic.oup.com/labmed/article/51/2/143/5542818.</mixed-citation><mixed-citation xml:lang="en">Ghanavat M., Haybar H., Pezeshki S.M.S., Shahjahani M., Jodat H., Elyasi M., Saki N. Cardiomyopathy in Thalassemia: Quick Review from Cellular Aspects to Diagnosis and Current Treatments. Lab Med. 2020;51(2):143–150. Available at: https://academic.oup.com/labmed/article/51/2/143/5542818.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Consolini R., Calleri A., Legitimo A., Massei F. Immunological evaluation of patients with beta-thalassemia major. Acta Haematol. 2001;105:7–12. Available at: https://pubmed.ncbi.nlm.nih.gov/25052967.</mixed-citation><mixed-citation xml:lang="en">Consolini R., Calleri A., Legitimo A., Massei F. Immunological evaluation of patients with beta-thalassemia major. Acta Haematol. 2001;105:7–12. Available at: https://pubmed.ncbi.nlm.nih.gov/25052967.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Capellini M., Cohen A., Eleftheriou A., Piga A., Porter J., Taher A. Guidelines for the clinical management of thalassemia (2nd ed.). Nicosia (CY): Thalassaemia International Federation; 2008. Available at: https://www.ncbi.nlm.nih.gov/books/NBK173968.</mixed-citation><mixed-citation xml:lang="en">Capellini M., Cohen A., Eleftheriou A., Piga A., Porter J., Taher A. Guidelines for the clinical management of thalassemia (2nd ed.). Nicosia (CY): Thalassaemia International Federation; 2008. Available at: https://www.ncbi.nlm.nih.gov/books/NBK173968.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">De Dreuzy E., Bhukhai K., Leboulch P., Payen E. Current and future alternative therapies for beta-thalassemia major. Biom J. 2016;39(1):24–38. Available at: https://pubmed.ncbi.nlm.nih.gov/27105596.</mixed-citation><mixed-citation xml:lang="en">De Dreuzy E., Bhukhai K., Leboulch P., Payen E. Current and future alternative therapies for beta-thalassemia major. Biom J. 2016;39(1):24–38. Available at: https://pubmed.ncbi.nlm.nih.gov/27105596.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Daher A.M., Al-Momen H., Jasim S.K. Deferasirox in thalassemia: a comparative study between an innovator drug and its copy among a sample of Iraqi patients. Ther Adv Drug Saf. 2019;10:2042098619880123. Available at: https://www.researchgate.net/publication/336388499.</mixed-citation><mixed-citation xml:lang="en">Daher A.M., Al-Momen H., Jasim S.K. Deferasirox in thalassemia: a comparative study between an innovator drug and its copy among a sample of Iraqi patients. Ther Adv Drug Saf. 2019;10:2042098619880123. Available at: https://www.researchgate.net/publication/336388499.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Dussiot M., Maciel T.T., Fricot A., Chartier C., Negre O., Veiga J. et al. An activin receptor IIA ligand trap corrects ineffective erythropoiesis in beta-thalassemia. Nat Med. 2014;20:398–407. Available at: https://www.nature.com/articles/nm.3468.</mixed-citation><mixed-citation xml:lang="en">Dussiot M., Maciel T.T., Fricot A., Chartier C., Negre O., Veiga J. et al. An activin receptor IIA ligand trap corrects ineffective erythropoiesis in beta-thalassemia. Nat Med. 2014;20:398–407. Available at: https://www.nature.com/articles/nm.3468.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">El-Beshlawy A., El-Ghamrawy M. Recent trends in treatment of thalassemia. Blood Cells Mol Dis. 2019;76:53–58. Available at: https://www.researchgate.net/publication/330860612.</mixed-citation><mixed-citation xml:lang="en">El-Beshlawy A., El-Ghamrawy M. Recent trends in treatment of thalassemia. Blood Cells Mol Dis. 2019;76:53–58. Available at: https://www.researchgate.net/publication/330860612.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Giardine B., Borg J., Viennas E., Pavlidic C.P., Moradkhani K., Joly P. et al. Updates of the Hb Var database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2014;42(Database issue):D1063–D1069. https://doi.org/10.1093/nar/gkt911.</mixed-citation><mixed-citation xml:lang="en">Giardine B., Borg J., Viennas E., Pavlidic C.P., Moradkhani K., Joly P. et al. Updates of the Hb Var database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2014;42(Database issue):D1063–D1069. https://doi.org/10.1093/nar/gkt911.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Haghpanah S., Zarei T., Zahedi Z., Karimi M. Compliance and satisfaction with deferasirox (Exjade®) compared with deferoxamine in patients with transfusion-dependent beta-thalassemia. Hematology. 2014;19(4):187–191. Available at: https://www.researchgate.net/publication/257202367.</mixed-citation><mixed-citation xml:lang="en">Haghpanah S., Zarei T., Zahedi Z., Karimi M. Compliance and satisfaction with deferasirox (Exjade®) compared with deferoxamine in patients with transfusion-dependent beta-thalassemia. Hematology. 2014;19(4):187–191. Available at: https://www.researchgate.net/publication/257202367.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Huang C.W., Jiang H. Research advances in transplantation for thalassemia major. Zhongguo Dang Dai Er Ke Za Zhi. 2020;22(1):77–81. Available at: https://www.researchgate.net/publication/338675330_Research_advances_in_transplantation_for_thalassemia_major.</mixed-citation><mixed-citation xml:lang="en">Huang C.W., Jiang H. Research advances in transplantation for thalassemia major. Zhongguo Dang Dai Er Ke Za Zhi. 2020;22(1):77–81. Available at: https://www.researchgate.net/publication/338675330_Research_advances_in_transplantation_for_thalassemia_major.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">.Jang J.H., Lee J.H., Yoon S.S., Jo D.Y., Kim H.J., Chung J., Lee J.W. Korean guidline for iron chelator therapy in transfusion-indused iron overload. J Korean Med Sci. 2013;28:1563–1572. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835496.</mixed-citation><mixed-citation xml:lang="en">.Jang J.H., Lee J.H., Yoon S.S., Jo D.Y., Kim H.J., Chung J., Lee J.W. Korean guidline for iron chelator therapy in transfusion-indused iron overload. J Korean Med Sci. 2013;28:1563–1572. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835496.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Karimi M., Arandi N., Haghpanah S., Ansari S., Azarkeyvan A., Bordbar M., Safaei S. Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia Intermedia. Hemoglobin. 2015;39(5):327–329. Available at: https://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1057735.</mixed-citation><mixed-citation xml:lang="en">Karimi M., Arandi N., Haghpanah S., Ansari S., Azarkeyvan A., Bordbar M., Safaei S. Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia Intermedia. Hemoglobin. 2015;39(5):327–329. Available at: https://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1057735.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Khera R., Singh T., Khuana N., Gupta N., Dubey A.P. HPLC in characterization of hemoglobin profile in thalassemia syndromes and hemoglobin pathies: a clinic hematological correlation. Indian. J Hematol Blood Transfus. 2015;31(1):110–115. Available at: https://www.hindawi.com/journals/isrn/2014/257805.</mixed-citation><mixed-citation xml:lang="en">Khera R., Singh T., Khuana N., Gupta N., Dubey A.P. HPLC in characterization of hemoglobin profile in thalassemia syndromes and hemoglobin pathies: a clinic hematological correlation. Indian. J Hematol Blood Transfus. 2015;31(1):110–115. Available at: https://www.hindawi.com/journals/isrn/2014/257805.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Kontoghiorghe C.N., Kontoghiorghes G.J. Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. Drug Des Dev Ther. 2016;10:465–481. Available at: https://www.semanticscholar.org.</mixed-citation><mixed-citation xml:lang="en">Kontoghiorghe C.N., Kontoghiorghes G.J. Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. Drug Des Dev Ther. 2016;10:465–481. Available at: https://www.semanticscholar.org.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Langlois S., Ford J.C., Chitayat D.; CCMG prenatal diagnosis committee; SOGC genetics committee. Carrier screening for thalassemia and hemoglobinopathies in Canada. J Obstet Gynaecol Can. 2008;30(10):950–959. Available at: https://www.jogc.com/article/S1701-2163(16)32975-9/fulltext.</mixed-citation><mixed-citation xml:lang="en">Langlois S., Ford J.C., Chitayat D.; CCMG prenatal diagnosis committee; SOGC genetics committee. Carrier screening for thalassemia and hemoglobinopathies in Canada. J Obstet Gynaecol Can. 2008;30(10):950–959. Available at: https://www.jogc.com/article/S1701-2163(16)32975-9/fulltext.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Lombardi G., Matera R., Minervini M., Cascavilla N., D’Arcangelo P., Carotenuto M. et al. Serum levels of cytokines and soluble antigens in polytransfused patients with beta thalassemia major: relationship to immune status. Hematologica. 1994;79(5):406–412. Available at: https://pubmed.ncbi.nlm.nih.gov/7843626.</mixed-citation><mixed-citation xml:lang="en">Lombardi G., Matera R., Minervini M., Cascavilla N., D’Arcangelo P., Carotenuto M. et al. Serum levels of cytokines and soluble antigens in polytransfused patients with beta thalassemia major: relationship to immune status. Hematologica. 1994;79(5):406–412. Available at: https://pubmed.ncbi.nlm.nih.gov/7843626.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Pattanapanyasat K., Thepthai C., Lamchiagdhase P. et al. Lymphocyte subsets and specific T-cell immune response in thalassemia. Cytometry. 2000;42:11–17. Available at: https://www.researchgate.net/publication/12635205.</mixed-citation><mixed-citation xml:lang="en">Pattanapanyasat K., Thepthai C., Lamchiagdhase P. et al. Lymphocyte subsets and specific T-cell immune response in thalassemia. Cytometry. 2000;42:11–17. Available at: https://www.researchgate.net/publication/12635205.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Risoluti R., Materazzi S., Sorrentino F., Bozzi C., Caprari P. Update on thalassemia diagnosis: New insights and methods. Talanta. 2018;183:216–222. Available at: https://www.researchgate.net/publication/323283581.</mixed-citation><mixed-citation xml:lang="en">Risoluti R., Materazzi S., Sorrentino F., Bozzi C., Caprari P. Update on thalassemia diagnosis: New insights and methods. Talanta. 2018;183:216–222. Available at: https://www.researchgate.net/publication/323283581.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
