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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">milmed</journal-id><journal-title-group><journal-title xml:lang="ru">Военная медицина</journal-title><trans-title-group xml:lang="en"><trans-title>Military Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-5044</issn><publisher><publisher-name>Белорусский государственный медицинский университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.51922/2074-5044.2021.4.121</article-id><article-id custom-type="elpub" pub-id-type="custom">milmed-992</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>ОБЗОРЫ И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Ответы адаптивной системы иммунитета на SARS-COV-2</article-title><trans-title-group xml:lang="en"><trans-title>Responses of the adaptive system of immunity to SARS-COV-2</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>Цыганков</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Cygankov</surname><given-names>A. M.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Янченко</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Yanchenko</surname><given-names>V. V.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>УО «Витебский государственный ордена Дружбы народов медицинский университет»</institution><country>Belarus</country></aff><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>01</day><month>11</month><year>2026</year></pub-date><volume>0</volume><issue>4</issue><fpage>121</fpage><lpage>128</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Цыганков А.М., Янченко В.В., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Цыганков А.М., Янченко В.В.</copyright-holder><copyright-holder xml:lang="en">Cygankov A.M., Yanchenko V.V.</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://milmed.ejournal.by/jour/article/view/992">https://milmed.ejournal.by/jour/article/view/992</self-uri><abstract><p>Адаптивная система иммунитета (далее СИ) важна для борьбы с вирусными инфекциями. Основными компонентами адаптивной иммунной системы являются В-лимфоциты, CD4 и CD8 Т-лимфоциты. В статье нами был проанализированы публикации, посвященные гуморальным и клеточным ответам людей на инфицирование SARS-CoV-2. Болезнь COVID-19 привела к высокой заболеваемости и смертности во всем мире за короткий срок. Научные достижения в понимании новой болезни были необычайно быстрыми, что является свидетельством работы международного научного сообщества, как в академических, так и в промышленных кругах в крайне напряженных условиях. В этой статье мы рассмотрим нынешнее понимание ответов адаптивного иммунитета при COVID-19 и вакцинации. Следует учитывать, что иммунный ответ способствует не только защите хозяина, но и иммунопатологии. Получив ответы на вопросы, касающиеся адаптивного иммунного ответа на SARS-CoV-2, можно решать практические задачи, которые стоят перед специалистами здравоохранения и обществом.</p></abstract><trans-abstract xml:lang="en"><p>The adaptive immune system is important for fighting viral infections. The main components of the adaptive immune system are B-lymphocytes, CD4 and CD8 T-lymphocytes. In this article we reviewed publications dealing with humoral and cellular responses in humans to SARS-CoV-2 infection. The COVID-19 disease in question has resulted in high morbidity and mortality worldwide in a short period of time. Scientific advances in understanding the new disease have been extraordinarily rapid, a testament to the work of the international scientific community, both in academia and industry, under extremely stressful conditions. In this article we will look at the current understanding of adaptive immunity responses in COVID-19 and vaccination. It should be borne in mind that the immune response contributes not only to host protection but also to immunopathology. By obtaining answers to questions concerning the adaptive immune response to SARS-CoV-2, the practical challenges facing health professionals and society can be addressed.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>лимфоциты</kwd><kwd>адаптивный иммунный ответ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>lymphocytes</kwd><kwd>adaptive immune response</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">Костинов М. П., Маркелова Е. В., Свитич О. А., Полищук В. Б. Иммунные механизмы SARS-CoV-2 и потенциальные препараты для профилактики и лечения COVID-19. Пульмонология. – 2020. – Т. 30. – № 5. – С. 700–708.</mixed-citation><mixed-citation xml:lang="en">Kostinov M. P., Markelova E. V., Svitich O. A., Polishchuk V. B. Immunnye mekhanizmy SARS-CoV-2 i potencial‘nye preparaty dlya profilaktiki i lecheniya COVID-19. Pul‘monologiya. – 2020. – T. 30. – № 5. – S. 700–708.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Смирнов В. С., Тотолян А. А. Врожденный иммунитет при коронавирусной инфекции // Инфекция и иммунитет. – 2020. – Т. 10. – № 2. – С. 259–268.</mixed-citation><mixed-citation xml:lang="en">Smirnov V. S., Totolyan A. A. Vrozhdennyj immunitet pri koronavirusnoj infekcii // Infekciya i immunitet. – 2020. – T. 10. – № 2. – S. 259–268.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Цыганков А. М., Янченко В. В. Защитные механизмы человека против вирусов, вызывающих острые респираторные инфекции. Клиническая инфектология и паразитология. – 2021. – Т. 10. – № 1. – С. 88–103.</mixed-citation><mixed-citation xml:lang="en">Cygankov A. M., Yanchenko V. V. Zashchitnye mekhanizmy cheloveka protiv virusov, vyzyvayushchih ostrye respiratornye infekcii. Klinicheskaya infektologiya i parazitologiya. – 2021. – T. 10. – № 1. – S. 88–103.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Харченко Е. П. Коронавирус SARS-CoV-2: сложности патогенеза, поиски вакцин и будущие пандемии // Эпидемиология и Вакцинопрофилактика. – 2020. – Т. 19. – №. 3. – С. 4–20.</mixed-citation><mixed-citation xml:lang="en">Harchenko E. P. Koronavirus SARS-CoV-2: slozhnosti patogeneza, poiski vakcin i budushchie pandemii // Epidemiologiya i Vakcinoprofilaktika. – 2020. – T. 19. – № 3. – S. 4–20.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Braun J. et al. SARS-CoV-2-reactive T cells in healthy donors and patients with COVID-19 // Nature. – 2020. – Т. 587. – № 7833. – Р. 270–274.</mixed-citation><mixed-citation xml:lang="en">Braun J. et al. SARS-CoV-2-reactive T cells in healthy donors and patients with COVID-19 // Nature. – 2020. – T. 587. – № 7833. – R. 270–274.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Carsetti R. et al. Different Innate and Adaptive Immune Responses to SARS-CoV-2 Infection of Asymptomatic, Mild, and Severe Cases //Frontiers in immunology. – 2020. – Т. 11. – Р. 33–65.</mixed-citation><mixed-citation xml:lang="en">Carsetti R. et al. Different Innate and Adaptive Immune Responses to SARS-CoV-2 Infection of Asymptomatic, Mild, and Severe Cases // Frontiers in immunology. – 2020. – T. 11. – R. 33–65.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Dan J. M. et al. Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection // Science. – 2021. – Т. 371. – № 6529. – Р. 40–63.</mixed-citation><mixed-citation xml:lang="en">Dan J. M. et al. Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection // Science. – 2021. – T. 371. – № 6529. – R. 40–63.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Diao B. et al. Reduction and functional exhaustion of T cells in patients with coronavirus disease 2019 (COVID-19) // Frontiers in immunology. – 2020. – Т. 11. – Р. 82–87.</mixed-citation><mixed-citation xml:lang="en">Diao B. et al. Reduction and functional exhaustion of T cells in patients with coronavirus disease 2019 (COVID-19) // Frontiers in immunology. – 2020. – T. 11. – S R. 82–87.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Dorp L. et al. No evidence for increased transmissibility from recurrent mutations in SARS-CoV-2 // Nature communications. – 2020. – Т. 11. – № 1. – Р. 1–8.</mixed-citation><mixed-citation xml:lang="en">Dorp L. et al. No evidence for increased transmissibility from recurrent mutations in SARS-CoV-2 // Nature communications. – 2020. – T. 11. – № 1. – R. 1–8.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Edridge A. W. D. et al. Seasonal coronavirus protective immunity is short-lasting // Nature medicine. – 2020. – Т. 26. – № 11. – Р. 1691–1693.</mixed-citation><mixed-citation xml:lang="en">Edridge A. W. D. et al. Seasonal coronavirus protective immunity is short-lasting // Nature medicine. – 2020. – T. 26. – № 11. – R. 1691–1693.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Gaebler C. et al. Evolution of antibody immunity to SARS-CoV-2 // Nature. – 2021. – №. 1. – Р. 1–6.</mixed-citation><mixed-citation xml:lang="en">Gaebler C. et al. Evolution of antibody immunity to SARS-CoV-2 // Nature. – 2021. – № 1. – R. 1–6.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Gutierrez L., Beckford J., Alachkar H. Deciphering the TКR Repertoire to Solve the COVID-19 Mystery // Trends in Pharmacological Sciences. – 2020. – Т. 41. – № 8. – Р. 518–530.</mixed-citation><mixed-citation xml:lang="en">Gutierrez L., Beckford J., Alachkar H. Deciphering the TKR Repertoire to Solve the COVID-19 Mystery // Trends in Pharmacological Sciences. – 2020. – T. 41. – № 8. – R. 518–530.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Habel J. R. et al. Suboptimal SARS-CoV-2 – specific CD8+ T cell response associated with the prominent HLA-A* 02: 01 phenotype //Proceedings of the National Academy of Sciences. – 2020. – Т. 117. – № 39. – Р. 24384–24391.</mixed-citation><mixed-citation xml:lang="en">Habel J. R. et al. Suboptimal SARS-CoV-2 – specific CD8+ T cell response associated with the prominent HLA-A* 02: 01 phenotype // Proceedings of the National Academy of Sciences. – 2020. – T. 117. – № 39. – R. 24384–24391.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Hartenian E. et al. The molecular virology of Coronaviruses //Journal of Biological Chemistry. – 2020. – Т. 295. – № 37. – Р. 12910–12934.</mixed-citation><mixed-citation xml:lang="en">Hartenian E. et al. The molecular virology of Coronaviruses // Journal of Biological Chemistry. – 2020. – T. 295. – № 37. – R. 12910–12934.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Hartley G. E. et al. Rapid generation of durable B cell memory to SARS-CoV-2 spike and nucleocapsid proteins in COVID-19 and convalescence //Science Immunology. – 2020. – Т. 5. – № 54. Р. 88–91.</mixed-citation><mixed-citation xml:lang="en">Hartley G. E. et al. Rapid generation of durable B cell memory to SARS-CoV-2 spike and nucleocapsid proteins in COVID-19 and convalescence // Science Immunology. – 2020. – T. 5. – № 54. R. 88–91.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Jarjour N. N., Masopust D., Jameson S. C. T cell memory: Understanding COVID-19 //Immunity. – 2021. – Т. 54. – № 1. – Р. 14–23.</mixed-citation><mixed-citation xml:lang="en">Jarjour N. N., Masopust D., Jameson S. C. T cell memory: Understanding COVID-19 // Immunity. – 2021. – T. 54. – № 1. – R. 14–23.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Krammer F. SARS-CoV-2 vaccines in development // Nature. – 2020. – Т. 586. – № 7830. – Р. 516–527.</mixed-citation><mixed-citation xml:lang="en">Krammer F. SARS-CoV-2 vaccines in development // Nature. – 2020. – T. 586. – №. 7830. – R. 516–527.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar B. V., Connors T. J., Farber D. L. Human T cell development, localization, and function throughout life // Immunity. – 2018. – Т. 48. – № 2. – Р. 202–213.</mixed-citation><mixed-citation xml:lang="en">Kumar B. V., Connors T. J., Farber D. L. Human T cell development, localization, and function throughout life // Immunity. – 2018. – T. 48. – № 2. – R. 202–213.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Li G. et al. Coronavirus infections and immune responses // Journal of medical virology. – 2020. – Т. 92. – № 4. – Р. 424–432.</mixed-citation><mixed-citation xml:lang="en">Li G. et al. Coronavirus infections and immune res-ponses // Journal of medical virology. – 2020. – T. 92. – № 4. – R. 424–432.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Lin M. et al. Association of HLA class I with severe acute respiratory syndrome coronavirus infection // BMC Medical Genetics. – 2003. – Т. 4. – № 1. – Р. 1–7.</mixed-citation><mixed-citation xml:lang="en">Lin M. et al. Association of HLA class I with severe acute respiratory syndrome coronavirus infection // BMC Medical Genetics. – 2003. – T. 4. – № 1. – R. 1–7.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Liu J. et al. Longitudinal characteristics of lymphocyte responses and cytokine profiles in the peripheral blood of SARS-CoV-2 infected patients //EBioMedicine. – 2020. – Т. 55. – Р. 1027–1063.</mixed-citation><mixed-citation xml:lang="en">Liu J. et al. Longitudinal characteristics of lymphocyte responses and cytokine profiles in the peripheral blood of SARS-CoV-2 infected patients // EBioMedicine. – 2020. – T. 55. –R. 1027–1063.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Maggi E., Canonica G. W., Moretta L. COVID-19: Unanswered Questions on Immune Response and Pathogenesis // The Journal of allergy and clinical immunology. – 2020. – Т. 146. – № 1. – Р. 18–22.</mixed-citation><mixed-citation xml:lang="en">Maggi E., Canonica G. W., Moretta L. COVID-19: Unanswered Questions on Immune Response and Pathogenesis // The Journal of allergy and clinical immunology. – 2020. – T. 146. – № 1. – R. 18–22.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Mathew D. et al. Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications // Science. – 2020. – Т. 369. – № 6508. – Р. 5–11.</mixed-citation><mixed-citation xml:lang="en">Mathew D. et al. Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications // Science. – 2020. – T. 369. – № 6508. – R. 5–11.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Melenotte C. et al. Immune responses during COVID-19 infection // OncoImmunology. – 2020. – Т. 9. – № 1. – Р. 1807–1836.</mixed-citation><mixed-citation xml:lang="en">Melenotte C. et al. Immune responses during COVID-19 infection // OncoImmunology. – 2020. – T. 9. – № 1. – R. 1807–1836.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Minervina A. A. et al. Longitudinal high-throughput TКR repertoire profiling reveals the dynamics of T-cell memory formation after mild COVID-19 infection // Elife. – 2021. – Т. 10. – Р. 635–702.</mixed-citation><mixed-citation xml:lang="en">Minervina A. A. et al. Longitudinal high-throughput TKR repertoire profiling reveals the dynamics of T-cell memory formation after mild COVID-19 infection // Elife. – 2021. – T. 10. – R. 635–702.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Mustapha J. O. et al. Understanding the implications of SARS-CoV-2 re-infections on immune response milieu, laboratory tests and control measures against COVID-19 // Heliyon. – 2021. – Р. 51–59.</mixed-citation><mixed-citation xml:lang="en">Mustapha J. O. et al. Understanding the implications of SARS-CoV-2 re-infections on immune response milieu, laboratory tests and control measures against COVID-19 // Heliyon. – 2021. – R. 51–59.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Ng K. W. et al. Preexisting and de novo humoral immunity to SARS-CoV-2 in humans // Science. – 2020. – Т. 370. – № 6522. – Р. 1339–1343.</mixed-citation><mixed-citation xml:lang="en">Ng K. W. et al. Preexisting and de novo humoral immunity to SARS-CoV-2 in humans // Science. – 2020. – T. 370. – № 6522. – R. 1339–1343.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Nguyen A. et al. Human leukocyte antigen susceptibility map for severe acute respiratory syndrome coronavirus 2 // Journal of virology. – 2020. – Т. 94. – №. 13. – Р. 510–520.</mixed-citation><mixed-citation xml:lang="en">Nguyen A. et al. Human leukocyte antigen susceptibility map for severe acute respiratory syndrome coronavirus 2 // Journal of virology. – 2020. – T. 94. – № 13. – R. 510–520.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Noorimotlagh Z. et al. Immune and bioinformatics identification of T cell and B cell epitopes in the protein structure of SARS-CoV-2: A systematic review // International immunopharmacology. – 2020. – Т. 86. – P. 106–122.</mixed-citation><mixed-citation xml:lang="en">Noorimotlagh Z. et al. Immune and bioinformatics identification of T cell and B cell epitopes in the protein structure of SARS-CoV-2: A systematic review // International immunopharmacology. – 2020. – T. 86. – P. 106–122.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Peng Y. et al. Broad and strong memory CD4+ and CD8+ T cells induced by SARS-CoV-2 in UK convalescent individuals following COVID-19 // Nature immunology. – 2020. – Т. 21. – № 11. – Р. 1336–1345.</mixed-citation><mixed-citation xml:lang="en">Peng Y. et al. Broad and strong memory CD4+ and CD8+ T cells induced by SARS-CoV-2 in UK convalescent individuals following COVID-19 // Nature immunology. – 2020. – T. 21. – № 11. – R. 1336–1345.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Rodda L. B. et al. Functional SARS-CoV-2-specific immune memory persists after mild COVID-19 // Cell. – 2021. – Т. 184. – № 1. – Р. 169–183.</mixed-citation><mixed-citation xml:lang="en">Rodda L. B. et al. Functional SARS-CoV-2-specific immune memory persists after mild COVID-19 // Cell. – 2021. – T. 184. – № 1. – R. 169–183.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Rodriguez-Morales A. J. et al. Clinical, laboratory and imaging features of COVID-19: A systematic review and meta-analysis // Travel medicine and infectious disease. – 2020. – Т. 34. – С. 1016–1023.</mixed-citation><mixed-citation xml:lang="en">Rodriguez-Morales A. J. et al. Clinical, laboratory and imaging features of COVID-19: A systematic review and meta-analysis // Travel medicine and infectious disease. – 2020. – T. 34. – S. 1016–1023.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Saini S. K. et al. SARS-CoV-2 genome-wide T cell epitope mapping reveals immunodominance and substantial CD8+ T cell activation in COVID-19 patients // Science Immunology. – 2021. – Т. 6. – № 58. – Р. 20–34.</mixed-citation><mixed-citation xml:lang="en">Saini S. K. et al. SARS-CoV-2 genome-wide T cell epitope mapping reveals immunodominance and substantial CD8+ T cell activation in COVID-19 patients // Science Immunology. – 2021. – T. 6. – № 58. – R. 20–34.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Schulien I. et al. Characterization of pre-existing and induced SARS-CoV-2-specific CD8+ T cells // Nature medicine. – 2021. – Т. 27. – № 1. – Р. 78–85.</mixed-citation><mixed-citation xml:lang="en">Schulien I. et al. Characterization of pre-existing and induced SARS-CoV-2-specific CD8+ T cells // Nature medicine. – 2021. – T. 27. – № 1. – R. 78–85.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Sekine T. et al. Robust T cell immunity in convalescent individuals with asymptomatic or mild COVID-19 // Cell. – 2020. – Т. 183. – № 1. – Р. 158–168.</mixed-citation><mixed-citation xml:lang="en">Sekine T. et al. Robust T cell immunity in convalescent individuals with asymptomatic or mild COVID-19 // Cell. – 2020. – T. 183. – № 1. – R. 158–168.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Sette A., Crotty S. Adaptive immunity to SARS-CoV-2 and COVID-19 //Cell. – 2021. – Т. 184. – № 4. – Р. 861–880.</mixed-citation><mixed-citation xml:lang="en">Sette A., Crotty S. Adaptive immunity to SARS-CoV-2 and COVID-19 // Cell. – 2021. – T. 184. – № 4. – R. 861–880.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Sunil K. S. et al. SARS-CoV-2 genome-wide T cell epitope mapping reveals immunodominance and substantial CD8+ T cell activation in COVID-19 patients. // Science Immunology. – 2021. – Т. 58. – № 6. – Р. 1–22.</mixed-citation><mixed-citation xml:lang="en">Sunil K. S. et al. SARS-CoV-2 genome-wide T cell epitope mapping reveals immunodominance and substantial CD8+ T cell activation in COVID-19 patients. // Science Immunology. – 2021. – T. 58. – № 6. – R. 1–22.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Sterlin D. et al. IgA dominates the early neutralizing antibody response to SARS-CoV-2 // Science translational medicine. – 2021. – Т. 13. – № 577. – Р. 22–32.</mixed-citation><mixed-citation xml:lang="en">Sterlin D. et al. IgA dominates the early neutralizing antibody response to SARS-CoV-2 // Science translational medicine. – 2021. – T. 13. – № 577. – R. 22–32.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Tay M. Z. et al. The trinity of COVID-19: immunity, inflammation and intervention // Nature Reviews Immunology. – 2020. – Т. 20. – № 6. – Р. 363–374.</mixed-citation><mixed-citation xml:lang="en">Tay M. Z. et al. The trinity of COVID-19: immunity, inflammation and intervention // Nature Reviews Immunology. – 2020. – T. 20. – № 6. – R. 363–374.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Z. et al. Exposure to SARS-CoV-2 generates T-cell memory in the absence of a detectable viral infection // Nature Communications. – 2021. – Т. 12. – № 1. – Р. 1–8.</mixed-citation><mixed-citation xml:lang="en">Wang Z. et al. Exposure to SARS-CoV-2 generates T-cell memory in the absence of a detectable viral infection // Nature Communications. – 2021. – T. 12. – № 1. – R. 1–8.</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>
