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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Infection and Immunity</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Infection and Immunity</journal-title><trans-title-group xml:lang="ru"><trans-title>Инфекция и иммунитет</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2220-7619</issn><issn publication-format="electronic">2313-7398</issn><publisher><publisher-name xml:lang="en">SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">16874</article-id><article-id pub-id-type="doi">10.15789/2220-7619-EOU-16874</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Autoimmune disorders in patients with granulomatosis diseases after COVID-19: T- and B-cells subsets function</article-title><trans-title-group xml:lang="ru"><trans-title>Аутоиммунные нарушения у больных гранулематозными заболеваниями после COVID-19: функционирование субпопуляций Т- и В-клеток</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Starshinova</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Старшинова</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>DSc (Medicine), Head Researcher, Laboratory of Probabilistic Methods of Analysis, Mathematics Department; Head of the Research Department</p></bio><bio xml:lang="ru"><p>д.м.н., главный научный сотрудник лаборатории вероятностных методов анализа математического факультета; начальник Управления научными исследованиями</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kudryavtsev</surname><given-names>I. V.</given-names></name><name xml:lang="ru"><surname>Кудрявцев</surname><given-names>И. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD (Biology), Head of the Cell Immunology Laboratory, Department of Immunology</p></bio><bio xml:lang="ru"><p>к.б.н., зав. лабораторией клеточной иммунологии отдела иммунологии</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rubinstein</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Рубинштейн</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Junior Researcher, Cell Immunology Laboratory, Department of Immunology</p></bio><bio xml:lang="ru"><p>младший научный сотрудник лаборатории клеточной иммунологии отдела иммунологии</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Malkova</surname><given-names>A.</given-names></name><name xml:lang="ru"><surname>Малкова</surname><given-names>А.</given-names></name></name-alternatives><address><country country="IL">Israel</country></address><bio xml:lang="en"><p>PhD Student, Department of Molecular Biology, Faculty of Natural Sciences</p></bio><bio xml:lang="ru"><p>аспирант кафедры молекулярной биологии факультета естественных наук</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ling</surname><given-names>H.</given-names></name><name xml:lang="ru"><surname>Лин</surname><given-names>Х.</given-names></name></name-alternatives><address><country country="CN">China</country></address><bio xml:lang="en"><p>DSc (Medicine), Department of Microbiology, Immunology, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology</p></bio><bio xml:lang="ru"><p>д.м.н., кафедра микробиологии, иммунологии; ключевая лаборатория инфекций и иммунитета провинции Хэйлунцзян; ключевая лаборатория биологии патогенов</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zhuang</surname><given-names>M.</given-names></name><name xml:lang="ru"><surname>Чжуан</surname><given-names>М.</given-names></name></name-alternatives><address><country country="CN">China</country></address><bio xml:lang="en"><p>DSc (Medicine), Department of Microbiology, Immunology, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology</p></bio><bio xml:lang="ru"><p>д.м.н., кафедра микробиологии, иммунологии; ключевая лаборатория инфекций и иммунитета провинции Хэйлунцзян; ключевая лаборатория биологии патогенов</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Starshinova</surname><given-names>A. Yu.</given-names></name><name xml:lang="ru"><surname>Старшинова</surname><given-names>А. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Student of Medicine Department</p></bio><bio xml:lang="ru"><p>студент медицинского факультета</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Dovgaluk</surname><given-names>I. F.</given-names></name><name xml:lang="ru"><surname>Довгалюк</surname><given-names>И. Ф.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>DSc (Medicine), Professor, Leading Researcher, Head of Pediatric Tuberculosis Department</p></bio><bio xml:lang="ru"><p>д.м.н., профессор, ведущий научный сотрудник, зав. отделением детского туберкулеза</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff7"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kudlay</surname><given-names>D. A.</given-names></name><name xml:lang="ru"><surname>Кудлай</surname><given-names>Д. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>DSc (Medicine), Professor of Pharmacology Department, Institute of Pharmacy; Leading Researcher, Laboratory of Personalized Medicine and Molecular Immunology</p></bio><bio xml:lang="ru"><p>д.м.н., профессор кафедры фармакологии Института фармации; ведущий научный сотрудник лаборатории персонализированной медицины и молекулярной иммунологии</p></bio><email>arrubin6@mail.ru</email><xref ref-type="aff" rid="aff8"/><xref ref-type="aff" rid="aff9"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">St. Petersburg State University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО Санкт-Петербургский государственный университет</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Almazov National Medical Research Centre</institution></aff><aff><institution xml:lang="ru">ФГБУ Национальный медицинский исследовательский центр имени Алмазова</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Institution of Experimental Medicine</institution></aff><aff><institution xml:lang="ru">ФГБНУ Институт экспериментальной медицины</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Ariel University</institution></aff><aff><institution xml:lang="ru">Университет Ариэль</institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">Harbin Medical University</institution></aff><aff><institution xml:lang="ru">Харбинский медицинский университет</institution></aff></aff-alternatives><aff-alternatives id="aff6"><aff><institution xml:lang="en">St. Petersburg State Pediatric Medical University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО Санкт-Петербургский государственный педиатрический медицинский университет</institution></aff></aff-alternatives><aff-alternatives id="aff7"><aff><institution xml:lang="en">St. Petersburg Research Institute of Phthisiopulmonology</institution></aff><aff><institution xml:lang="ru">ФГБУ Санкт-Петербургский научно-исследовательский институт фтизиопульмонологии Министерства здравоохранения Российской Федерации</institution></aff></aff-alternatives><aff-alternatives id="aff8"><aff><institution xml:lang="en">I.M. Sechenov First Moscow State Medical University</institution></aff><aff><institution xml:lang="ru">ФГАОУ ВО Первый Московский государственный медицинский университет имени И.М. Сеченова Министерства здравоохранения Российской Федерации (Сеченовский Университет)</institution></aff></aff-alternatives><aff-alternatives id="aff9"><aff><institution xml:lang="en">Institute of Immunology FMBA of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ ГНЦ Институт иммунологии ФМБА России</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2024-03-25" publication-format="electronic"><day>25</day><month>03</month><year>2024</year></pub-date><pub-date date-type="pub" iso-8601-date="2024-06-05" publication-format="electronic"><day>05</day><month>06</month><year>2024</year></pub-date><volume>14</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>251</fpage><lpage>266</lpage><history><date date-type="received" iso-8601-date="2023-10-04"><day>04</day><month>10</month><year>2023</year></date><date date-type="accepted" iso-8601-date="2024-03-21"><day>21</day><month>03</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Starshinova A.A., Kudryavtsev I.V., Rubinstein A.A., Malkova A., Ling H., Zhuang M., Starshinova A.Y., Dovgaluk I.F., Kudlay D.A.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Старшинова А.А., Кудрявцев И.В., Рубинштейн А.А., Малкова А., Лин Х., Чжуан М., Старшинова А.Ю., Довгалюк И.Ф., Кудлай Д.А.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Starshinova A.A., Kudryavtsev I.V., Rubinstein A.A., Malkova A., Ling H., Zhuang M., Starshinova A.Y., Dovgaluk I.F., Kudlay D.A.</copyright-holder><copyright-holder xml:lang="ru">Старшинова А.А., Кудрявцев И.В., Рубинштейн А.А., Малкова А., Лин Х., Чжуан М., Старшинова А.Ю., Довгалюк И.Ф., Кудлай Д.А.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://iimmun.ru/iimm/article/view/16874">https://iimmun.ru/iimm/article/view/16874</self-uri><abstract xml:lang="en"><p>Sarcoidosis and tuberculosis are both granulomatous diseases that have many similarities, making the differential diagnosis of sarcoidosis and tuberculosis difficult, as well as leading to inappropriate treatment selection of both diseases. Autoimmune inflammation (AI) is one of the processes identified tuberculosis and sarcoidosis. Current evidences about the risk and clinical outcomes of COVID-19 infection in patient with sarcoidosis and M. tuberculosis co-infection are still not well understood. SARS-CoV-2 has direct damage to the epithelial cells of the respiratory system, and in-directly due to circulatory disorders. Materials and methods. In the study we analyzed characteristics of autoimmune response in patients with granulomatosis diseases (tuberculosis and sarcoidosis) after COVID-19. We have analyzed articles for the period of December 2019 to March 2023, published in international database (“Medline”, “PubMed”, “Scopus”). The keywords we used “COVID-19”, “SARS-CoV-2”, “tuberculosis”, “sarcoidosis”, “granulomatosis diseases”, “T cells”, “B cells”, “Treg”, “follicular Treg” and “Treg subsets”. The narrative review was carried out in accordance with the PRISMA protocol (http://www.prisma-statement.org) used for this type of study (ID-423604). Results. The influence of COVID-19 infection can also make a significant contribution to the violation of the T- and B-cell immune response, the violation of the nature of cellular metabolism, which will affect the course of granulomatous inflammation in various ways. According to the different researches, autoimmune inflammation can be an important protective mechanism in sarcoidosis and, at the same time, exacerbates the course of tuberculosis infection with the disease progression and pathogen drug resistance formation subsequently. The study of immune response features in patients with COVID-19 showed the presence of several similar characteristics in cellular components of the immune response. Conclusion. Evidence of the presence of autoimmune inflammation in patients with these granulomatous lung diseases, the development of patient immunotypes, including the transferred COVID-19, will be a significant contribution to the development of personalized patient management tactics, taking into account the identified violations of the immune response mechanisms.</p></abstract><trans-abstract xml:lang="ru"><p>Саркоидоз и туберкулез являются гранулематозными патологиями, имеющими большое количество схожих черт, из-за которых возникают трудности в дифференциальной диагностике этих заболеваний, что в дальнейшем приводит к неправильному выбору тактики лечения пациентов. Аутоиммунное воспаление (АВ) является одним из процессов, выявленных как при туберкулезе, так и при саркоидозе. Текущие данные о риске и клинических исходах инфекции COVID-19 у пациентов с саркоидозом либо с сочетанной инфекцией M. tuberculosis все еще недостаточно изучены. SARS-CoV-2 оказывает как прямое патологическое действие на эпителиальные клетки дыхательной системы, так и опосредованное за счет нарушений кровообращения. Материалы и методы. В этом исследовании мы изучили особенности аутоиммунного ответа у пациентов с гранулематозными заболеваниями (туберкулезом и саркоидозом) после COVID-19. Мы проанализировали статьи с декабря 2019 по март 2023 г., опубликованные в международных базах данных («Medline», «PubMed», «Scopus»). Ключевые слова, которые мы использовали: «COVID-19», «SARS-CoV-2», «туберкулез», «саркоидоз», «гранулематозные заболевания», «Т-клетки», «В-клетки», «Treg», «фолликулярный Treg» и «Подмножества Treg». Описательный обзор проводился в соответствии с протоколом PRISMA (http://www.prisma-statement.org), используемым для этого типа исследования (ID-423604). Результаты. COVID-19 вносит существенный вклад в нарушение Т- и В-клеточного иммунного ответа. Коронавирусная инфекция может изменить и характер клеточного метаболизма, что отразится на течении гранулематозного воспаления. По данным различных исследований, аутоиммунный компонент может быть важным защитным механизмом при саркоидозе и, в то же время, он способен усугублять течение туберкулезной инфекции, приводить к прогрессированию заболевания с формированием в дальнейшем лекарственной устойчивости возбудителя. Изучение особенностей иммунного ответа у пациентов с COVID-19 и пациентов с интерстициальными заболеваниями легких показало наличие ряда схожих характеристик у клеточных компонентов иммунного ответа. Заключение. Доказательства наличия аутоиммунного воспаления у пациентов с данными гранулематозными заболеваниями легких, определение иммунотипов пациентов, в том числе перенесших COVID-19, будут вносить существенный вклад в разработку персонализированной тактики ведения пациентов с учетом выявленных нарушений механизмов иммунного ответа.</p></trans-abstract><kwd-group xml:lang="en"><kwd>autoimmunity</kwd><kwd>tuberculosis</kwd><kwd>sarcoidosis</kwd><kwd>granulomatosis diseases</kwd><kwd>T cell</kwd><kwd>B cell</kwd><kwd>Treg</kwd><kwd>follicular Treg</kwd><kwd>Treg subsets</kwd><kwd>prognosis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>аутоиммунитет</kwd><kwd>туберкулез</kwd><kwd>саркоидоз</kwd><kwd>гранулематозные заболевания</kwd><kwd>Т-клетки</kwd><kwd>В-клетки</kwd><kwd>Treg</kwd><kwd>фолликулярные Treg</kwd><kwd>субпопуляции Treg</kwd><kwd>прогноз</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="en">Ministry of Science and Higher Education of the Russian Federation</institution></institution-wrap><institution-wrap><institution xml:lang="ru">Министерство науки и высшего образования Российской Федерации</institution></institution-wrap></funding-source><award-id>075-15-2024-631</award-id></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Abebe F. Immunological basis of early clearance of Mycobacterium tuberculosis infection: the role of natural killer cells. Clin. Exp. Immunol., 2021, vol. 204, no. 1, pp. 32–40. doi: 10.1111/cei.13565</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Abreu M.T., Carvalheiro H., Rodrigues-Sousa T., Domingos A., Segorbe-Luis A., Rodrigues-Santos P., Souto-Carneiro M.M. Alterations in the peripheral blood B cell subpopulations of multidrug-resistant tuberculosis patients. Clin. Exp. Med., 2014, vol. 14, pp. 423–429. doi: 10.1007/s10238-013-0258-1</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Adamo S., Michler J., Zurbuchen Y., Cervia C., Taeschler P., Raeber M.E., Baghai Sain S., Nilsson J., Moor A.E., Boyman O. Signature of long-lived memory CD8+ T cells in acute SARS-CoV-2 infection. Nature, 2022, vol. 602, no. 7895, pp. 148–155. doi: 10.1038/s41586-021-04280-x</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Ahmed A., Adiga V., Nayak S., Uday Kumar J.A.J., Dhar C., Sahoo P.N., Sundararaj B.K., Souza G.D., Vyakarnam A. Circulating HLA-DR+CD4+ effector memory T cells resistant to CCR5 and PD-L1 mediated suppression compromise regulatory T cell function in tuberculosis. PLoS Pathog. 2018, vol. 14, no. 9: e1007289. doi: 10.1371/journal.ppat.1007289</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Akiyama M., Yasuoka H., Yamaoka K., Suzuki K., Kaneko Y., Kondo H., Kassai Y., Koga K., Miyazaki T., Morita R., Yoshimura A., Takeuchi T. Enhanced IgG4 production by follicular helper 2 T cells and the involvement of follicular helper 1 T cells in the pathogenesis of IgG4-related disease. Arthritis. Res. Ther., 2016, no. 18: 167. doi: 10.1186/s13075-016-1064-4</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Аkthivel P., Bruder D., Mechanism of granuloma formation in sarcoidosis. Curr. Opin. Hematol., 2017, vol. 24, pp. 59–65. doi: 10.1097/MOH.0000000000000301</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Al Balushi A., AlShekaili J., Al Kindi M., Ansari Z., Al-Khabori M., Khamis F., Ambusaidi Z., Al Balushi A., Al Huraizi A., Al Sulaimi S., Al Fahdi F., Al Balushi I., Pandak N., Fletcher T., Nasr I. Immunological predictors of disease severity in patients with COVID-19. Int. J. Infect. Dis., 2021, vol. 110, pp. 83–92. doi: 10.1016/j.ijid.2021.06.056</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Alosaimi B., Mubarak A., Hamed M.E., Almutairi A.Z., Alrashed A.A., AlJuryyan A., Enani M., Alenzi F.Q., Alturaiki W. Complement Anaphylatoxins and Inflammatory Cytokines as Prognostic Markers for COVID-19 Severity and In-Hospital Mortality. Front. Immunol., 2021, no. 12: 668725. doi: 10.3389/fimmu.2021.668725</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Annunziato F., Romagnani C., Romagnani S. The 3 major types of innate and adaptive cell-mediated effector immunity. J. Allergy Clin. Immunol., 2015, vol. 135, no. 3, pp. 626–35. doi: 10.1016/j.jaci.2014.11.001</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Bagavant H., Cizio K., Araszkiewicz A.M., Papinska J.A., Garman L., Li C., Pezant N., Drake W.P., Montgomery C.G., Deshmukh U.S. Systemic immune response to vimentin and granuloma formation in a model of pulmonary sarcoidosis. J. Transl. Autoimmun., 2022, no. 5: 100153. doi: 10.1016/j.jtauto.2022.100153</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Belyaeva I.V., Kosova A.N., Vasiliev A.G. Tuberculosis and Autoimmunity. Pathophysiology, 2022, vol. 29, no. 3, pp. 469–470. doi: 10.3390/pathophysiology29020022</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Billiau A., Matthys P. Modes of action of Freund’s adjuvants in experimental models of autoimmune diseases. J. Leukoc. Biol., 2001, vol. 70, no. 6, pp. 849–860</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Billottet C., Quemener C., Bikfalvi A. CXCR3, a double-edged sword in tumor progression and angiogenesis. Biochim. Biophys. Acta, 2013, vol. 1836, no. 2, pp. 287–295. doi: 10.1016/j.bbcan.2013.08.002</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Blank M., Barzilai O., Shoenfeld Y. Molecular mimicry and auto-immunity. Clin. Rev. Allergy Immunol., 2007, vol. 32, no. 1, pp. 111–118. doi: 10.1007/BF02686087</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Boechat J.L., Chora I., Morais A., Delgado L. The immune response to SARS-CoV-2 and COVID-19 immunopathology — current perspectives. Pulmonology, 2021, vol. 27, no. 5, pp. 423–437. doi: 10.1016/j.pulmoe.2021.03.008</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Borham M., Oreiby A., El-Gedawy A., Hegazy Y., Khalifa H.O., Al-Gaabary M., Matsumoto T. Review on Bovine Tuberculosis: An Emerging Disease Associated with Multidrug-Resistant Mycobacterium Species. Pathogens, 2022, vol. 11, no. 7: 715. doi: 10.3390/pathogens11070715</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Broos C.E., van Nimwegen M., Hoogsteden H.C., Hendriks R.W., Kool M., van den Blink B. Granuloma formation in pulmonary sarcoidosis. Front. Immunol., 2013, no. 4: 437. doi: 10.3389/fimmu.2013.00437</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Broos C.E., van Nimwegen M., Kleinjan A., et al. Impaired survival of regulatory T cells in pulmonary sarcoidosis. Respir Res. 2015, vol. 16, no. 1: 108. doi: 10.1186/s12931-015-0265-8</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Busuttil A., Weigt S.S., Keane M.P., Xue Y.Y., Palchevskiy V., Burdick M.D., Huang C., Zisman D.A., Fishbein M., Lynch J.P.3rd, Strieter R.M., Elashoff R.M., Belperio J.A. CXCR3 ligands are augmented during the pathogenesis of pulmonary sarcoidosis. Eur. Respir. J., 2009, vol. 34, no. 3, pp. 676–686. doi: 10.1183/09031936.00157508</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Cain H., Kraus B. Immunofluorescence microscopic demonstration of vimentin filaments in asteroid bodies of sarcoidosis. A comparison with electron microscopic findings. Virchows Arch. B Cell. Pathol. Incl. Mol. Pathol., 1983, vol. 42, no. 2, pp. 213–226. doi: 10.1007/bf02890384</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Cardona P., Cardona P.-J. Regulatory T Cells in Mycobacterium tuberculosis Infection. Front. Immunol., 2019, vol. 10: 2139. doi: 10.3389/fimmu.2019.02139</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Caso F., Costa L., Ruscitti P., Navarini L., Del Puente A., Giacomelli R., Scarpa R. Could Sars-coronavirus-2 trigger autoimmune and/or autoinflammatory mechanisms in genetically predisposed subjects? Autoimmun. Rev., 2020, vol. 19, no. 5: 102524. doi: 10.1016/j.autrev.2020.102524</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Chen X., Huang J., Huang Y., Chen J., Huang Y., Jiang X., Shi Y. Characteristics of immune cells and cytokines in patients with coronavirus disease 2019 in Guangzhou, China. Hum. Immunol., 2020, vol. 81, no. 12, pp. 702–708. doi: 10.1016/j.humimm.2020.08.006</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Chen X., Zhang M., Liao M., Graner M.W., Wu C., Yang Q., Liu H., Zhou B Reduced Th17 response in patients with tuberculosis correlates with IL-6R expression on CD4+ T Cells. Am. J. Respir. Crit. Care Med., 2010, vol. 181, no. 7, pp. 734–742. doi: 10.1164/rccm.200909-1463OC</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Chen Y.C., Chin C.H., Liu S.F., Wu C.C., Tsen C.C., Wang Y.H., Chao T.Y., Lie C.H., Chen C.J., Wang C.C., Lin M.C. Prognostic values of serum IP-10 and IL-17 in patients with pulmonary tuberculosis. Dis. Markers, 2011, vol. 31, no. 2, pp. 101–110. doi: 10.3233/DMA-2011-0808</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Cheng M.P., Butler-Laporte G., Parkes L.O., Bold T.D., Fritzler M.J., Behr M.A. Prevalence of Auto-antibodies in Pulmonary Tuberculosis. Open Forum Infect. Dis., 2019, vol. 6, no. 4: ofz114. doi: 10.1093/ofid/ofz114</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Chiacchio T., Casetti R., Butera O., Vanini V., Carrara S., Girardi E., Di Mitri D., Battistini L., Martini F., Borsellino G., Goletti D. Characterization of regulatory T cells identified as CD4(+)CD25(high)CD39(+) in patients with active tuberculosis. Clin. Exp. Immunol., 2009, vol. 156, no. 3, pp. 463–70. doi: 10.1111/j.1365-2249.2009.03908.x</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Cinetto F., Scarpa R., Dell’Edera A., Jones M.G., Immunology of sarcoidosis: old companions, new relationships. Curr. Opin. Pulm. Med., 2020, vol. 26, pp. 535–543. doi: 10.1097/MCP.0000000000000711</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>D’Alessandro M., Bergantini L., Cameli P., Mezzasalma F., Refini R.M., Pieroni M., Sestini P., Bargagli E. Adaptive immune system in pulmonary sarcoidosis — comparison of peripheral and alveolar biomarkers. Clin. Exp. Immunol., 2021, vol. 205, no. 3, pp. 406–416. doi: 10.1111/cei.13635</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>D’Alessandro M., Bergantini L., Gangi S., Cameli P., Armati M., Fanetti M., Mezzasalma F., Baglioni S., Sarc-Si Study Group, Bargagli E. Imbalance of Lymphocyte Subsets and CD45RA-Expressing Cells in Intrathoracic Lymph Nodes, Alveolar Compartment and Bloodstream of Pulmonary Sarcoidosis Patients. Int. J. Mol. Sci., 2023, vol. 24, no. 12: 10344. doi: 10.3390/ijms241210344</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>De Biasi S., Lo Tartaro D., Meschiari M., Gibellini L., Bellinazzi C., Borella R., Fidanza L., Mattioli M., Paolini A., Gozzi L., Jaacoub D., Faltoni M., Volpi S., Milić J., Sita M., Sarti M., Pucillo C., Girardis M., Guaraldi G., Mussini C., Cossarizza A. Expansion of plasmablasts and loss of memory B cells in peripheral blood from COVID-19 patients with pneumonia. Eur. J. Immunol., 2020, vol. 50, no. 9, pp. 1283–1294. doi: 10.1002/eji.202048838</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Ding J., Dai J., Cai H., Gao Q., Wen Y. Extensively disturbance of regulatory T cells — Th17 cells balance in stage II pulmonary sarcoidosis. Int. J. Med. Sci., 2017, vol. 14, no. 11, pp. 1136–1142. doi: 10.7150/ijms.18838</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Dubaniewicz A. Mycobacterium tuberculosis heat shock proteins and autoimmunity in sarcoidosis. Autoimmun. Rev., 2010, vol. 9, no. 6, pp. 419–424. doi: 10.1016/j.autrev.2009.11.015</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Elkington P., Tebruegge M., Mansour S. Tuberculosis: an Infection-Initiated Autoimmune Disease? Trends Immunol., 2016, vol. 37, no. 12, pp. 815–818. doi: 10.1016/j.it.2016.09.007</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Erre G.L., Cossu D., Masala S., Mameli G., Cadoni M.L., Serdino S., Longu M.G., Passiu G., Sechi L.A. Mycobacterium tuberculosis lipoarabinomannan antibodies are associated to rheumatoid arthritis in Sardinian patients. Clin. Rheumatol., 2014, vol. 33, no. 12, pp. 1725–1729. doi: 10.1007/s10067-014-2678-z</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Fathi F., Sami R., Mozafarpoor S., Hafezi H., Motedayyen H., Arefnezhad R., Eskandari N. Immune system changes during COVID-19 recovery play key role in determining disease severity. Int. J. Immunopathol. Pharmacol., 2020, no. 34: 2058738420966497. doi: 10.1177/2058738420966497</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Ferrantelli F., Chiozzini C., Manfredi F., Leone P., Spada M., Di Virgilio A., Giovannelli A., Sanchez M., Cara A., Michelini Z., Federico M. Strong SARS-CoV-2 N-Specific CD8+ T Immunity Induced by Engineered Extracellular Vesicles Associates with Protection from Lethal Infection in Mice. Viruses, 2022, vol. 14, no. 2: 329. doi: 10.3390/v14020329</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Fischer A., Ellinghaus D., Nutsua M., Hofmann S., Montgomery C.G., Iannuzzi M.C., Rybicki B.A., Petrek M., Mrazek F., Pabst S., Grohé C., Grunewald J., Ronninger M., Eklund A., Padyukov L., Mihailovic-Vucinic V., Jovanovic D., Sterclova M., Homolka J., Nöthen M.M., Herms S., Gieger C., Strauch K., Winkelmann J., Boehm B.O., Brand S., Büning C., Schürmann M., Ellinghaus E., Baurecht H., Lieb W., Nebel A., Müller-Quernheim J., Franke A., Schreiber S.; GenPhenReSa Consortium. Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk. Am. J. Respir. Crit. Care Med., 2015, vol. 192, no. 6, pp. 727–736. doi: 10.1164/rccm.201503-0418OC</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Fischer A., Rybicki B.A. Granuloma genes in sarcoidosis: what is new? Curr. Opin. Pulm. Med., 2015, vol. 21, no. 5, pp. 510–516. doi: 10.1097/MCP.0000000000000189</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Gong F., Dai Y., Zheng T., Cheng L., Zhao D., Wang H., Liu M., Pei H., Jin T., Yu D., Zhou P. Peripheral CD4+ T cell subsets and antibody response in COVID-19 convalescent individuals. J. Clin. Invest., 2020, vol. 130, no. 12, pp. 6588–6599. doi: 10.1172/JCI141054</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Groom J.R., Luster A.D. CXCR3 ligands: redundant, collaborative and antagonistic functions. Immunol. Cell. Biol., 2011, vol. 89, no. 2, pp. 207–215. doi: 10.1038/icb.2010.158</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Gutiérrez-Bautista J.F., Rodriguez-Nicolas A., Rosales-Castillo A., Jiménez P., Garrido F., Anderson P., Ruiz-Cabello F., López-Ruz M.Á. Negative Clinical Evolution in COVID-19 Patients Is Frequently Accompanied With an Increased Proportion of Undifferentiated Th Cells and a Strong Underrepresentation of the Th1 Subset. Front. Immunol., 2020, no. 11: 596553. doi: 10.3389/fimmu.2020.596553</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Guyot-Revol V., Innes J.A., Hackforth S., Hinks T., Lalvani A. Regulatory T cells are expanded in blood and disease sites in patients with tuberculosis. Am. J. Respir. Crit. Care Med., 2006, vol. 173, pp. 803–810. doi: 10.1164/rccm.200508-1294OC</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Habel J.R., Nguyen T.H.O., van de Sandt C.E., Juno J.A., Chaurasia P., Wragg K., Koutsakos M., Hensen L., Jia X., Chua B., Zhang W., Tan H.X., Flanagan K.L., Doolan D.L., Torresi J., Chen W., Wakim L.M., Cheng A.C., Doherty P.C., Petersen J., Rossjohn J., Wheatley A.K., Kent S.J., Rowntree L.C., Kedzierska K. Suboptimal SARS-CoV-2-specific CD8+ T cell response associated with the prominent HLA-A*02:01 phenotype. Proc. Natl Acad. Sci. USA, 2020, vol. 117, no. 39, pp. 24384–24391. doi: 10.1073/pnas.2015486117</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Halim L., Romano M., McGregor R., Correa I., Pavlidis P., Grageda N., Hoong S.J., Yuksel M., Jassem W., Hannen R.F., Ong M., Mckinney O., Hayee B., Karagiannis S.N., Powell N., Lechler R.I., Nova-Lamperti E., Lombardi G. An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment. Cell. Rep., 2017, vol. 20, no. 3, pp. 757–770. doi: 10.1016/j.celrep.2017.06.079</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Hingley-Wilson S.M., Connell D., Pollock K., Hsu T., Tchilian E., Sykes A., Grass L., Potiphar L., Bremang S., Kon O.M., Jacobs W.R. Jr., Lalvani A. ESX1-dependent fractalkine mediates chemotaxis and Mycobacterium tuberculosis infection in humans. Tuberculosis (Edinb.), 2014, vol. 94, no. 3, pp. 262–270. doi: 10.1016/j.tube.2014.01.004</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Hu B., Huang S., Yin L. The cytokine storm and COVID-19. J. Med. Virol., 2021, vol. 93, no. 1, pp. 250–256. doi: 10.1002/jmv.26232</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Huang H., Lu Z., Jiang C., Liu J., Wang Y., Xu Z. Imbalance between Th17 and regulatory T-Cells in sarcoidosis. Int. J. Mol. Sci., 2013, vol. 14, no. 11, pp. 21463–21473. doi: 10.3390/ijms141121463</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Joosten S.A., van Meijgaarden K.E., Del Nonno F., Baiocchini A., Petrone L., Vanini V., Smits H.H., Palmieri F., Goletti D., Ottenhoff T.H. Patients with Tuberculosis Have a Dysfunctional Circulating B-Cell Compartment, Which Normalizes following Successful Treatment. PLoS Pathog., 2016, vol. 12, no. 6: e1005687. doi: 10.1371/journal.ppat.1005687</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Kakumanu P., Yamagata H., Sobel E.S., Reeves W.H., Chan E.K., Satoh M. Patients with pulmonary tuberculosis are frequently positive for anti-cyclic citrullinated peptide antibodies, but their sera also react with unmodified arginine-containing peptide. Arthritis Rheum., 2008, vol. 58, no. 6, pp. 1576–1581. doi: 10.1002/art.23514</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Kalfaoglu B., Almeida-Santos J., Tye C.A., Satou Y., Ono M. T-Cell Hyperactivation and Paralysis in Severe COVID-19 Infection Revealed by Single-Cell Analysis. Front. Immunol., 2020, no. 11: 589380. doi: 10.3389/fimmu.2020.589380</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Kalinina O., Golovkin A., Zaikova E., Aquino A., Bezrukikh V., Melnik O., Vasilieva E., Karonova T., Kudryavtsev I., Shlyakhto E. Cytokine Storm Signature in Patients with Moderate and Severe COVID-19. Int. J. Mol. Sci., 2022, vol. 23, no. 16: 8879. doi: 10.3390/ijms23168879</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Kanduc D., Shoenfeld Y. On the molecular determinants of the SARS-CoV-2 attack. Clin. Immunol., 2020, no. 215: 108426. doi: 10.1016/j.clim.2020.108426</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Kaneko N., Kuo H.H., Boucau J., Farmer J.R., Allard-Chamard H., Mahajan V.S., Piechocka-Trocha A., Lefteri K., Osborn M., Bals J., Bartsch Y.C., Bonheur N., Caradonna T.M., Chevalier J., Chowdhury F., Diefenbach T.J., Einkauf K., Fallon J., Feldman J., Finn K.K., Garcia-Broncano P., Hartana C.A., Hauser B.M., Jiang C., Kaplonek P., Karpell M., Koscher E.C., Lian X., Liu H., Liu J., Ly N.L., Michell A.R., Rassadkina Y., Seiger K., Sessa L., Shin S., Singh N., Sun W., Sun X., Ticheli H.J., Waring M.T., Zhu A.L., Alter G., Li J.Z., Lingwood D., Schmidt A.G., Lichterfeld M., Walker B.D., Yu X.G., Padera R.F. Jr., Pillai S.; Massachusetts Consortium on Pathogen Readiness Specimen Working Group. Loss of Bcl-6-Expressing T Follicular Helper Cells and Germinal Centers in COVID-19. Cell, 2020, vol. 183, no. 1, pp. 143–157.e13. doi: 10.1016/j.cell.2020.08.025</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Kim S.H., Kim J., Jang J.Y., Noh H., Park J., Jeong H., Jeon D., Uhm C., Oh H., Cho K., Jeon Y., On D, Yoon S., Lim S.Y., Kim S.P., Lee Y.W., Jang H.J., Park I.H., Oh J., Seo J.S., Kim J.J., Seok S.H., Lee Y.J., Hong S.M., An S.H., Kim S.Y., Kim Y.B., Hwang J.Y., Lee H.J., Kim H.B., Choi K.S., Park J.W., Seo J.Y., Yun J.W., Shin J.S., Lee H.Y., Kim K., Lee D., Lee H., Nam K.T., Seong J.K. Mouse models of lung-specific SARS-CoV-2 infection with moderate pathological traits. Front. Immunol., 2022, no. 13: 1055811. doi: 10.3389/fimmu.2022.1055811</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Kita S., Tsuda T., Sugisaki K., Miyazaki E., Matsumoto T. Characterization of distribution of T lymphocyte subsets and activated T lymphocytes infiltrating into sarcoid lesions. Intern. Med., 1995, vol. 34, no. 9, pp. 847–855. doi: 10.2169/internalmedicine.34.847</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Korobova Z.R., Arsentieva N.A., Liubimova N.E., Batsunov O.K., Dedkov V.G., Gladkikh A.S., Sharova A.A., Adish Z., Chernykh E.I., Kaschenko V.A., Ratnikov V.A., Gorelov V.P., Stanevich O.V., Kulikov A.N., Pevtsov D.E., Totolian A.A. Cytokine Profiling in Different SARS-CoV-2 Genetic Variants. Int. J. Mol. Sci., 2022, vol. 23, no. 22: 14146. doi: 10.3390/ijms232214146</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Koutsakos M., Rowntree L.C., Hensen L., Chua B.Y., van de Sandt C.E., Habel J.R., Zhang W., Jia X., Kedzierski L., Ashhurst T.M., Putri G.H., Marsh-Wakefield F., Read M.N., Edwards D.N., Clemens E.B., Wong C.Y., Mordant F.L., Juno J.A., Amanat F., Audsley J., Holmes N.E., Gordon C.L., Smibert O.C., Trubiano J.A., Hughes C.M., Catton M., Denholm J.T., Tong S.Y.C., Doolan D.L., Kotsimbos T.C., Jackson D.C., Krammer F., Godfrey D.I., Chung A.W., King N.J.C., Lewin S.R., Wheatley A.K., Kent S.J., Subbarao K., McMahon J., Thevarajan I., Nguyen T.H.O., Cheng A.C., Kedzierska K. Integrated immune dynamics define correlates of COVID-19 severity and antibody responses. Cell. Rep. Med., 2021, vol. 2, no. 3: 100208. doi: 10.1016/j.xcrm.2021.100208</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Kozlov V.A., Savchenko A.A., Kudryavtsev I.V., Kozlov I.G., Kudlay D.A., Prodeus A.P., Borisov, A.G. Clinical Immunology. Krasnoyarsk: Polycor, Russia, 2020. 386 p. (In Russ.)</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Kozlov V.A., Tikhonova E.P., Savchenko A.A., Kudryavtsev I.V., Andronova N.V., Anisimova E.N., Golovkin A.S., Demina D.V., Zdzitovetsky D. .E., Kalinina Yu.S., Kasparov E.V., Kozlov I.G., Korsunsky I.A., Kudlay D.A., Kuzmina T.Yu., Minoranskaya N.S., Prodeus A.P. ., Starikova E.A., Cherdantsev D.V., Chesnokov A.B., Gear P.A., Borisov A.G. Clinical immunology. A practical guide for infectious disease specialists. Krasnoyarsk: Polikor, 2021. 563 p. (In Russ.). doi: 10.17513/np.438</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Kratzer B., Trapin D., Ettel P., Körmöczi U., Rottal A., Tuppy F., Feichter M., Gattinger P., Borochova K., Dorofeeva Y., Tulaeva I., Weber M., Grabmeier-Pfistershammer K., Tauber P.A., Gerdov M., Mühl B., Perkmann T., Fae I., Wenda S., Führer H., Henning R., Valenta R., Pickl W.F. Immunological imprint of COVID-19 on human peripheral blood leukocyte populations. Allergy, 2021, vol. 76, no. 3, pp. 751–765. doi: 10.1111/all.14647</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Kudryavtsev I., Rubinstein A., Golovkin A., Kalinina O., Vasilyev K., Rudenko L., Isakova-Sivak I. Dysregulated Immune Responses in SARS-CoV-2-Infected Patients: A Comprehensive Overview. Viruses, 2022, vol. 14, no. 5: 1082. doi: 10.3390/v14051082</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Kudryavtsev I., Serebriakova M., Starshinova A., Zinchenko Y., Basantsova N., Malkova A., Soprun L., Churilov L.P., Toubi E., Yablonskiy P., Shoenfeld Y. Imbalance in B cell and T Follicular Helper Cell Subsets in Pulmonary Sarcoidosis. Sci. Rep., 2020, vol. 10, no. 1: 1059. doi: 10.1038/s41598-020-57741-0</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Kudryavtsev I., Zinchenko Y., Starshinova A., Serebriakova M., Malkova A., Akisheva T., Kudlay D., Glushkova A., Yablonskiy P., Shoenfeld Y. Circulating Regulatory T Cell Subsets in Patients with Sarcoidosis. Diagnostics (Basel)., 2023, vol. 13, no. 8: 1378. doi: 10.3390/diagnostics13081378</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Kudryavtsev I.V., Arsentieva N.A., Batsunov O.K., Korobova Z.R., Khamitova I.V., Isakov D.V., Kuznetsova R.N., Rubinstein A.A., Stanevich O.V., Lebedeva A.A., Vorobyov E.A., Vorobyova S.V., Kulikov A.N., Sharapova M.A., Pevtcov D.E., Totolian A.A. Alterations in B Cell and Follicular T-Helper Cell Subsets in Patients with Acute COVID-19 and COVID-19 Convalescents. Curr. Issues Mol. Biol., 2021, vol. 44, no. 1, pp. 194–205. doi: 10.3390/cimb44010014</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Kudryavtsev I.V., Arsentieva N.A., Korobova Z.R., Isakov D.V., Rubinstein A.A., Batsunov O.K., Khamitova I.V., Kuznetsova R.N., Savin T.V., Akisheva T.V., Stanevich O.V., Lebedeva A.A., Vorobyov E.A., Vorobyova S.V., Kulikov A.N., Sharapova M.A., Pevtsov D.E., Totolian A.A. Heterogenous CD8+ T Cell Maturation and ‘Polarization’ in Acute and Convalescent COVID-19 Patients. Viruses, 2022, vol. 14, no. 9: 1906. doi: 10.3390/v14091906</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Kudryavtsev I.V., Lazareva N.M., Baranova O.P., Golovkin A.S., Isakov D.V., Serebriakova M.K., Ses T.P., Ilkovich M.M., Totolian Areg A. CD39+ expression by regulatory T cells in pulmonary sarcoidosis and Lofgren’s syndrome. Medical Immunol. (Russia), 2019, vol. 21, no. 3, pp. 467–478. doi: 10.15789/1563-0625-2019-3-467-478</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Kudryavtsev I.V., Lazareva N.M., Baranova O.P., Serebriakova M.K., Ses’ T.P., Ilkovich M.M., Totolian A.A. Peripheral blood T helper cell subsets in Löfgren’s and non-Löfgren’s syndrome patients. Medical Immunology (Russia), 2022, vol. 24, no. 3, pp. 573–586. (In Russ.). doi: 10.15789/1563-0625-PBT-2468</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Kudryavtsev I.V., Serebriakova M.K., Starshinova A.A., Zinchenko Yu.S., Basantsova N.Yu., Belyaeva E.N., Pavlova M.V., Yablonskiy P.K. Altered peripheral blood Th17 and follicular T-helper subsets in patients with pulmonary tuberculosis. Russian Journal of Infection and Immunity, 2019, vol. 9, no. 2, pp. 304–314. doi: 10.15789/2220-7619-2019-2-304-314</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Kumar P., Saini S., Khan S., Surendra Lele S., Prabhakar B.S. Restoring self-tolerance in autoimmune diseases by enhancing regulatory T-cells. Cell. Immunol., 2019, vol. 339, pp. 41–49. doi: 10.1016/j.cellimm.2018.09.008</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Laing A.G., Lorenc A., Del Molino Del Barrio I., Das A., Fish M., Monin L., Muñoz-Ruiz M., McKenzie D.R., Hayday T.S., Francos-Quijorna I., Kamdar S., Joseph M., Davies D., Davis R., Jennings A., Zlatareva I., Vantourout P., Wu Y., Sofra V., Cano F., Greco M., Theodoridis E., Freedman J.D., Gee S., Chan J.N.E., Ryan S., Bugallo-Blanco E., Peterson P., Kisand K., Haljasmägi L., Chadli L., Moingeon P., Martinez L., Merrick B., Bisnauthsing K., Brooks K., Ibrahim M.A.A., Mason J., Lopez Gomez F., Babalola K., Abdul-Jawad S., Cason J., Mant C., Seow J., Graham C., Doores K.J., Di Rosa F., Edgeworth J., Shankar-Hari M., Hayday A.C. A dynamic COVID-19 immune signature includes associations with poor prognosis. Nat. Med., 2020, vol. 26, no. 10, pp. 1623–1635. doi: 10.1038/s41591-020-1038-6</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Lazareva N.M., Baranova O.P., Kudryavtsev I.V., Arsentieva N.A., Liubimova N.E., Ses’ T.P., Ilkovich M.M., Totolian A.A. CXCR3 chemokine receptor ligands in sarcoidosis. Medical Immunology (Russia), 2021, vol. 23, no. 1, pp. 73–86. (In Russ.). doi: 10.15789/1563-0625-CCR-2181</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Lazareva N.M., Baranova O.P., Kudryavtsev I.V., Isakov D.V., Arsentieva N.A., Liubimova N.E., Ses’ T.P., Ilkovich M.M., Totolian A.A. chemokines CCL17 and CCL22 in sarcoidosis. Medical Immunology (Russia), 2021, vol. 23, no. 4, pp. 791–798. (In Russ.). doi: 10.15789/1563-0625-CCA-2340</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Lazareva N., Kudryavtsev I., Baranova O., Serebriakova M., Ses’ T., Ilkovich M., Totolyan A. Peripheral blood cytotoxic T cells in patients with sarcoidosis. Russian Journal of Immunology, 2018, vol. 12, no. 3, pp. 348–353. doi: 10.31857/S102872210002408-3</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Li Y., Wei C., Xu H., Jia J., Wei Z., Guo R., Jia Y., Wu Y., Li Y., Qi X., Li Z., Gao X. The Immunoregulation of Th17 in Host against Intracellular Bacterial Infection. Mediators Inflamm., 2018, no. 2018: 6587296. doi: 10.1155/2018/6587296</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Lin L., Lu L., Cao W., Li T. Hypothesis for potential pathogenesis of SARS-CoV-2 infection — a review of immune changes in patients with viral pneumonia. Emerg. Microbes Infect., 2020, vol. 9, pp. 727–732. doi: 10.1080/22221751.2020.1746199</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Linke M., Pham H.T., Katholnig K., Schnöller T., Miller A., Demel F., Schütz B., Rosner M., Kovacic B., Sukhbaatar N., Niederreiter B., Blüml S., Kuess P., Sexl V., Müller M., Mikula M., Weckwerth W., Haschemi A., Susani M., Hengstschläger M., Gambello M.J., Weichhart T. Chronic signaling via the metabolic checkpoint kinase mTORC1 induces macrophage granuloma formation and marks sarcoidosis progression. Nat. Immunol., 2017, vol. 18, no. 3, pp. 293–302. doi: 10.1038/ni.3655</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Lo C.Y., Huang Y.C., Huang H.Y., Chung F.T., Lin C.W., Chung K.F., Wang C.H. Increased Th1 Cells with Disease Resolution of Active Pulmonary Tuberculosis in Non-Atopic Patients. Biomedicines, 2021, vol. 9, no. 7: 724. doi: 10.3390/biomedicines9070724</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Ly N.T.M., Ueda-Hayakawa I., Nguyen C.T.H., Okamoto H. Exploring the imbalance of circulating follicular helper CD4+ T cells in sarcoidosis patients. J. Dermatol. Sci., 2020, vol. 97, no. 3, pp. 216–224. doi: 10.1016/j.jdermsci.2020.02.002</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Lyadova I.V., Panteleev A.V. Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers. Mediators Inflamm, 2015, no. 2015: 854507. doi: 10.1155/2015/854507</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Machado Ribeiro F., Goldenberg T. Mycobacteria and autoimmunity. Lupus, 2015, vol. 24, no. 4–5, pp. 374–381. doi: 10.1177/0961203314559634</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Malkova A., Kudlay D., Kudryavtsev I., Starshinova A., Yablonskiy P., Shoenfeld Y. Immunogenetic Predictors of Severe COVID-19. Vaccines (Basel.), 2021, vol. 9, no. 3: 211. doi: 10.3390/vaccines9030211</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Mani R., Gupta M., Malik A., Tandon R., Prasad R., Bhatnagar R., Banerjee N. Adjuvant Potential of Poly-α-l-Glutamine from the Cell Wall of Mycobacterium tuberculosis. Infect. Immun., 2018, vol. 86, no. 10: pii: e00537-18. doi: 10.1128/IAI.00537-18</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Martonik D., Parfieniuk-Kowerda A., Rogalska M., Flisiak R. The Role of Th17 Response in COVID-19. Cells, 2021, vol. 10, no. 6: 1550. doi: 10.3390/cells10061550</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Mathew D., Giles J.R., Baxter A.E., Greenplate A.R., Wu J.E., Alanio C., Oldridge D.A., Kuri-Cervantes L., Pampena M.B., D’Andrea K., Manne S., Chen Z., Huang Y.J., Reilly J.P., Weisman A.R., Ittner C.A.G., Kuthuru O., Dougherty J., Nzingha K., Han N., Kim J., Pattekar A., Goodwin E.C., Anderson E.M., Weirick M.E., Gouma S., Arevalo C.P., Bolton M.J., Chen F., Lacey S.F., Hensley S.E., Apostolidis S., Huang A.C., Vella L.A.; UPenn COVID Processing Unit; Betts M.R., Meyer N.J., Wherry E.J. Deep immune profiling of COVID-19 patients reveals patient heterogeneity and distinct immunotypes with implications for therapeutic interventions. bioRxiv, 2020: 2020.05.20.106401 [Preprint]. doi: 10.1101/2020.05.20.106401</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Mertz P., Jeannel J., Guffroy A., Lescuyer S., Korganow A.S., Rondeau-Lutz M., Weber J.C. Granulomatous manifestations associated with COVID19 infection: Is there a link between these two diseases? Autoimmun Rev., 2021, vol. 20, no. 6: 102824. doi: 10.1016/j.autrev.2021.102824</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Miyara M., Amoura Z., Parizot C., Badoual C., Dorgham K., Trad S., Kambouchner M., Valeyre D., Chapelon-Abric C., Debré P., Piette J.C., Gorochov G. The immune paradox of sarcoidosis and regulatory T cells. J. Exp. Med., 2006, vol. 203, no. 2, pp. 359–370. doi: 10.1084/jem.20050648</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Mohebbi S.R., Baghaei K., Rostami-Nejad M., Nazemalhosseini Mojarad E., Mirjalali H., Yadegar A., Asri N., Abdoulahi S., Assadzadeh Aghdaei H. Significant changes of CD4, FOXP3, CD25, and IL6 expression level in Iranian COVID-19 patients. Gastroenterol. Hepatol. Bed. Bench., 2020, vol. 13, no. 4, pp. 388–392.</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Musaelyan A., Lapin S., Nazarov V., Tkachenko O., Gilburd B., Mazing A., Mikhailova L., Shoenfeld Y. Vimentin as antigenic target in autoimmunity: a comprehensive review. J. Autoimmun. Rev., 2018, vol. 17, no. 9, pp. 926–934. doi: 10.1016/j.autrev.2018.04.004</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Nureki S., Miyazaki E., Ando M., Ueno T., Fukami T., Kumamoto T., Sugisaki K., Tsuda T. Circulating levels of both Th1 and Th2 chemokines are elevated in patients with sarcoidosis. Respir. Med., 2008, vol. 102, no. 2, pp. 239–247. doi: 10.1016/j.rmed.2007.09.006</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Odak I., Barros-Martins J., Bošnjak B., Stahl K., David S., Wiesner O., Busch M., Hoeper M.M., Pink I., Welte T., Cornberg M., Stoll M., Goudeva L., Blasczyk R., Ganser A., Prinz I., Förster R., Koenecke C., Schultze-Florey C.R. Reappearance of effector T cells is associated with recovery from COVID-19. EBioMedicine, 2020, no. 57: 102885. doi: 10.1016/j.ebiom.2020.102885</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Ogongo P., Tezera L.B., Ardain A., Nhamoyebonde S., Ramsuran D., Singh A., Ng’oepe A, Karim F., Naidoo T., Khan K., Dullabh K.J., Fehlings M., Lee B.H., Nardin A., Lindestam Arlehamn C.S., Sette A., Behar S.M., Steyn A.J., Madansein R., Kløverpris H.N., Elkington P.T., Leslie A. Tissue-resident-like CD4+ T cells secreting IL-17 control Mycobacterium tuberculosis in the human lung. J. Clin. Invest., 2021, vol. 131, no. 10: e142014. doi: 10.1172/JCI142014</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Okamoto Yoshida Y., Umemura M., Yahagi A., O’Brien R.L., Ikuta K., Kishihara K., Hara H., Nakae S., Iwakura Y., Matsuzaki G. Essential role of IL-17A in the formation of a mycobacterial infection-induced granuloma in the lung. J. Immunol., 2010, vol. 184, no. 8, pp. 4414–4422. doi: 10.4049/jimmunol.0903332</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Patterson K.C., Chen E.S. The Pathogenesis of Pulmonary Sarcoidosis and Implications for Treatme Ribeiro F.M., Goldenberg T. Mycobacteria and autoimmunity. Lupus, 2015, vol. 24, no. 4–5, pp. 374–381. doi: 10.1177/0961203314559634</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Peng X., Ouyang J., Isnard S., Lin J., Fombuena B., Zhu B., Routy J.P. Sharing CD4+ T Cell Loss: When COVID-19 and HIV Collide on Immune System. Front. Immunol., 2020, no. 11: 596631. doi: 10.3389/fimmu.2020.596631</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Pérez-Gómez A., Gasca-Capote C., Vitallé J., Ostos F.J., Serna-Gallego A., Trujillo-Rodríguez M., Muñoz-Muela E., Giráldez-Pérez T., Praena-Segovia J., Navarro-Amuedo M.D., Paniagua-García M., García-Gutiérrez M., Aguilar-Guisado M., Rivas-Jeremías I., Jiménez-León M.R., Bachiller S., Fernández-Villar A., Pérez-González A., Gutiérrez-Valencia A., Rafii-El-Idrissi Benhnia M., Weiskopf D., Sette A., López-Cortés L.F., Poveda E., Ruiz-Mateos E.; Virgen del Rocío Hospital COVID-19 and COHVID-GS Working Teams. Deciphering the quality of SARS-CoV-2 specific T-cell response associated with disease severity, immune memory and heterologous response. Clin. Transl. Med., 2022, vol. 12, no. 4: e802. doi: 10.1002/ctm2.802</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Prasse A., Georges C.G., Biller H., Hamm H., Matthys H., Luttmann W., Virchow J.C. Jr. Th1 cytokine pattern in sarcoidosis is expressed by bronchoalveolar CD4+ and CD8+ T cells. Clin. Exp. Immunol., 2000, vol. 122, no. 2, pp. 241–248. doi: 10.1046/j.1365-2249.2000.01365.x</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Radziszewska A., Moulder Z., Jury E.C., Ciurtin C. CD8+ T Cell Phenotype and Function in Childhood and Adult-Onset Connective Tissue Disease. Int. J. Mol. Sci., 2022, vol. 23, no. 19: 11431. doi: 10.3390/ijms231911431</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Ramasamy A., Wang C., Brode W.M., Verduzco-Gutierrez M., Melamed E. Immunologic and Autoimmune-Related Sequelae of Severe Acute Respiratory Syndrome Coronavirus 2 Infection: Clinical Symptoms and Mechanisms of Disease. Phys. Med. Rehabil. Clin. N. Am., 2023, vol. 34, no. 3, pp. 623–642. doi: 10.1016/j.pmr.2023.04.004</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Ramstein J., Broos C.E., Simpson L.J., Ansel K.M., Sun S.A., Ho M.E., Woodruff P.G., Bhakta N.R.,Christian L., Nguyen C.P., Antalek B.J., Benn B.S., Hendriks R.W., van den Blink B., Kool M., Koth L.L. IFN-γ-producing T-Helper 17.1 Cells are increased in sarcoidosis and are more prevalent than T-Helper type 1 Cells. Am.J. Respir. Crit. Care Med., 2016, vol. 193, no. 11, pp. 1281–1291.</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Repac J., Mandić M., Lunić T., Božić B., Božić Nedeljković B. Mining the capacity of human-associated microorganisms to trigger rheumatoid arthritis-A systematic immunoinformatics analysis of T cell epitopes. PLoS One, 2021, vol. 16, no. 6: e0253918. doi: 10.1371/journal.pone.025391</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Richmond B.W., Ploetze K., Isom J., Chambers-Harris I., Braun N.A., Taylor T., Abraham S., Mageto Y., Culver D.A., Oswald-Richter K.A., Drake W.P. Sarcoidosis Th17 cells are ESAT-6 antigen specific but demonstrate reduced IFN-γ expression. J. Clin. Immunol., 2013, vol. 33, no. 2, pp. 446–455. doi: 10.1007/s10875-012-9817-6</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Rijnink W.F., Ottenhoff T.H., Joosten S.A. B-Cells and Antibodies as Contributors to Effector Immune Responses in Tuberculosis. Front. Immunol., 2021, vol. 12: 640168. doi: 10.3389/fimmu.2021.640168</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Rojas M., Herrán M., Ramírez-Santana C., Leung P.S.C., Anaya J.M., Ridgway W.M., Gershwin M.E. Molecular mimicry and autoimmunity in the time of COVID-19. J. Autoimmun., 2023, no. 139: 103070. doi: 10.1016/j.jaut.2023.103070</mixed-citation></ref><ref id="B105"><label>105.</label><mixed-citation>Samuel C.E. Antiviral actions of interferons. Clin. Microbiol. Rev., 2001, vol. 14, no. 4, pp. 778–809. doi: 10.1128/CMR.14.4.778-809.2001</mixed-citation></ref><ref id="B106"><label>106.</label><mixed-citation>San Segundo D., Arnáiz de Las Revillas F., Lamadrid-Perojo P., Comins-Boo A., González-Rico C., Alonso-Peña M., Irure-Ventura J., Olmos J.M., Fariñas M.C., López-Hoyos M. Innate and Adaptive Immune Assessment at Admission to Predict Clinical Outcome in COVID-19 Patients. Biomedicines, 2021, vol. 9, no. 8: 917. doi: 10.3390/biomedicines9080917</mixed-citation></ref><ref id="B107"><label>107.</label><mixed-citation>Saris A., Reijnders T.D.Y., Nossent E.J., Schuurman A.R., Verhoeff J., Asten S.V., Bontkes H., Blok S., Duitman J., Bogaard H.J., Heunks L., Lutter R., van der Poll T., Garcia Vallejo J.J.; ArtDECO consortium and the Amsterdam UMC COVID study group. Distinct cellular immune profiles in the airways and blood of critically ill patients with COVID-19. Thorax, 2021, vol. 76, no. 10, pp. 1010–1019. doi: 10.1136/thoraxjnl-2020-216256</mixed-citation></ref><ref id="B108"><label>108.</label><mixed-citation>Sattler A., Angermair S., Stockmann H., Heim K.M., Khadzhynov D., Treskatsch S., Halleck F., Kreis M.E., Kotsch K. SARS-CoV-2-specific T cell responses and correlations with COVID-19 patient predisposition. J. Clin. Invest., 2020, vol. 130, no. 12, pp. 6477–6489. doi: 10.1172/JCI140965</mixed-citation></ref><ref id="B109"><label>109.</label><mixed-citation>Saussine A., Tazi A., Feuillet S., Rybojad M., Juillard C., Bergeron A., Dessirier V., Bouhidel F., Janin A., Bensussan A., Bagot M., Bouaziz J.D. Active chronic sarcoidosis is characterized by increased transitional blood B cells, increased IL-10-producing regulatory B cells and high BAFF levels. PLoS One, 2012, vol. 7, no. 8: e43588. doi: 10.1371/journal.pone.0043588</mixed-citation></ref><ref id="B110"><label>110.</label><mixed-citation>Scadding J.G. Mycobacterium tuberculosis in the aetiology of sarcoidosis. Br. Med. J., 1960, vol. 2, no. 5213, pp. 1617–1623.</mixed-citation></ref><ref id="B111"><label>111.</label><mixed-citation>Schultheiß C., Paschold L., Simnica D., Mohme M., Willscher E., von Wenserski L., Scholz R., Wieters I., Dahlke C., Tolosa E., Sedding D.G., Ciesek S., Addo M., Binder M. Next-Generation Sequencing of T and B Cell Receptor Repertoires from COVID-19 Patients Showed Signatures Associated with Severity of Disease. Immunity, 2020, vol. 53, no. 2, pp. 442–455.e4. doi: 10.1016/j.immuni.2020.06.024</mixed-citation></ref><ref id="B112"><label>112.</label><mixed-citation>Sellares J., Strambu I., Crouser E.D., Freudenberg M.A., Gulati M., Hart S., Herzog E., Kolb M., Weichhart T., Drake W.P., Spitzer G., Singh N., Culver D.A. New advances in the development of sarcoidosis models: a synopsis of a symposium sponsored by the Foundation for Sarcoidosis Research. Sarcoidosis Vasc. Diffuse Lung. Dis., 2018, vol. 35, no. 1, pp. 2–4. doi: 10.36141/svdld.v35i1.7032</mixed-citation></ref><ref id="B113"><label>113.</label><mixed-citation>Semple P.L., Binder A.B., Davids M., Maredza A., van Zyl-Smit R.N., Dheda K. Regulatory T cells attenuate mycobacterial stasis in alveolar and blood-derived macrophages from patients with tuberculosis. Am. J. Respir. Crit. Care Med., 2013, vol. 187, no. 11, pp. 1249–58. doi: 10.1164/rccm.201210-1934OC</mixed-citation></ref><ref id="B114"><label>114.</label><mixed-citation>Sève P., Pacheco Y., Durupt F., Jamilloux Y., Gerfaud-Valentin M., Isaac S., Boussel L., Calender A., Androdias G., Valeyre D., El Jammal T. Sarcoidosis: A Clinical Overview from Symptoms to Diagnosis. Cells, 2021, vol. 10, no. 4: 766. doi: 10.3390/cells10040766</mixed-citation></ref><ref id="B115"><label>115.</label><mixed-citation>Sharma A., Balda S., Apreja M., Kataria K., Capalash N., Sharma P. COVID-19 Diagnosis: Current and Future Techniques. Int. J. Biol. Macromol., 2021, vol. 193 (Pt B), pp. 1835–1844. doi: 10.1016/j.ijbiomac.2021.11.016</mixed-citation></ref><ref id="B116"><label>116.</label><mixed-citation>Sharp M., Mustafa A.M., Farah N., Bonham C.A. Interstitial Lung Disease and Sarcoidosis. Clin. Chest Med., 2023, vol. 44, no. 3, pp. 575–584. doi: 10.1016/j.ccm.2023.06.003</mixed-citation></ref><ref id="B117"><label>117.</label><mixed-citation>Shoenfeld Y., Aron-Maor A., Tanai A., Ehrenfeld M. BCG and Autoimmunity: Another Two-Edged Sword. J. Autoimmun., 2001, vol. 16, pp. 235–240. doi: 10.1006/jaut.2000.0494</mixed-citation></ref><ref id="B118"><label>118.</label><mixed-citation>Song Z., Marzilli L., Greenlee B.M., Chen E.S., Silver R.F., Askin F.B., Teirstein A.S., Zhang Y., Cotter R.J., Moller D.R. Mycobacterial catalase-peroxidase is a tissue antigen and target of the adaptive immune response in systemic sarcoidosis. J. Exp. Med., 2005, vol. 201, pp. 755–776. doi: 10.1084/jem.20040429</mixed-citation></ref><ref id="B119"><label>119.</label><mixed-citation>Sosa-Hernández V.A., Torres-Ruíz J., Cervantes-Díaz R., Romero-Ramírez S., Páez-Franco J.C., Meza-Sánchez D.E., Juárez-Vega G., Pérez-Fragoso A., Ortiz-Navarrete V., Ponce-de-León A., Llorente L., Berrón-Ruiz L., Mejía-Domínguez N.R., Gómez-Martín D., Maravillas-Montero J.L. B Cell Subsets as Severity-Associated Signatures in COVID-19 Patients. Front. Immunol., 2020, vol. 11: 611004. doi: 10.3389/fimmu.2020.611004</mixed-citation></ref><ref id="B120"><label>120.</label><mixed-citation>Spoerl S., Kremer A.N., Aigner M., Eisenhauer N., Koch P., Meretuk L., Löffler P., Tenbusch M., Maier C., Überla K., Heinzerling L., Frey B., Lutzny-Geier G., Winkler T.H., Krönke G., Vetter M., Bruns H., Neurath M.F., Mackensen A., Kremer A.E., Völkl S. Upregulation of CCR4 in activated CD8+ T cells indicates enhanced lung homing in patients with severe acute SARS-CoV-2 infection. Eur. J. Immunol., 2021, vol. 51, no. 6, pp. 1436–1448. doi: 10.1002/eji.202049135</mixed-citation></ref><ref id="B121"><label>121.</label><mixed-citation>Starshinova A., Malkova А., Kudryavtsev I., Kudlay D., Zinchenko Y., Yablonskiy P. Tuberculosis and autoimmunity: common features. Tuberculosis (Edinb.), 2022, no. 134: 102202. doi: 10.1016/j.tube.2022.102202</mixed-citation></ref><ref id="B122"><label>122.</label><mixed-citation>Starshinova A., Zinchenko Y., Malkova A., Kudlay D., Kudryavtsev I., Yablonskiy P. Sarcoidosis and Autoimmune Inflammatory Syndrome Induced by Adjuvants. Life (Basel), 2023, vol. 13, no. 4: 1047. doi: 10.3390/life13041047</mixed-citation></ref><ref id="B123"><label>123.</label><mixed-citation>Starshinova A.A., Malkova A.M., Basantsova N.Y., Zinchenko Y.S., Kudryavtsev I.V., Ershov G.A., Soprun L.A., Mayevskaya V.A., Churilov L.P., Yablonskiy P.K. Sarcoidosis as an Autoimmune Disease. Front. Immunol., 2020, no. 10: 2933. doi: 10.3389/fimmu.2019.02933</mixed-citation></ref><ref id="B124"><label>124.</label><mixed-citation>Starshinova A.A., Malkova A.M., Zinchenko Yu.S., Basantsova N.Yu., Kudlay D.A. Autoimmune component in the etiology of sarcoidosis. Tuberculosis and Lung Diseases, 2020, vol. 98, no.5, pp. 54–62. doi: 10.21292/2075-1230-2020-98-5-54-62</mixed-citation></ref><ref id="B125"><label>125.</label><mixed-citation>Starshinova A.A., Malkova A.М., Zinchenko Yu.S., Basantsova N.Yu., Pavlova M.V., Belyaeva E.N., Lapin S.V., Masing A.V., Surkova E.A., Yablonsky P.K. Characteristics of autoimmune inflammation in patients with pulmonary tuberculosis. Medical Immunology (Russia), 2019, vol. 21, no. 5, pp. 911–918. doi: 10.15789/1563-0625-2019-5-911-918</mixed-citation></ref><ref id="B126"><label>126.</label><mixed-citation>Szekanecz Z., Balog A., Constantin T., Czirják L., Géher P., Kovács L., Kumánovics G., Nagy G., Rákóczi É., Szamosi S., Szűcs G., Vályi-Nagy I. COVID-19: autoimmunity, multisystemic inflammation and autoimmune rheumatic patients. Expert Rev. Mol. Med., 2022, vol. 24: e13. doi: 10.1017/erm.2022.10</mixed-citation></ref><ref id="B127"><label>127.</label><mixed-citation>Tan M., Liu Y., Zhou R., Deng X., Li F., Liang K., Shi Y. Immunopathological characteristics of coronavirus disease 2019 cases in Guangzhou, China. Immunology, 2020, vol. 160, no. 3, pp. 261–268. doi: 10.1111/imm.13223</mixed-citation></ref><ref id="B128"><label>128.</label><mixed-citation>Tana C., Cinetto F., Mantini C., Bernardinello N., Tana M., Ricci F., Ticinesi A., Meschi T., Scarpa R., Cipollone F., Giamberardino M.A., Spagnolo P. Sarcoidosis and COVID-19: At the Cross-Road between Immunopathology and Clinical Manifestation. Biomedicines, 2022, vol. 10, no. 10: 2525. doi: 10.3390/biomedicines10102525</mixed-citation></ref><ref id="B129"><label>129.</label><mixed-citation>Tchernev G., Ananiev J., Cardoso J.C., Wollina U., Verma S.B., Patterson J.W., Dourmishev L.A., Tronnier M., Okamoto H., Mizuno K., Kanazawa N., Gulubova M., Manolova I., Salaro C. Sarcoidosis and molecular mimicry — important etiopathogenetic aspects: current state and future directions. Wien Klin. Wochenschr., 2012, vol. 124, no. 7–8, pp. 227–238. doi: 10.1007/s00508-012-0154-9</mixed-citation></ref><ref id="B130"><label>130.</label><mixed-citation>Ten Berge B., Paats M.S., Bergen I.M., van den Blink B., Hoogsteden H.C., Lambrecht B.N., Hendriks R.W., Kleinjan A. Increased IL-17A expression in granulomas and in circulating memory T cells in sarcoidosis. Rheumatology (Oxford), 2012, vol. 51, no. 1, pp. 37–46. doi: 10.1093/rheumatology/ker316</mixed-citation></ref><ref id="B131"><label>131.</label><mixed-citation>Thillai M., Eberhardt C., Lewin A.M., Potiphar L., Hingley-Wilson S., Sridhar S., Macintyre J., Kon O.M., Wickremasinghe M., Wells A., Weeks M.E., Mitchell D., Lalvani A. Sarcoidosis and tuberculosis cytokine profiles: Indistinguishable in bronchoalveolar lavage but different in blood. PLoS One, 2012, vol. 7: e38083. doi: 10.1371/journal.pone.0038083</mixed-citation></ref><ref id="B132"><label>132.</label><mixed-citation>Trougakos I.P., Stamatelopoulos K., Terpos E., Tsitsilonis O.E., Aivalioti E., Paraskevis D., Kastritis E., Pavlakis G.N., Dimopoulos M.A. Insights to SARS-CoV-2 life cycle, pathophysiology, and rationalized treatments that target COVID-19 clinical complications. J. Biomed. Sci., 2021, vol. 28, no. 1: 9. doi: 10.1186/s12929-020-00703-5</mixed-citation></ref><ref id="B133"><label>133.</label><mixed-citation>Vasileva E.V., Kudryavtsev I.V., Maximov G.V., Verbov V.N., Serebriakova M.K., Tkachuk A.P., Totolian Areg A. Impact of HIV infection and tuberculosison the peripheral blood T-cell differentiation. Russian Journal of Infection and Immunity, 2017, vol. 7, no. 2, pp. 151–161. doi: 10.15789/2220-7619-2017-2-151-161</mixed-citation></ref><ref id="B134"><label>134.</label><mixed-citation>Velounias R.L., Tull T.J. Human B-cell subset identification and changes in inflammatory diseases. Clin. Exp. Immunol., 2022, vol. 210, no. 3, pp. 201–216. doi: 10.1093/cei/uxac104</mixed-citation></ref><ref id="B135"><label>135.</label><mixed-citation>Watad A., Rosenberg V., Tiosano S., Cohen Tervaert J.W., Yavne Y., Shoenfeld Y., Shalev V., Chodick G., Amital H. Silicone breast implants and the risk of autoimmune diseases: real world analysis. Ann. Rheum. Dis., 2018, vol. 77, pp. 1191–1192. doi: 10.1093/ije/dyy217</mixed-citation></ref><ref id="B136"><label>136.</label><mixed-citation>Weiskopf D., Schmitz K.S., Raadsen M.P., Grifoni A., Okba N.M.A., Endeman H., van den Akker J.P.C., Molenkamp R., Koopmans M.P.G., van Gorp E.C.M., Haagmans B.L., de Swart R.L., Sette A., de Vries R.D. Phenotype and kinetics of SARS-CoV-2-specific T cells in COVID-19 patients with acute respiratory distress syndrome. Sci. Immunol., 2020, vol. 5, no. 48: eabd2071. doi: 10.1126/sciimmunol.abd2071</mixed-citation></ref><ref id="B137"><label>137.</label><mixed-citation>WHO global lists of high burden countries for TB, multidrug/rifampicin-resistant TB (MDR/RR-TB) and TB/HIV, 2021–2025. WHO, 2021. 16 p.</mixed-citation></ref><ref id="B138"><label>138.</label><mixed-citation>WHO. Coronavirus disease (COVID-19) Pandemic. Geneva: WHO; 2020. URL: https://www.who.int/emergencies/diseases/novel-coronavirus-2019</mixed-citation></ref><ref id="B139"><label>139.</label><mixed-citation>Winau F., Weber S., Sad S., de Diego J., Hoops S.L., Breiden B., Sandhoff K., Brinkmann V., Kaufmann S.H., Schaible U.E. Apoptotic vesicles crossprime CD8 T cells and protect against tuberculosis. Immunity, 2006, vol. 24, no. 1, pp. 105–117. doi: 10.1016/j.immuni.2005.12.001</mixed-citation></ref><ref id="B140"><label>140.</label><mixed-citation>Winheim E., Rinke L., Lutz K., Reischer A., Leutbecher A., Wolfram L., Rausch L., Kranich J., Wratil P.R., Huber J.E., Baumjohann D., Rothenfusser S., Schubert B., Hilgendorff A., Hellmuth J.C., Scherer C., Muenchhoff M., von Bergwelt-Baildon M., Stark K., Straub T., Brocker T., Keppler O.T., Subklewe M., Krug A.B. Impaired function and delayed regeneration of dendritic cells in COVID-19. PLoS Pathog., 2021, vol. 17, no. 10: e1009742. doi: 10.1371/journal.ppat.100974</mixed-citation></ref><ref id="B141"><label>141.</label><mixed-citation>Wu D., Yang X.O. TH17 responses in cytokine storm of COVID-19: an emerging target of JAK2 inhibitor Fedratinib. J. Microbiol. Immunol. Infect., 2020, vol. 53, no. 3, pp. 368–370. doi: 10.1016/j.jmii.2020.03.005</mixed-citation></ref><ref id="B142"><label>142.</label><mixed-citation>Wu Y.E., Zhang S.W., Peng W.G., Li K.S., Li K., Jiang J.K., Lin J.H., Cai Y.M. Changes in lymphocyte subsets in the peripheral blood of patients with active pulmonary tuberculosis. J. Int. Med. Res., 2009, vol. 37, no. 6, pp. 1742–1749. doi: 10.1177/147323000903700610</mixed-citation></ref><ref id="B143"><label>143.</label><mixed-citation>Xu Z., Shi L., Wang Y., Zhang J., Huang L., Zhang C., Liu S., Zhao P., Liu H., Zhu L., Tai Y., Bai C., Gao T., Song J., Xia P., Dong J., Zhao J., Wang F.S. Pathological findings of COVID-19 associated with acute respiratory distress syndrome. Lancet Respir. Med., 2020, vol. 8, pp. 420–422. doi: 10.1016/S2213-2600(20)30076-X</mixed-citation></ref><ref id="B144"><label>144.</label><mixed-citation>Zaid Y., Doré É., Dubuc I., Archambault A.S., Flamand O., Laviolette M., Flamand N., Boilard É., Flamand L. Chemokines and eicosanoids fuel the hyperinflammation within the lungs of patients with severe COVID-19. J. Allergy Clin. Immunol., 2021, vol. 148, no. 2, pp. 368–380.e3. doi: 10.1016/j.jaci.2021.05.032</mixed-citation></ref><ref id="B145"><label>145.</label><mixed-citation>Zewdie M., Howe R., Hoff S.T., Doherty T.M., Getachew N., Tarekegne A., Tessema B., Yamuah L., Aseffa A., Abebe M. Ex-vivo characterization of regulatory T cells in pulmonary tuberculosis patients, latently infected persons, and healthy endemic controls. Tuberculosis, 2016, vol. 100, pp. 61–68. doi: 10.1016/j.tube.2016.06.007</mixed-citation></ref><ref id="B146"><label>146.</label><mixed-citation>Zhang H., Costabel U., Dai H. The Role of Diverse Immune Cells in Sarcoidosis. Front. Immunol., 2021, no. 12: 788502. doi: 10.3389/fimmu.2021.788502</mixed-citation></ref><ref id="B147"><label>147.</label><mixed-citation>Zhang M., Zhang S. T Cells in Fibrosis and Fibrotic Diseases. Front. Immunol., 2020, no. 11: 1142. doi: 10.3389/fimmu.2020.01142</mixed-citation></ref><ref id="B148"><label>148.</label><mixed-citation>Zhang M., Zheng X., Zhang J., Zhu Y., Zhu X., Liu H., Zeng M, Graner M.W., Zhou B., Chen X. CD19+CD1d+CD5+ B cell frequencies are increased in patients with tuberculosis and suppress Th17 responses. Cell. Immunol., 2012, vol. 274, no. 1–2, pp. 89–97. doi: 10.1016/j.cellimm.2012.01.007</mixed-citation></ref><ref id="B149"><label>149.</label><mixed-citation>Zheng H.Y., Zhang M., Yang C.X., Zhang N., Wang X.C., Yang X.P., Dong X.Q., Zheng Y.T. Elevated exhaustion levels and reduced functional diversity of T cells in peripheral blood may predict severe progression in COVID-19 patients. Cell. Mol. Immunol., 2020, vol. 17, no. 5, pp. 541–543. doi: 10.1038/s41423-020-0401-3</mixed-citation></ref><ref id="B150"><label>150.</label><mixed-citation>Zhou E.R., Arce S. Key Players and Biomarkers of the Adaptive Immune System in the Pathogenesis of Sarcoidosis. Int. J. Mol. Sci., 2020, vol. 21, no. 19: 7398. doi: 10.3390/ijms21197398</mixed-citation></ref><ref id="B151"><label>151.</label><mixed-citation>Zhuang Z., Lai X., Sun J., Chen Z., Zhang Z., Dai J., Liu D., Li Y., Li F., Wang Y., Zhu A., Wang J., Yang W., Huang J., Li X., Hu L., Wen L., Zhuo J., Zhang Y., Chen D., Li S., Huang S., Shi Y., Zheng K., Zhong N., Zhao J., Zhou D., Zhao J. Mapping and role of T cell response in SARS-CoV-2-infected mice. J. Exp. Med., 2021, vol. 218, no. 4: e20202187. doi: 10.1084/jem.20202187</mixed-citation></ref></ref-list></back></article>
