<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Biotherapy</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Biotherapy</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский биотерапевтический журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9784</issn><issn publication-format="electronic">1726-9792</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1324</article-id><article-id pub-id-type="doi">10.17650/1726-9784-2022-21-2-19-32</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Modern antiviral biomedical cell products and their applications for COVID-19 therapy</article-title><trans-title-group xml:lang="ru"><trans-title>Современные противовирусные биомедицинские клеточные продукты и перспективы их применения в терапии COVID-19</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0769-1695</contrib-id><name-alternatives><name xml:lang="en"><surname>Chikileva</surname><given-names>I. O.</given-names></name><name xml:lang="ru"><surname>Чикилева</surname><given-names>И. О.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Irina Olegovna Chikileva</p><p>24, Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>Ирина Олеговна Чикилева</p><p>115478 Москва, Каширское шоссе, 24</p></bio><email>irinatchikileva@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9374-3158</contrib-id><name-alternatives><name xml:lang="en"><surname>Shubina</surname><given-names>I. Zh.</given-names></name><name xml:lang="ru"><surname>Шубина</surname><given-names>И. Ж.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Irina Zh. Shubina</p><p>24, Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0132-167X</contrib-id><name-alternatives><name xml:lang="en"><surname>Kiselevskiy</surname><given-names>M. V.</given-names></name><name xml:lang="ru"><surname>Киселевский</surname><given-names>М. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Mikhail V. Kiselevskiy</p><p>24, Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N. N. Blokhin National Medical Center of Oncology, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н. Н. Блохина» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-07-26" publication-format="electronic"><day>26</day><month>07</month><year>2022</year></pub-date><volume>21</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>19</fpage><lpage>32</lpage><history><date date-type="received" iso-8601-date="2022-07-26"><day>26</day><month>07</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-07-26"><day>26</day><month>07</month><year>2022</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://bioterapevt.abvpress.ru/jour/article/view/1324">https://bioterapevt.abvpress.ru/jour/article/view/1324</self-uri><abstract xml:lang="en"><p>Several types of COVID-19 vaccines have been developed in a short period of time. However, the groups at risk of severe COVID-19 (the elderly, people with suppressed immunity, such as oncological patients, or organ transplantation patients) are the least likely to develop an adequate immune response to vaccination. Therefore, in order to obtain protective reactions in these groups, it is advisable to use such biomedical cell products (BMCP) as dendritic cell (DC) based vaccines loaded with SARS-CoV-2 antigens <italic>ex vivo</italic> under optimal conditions. In some cases, when vaccination has not been carried out in a timely manner and the risk of a serious disease is high, it is worth-while to take immediate measures to protect the body from the virus that has infected the organism.</p><p>For this protective action lymphocytes with chimeric antigen receptors (CAR) may be suitable. Such receptors recognize antigens using modified antibody domains, without need for presentation within molecules of major histocompatibility complex. Therefore, it is possible to use donor effector CAR lymphocytes, which were prepared in advance, for emergency needs. CAR lymphocytes are currently used primarily for tumor therapy. Until 2020, there was limited research on antiviral CAR lymphocytes. However, the COVID-19 pandemic has led to a dramatic intensification of such activities. DCs, which are considered to be the most effective antigen-presenting cells, were also originally used as anti-tumor vaccines. The safety of DC vaccines, their high effectiveness in the presentation of target antigens quickly led researchers to try using DCs also as a therapeutic agent for chronic viral diseases such as hepatitis B and C, human immunodeficiecy virus.</p><p>This review summarizes the data on antiviral BMCPs that have been developed so far, with a particular focus on products against COVID-19. It discusses how the results of previous studies can be used to increase the efficiency of anti-COVID-19 BMCP.</p></abstract><trans-abstract xml:lang="ru"><p>За короткий промежуток времени было разработано несколько типов вакцин против COVID-19. Однако именно группы риска по тяжелому течению COVID-19 (пожилые люди, лица с подавленным иммунитетом, такие как онкологические пациенты или пациенты после пересадки органов) хуже всего развивают адекватный иммунный ответ на вакцинацию. Поэтому для получения защитных реакций у данных групп следует применять вакцины на основе таких биомедицинских клеточных продуктов (БМКП), как дендритные клетки (ДК), нагруженные антигенами SARS-CoV-2 <italic>ex vivo</italic> в оптимальных условиях. В некоторых случаях, когда вакцинация не была проведена своевременно, а риск тяжелого заболевания велик, целесообразно немедленно предпринять меры для защиты организма от вируса, инфицировавшего организм.</p><p>Для подобного протективного действия могут использоваться другие БМКП – лимфоциты с химерным рецептором антигенов (chimeric antigen receptors, CAR). Такие рецепторы распознают антигены при помощи модифицированных доменов антител, то есть вне контекста молекул главного комплекса гистосовместимости. Поэтому возможно применение для экстренных нужд донорских эффекторных CAR-лимфоцитов, которые были заготовлены заранее. CAR-лимфоциты в настоящее время используются главным образом для противоопухолевой терапии. До 2020 г. велось достаточно ограниченное количество исследований противовирусных CAR-лимфоцитов. Однако пандемия COVID-19 привела к резкой интенсификации подобных работ. ДК, которые считаются наиболее эффективными антигенпрезентирующими клетками, тоже первоначально использовались в качестве противоопухолевых вакцин. Безопасность ДК-вакцин, их высокая эффективность в случае присутствия целевого антигена достаточно быстро привели к тому, что экспериментаторы стали пытаться применять ДК также в качестве терапевтического агента при хронических вирусных заболеваниях типа гепатитов B и C, вирусе иммунодефицита человека.</p><p>В настоящем обзоре суммируются данные о противовирусных БМКП, которые были разработаны к настоящему времени, особое внимание уделяется продуктам против COVID-19. Обсуждается, каким образом результаты предыдущих исследований могут быть применены для увеличения эффективности БМКП, направленных против COVID-19.</p></trans-abstract><kwd-group xml:lang="en"><kwd>COVID-19</kwd><kwd>biomedical cell products</kwd><kwd>chimeric antigen receptors</kwd><kwd>dendritic cells</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>COVID-19</kwd><kwd>биомедицинские клеточные продукты</kwd><kwd>химерные рецепторы антигенов</kwd><kwd>дендритные клетки</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Li C.X., Noreen S., Zhang L.X. et al. A critical analysis of SARS-CoV-2 (COVID-19) complexities, emerging variants, and therapeutic interventions and vaccination strategies. Biomed Pharmacother 2022;146:112550. DOI: 10.1016/j.biopha.2021.112550</mixed-citation><mixed-citation xml:lang="ru">Li C.X., Noreen S., Zhang L.X. et al. A critical analysis of SARS-CoV-2 (COVID-19) complexities, emerging variants, and therapeutic interventions and vaccination strategies. Biomed Pharmacother 2022;146:112550. DOI: 10.1016/j.biopha.2021.112550</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Sarubbo F., El Haji K., Vidal-Balle A., Bargay Lleonart J. Neurological consequences of COVID-19 and brain related pathogenic mechanisms: a new challenge for neuroscience. Brain Behav Immun Health 2022;19:100399. DOI: 10.1016/j.bbih.2021.100399</mixed-citation><mixed-citation xml:lang="ru">Sarubbo F., El Haji K., Vidal-Balle A., Bargay Lleonart J. Neurological consequences of COVID-19 and brain related pathogenic mechanisms: a new challenge for neuroscience. Brain Behav Immun Health 2022;19:100399. DOI: 10.1016/j.bbih.2021.100399</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Jean S.S., Lee P.I., Hsueh P.R. Treatment options for COVID-19: the reality and challenges. J Microbiol Immunol Infect 2020;53(3):436–43. DOI: 10.1016/j.jmii.2020.03.034</mixed-citation><mixed-citation xml:lang="ru">Jean S.S., Lee P.I., Hsueh P.R. Treatment options for COVID-19: the reality and challenges. J Microbiol Immunol Infect 2020;53(3):436–43. DOI: 10.1016/j.jmii.2020.03.034</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Zinatizadeh M.R., Zarandi P.K., Zinatizadeh M. et al. Efficacy of mRNA, adenoviral vector, and perfusion protein COVID-19 vaccines. Biomed Pharmacother 2022;146:112527. DOI: 10.1016/j.biopha.2021.112527</mixed-citation><mixed-citation xml:lang="ru">Zinatizadeh M.R., Zarandi P.K., Zinatizadeh M. et al. Efficacy of mRNA, adenoviral vector, and perfusion protein COVID-19 vaccines. Biomed Pharmacother 2022;146:112527. DOI: 10.1016/j.biopha.2021.112527</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Logunov D.Y., Dolzhikova I.V., Shcheblyakov D.V. et al. Safety and efficacy of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine: an interim analysis of a randomised controlled phase 3 trial in Russia. Lancet 2021;397(10275):671–81. DOI: 10.1016/S0140-6736(21)00234-8</mixed-citation><mixed-citation xml:lang="ru">Logunov D.Y., Dolzhikova I.V., Shcheblyakov D.V. et al. Safety and efficacy of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine: an interim analysis of a randomised controlled phase 3 trial in Russia. Lancet 2021;397(10275):671–81. DOI: 10.1016/S0140-6736(21)00234-8</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Galmiche S., Luong Nguyen L.B., Tartour E. et al. Immunological and clinical efficacy of COVID-19 vaccines in immuno-compromised populations: a systematic review. Clin Microbiol Infect 2022;28(2):163–77. DOI: 10.1016/j.cmi.2021.09.036</mixed-citation><mixed-citation xml:lang="ru">Galmiche S., Luong Nguyen L.B., Tartour E. et al. Immunological and clinical efficacy of COVID-19 vaccines in immuno-compromised populations: a systematic review. Clin Microbiol Infect 2022;28(2):163–77. DOI: 10.1016/j.cmi.2021.09.036</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Zhou R., To K.K., Wong Y.C. et al. Acute SARS-CoV-2 infection impairs dendritic cell and T cell responses. Immunity 2020;53(4):864–77.e.5. DOI: 10.1016/j.immuni.2020.07.026</mixed-citation><mixed-citation xml:lang="ru">Zhou R., To K.K., Wong Y.C. et al. Acute SARS-CoV-2 infection impairs dendritic cell and T cell responses. Immunity 2020;53(4):864–77.e.5. DOI: 10.1016/j.immuni.2020.07.026</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Filin I.Y., Kitaeva K.V., Rutland C.S. et al. Recent advances in experimental dendritic cell vaccines for cancer. Front Oncol 2021;11:730824. DOI: 10.3389/fonc.2021.730824</mixed-citation><mixed-citation xml:lang="ru">Filin I.Y., Kitaeva K.V., Rutland C.S. et al. Recent advances in experimental dendritic cell vaccines for cancer. Front Oncol 2021;11:730824. DOI: 10.3389/fonc.2021.730824</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Zhang X., Gordon J.R., Xiang J. Advances in dendritic cell-based vaccine of cancer. Cancer Biother Radiopharm 2002;17(6):601–19. DOI: 10.1089/108497802320970217</mixed-citation><mixed-citation xml:lang="ru">Zhang X., Gordon J.R., Xiang J. Advances in dendritic cell-based vaccine of cancer. Cancer Biother Radiopharm 2002;17(6):601–19. DOI: 10.1089/108497802320970217</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Sadeghzadeh M., Bornehdeli S., Mohahammadrezakhani H. et al. Dendritic cell therapy in cancer treatment; the state-of-the-art. Life Sci 2020;254:117580. DOI: 10.1016/j.lfs.2020.117580</mixed-citation><mixed-citation xml:lang="ru">Sadeghzadeh M., Bornehdeli S., Mohahammadrezakhani H. et al. Dendritic cell therapy in cancer treatment; the state-of-the-art. Life Sci 2020;254:117580. DOI: 10.1016/j.lfs.2020.117580</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Saadeldin M.K., Abdel-Aziz A.K., Abdellatif A. Dendritic cell vaccine immunotherapy; the beginning of the end of cancer and COVID-19. A hypothesis. Med Hypotheses 2021;146:110365. DOI: 10.1016/j.mehy.2020.110365</mixed-citation><mixed-citation xml:lang="ru">Saadeldin M.K., Abdel-Aziz A.K., Abdellatif A. Dendritic cell vaccine immunotherapy; the beginning of the end of cancer and COVID-19. A hypothesis. Med Hypotheses 2021;146:110365. DOI: 10.1016/j.mehy.2020.110365</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Brusko M.A., Stewart J.M., Posgai A.L. et al. Immunomodulatory dual-sized microparticle system conditions human antigen presenting cells into a tolerogenic phenotype in vitro and inhibits type 1 diabetes-specific autoreactive T cell responses. Front Immunol 2020;11:574447. DOI: 10.3389/fimmu.2020.574447</mixed-citation><mixed-citation xml:lang="ru">Brusko M.A., Stewart J.M., Posgai A.L. et al. Immunomodulatory dual-sized microparticle system conditions human antigen presenting cells into a tolerogenic phenotype in vitro and inhibits type 1 diabetes-specific autoreactive T cell responses. Front Immunol 2020;11:574447. DOI: 10.3389/fimmu.2020.574447</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Adorini L., Penna G., Giarratana N., Uskokovic M. Tolerogenic dendritic cells induced by vitamin D receptor ligands enhance regulatory T cells inhibiting allograft rejection and autoimmune diseases. J Cell Biochem 2003;88(2):227–33. DOI: 10.1002/jcb.10340</mixed-citation><mixed-citation xml:lang="ru">Adorini L., Penna G., Giarratana N., Uskokovic M. Tolerogenic dendritic cells induced by vitamin D receptor ligands enhance regulatory T cells inhibiting allograft rejection and autoimmune diseases. J Cell Biochem 2003;88(2):227–33. DOI: 10.1002/jcb.10340</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Shen C., Wang Z., Zhao F. et al. Treatment of 5 critically ill patients with COVID-19 with convalescent plasma. JAMA 2020;323(16):1582–9. DOI: 10.1001/jama.2020.4783</mixed-citation><mixed-citation xml:lang="ru">Shen C., Wang Z., Zhao F. et al. Treatment of 5 critically ill patients with COVID-19 with convalescent plasma. JAMA 2020;323(16):1582–9. DOI: 10.1001/jama.2020.4783</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Tosta E. The protective immunity induced by SARS-CoV-2 infection and vaccination: a critical appraisal. Explor Immunol 2021;1:199–225. DOI: 10.37349/ei.2021.00014</mixed-citation><mixed-citation xml:lang="ru">Tosta E. The protective immunity induced by SARS-CoV-2 infection and vaccination: a critical appraisal. Explor Immunol 2021;1:199–225. DOI: 10.37349/ei.2021.00014</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Zohar T., Loos C., Fischinger S. et al. Compromised humoral functional evolution tracks with SARS-CoV-2 mortality. Cell 2020;183(6):1508–19.e12. DOI: 10.1016/j.cell.2020.10.052</mixed-citation><mixed-citation xml:lang="ru">Zohar T., Loos C., Fischinger S. et al. Compromised humoral functional evolution tracks with SARS-CoV-2 mortality. Cell 2020;183(6):1508–19.e12. DOI: 10.1016/j.cell.2020.10.052</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Wu Y., Huang Z., Harrison R. et al. Engineering CAR T cells for enhanced efficacy and safety. APL Bioeng 2022;6(1):011502. DOI: 10.1063/5.0073746</mixed-citation><mixed-citation xml:lang="ru">Wu Y., Huang Z., Harrison R. et al. Engineering CAR T cells for enhanced efficacy and safety. APL Bioeng 2022;6(1):011502. DOI: 10.1063/5.0073746</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Maus M.V., Grupp S.A., Porter D.L., June C.H. Antibody-modified T cells: CARs take the front seat for hematologic malignancies. Blood 2014;123(17):2625–35. DOI: 10.1182/blood-2013-11-492231</mixed-citation><mixed-citation xml:lang="ru">Maus M.V., Grupp S.A., Porter D.L., June C.H. Antibody-modified T cells: CARs take the front seat for hematologic malignancies. Blood 2014;123(17):2625–35. DOI: 10.1182/blood-2013-11-492231</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Pule M.A., Savoldo B., Myers G.D. et al. Virus-specific T cells engineered to coexpress tumor-specific receptors: persistence and antitumor activity in individuals with neuroblastoma. Nat Med 2008;14(11):1264–70. DOI: 10.1038/nm.1882</mixed-citation><mixed-citation xml:lang="ru">Pule M.A., Savoldo B., Myers G.D. et al. Virus-specific T cells engineered to coexpress tumor-specific receptors: persistence and antitumor activity in individuals with neuroblastoma. Nat Med 2008;14(11):1264–70. DOI: 10.1038/nm.1882</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Loskog A., Giandomenico V., Rossig C. et al. Addition of the CD28 signaling domain to chimeric T-cell receptors enhances chimeric T-cell resistance to T regulatory cells. Leukemia 2006;20(10):1819–28. DOI: 10.1038/sj.leu.2404366</mixed-citation><mixed-citation xml:lang="ru">Loskog A., Giandomenico V., Rossig C. et al. Addition of the CD28 signaling domain to chimeric T-cell receptors enhances chimeric T-cell resistance to T regulatory cells. Leukemia 2006;20(10):1819–28. DOI: 10.1038/sj.leu.2404366</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Hombach A.A., Abken H. Costimulation by chimeric antigen receptors revisited the T cell antitumor response benefits from combined CD28‒OX40 signalling. Int J Cancer 2011;129(12):2935–44. DOI: 10.1002/ijc.25960</mixed-citation><mixed-citation xml:lang="ru">Hombach A.A., Abken H. Costimulation by chimeric antigen receptors revisited the T cell antitumor response benefits from combined CD28‒OX40 signalling. Int J Cancer 2011;129(12):2935–44. DOI: 10.1002/ijc.25960</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Finney H.M., Akbar A.N., Lawson A.D. Activation of resting human primary T cells with chimeric receptors: costimulation from CD28, inducible costimulator, CD134, and CD137 in series with signals from the TCRζ chain. J Immunol 2004;172(1): 104–13. DOI: 10.4049/jimmunol.172.1.104</mixed-citation><mixed-citation xml:lang="ru">Finney H.M., Akbar A.N., Lawson A.D. Activation of resting human primary T cells with chimeric receptors: costimulation from CD28, inducible costimulator, CD134, and CD137 in series with signals from the TCRζ chain. J Immunol 2004;172(1): 104–13. DOI: 10.4049/jimmunol.172.1.104</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Maude S.L., Frey N., Shaw P.A. et al. Chimeric antigen receptor T cells for sustained remissions in leukemia. N Engl J Med 2014;371(16):1507–17. DOI: 10.1056/NEJMoa1407222</mixed-citation><mixed-citation xml:lang="ru">Maude S.L., Frey N., Shaw P.A. et al. Chimeric antigen receptor T cells for sustained remissions in leukemia. N Engl J Med 2014;371(16):1507–17. DOI: 10.1056/NEJMoa1407222</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Zhang Y., Li P., Fang H. et al. Paving the way towards universal chimeric antigen receptor therapy in cancer treatment: current landscape and progress. Front Immunol 2020;11:604915. DOI: 10.3389/fimmu.2020.604915</mixed-citation><mixed-citation xml:lang="ru">Zhang Y., Li P., Fang H. et al. Paving the way towards universal chimeric antigen receptor therapy in cancer treatment: current landscape and progress. Front Immunol 2020;11:604915. DOI: 10.3389/fimmu.2020.604915</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Wu J., Mishra H.K., Walcheck B. Role of ADAM17 as a regulatory checkpoint of CD16A in NK cells and as a potential target for cancer immunotherapy. J Leukoc Biol 2019;105(6):1297–303. DOI: 10.1002/JLB.2MR1218-501R</mixed-citation><mixed-citation xml:lang="ru">Wu J., Mishra H.K., Walcheck B. Role of ADAM17 as a regulatory checkpoint of CD16A in NK cells and as a potential target for cancer immunotherapy. J Leukoc Biol 2019;105(6):1297–303. DOI: 10.1002/JLB.2MR1218-501R</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Walcheck B., Wu J. iNK-CD64/16A cells: a promising approach for ADCC? Expert Opin Biol Ther 2019;19(12):1229–32. DOI: 10.1080/14712598.2019.1667974.</mixed-citation><mixed-citation xml:lang="ru">Walcheck B., Wu J. iNK-CD64/16A cells: a promising approach for ADCC? Expert Opin Biol Ther 2019;19(12):1229–32. DOI: 10.1080/14712598.2019.1667974.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Phase I–II Trial of dendritic cell vaccine to prevent COVID-19 in adults. Available at: https://clinicaltrials.gov/ct2/show/NCT04386252.</mixed-citation><mixed-citation xml:lang="ru">Phase I–II Trial of dendritic cell vaccine to prevent COVID-19 in adults. Available at: https://clinicaltrials.gov/ct2/show/NCT04386252.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Immunity and safety of Covid-19 synthetic minigene vaccine. Available at: https://clinicaltrials.gov/ct2/show/NCT04276896?term=DC&amp;cond=SARS+CoV+2+Infection&amp;draw=2&amp;rank=1.</mixed-citation><mixed-citation xml:lang="ru">Immunity and safety of Covid-19 synthetic minigene vaccine. Available at: https://clinicaltrials.gov/ct2/show/NCT04276896?term=DC&amp;cond=SARS+CoV+2+Infection&amp;draw=2&amp;rank=1.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Zhou Q., Gu H., Sun S. et al. Large-sized graphene oxide nanosheets increase DC-T-cell synaptic contact and the efficacy of DC vaccines against SARS-CoV-2. Adv Mater 2021;33(40):e2102528. DOI: 10.1002/adma.202102528</mixed-citation><mixed-citation xml:lang="ru">Zhou Q., Gu H., Sun S. et al. Large-sized graphene oxide nanosheets increase DC-T-cell synaptic contact and the efficacy of DC vaccines against SARS-CoV-2. Adv Mater 2021;33(40):e2102528. DOI: 10.1002/adma.202102528</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Reuter T., Heldmann M., Schimmer S. et al. Protection of mice against Friend retrovirus infection by vaccination with antigen-loaded, spleen-derived dendritic cells. Vaccine 2004;22(21–22):2686–9. DOI: 10.1016/j.vaccine.2004.01.005</mixed-citation><mixed-citation xml:lang="ru">Reuter T., Heldmann M., Schimmer S. et al. Protection of mice against Friend retrovirus infection by vaccination with antigen-loaded, spleen-derived dendritic cells. Vaccine 2004;22(21–22):2686–9. DOI: 10.1016/j.vaccine.2004.01.005</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Norton T.D., Miller E.A. Recent advances in lentiviral vaccines for HIV-1 infection. Front Immunol 2016;7:243. DOI: 10.3389/fimmu.2016.00243</mixed-citation><mixed-citation xml:lang="ru">Norton T.D., Miller E.A. Recent advances in lentiviral vaccines for HIV-1 infection. Front Immunol 2016;7:243. DOI: 10.3389/fimmu.2016.00243</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Mohamed H., Miller V., Jennings S.R. et al. The evolution of dendritic cell immunotherapy against HIV-1 infection: improvements and outlook. J Immunol Res 2020;2020:9470102. DOI: 10.1155/2020/9470102</mixed-citation><mixed-citation xml:lang="ru">Mohamed H., Miller V., Jennings S.R. et al. The evolution of dendritic cell immunotherapy against HIV-1 infection: improvements and outlook. J Immunol Res 2020;2020:9470102. DOI: 10.1155/2020/9470102</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Norton T.D., Zhen A., Tada T. et al. Lentiviral vector-based dendritic cell vaccine suppresses HIV replication in humanized mice. Mol Ther 2019;27(5):960–73. DOI: 10.1016/j.ymthe.2019.03.008</mixed-citation><mixed-citation xml:lang="ru">Norton T.D., Zhen A., Tada T. et al. Lentiviral vector-based dendritic cell vaccine suppresses HIV replication in humanized mice. Mol Ther 2019;27(5):960–73. DOI: 10.1016/j.ymthe.2019.03.008</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Miller E., Spadaccia M., Sabado R. et al. Autologous aldrithiol-2-inactivated HIV-1 combined with polyinosinic-polycytidylic acid-poly-L-lysine carboxymethylcellulose as a vaccine platform for therapeutic dendritic cell immunotherapy. Vaccine 2015;33(2):388–95. DOI: 10.1016/j.vaccine.2014.10.054</mixed-citation><mixed-citation xml:lang="ru">Miller E., Spadaccia M., Sabado R. et al. Autologous aldrithiol-2-inactivated HIV-1 combined with polyinosinic-polycytidylic acid-poly-L-lysine carboxymethylcellulose as a vaccine platform for therapeutic dendritic cell immunotherapy. Vaccine 2015;33(2):388–95. DOI: 10.1016/j.vaccine.2014.10.054</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Hong B., Lee S.H., Song X.T. et al. A super TLR agonist to improve efficacy of dendritic cell vaccine in induction of anti-HCV immunity. PLoS One 2012;7(11):e48614. DOI: 10.1371/journal.pone.0048614</mixed-citation><mixed-citation xml:lang="ru">Hong B., Lee S.H., Song X.T. et al. A super TLR agonist to improve efficacy of dendritic cell vaccine in induction of anti-HCV immunity. PLoS One 2012;7(11):e48614. DOI: 10.1371/journal.pone.0048614</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Zhou Y., Zhao F., Chen L. et al. Development of a dendritic cell vaccine encoding multiple cytotoxic T lymphocyte epitopes targeting hepatitis C virus. Int J Mol Med 2013;32(4):901–9. DOI: 10.3892/ijmm.2013.1466</mixed-citation><mixed-citation xml:lang="ru">Zhou Y., Zhao F., Chen L. et al. Development of a dendritic cell vaccine encoding multiple cytotoxic T lymphocyte epitopes targeting hepatitis C virus. Int J Mol Med 2013;32(4):901–9. DOI: 10.3892/ijmm.2013.1466</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Mekonnen Z.A., Masavuli M.G., Yu W. et al. Enhanced T cell responses induced by a necrotic dendritic cell vaccine, expressing HCV NS3. Front Microbiol 2020;11:559105. DOI: 10.3389/fmicb.2020.559105</mixed-citation><mixed-citation xml:lang="ru">Mekonnen Z.A., Masavuli M.G., Yu W. et al. Enhanced T cell responses induced by a necrotic dendritic cell vaccine, expressing HCV NS3. Front Microbiol 2020;11:559105. DOI: 10.3389/fmicb.2020.559105</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Ostanin A.A., Chernykh E.R. Autologous dendritic cell vaccine for treatment of patients with chronic HCV-infection. Available at: https://clinicaltrials.gov/ct2/show/study/NCT03119025?term=DC+vaccine&amp;cond=Hepatitis+C&amp;draw=2&amp;rank=1.</mixed-citation><mixed-citation xml:lang="ru">Ostanin A.A., Chernykh E.R. Autologous dendritic cell vaccine for treatment of patients with chronic HCV-infection. Available at: https://clinicaltrials.gov/ct2/show/study/NCT03119025?term=DC+vaccine&amp;cond=Hepatitis+C&amp;draw=2&amp;rank=1.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Chernykh E., Leplina O., Oleynik E. et al. Immunotherapy with interferon-α-induced dendritic cells for chronic HCV infection (the results of pilot clinical trial). Immunol Res 2018;66(1):31–43. DOI: 10.1007/s12026-017-8967-2</mixed-citation><mixed-citation xml:lang="ru">Chernykh E., Leplina O., Oleynik E. et al. Immunotherapy with interferon-α-induced dendritic cells for chronic HCV infection (the results of pilot clinical trial). Immunol Res 2018;66(1):31–43. DOI: 10.1007/s12026-017-8967-2</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Phase I–II vaccination of autologous dendritic cells transduced with adenoviral vector encoding NS3 in hepatitis C encoding NS3 in hepatitis C. Available at: https://clinicaltrials.gov/ct2/show/study/NCT02309086?term=DC+vaccine&amp;cond=Hepatitis+C&amp;draw=2&amp;rank=2.</mixed-citation><mixed-citation xml:lang="ru">Phase I–II vaccination of autologous dendritic cells transduced with adenoviral vector encoding NS3 in hepatitis C encoding NS3 in hepatitis C. Available at: https://clinicaltrials.gov/ct2/show/study/NCT02309086?term=DC+vaccine&amp;cond=Hepatitis+C&amp;draw=2&amp;rank=2.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Chen M., Li Y.G., Zhang D.Z. et al. Therapeutic effect of autologous dendritic cell vaccine on patients with chronic hepatitis B: a clinical study. World J Gastroenterol 2005;11(12):1806–8. DOI: 10.3748/wjg.v11.i12.1806</mixed-citation><mixed-citation xml:lang="ru">Chen M., Li Y.G., Zhang D.Z. et al. Therapeutic effect of autologous dendritic cell vaccine on patients with chronic hepatitis B: a clinical study. World J Gastroenterol 2005;11(12):1806–8. DOI: 10.3748/wjg.v11.i12.1806</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. A Clinical Trial on Hepatitis B Vaccine Activated-Dendritic Cells Combined With Anti-HBV Drugs in CHB (CTHBVACADCHB). Available at: https://clinicaltrials.gov/ct2/show/NCT02615639?term=DC+vaccine&amp;cond=Hepatitis+B&amp;draw=2&amp;rank=1.</mixed-citation><mixed-citation xml:lang="ru">A Clinical Trial on Hepatitis B Vaccine Activated-Dendritic Cells Combined With Anti-HBV Drugs in CHB (CTHBVACADCHB). Available at: https://clinicaltrials.gov/ct2/show/NCT02615639?term=DC+vaccine&amp;cond=Hepatitis+B&amp;draw=2&amp;rank=1.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Luo J., Li J., Chen R.L. et al. Autologus dendritic cell vaccine for chronic hepatitis B carriers: a pilot, open label, clinical trial in human volunteers. Vaccine 2010;28(13):2497–504. DOI: 10.1016/j.vaccine.2010.01.038</mixed-citation><mixed-citation xml:lang="ru">Luo J., Li J., Chen R.L. et al. Autologus dendritic cell vaccine for chronic hepatitis B carriers: a pilot, open label, clinical trial in human volunteers. Vaccine 2010;28(13):2497–504. DOI: 10.1016/j.vaccine.2010.01.038</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Akbar S.M., Furukawa S., Horiike N. et al. Safety and immuno-genicity of hepatitis B surface antigen-pulsed dendritic cells in patients with chronic hepatitis B. J Viral Hepat 2011;18(6):408–14. DOI: 10.1111/j.1365-2893.2010.01320.x</mixed-citation><mixed-citation xml:lang="ru">Akbar S.M., Furukawa S., Horiike N. et al. Safety and immuno-genicity of hepatitis B surface antigen-pulsed dendritic cells in patients with chronic hepatitis B. J Viral Hepat 2011;18(6):408–14. DOI: 10.1111/j.1365-2893.2010.01320.x</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Wei M.J., Pan X.N., Wei K.P. et al. Efficacy of HBV-pulsed DCs in combination with entecavir in patients with chronic hepatitis B infection. Int Immunopharmacol 2015;27(2):238–43. DOI: 10.1016/j.intimp.2015.06.019</mixed-citation><mixed-citation xml:lang="ru">Wei M.J., Pan X.N., Wei K.P. et al. Efficacy of HBV-pulsed DCs in combination with entecavir in patients with chronic hepatitis B infection. Int Immunopharmacol 2015;27(2):238–43. DOI: 10.1016/j.intimp.2015.06.019</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Yang J.Y., Cao D.Y., Liu W.C. et al. Dendritic cell generated from CD34 + hematopoietic progenitors can be transfected with adenovirus containing gene of HBsAg and induce antigen-specific cytotoxic T cell responses. Cell Immunol 2006;240(1):14–21. DOI: 10.1016/j.cellimm.2006.06.005</mixed-citation><mixed-citation xml:lang="ru">Yang J.Y., Cao D.Y., Liu W.C. et al. Dendritic cell generated from CD34 + hematopoietic progenitors can be transfected with adenovirus containing gene of HBsAg and induce antigen-specific cytotoxic T cell responses. Cell Immunol 2006;240(1):14–21. DOI: 10.1016/j.cellimm.2006.06.005</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Long J., Zhou B., Li H. et al. Improvement of HBsAg gene-modified dendritic cell-based vaccine efficacy by optimizing immunization method or the application of β-glucosylceramide. Immunol Invest 2013;42(2):137–55. DOI: 10.3109/08820139.2012.744418</mixed-citation><mixed-citation xml:lang="ru">Long J., Zhou B., Li H. et al. Improvement of HBsAg gene-modified dendritic cell-based vaccine efficacy by optimizing immunization method or the application of β-glucosylceramide. Immunol Invest 2013;42(2):137–55. DOI: 10.3109/08820139.2012.744418</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Chemaly R.F., Ullmann A.J., Stoelben S. et al. Letermovir for cytomegalovirus prophylaxis in hematopoietic-cell transplantation. N Engl J Med 2014;370(19):1781–9. DOI: 10.1056/NEJMoa1309533</mixed-citation><mixed-citation xml:lang="ru">Chemaly R.F., Ullmann A.J., Stoelben S. et al. Letermovir for cytomegalovirus prophylaxis in hematopoietic-cell transplantation. N Engl J Med 2014;370(19):1781–9. DOI: 10.1056/NEJMoa1309533</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Van Craenenbroeck A.H., Smits E.L., Anguille S. et al. Induction of cytomegalovirus-specific T cell responses in healthy volunteers and allogeneic stem cell recipients using vaccination with messenger RNA-transfected dendritic cells. Transplantation 2015;99(1):120–7. DOI: 10.1097/TP.0000000000000272</mixed-citation><mixed-citation xml:lang="ru">Van Craenenbroeck A.H., Smits E.L., Anguille S. et al. Induction of cytomegalovirus-specific T cell responses in healthy volunteers and allogeneic stem cell recipients using vaccination with messenger RNA-transfected dendritic cells. Transplantation 2015;99(1):120–7. DOI: 10.1097/TP.0000000000000272</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Ma C.K.K., Clancy L., Simms R. et al. Adjuvant peptide pulsed dendritic cell vaccination in addition to T cell adoptive immunotherapy for cytomegalovirus infection in allogeneic hematopoietic stem cell transplantation recipients. Biol Blood Marrow Transplant 2018;24(1):71–7. DOI: 10.1016/j.bbmt.2017.08.028</mixed-citation><mixed-citation xml:lang="ru">Ma C.K.K., Clancy L., Simms R. et al. Adjuvant peptide pulsed dendritic cell vaccination in addition to T cell adoptive immunotherapy for cytomegalovirus infection in allogeneic hematopoietic stem cell transplantation recipients. Biol Blood Marrow Transplant 2018;24(1):71–7. DOI: 10.1016/j.bbmt.2017.08.028</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Cytomegalovirus (CMV) RNA-pulsed dendritic cells for pediatric patients and young adults with WHO grade IV glioma, recurrent malignant glioma, or recurrent medulloblastoma (ATTAC-P). Available at: https://clinicaltrials.gov/ct2/show/study/NCT03615404?term=DC&amp;cond=CMV&amp;draw=2&amp;rank=1.</mixed-citation><mixed-citation xml:lang="ru">Cytomegalovirus (CMV) RNA-pulsed dendritic cells for pediatric patients and young adults with WHO grade IV glioma, recurrent malignant glioma, or recurrent medulloblastoma (ATTAC-P). Available at: https://clinicaltrials.gov/ct2/show/study/NCT03615404?term=DC&amp;cond=CMV&amp;draw=2&amp;rank=1.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Ueno K., Kinjo Y., Okubo Y. et al. Dendritic cell-based immunization ameliorates pulmonary infection with highly virulent Cryptococcus gattii. Infect Immun 2015;83(4):1577–86. DOI: 10.1128/IAI.02827-14</mixed-citation><mixed-citation xml:lang="ru">Ueno K., Kinjo Y., Okubo Y. et al. Dendritic cell-based immunization ameliorates pulmonary infection with highly virulent Cryptococcus gattii. Infect Immun 2015;83(4):1577–86. DOI: 10.1128/IAI.02827-14</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Ueno K., Urai M., Ohkouchi K. et al. Dendritic cell-based vaccine against fungal infection. Methods Mol Biol 2016;1403:537–49. DOI: 10.1007/978-1-4939-3387-7_30</mixed-citation><mixed-citation xml:lang="ru">Ueno K., Urai M., Ohkouchi K. et al. Dendritic cell-based vaccine against fungal infection. Methods Mol Biol 2016;1403:537–49. DOI: 10.1007/978-1-4939-3387-7_30</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54. Ueno K., Urai M., Takatsuka S. et al. Immunization with antigen-pulsed dendritic cells against highly virulent Cryptococcus gattii infection: analysis of cytokine-producing T cells. Methods Mol Biol 2017;1625:327–39. DOI: 10.1007/978-1-4939-7104-6_22</mixed-citation><mixed-citation xml:lang="ru">Ueno K., Urai M., Takatsuka S. et al. Immunization with antigen-pulsed dendritic cells against highly virulent Cryptococcus gattii infection: analysis of cytokine-producing T cells. Methods Mol Biol 2017;1625:327–39. DOI: 10.1007/978-1-4939-7104-6_22</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55. Silva L.B.R., Dias L.S., Rittner G.M.G. et al. Dendritic cells primed with Paracoccidioides brasiliensis peptide P10 are therapeutic in immunosuppressed mice with paracoccidioidomycosis. Front Microbiol 2017;8:1057. DOI: 10.3389/fmicb.2017.01057</mixed-citation><mixed-citation xml:lang="ru">Silva L.B.R., Dias L.S., Rittner G.M.G. et al. Dendritic cells primed with Paracoccidioides brasiliensis peptide P10 are therapeutic in immunosuppressed mice with paracoccidioidomycosis. Front Microbiol 2017;8:1057. DOI: 10.3389/fmicb.2017.01057</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56. Grifoni A., Weiskopf D., Ramirez S.I. et al. Targets of T cell responses to SARS-CoV-2 coronavirus in humans with COVID-19 disease and unexposed individuals. Cell 2020;181(7):1489–501.e15. DOI: 10.1016/j.cell.2020.05.015</mixed-citation><mixed-citation xml:lang="ru">Grifoni A., Weiskopf D., Ramirez S.I. et al. Targets of T cell responses to SARS-CoV-2 coronavirus in humans with COVID-19 disease and unexposed individuals. Cell 2020;181(7):1489–501.e15. DOI: 10.1016/j.cell.2020.05.015</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57. Premkumar L., Segovia-Chumbez B., Jadi R. et al. The receptor binding domain of the viral spike protein is an immunodominant and highly specific target of antibodies in SARS-CoV-2 patients. Sci Immunol 2020;5(48):eabc8413. DOI: 10.1126/sciimmunol.abc8413</mixed-citation><mixed-citation xml:lang="ru">Premkumar L., Segovia-Chumbez B., Jadi R. et al. The receptor binding domain of the viral spike protein is an immunodominant and highly specific target of antibodies in SARS-CoV-2 patients. Sci Immunol 2020;5(48):eabc8413. DOI: 10.1126/sciimmunol.abc8413</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">58. Hoffmann M., Kleine-Weber H., Schroeder S. et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 2020;181(2):271–80.e8. DOI: 10.1016/j.cell.2020.02.052</mixed-citation><mixed-citation xml:lang="ru">Hoffmann M., Kleine-Weber H., Schroeder S. et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 2020;181(2):271–80.e8. DOI: 10.1016/j.cell.2020.02.052</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">59. Letko M., Marzi A., Munster V. Functional assessment of cell entry and receptor usage for SARS-CoV-2 and other lineage B betacoronaviruses. Nat Microbiol 2020;5(4):562–9. DOI: 10.1038/s41564-020-0688-y</mixed-citation><mixed-citation xml:lang="ru">Letko M., Marzi A., Munster V. Functional assessment of cell entry and receptor usage for SARS-CoV-2 and other lineage B betacoronaviruses. Nat Microbiol 2020;5(4):562–9. DOI: 10.1038/s41564-020-0688-y</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">60. Hoffmann M., Kleine-Weber H., Pöhlmann S. A Multibasic cleavage site in the spike protein of SARS-CoV-2 is essential for infection of human lung cells. Mol Cell 2020;78(4):779–84.e5. DOI: 10.1016/j.molcel.2020.04.022</mixed-citation><mixed-citation xml:lang="ru">Hoffmann M., Kleine-Weber H., Pöhlmann S. A Multibasic cleavage site in the spike protein of SARS-CoV-2 is essential for infection of human lung cells. Mol Cell 2020;78(4):779–84.e5. DOI: 10.1016/j.molcel.2020.04.022</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">61. Cao Y., Su B., Guo X. et al. Potent neutralizing antibodies against SARS-CoV-2 identified by high-throughput single-cell sequencing of convalescent patientsʼ B cells. Cell 2020;182(1):73–84.e16. DOI: 10.1016/j.cell.2020.05.025</mixed-citation><mixed-citation xml:lang="ru">Cao Y., Su B., Guo X. et al. Potent neutralizing antibodies against SARS-CoV-2 identified by high-throughput single-cell sequencing of convalescent patientsʼ B cells. Cell 2020;182(1):73–84.e16. DOI: 10.1016/j.cell.2020.05.025</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">62. Shi R., Shan C., Duan X. et al. A human neutralizing antibody targets the receptor-binding site of SARS-CoV-2. Nature 2020;584(7819):120–4. DOI: 10.1038/s41586-020-2381-y</mixed-citation><mixed-citation xml:lang="ru">Shi R., Shan C., Duan X. et al. A human neutralizing antibody targets the receptor-binding site of SARS-CoV-2. Nature 2020;584(7819):120–4. DOI: 10.1038/s41586-020-2381-y</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">63. Guo X., Kazanova A., Thurmond S. et al. Effective chimeric antigen receptor T cells against SARS-CoV-2. iScience 2021;24(11):103295. DOI: 10.1016/j.isci.2021.103295</mixed-citation><mixed-citation xml:lang="ru">Guo X., Kazanova A., Thurmond S. et al. Effective chimeric antigen receptor T cells against SARS-CoV-2. iScience 2021;24(11):103295. DOI: 10.1016/j.isci.2021.103295</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">64. Tian X., Li C., Huang A. et al. Potent binding of 2019 novel coronavirus spike protein by a SARS coronavirus-specific human monoclonal antibody. Emerg Microbes Infect 2020;9(1):382–5. DOI: 10.1080/22221751.2020.1729069</mixed-citation><mixed-citation xml:lang="ru">Tian X., Li C., Huang A. et al. Potent binding of 2019 novel coronavirus spike protein by a SARS coronavirus-specific human monoclonal antibody. Emerg Microbes Infect 2020;9(1):382–5. DOI: 10.1080/22221751.2020.1729069</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">65. Mehrabadi A.Z., Ranjbar R., Farzanehpour M. et al. Therapeutic potential of CAR T cell in malignancies: a scoping review. Biomed Pharmacother 2022;146:112512. DOI: 10.1016/j.biopha.2021.112512</mixed-citation><mixed-citation xml:lang="ru">Mehrabadi A.Z., Ranjbar R., Farzanehpour M. et al. Therapeutic potential of CAR T cell in malignancies: a scoping review. Biomed Pharmacother 2022;146:112512. DOI: 10.1016/j.biopha.2021.112512</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">66. Björkström N.K., Strunz B., Ljunggren H.G. Natural killer cells in antiviral immunity. Nat Rev Immunol 2022;22(2):112–23. DOI: 10.1038/s41577-021-00558-3</mixed-citation><mixed-citation xml:lang="ru">Björkström N.K., Strunz B., Ljunggren H.G. Natural killer cells in antiviral immunity. Nat Rev Immunol 2022;22(2):112–23. DOI: 10.1038/s41577-021-00558-3</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">67. Carlsten M., Childs R.W. Genetic manipulations of NK cells for cancer immunotherapy. Front Immunol 2015;6:266. DOI: 10.3389/fimmu.2015.00266</mixed-citation><mixed-citation xml:lang="ru">Carlsten M., Childs R.W. Genetic manipulations of NK cells for cancer immunotherapy. Front Immunol 2015;6:266. DOI: 10.3389/fimmu.2015.00266</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">68. Simonetta F., Alvarez M., Negrin R.S. Natural killer cells in graft-versus-host-disease after allogeneic hematopoietic cell transplantation. Front Immunol 2017;8:465. DOI: 10.3389/fimmu.2017.00465</mixed-citation><mixed-citation xml:lang="ru">Simonetta F., Alvarez M., Negrin R.S. Natural killer cells in graft-versus-host-disease after allogeneic hematopoietic cell transplantation. Front Immunol 2017;8:465. DOI: 10.3389/fimmu.2017.00465</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><citation-alternatives><mixed-citation xml:lang="en">69. Shah N., Li L., McCarty J. et al. Phase I study of cord bloodderived natural killer cells combined with autologous stem cell transplantation in multiple myeloma. Br J Haematol 2017;177(3):457–66. DOI: 10.1111/bjh.14570</mixed-citation><mixed-citation xml:lang="ru">Shah N., Li L., McCarty J. et al. Phase I study of cord bloodderived natural killer cells combined with autologous stem cell transplantation in multiple myeloma. Br J Haematol 2017;177(3):457–66. DOI: 10.1111/bjh.14570</mixed-citation></citation-alternatives></ref><ref id="B70"><label>70.</label><citation-alternatives><mixed-citation xml:lang="en">70. Heipertz E.L., Zynda E.R., Stav-Noraas T.E. et al. Current perspectives on “off-the-shelf” allogeneic NK and CAR-NK cell therapies. Front Immunol 2021;12:732135. DOI: 10.3389/fimmu.2021.732135</mixed-citation><mixed-citation xml:lang="ru">Heipertz E.L., Zynda E.R., Stav-Noraas T.E. et al. Current perspectives on “off-the-shelf” allogeneic NK and CAR-NK cell therapies. Front Immunol 2021;12:732135. DOI: 10.3389/fimmu.2021.732135</mixed-citation></citation-alternatives></ref><ref id="B71"><label>71.</label><citation-alternatives><mixed-citation xml:lang="en">71. Mo F., Mamonkin M., Brenner M.K., Heslop H.E. Taking T-cell oncotherapy off-the-shelf. Trends Immunol 2021;42(3):261–72. DOI: 10.1016/j.it.2021.01.004</mixed-citation><mixed-citation xml:lang="ru">Mo F., Mamonkin M., Brenner M.K., Heslop H.E. Taking T-cell oncotherapy off-the-shelf. Trends Immunol 2021;42(3):261–72. DOI: 10.1016/j.it.2021.01.004</mixed-citation></citation-alternatives></ref><ref id="B72"><label>72.</label><citation-alternatives><mixed-citation xml:lang="en">72. Ma M., Badeti S., Geng K., Liu D. Efficacy of targeting SARS-CoV-2 by CAR-NK cells. bioRxiv 2020;2020.08.11:247320. Preprint. DOI: 10.1101/2020.08.11.247320</mixed-citation><mixed-citation xml:lang="ru">Ma M., Badeti S., Geng K., Liu D. Efficacy of targeting SARS-CoV-2 by CAR-NK cells. bioRxiv 2020;2020.08.11:247320. Preprint. DOI: 10.1101/2020.08.11.247320</mixed-citation></citation-alternatives></ref><ref id="B73"><label>73.</label><citation-alternatives><mixed-citation xml:lang="en">73. Ma M., Badeti S., Chen C.H. et al. CAR-NK cells effectively target the D614 and G614 SARS-CoV-2-infected cells. bioRxiv 2021;2021.01.14:426742. Preprint. DOI: 10.1101/2021.01.14.426742</mixed-citation><mixed-citation xml:lang="ru">Ma M., Badeti S., Chen C.H. et al. CAR-NK cells effectively target the D614 and G614 SARS-CoV-2-infected cells. bioRxiv 2021;2021.01.14:426742. Preprint. DOI: 10.1101/2021.01.14.426742</mixed-citation></citation-alternatives></ref><ref id="B74"><label>74.</label><citation-alternatives><mixed-citation xml:lang="en">74. Ma M.T., Badeti S., Chen C.H. et al. CAR-NK cells effectively target SARS-CoV-2-spike-expressing cell lines in vitro. Front Immunol 2021;12:652223. DOI: 10.3389/fimmu.2021.652223</mixed-citation><mixed-citation xml:lang="ru">Ma M.T., Badeti S., Chen C.H. et al. CAR-NK cells effectively target SARS-CoV-2-spike-expressing cell lines in vitro. Front Immunol 2021;12:652223. DOI: 10.3389/fimmu.2021.652223</mixed-citation></citation-alternatives></ref><ref id="B75"><label>75.</label><citation-alternatives><mixed-citation xml:lang="en">75. Pinto D., Park Y.J., Beltramello M. et al. Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody. Nature 2020;583(7815):290–5. DOI: 10.1038/s41586-020-2349-y</mixed-citation><mixed-citation xml:lang="ru">Pinto D., Park Y.J., Beltramello M. et al. Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody. Nature 2020;583(7815):290–5. DOI: 10.1038/s41586-020-2349-y</mixed-citation></citation-alternatives></ref><ref id="B76"><label>76.</label><citation-alternatives><mixed-citation xml:lang="en">76. Fu W., Lei C., Ma Z. et al. CAR macrophages for SARS-CoV-2 immunotherapy. Front Immunol 2021;12:669103. DOI: 10.3389/fimmu.2021.669103</mixed-citation><mixed-citation xml:lang="ru">Fu W., Lei C., Ma Z. et al. CAR macrophages for SARS-CoV-2 immunotherapy. Front Immunol 2021;12:669103. DOI: 10.3389/fimmu.2021.669103</mixed-citation></citation-alternatives></ref><ref id="B77"><label>77.</label><citation-alternatives><mixed-citation xml:lang="en">77. Christodoulou I., Rahnama R., Ravich J.W. et al. Glycoprotein targeted CAR-NK cells for the treatment of SARS-CoV-2 infection. Front Immunol 2021;12:763460. DOI: 10.3389/fimmu.2021.763460</mixed-citation><mixed-citation xml:lang="ru">Christodoulou I., Rahnama R., Ravich J.W. et al. Glycoprotein targeted CAR-NK cells for the treatment of SARS-CoV-2 infection. Front Immunol 2021;12:763460. DOI: 10.3389/fimmu.2021.763460</mixed-citation></citation-alternatives></ref><ref id="B78"><label>78.</label><citation-alternatives><mixed-citation xml:lang="en">78. A phase I/II study of universal off-the-shelf NKG2D-ACE2 CAR-NK cells for therapy of COVID-19. Available at: https://clinicaltrials.gov/ct2/show/NCT04324996?term=CAR&amp;cond=COVID-19&amp;draw=2&amp;rank=1.</mixed-citation><mixed-citation xml:lang="ru">A phase I/II study of universal off-the-shelf NKG2D-ACE2 CAR-NK cells for therapy of COVID-19. Available at: https://clinicaltrials.gov/ct2/show/NCT04324996?term=CAR&amp;cond=COVID-19&amp;draw=2&amp;rank=1.</mixed-citation></citation-alternatives></ref><ref id="B79"><label>79.</label><citation-alternatives><mixed-citation xml:lang="en">79. Sohail A., Yu Z., Arif R. et al. Piecewise differentiation of the fractional order CAR-T cells-SARS-2 virus model. Results Phys 2022;33:105046. DOI: 10.1016/j.rinp.2021.105046</mixed-citation><mixed-citation xml:lang="ru">Sohail A., Yu Z., Arif R. et al. Piecewise differentiation of the fractional order CAR-T cells-SARS-2 virus model. Results Phys 2022;33:105046. DOI: 10.1016/j.rinp.2021.105046</mixed-citation></citation-alternatives></ref><ref id="B80"><label>80.</label><citation-alternatives><mixed-citation xml:lang="en">80. Al-Utaibi K.A., Nutini A., Sohail A. et al. Forecasting the action of CAR-T cells against SARS-corona virus-II infection with branching process. Model Earth Syst Environ 2021:1–9. Online ahead of print. DOI: 10.1007/s40808-021-01312-3</mixed-citation><mixed-citation xml:lang="ru">Al-Utaibi K.A., Nutini A., Sohail A. et al. Forecasting the action of CAR-T cells against SARS-corona virus-II infection with branching process. Model Earth Syst Environ 2021:1–9. Online ahead of print. DOI: 10.1007/s40808-021-01312-3</mixed-citation></citation-alternatives></ref><ref id="B81"><label>81.</label><citation-alternatives><mixed-citation xml:lang="en">81. Zhu T., Xiao Y., Meng X. et al. Nanovesicles derived from bispecific CAR-T cells targeting the spike protein of SARS-CoV-2 for treating COVID-19. J Nanobiotechnology 2021;19(1):391. DOI: 10.1186/s12951-021-01148-0</mixed-citation><mixed-citation xml:lang="ru">Zhu T., Xiao Y., Meng X. et al. Nanovesicles derived from bispecific CAR-T cells targeting the spike protein of SARS-CoV-2 for treating COVID-19. J Nanobiotechnology 2021;19(1):391. DOI: 10.1186/s12951-021-01148-0</mixed-citation></citation-alternatives></ref><ref id="B82"><label>82.</label><citation-alternatives><mixed-citation xml:lang="en">82. Bednar C., Ensser A. CARs – a new perspective to HCMV treatment. Viruses 2021;13(8):1563. DOI: 10.3390/v13081563</mixed-citation><mixed-citation xml:lang="ru">Bednar C., Ensser A. CARs – a new perspective to HCMV treatment. Viruses 2021;13(8):1563. DOI: 10.3390/v13081563</mixed-citation></citation-alternatives></ref><ref id="B83"><label>83.</label><citation-alternatives><mixed-citation xml:lang="en">83. Seif M., Einsele H., Löffler J. CAR T cells beyond cancer: hope for immunomodulatory therapy of infectious diseases. Front Immunol 2019;10:2711. DOI: 10.3389/fimmu.2019.02711</mixed-citation><mixed-citation xml:lang="ru">Seif M., Einsele H., Löffler J. CAR T cells beyond cancer: hope for immunomodulatory therapy of infectious diseases. Front Immunol 2019;10:2711. DOI: 10.3389/fimmu.2019.02711</mixed-citation></citation-alternatives></ref><ref id="B84"><label>84.</label><citation-alternatives><mixed-citation xml:lang="en">84. Slabik C., Kalbarczyk M., Danisch S. et al. CAR-T cells targeting Epstein-Barr virus gp350 validated in a humanized mouse model of EBV Infection and lymphoproliferative disease. Mol Ther Oncolytics 2020;18:504–24. DOI: 10.1016/j.omto.2020.08.005</mixed-citation><mixed-citation xml:lang="ru">Slabik C., Kalbarczyk M., Danisch S. et al. CAR-T cells targeting Epstein-Barr virus gp350 validated in a humanized mouse model of EBV Infection and lymphoproliferative disease. Mol Ther Oncolytics 2020;18:504–24. DOI: 10.1016/j.omto.2020.08.005</mixed-citation></citation-alternatives></ref><ref id="B85"><label>85.</label><citation-alternatives><mixed-citation xml:lang="en">85. Tang X., Zhou Y., Li W. et al. T cells expressing a LMP1-specific chimeric antigen receptor mediate antitumor effects against LMP1-positive nasopharyngeal carcinoma cells in vitro and in vivo. J Biomed Res 2014;28(6):468–75. DOI: 10.7555/JBR.28.20140066</mixed-citation><mixed-citation xml:lang="ru">Tang X., Zhou Y., Li W. et al. T cells expressing a LMP1-specific chimeric antigen receptor mediate antitumor effects against LMP1-positive nasopharyngeal carcinoma cells in vitro and in vivo. J Biomed Res 2014;28(6):468–75. DOI: 10.7555/JBR.28.20140066</mixed-citation></citation-alternatives></ref><ref id="B86"><label>86.</label><citation-alternatives><mixed-citation xml:lang="en">86. Kieser A., Sterz K.R. The latent membrane protein 1 (LMP1). Curr Top Microbiol Immunol 2015;391:119–49. DOI: 10.1007/978-3-319-22834-1_4</mixed-citation><mixed-citation xml:lang="ru">Kieser A., Sterz K.R. The latent membrane protein 1 (LMP1). Curr Top Microbiol Immunol 2015;391:119–49. DOI: 10.1007/978-3-319-22834-1_4</mixed-citation></citation-alternatives></ref><ref id="B87"><label>87.</label><citation-alternatives><mixed-citation xml:lang="en">87. LMP1 CAR-T for Patients With LMP1 positive infectious diseases and hematological malignancies. Available at: https://www.clinicaltrials.gov/ct2/show/NCT04657965?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=3.</mixed-citation><mixed-citation xml:lang="ru">LMP1 CAR-T for Patients With LMP1 positive infectious diseases and hematological malignancies. Available at: https://www.clinicaltrials.gov/ct2/show/NCT04657965?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=3.</mixed-citation></citation-alternatives></ref><ref id="B88"><label>88.</label><citation-alternatives><mixed-citation xml:lang="en">88. Maldini C.R., Ellis G.I., Riley J.L. CAR T cells for infection, autoimmunity and allotransplantation. Nat Rev Immunol 2018;18(10):605–16. DOI: 10.1038/s41577-018-0042-2</mixed-citation><mixed-citation xml:lang="ru">Maldini C.R., Ellis G.I., Riley J.L. CAR T cells for infection, autoimmunity and allotransplantation. Nat Rev Immunol 2018;18(10):605–16. DOI: 10.1038/s41577-018-0042-2</mixed-citation></citation-alternatives></ref><ref id="B89"><label>89.</label><citation-alternatives><mixed-citation xml:lang="en">89. Liu L., Patel B., Ghanem M.H. et al.Novel CD4-based bispecific chimeric antigen receptor designed for enhanced anti-HIV potency and absence of HIV entry receptor activity. J Virol 2015;89(13):6685–94. DOI: 10.1128/JVI.00474-15</mixed-citation><mixed-citation xml:lang="ru">Liu L., Patel B., Ghanem M.H. et al.Novel CD4-based bispecific chimeric antigen receptor designed for enhanced anti-HIV potency and absence of HIV entry receptor activity. J Virol 2015;89(13):6685–94. DOI: 10.1128/JVI.00474-15</mixed-citation></citation-alternatives></ref><ref id="B90"><label>90.</label><citation-alternatives><mixed-citation xml:lang="en">90. Zhen A., Peterson C.W., Carrillo M.A. et al. Long-term persistence and function of hematopoietic stem cell-derived chimeric antigen receptor T cells in a nonhuman primate model of HIV/AIDS. PLoS Pathog 2017;13(12):e1006753. DOI: 10.1371/journal.ppat.1006753</mixed-citation><mixed-citation xml:lang="ru">Zhen A., Peterson C.W., Carrillo M.A. et al. Long-term persistence and function of hematopoietic stem cell-derived chimeric antigen receptor T cells in a nonhuman primate model of HIV/AIDS. PLoS Pathog 2017;13(12):e1006753. DOI: 10.1371/journal.ppat.1006753</mixed-citation></citation-alternatives></ref><ref id="B91"><label>91.</label><citation-alternatives><mixed-citation xml:lang="en">91. Leslie G.J., Wang J., Richardson M.W. et al. Potent and broad inhibition of HIV-1 by a peptide from the gp41 heptad repeat-2 domain conjugated to the CXCR4 amino terminus. PLoS Pathog 2016;12(1):e1005983. DOI: 10.1371/journal.ppat.1005983</mixed-citation><mixed-citation xml:lang="ru">Leslie G.J., Wang J., Richardson M.W. et al. Potent and broad inhibition of HIV-1 by a peptide from the gp41 heptad repeat-2 domain conjugated to the CXCR4 amino terminus. PLoS Pathog 2016;12(1):e1005983. DOI: 10.1371/journal.ppat.1005983</mixed-citation></citation-alternatives></ref><ref id="B92"><label>92.</label><citation-alternatives><mixed-citation xml:lang="en">92. Maldini C.R., Gayout K., Leibman R.S. et al. HIV-resistant and HIV-specific CAR-modified CD4+ T cells mitigate HIV disease progression and confer CD4+ T cell help in vivo. Mol Ther 2020;28(7):1585–99. DOI: 10.1016/j.ymthe.2020.05.012</mixed-citation><mixed-citation xml:lang="ru">Maldini C.R., Gayout K., Leibman R.S. et al. HIV-resistant and HIV-specific CAR-modified CD4+ T cells mitigate HIV disease progression and confer CD4+ T cell help in vivo. Mol Ther 2020;28(7):1585–99. DOI: 10.1016/j.ymthe.2020.05.012</mixed-citation></citation-alternatives></ref><ref id="B93"><label>93.</label><citation-alternatives><mixed-citation xml:lang="en">93. Jiang Z., Liang H., Pan H. et al. HIV-1-specific CAR-T cells with cell-intrinsic PD-1 checkpoint blockade enhance anti-HIV efficacy in vivo. Front Microbiol 2021;12:684016. DOI: 10.3389/fmicb.2021.684016</mixed-citation><mixed-citation xml:lang="ru">Jiang Z., Liang H., Pan H. et al. HIV-1-specific CAR-T cells with cell-intrinsic PD-1 checkpoint blockade enhance anti-HIV efficacy in vivo. Front Microbiol 2021;12:684016. DOI: 10.3389/fmicb.2021.684016</mixed-citation></citation-alternatives></ref><ref id="B94"><label>94.</label><citation-alternatives><mixed-citation xml:lang="en">94. Pampusch M.S., Abdelaal H.M., Cartwright E.K. et al. CAR/ CXCR5-T cell immunotherapy is safe and potentially efficacious in promoting sustained remission of SIV infection. PLoS Pathog 2022;18(2):e1009831. DOI: 10.1371/journal.ppat.1009831</mixed-citation><mixed-citation xml:lang="ru">Pampusch M.S., Abdelaal H.M., Cartwright E.K. et al. CAR/ CXCR5-T cell immunotherapy is safe and potentially efficacious in promoting sustained remission of SIV infection. PLoS Pathog 2022;18(2):e1009831. DOI: 10.1371/journal.ppat.1009831</mixed-citation></citation-alternatives></ref><ref id="B95"><label>95.</label><citation-alternatives><mixed-citation xml:lang="en">95. Lim R.M., Rong L., Zhen A., Xie J. A universal CAR-NK cell targeting various epitopes of HIV-1 gp160. ACS Chem Biol 2020;15(8):2299–310. DOI: 10.1021/acschembio.0c00537</mixed-citation><mixed-citation xml:lang="ru">Lim R.M., Rong L., Zhen A., Xie J. A universal CAR-NK cell targeting various epitopes of HIV-1 gp160. ACS Chem Biol 2020;15(8):2299–310. DOI: 10.1021/acschembio.0c00537</mixed-citation></citation-alternatives></ref><ref id="B96"><label>96.</label><citation-alternatives><mixed-citation xml:lang="en">96. Kim G.B., Hege K., Riley J.L. CAR talk: how cancer-specific CAR T cells can instruct how to build CAR T cells to cure HIV. Front Immunol 2019;10:2310. DOI: 10.3389/fimmu.2019.02310</mixed-citation><mixed-citation xml:lang="ru">Kim G.B., Hege K., Riley J.L. CAR talk: how cancer-specific CAR T cells can instruct how to build CAR T cells to cure HIV. Front Immunol 2019;10:2310. DOI: 10.3389/fimmu.2019.02310</mixed-citation></citation-alternatives></ref><ref id="B97"><label>97.</label><citation-alternatives><mixed-citation xml:lang="en">97. CD4 CAR+ ZFN-modified T cells in HIV therapy. Available at: https://clinicaltrials.gov/ct2/show/NCT03617198.</mixed-citation><mixed-citation xml:lang="ru">CD4 CAR+ ZFN-modified T cells in HIV therapy. Available at: https://clinicaltrials.gov/ct2/show/NCT03617198.</mixed-citation></citation-alternatives></ref><ref id="B98"><label>98.</label><citation-alternatives><mixed-citation xml:lang="en">98. CAR-T cells for HIV infection. Available at: https://www.clinicaltrials.gov/ct2/show/NCT04648046?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=1.</mixed-citation><mixed-citation xml:lang="ru">CAR-T cells for HIV infection. Available at: https://www.clinicaltrials.gov/ct2/show/NCT04648046?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=1.</mixed-citation></citation-alternatives></ref><ref id="B99"><label>99.</label><citation-alternatives><mixed-citation xml:lang="en">99. Third-Generation CAR-T-cell Therapy in Individuals With HIV-1 Infection (TCTIWHI). Available at: https://www.clinicaltrials.gov/ct2/show/NCT04863066?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=2.</mixed-citation><mixed-citation xml:lang="ru">Third-Generation CAR-T-cell Therapy in Individuals With HIV-1 Infection (TCTIWHI). Available at: https://www.clinicaltrials.gov/ct2/show/NCT04863066?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=2.</mixed-citation></citation-alternatives></ref><ref id="B100"><label>100.</label><citation-alternatives><mixed-citation xml:lang="en">100. The effect of chimeric antigen receptor (CAR)-T cell therapy on the reconstitution of HIV-specific immune function. Available at: https://www.clinicaltrials.gov/ct2/show/NCT03240328?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=10.</mixed-citation><mixed-citation xml:lang="ru">The effect of chimeric antigen receptor (CAR)-T cell therapy on the reconstitution of HIV-specific immune function. Available at: https://www.clinicaltrials.gov/ct2/show/NCT03240328?term=CAR&amp;cond=Infections&amp;draw=2&amp;rank=10.</mixed-citation></citation-alternatives></ref><ref id="B101"><label>101.</label><citation-alternatives><mixed-citation xml:lang="en">101. Meng Z., Chen Y., Lu M. Advances in targeting the innate and adaptive immune systems to cure chronic hepatitis B virus infection. Front Immunol 2020;10:3127. DOI: 10.3389/fimmu.2019.03127</mixed-citation><mixed-citation xml:lang="ru">Meng Z., Chen Y., Lu M. Advances in targeting the innate and adaptive immune systems to cure chronic hepatitis B virus infection. Front Immunol 2020;10:3127. DOI: 10.3389/fimmu.2019.03127</mixed-citation></citation-alternatives></ref><ref id="B102"><label>102.</label><citation-alternatives><mixed-citation xml:lang="en">102. Bohne F., Chmielewski M., Ebert G. et al. T cells redirected against hepatitis B virus surface proteins eliminate infected hepatocytes. Gastroenterology 2008;134(1):239–47. DOI: 10.1053/j.gastro.2007.11.002</mixed-citation><mixed-citation xml:lang="ru">Bohne F., Chmielewski M., Ebert G. et al. T cells redirected against hepatitis B virus surface proteins eliminate infected hepatocytes. Gastroenterology 2008;134(1):239–47. DOI: 10.1053/j.gastro.2007.11.002</mixed-citation></citation-alternatives></ref><ref id="B103"><label>103.</label><citation-alternatives><mixed-citation xml:lang="en">103. Krebs K., Böttinger N., Huang L.R. et al. T cells expressing a chimeric antigen receptor that binds hepatitis B virus envelope proteins control virus replication in mice. Gastroenterology 2013;145(2):456–65. DOI: 10.1053/j.gastro.2013.04.047</mixed-citation><mixed-citation xml:lang="ru">Krebs K., Böttinger N., Huang L.R. et al. T cells expressing a chimeric antigen receptor that binds hepatitis B virus envelope proteins control virus replication in mice. Gastroenterology 2013;145(2):456–65. DOI: 10.1053/j.gastro.2013.04.047</mixed-citation></citation-alternatives></ref><ref id="B104"><label>104.</label><citation-alternatives><mixed-citation xml:lang="en">104. Kruse R.L., Shum T., Tashiro H. et al. HBsAg-redirected T cells exhibit antiviral activity in HBV-infected human liver chimeric mice. Cytotherapy 2018;20(5):697–705. DOI: 10.1016/j.jcyt.2018.02.002</mixed-citation><mixed-citation xml:lang="ru">Kruse R.L., Shum T., Tashiro H. et al. HBsAg-redirected T cells exhibit antiviral activity in HBV-infected human liver chimeric mice. Cytotherapy 2018;20(5):697–705. DOI: 10.1016/j.jcyt.2018.02.002</mixed-citation></citation-alternatives></ref><ref id="B105"><label>105.</label><citation-alternatives><mixed-citation xml:lang="en">105. Klopp A., Schreiber S., Kosinska A.D. et al. Depletion of T cells via inducible caspase 9 increases safety of adoptive T-Cell therapy against chronic hepatitis B. Front Immunol 2021;12:734246. DOI: 10.3389/fimmu.2021.734246</mixed-citation><mixed-citation xml:lang="ru">Klopp A., Schreiber S., Kosinska A.D. et al. Depletion of T cells via inducible caspase 9 increases safety of adoptive T-Cell therapy against chronic hepatitis B. Front Immunol 2021;12:734246. DOI: 10.3389/fimmu.2021.734246</mixed-citation></citation-alternatives></ref><ref id="B106"><label>106.</label><citation-alternatives><mixed-citation xml:lang="en">106. Festag M.M., Festag J., Fräßle S.P. et al. Evaluation of a fully human, hepatitis B virus-specific chimeric antigen receptor in an immunocompetent mouse model. Mol Ther 2019;27(5):947–59. DOI: 10.1016/j.ymthe.2019.02.001</mixed-citation><mixed-citation xml:lang="ru">Festag M.M., Festag J., Fräßle S.P. et al. Evaluation of a fully human, hepatitis B virus-specific chimeric antigen receptor in an immunocompetent mouse model. Mol Ther 2019;27(5):947–59. DOI: 10.1016/j.ymthe.2019.02.001</mixed-citation></citation-alternatives></ref><ref id="B107"><label>107.</label><citation-alternatives><mixed-citation xml:lang="en">107. Sautto G.A., Wisskirchen K., Clementi N. et al. Chimeric antigen receptor (CAR)-engineered T cells redirected against hepatitis C virus (HCV) E2 glycoprotein. Gut 2016;65(3):512–23. DOI: 10.1136/gutjnl-2014-308316</mixed-citation><mixed-citation xml:lang="ru">Sautto G.A., Wisskirchen K., Clementi N. et al. Chimeric antigen receptor (CAR)-engineered T cells redirected against hepatitis C virus (HCV) E2 glycoprotein. Gut 2016;65(3):512–23. DOI: 10.1136/gutjnl-2014-308316</mixed-citation></citation-alternatives></ref></ref-list></back></article>
