<?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">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">733</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2023-22-2-166-174</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Pathogenesis, treatment and prevention of diseases caused by Epstein–Barr virus</article-title><trans-title-group xml:lang="ru"><trans-title>Патогенез, лечение и профилактика заболеваний, вызванных вирусом Эпштейна–Барр</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1643-5960</contrib-id><name-alternatives><name xml:lang="en"><surname>Rumyantsev</surname><given-names>A. G.</given-names></name><name xml:lang="ru"><surname>Румянцев</surname><given-names>А. Г.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Alexander G. Rumyantsev, Member of the RAS, Dr. Med. Sci., Professor, Academic Supervisor</p><p>Moscow</p></bio><bio xml:lang="ru"><p>Александр Григорьевич Румянцев, кадемик РАН, д-р мед. наук, профессор, научный руководитель</p><p>117997</p><p>ул. Саморы Машела, 1</p><p>Москва</p></bio><email>alexrum47@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-07-08" publication-format="electronic"><day>08</day><month>07</month><year>2023</year></pub-date><volume>22</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>166</fpage><lpage>174</lpage><history><date date-type="received" iso-8601-date="2023-03-22"><day>22</day><month>03</month><year>2023</year></date><date date-type="accepted" iso-8601-date="2023-05-25"><day>25</day><month>05</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/733">https://hemoncim.com/jour/article/view/733</self-uri><abstract xml:lang="en"><p>   Studying diseases associated with viruses belonging to the family of <italic>Herpesviridae</italic> is an important challenge for medical researchers and clinicians because of the specific tropism of herpesviruses for immune cells, life-long persistence in human target cells, the ability to reactivate and the potential to cause a wide variety of clinical manifestations. Unlike other members of <italic>Herpesviridae</italic>, Epstein–Barr virus (EBV), also known as human herpes 4, displays tropism for B cells and mucosal epithelial cells, has the capacity to cause not only productive infection (infectious mononucleosis), but also establish various types of latency in cells, causes benign and malignant transformation of immune system cells (hemoblastoses) and mucosal epithelial cells (oral cavity cancer and gastric cancer). EBV causes 200 000 deaths worldwide every year, the majority of which are attributable to cancers associated with EBV persistence. Moreover, EBV is associated with a group of autoimmune disorders, such as multiple sclerosis, and secondary immunodeficiencies occurring in patients with infection of immune system cells. Mechanisms of the interaction between EBV and human cells implicated in cancer induction should be a focus of further research in fundamental virology, oncology and medicine as a whole. The interactions between EBV and target cells in mother-fetus-child system appear to be the most complicated. The inevitability of facing the virus and associated long-term consequences is determined by the time and mode of mother-to-child transmission of EBV, the presence of innate immune defense factors, genetics and molecular mechanisms of EBV latency. Recent scientific insights allow us to establish control over the evolution of EBV interactions with its host and to identify promising approaches to the prevention and treatment of previously incurable diseases associated with EBV.</p></abstract><trans-abstract xml:lang="ru"><p>Изучение заболеваний, ассоциированных с вирусами семейства <italic>Herpesviridae</italic>, является важной научно-практической проблемой медицины в связи со специфической тропностью вирусов к клеткам иммунной системы, пожизненной персистенцией в клетках-мишенях человека, способностью вируса к реактивации и широким диапазоном клинических форм заболеваний. Вирус Эпштейна–Барр (Epstein–Barr virus, EBV), или вирус герпеса человека 4-го типа, отличается от других вирусов семейства <italic>Herpesviridae</italic> тропностью к В-лимфоцитам и клеткам эпителия слизистых, способностью помимо продуктивной формы инфекции, какой является инфекционный мононуклеоз, проявлять различные варианты латентного состояния в клетках, вызывать доброкачественную и злокачественную трансформацию клеток иммунной системы (гемобластозы) и слизистых (рак полости рта и желудка). С онкогенными последствиями персистенции EBV связана основная часть из 200 000 смертей в год в мире. Кроме того, EBV ассоциирован с группой аутоиммунных расстройств, таких как рассеянный склероз и вторичные иммунодефициты, сопровождающие инфекции иммунной системы. Механизмы, определяющие взаимодействие EBV и клеток человека в индукции опухолей, являются точкой развития фундаментальной вирусологии, онкологии и медицины в целом. Самым сложным является взаимодействие EBV с клеточными мишенями в системе «мать–плод–ребенок». Неизбежность встречи с вирусом и отдаленных результатов этой встречи определяется временем и путями заражения матери и ребенка, наличием врожденных факторов иммунной защиты, генетикой и молекулярными механизмами латентности вируса. Новые научные данные, полученные в последние годы, позволяют установить контроль за эволюцией взаимоотношений EBV и хозяина, а также наметить перспективные опции лечения и профилактики ранее неизлечимых заболеваний, ассоциированных с EBV.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Epstein–Barr virus</kwd><kwd>herpesvirus family</kwd><kwd>immune system</kwd><kwd>genetics</kwd><kwd>latent course</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>вирус Эпштейна–Барр</kwd><kwd>семейство герпесвирусов</kwd><kwd>иммунная система</kwd><kwd>генетика</kwd><kwd>латентное течение</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Not specified</funding-statement><funding-statement xml:lang="ru">Не указано</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Румянцев А. Г. Заболевания, вызываемые герпесвирусами. Механизмы повреждения, патогенетическая терапия и профилактика / А. Г. Румянцев // Педиатрия. Журнал им. Г. Н. Сперанского. – 2023. – 102 (2): 116–23. DOI: 10.24110/0031-403X-2023-102-2-116-123</mixed-citation><mixed-citation xml:lang="ru">Румянцев А. Г. Заболевания, вызываемые герпесвирусами. Механизмы повреждения, патогенетическая терапия и профилактика / А. Г. Румянцев // Педиатрия. Журнал им. Г. Н. Сперанского. – 2023. – 102 (2): 116–23. DOI: 10.24110/0031-403X-2023-102-2-116-123</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Epstein M. A., Achong B. G., Barr Y. M. Virus Particles in Cultured Lymphoblasts from Burkitt’s Lymphoma. Lancet 1964; 1 (7335): 702–3. DOI: 10.1016/S0140-6736(64)91524-7</mixed-citation><mixed-citation xml:lang="ru">Epstein M. A., Achong B. G., Barr Y. M. Virus Particles in Cultured Lymphoblasts from Burkitt’s Lymphoma. Lancet 1964; 1 (7335): 702–3. DOI: 10.1016/S0140-6736(64)91524-7</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Luzuriaga K., Sullivan J. L. Infectious mononucleosis. N Engl J Med 2010; 362 (21): 1993–2000. DOI: 10.1056/nejmcp1001116</mixed-citation><mixed-citation xml:lang="ru">Luzuriaga K., Sullivan J. L. Infectious mononucleosis. N Engl J Med 2010; 362 (21): 1993–2000. DOI: 10.1056/nejmcp1001116</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Chandran В., Hutt-Fletcher L. Gammaherpesviruses entry and early events during infection. In: Arvin A., Campadelli-Fiume G., Mocarski E., Moore P. S., Roizman B., Whitley R., Yamanishi K. (eds.). Human herpes-viruses: Biology, therapy, and immunoprophylaxis. Cambridge: Cambridge University Press; 2007.</mixed-citation><mixed-citation xml:lang="ru">Chandran В., Hutt-Fletcher L. Gammaherpesviruses entry and early events during infection. In: Arvin A., Campadelli-Fiume G., Mocarski E., Moore P. S., Roizman B., Whitley R., Yamanishi K. (eds.). Human herpes-viruses: Biology, therapy, and immunoprophylaxis. Cambridge: Cambridge University Press; 2007.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Chesnokova L. S., Valencia S. M., Hutt-Fletcher L. M. The BDLF3 gene product of Epstein–Barr virus, gpl50, mediates non-productive binding to heparan sulfate on epithelial cells and only the binding domain of CD21 is required for infection. Virology 2016; 494: 23–8. DOI: 10.1016/j.virol.2016.04.002</mixed-citation><mixed-citation xml:lang="ru">Chesnokova L. S., Valencia S. M., Hutt-Fletcher L. M. The BDLF3 gene product of Epstein–Barr virus, gpl50, mediates non-productive binding to heparan sulfate on epithelial cells and only the binding domain of CD21 is required for infection. Virology 2016; 494: 23–8. DOI: 10.1016/j.virol.2016.04.002</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Zhang H., Li Y., Wang H. B., Zhang A., Chen M. L., Fang Z. X., et al. Ephrin receptor A2 is an epithelialcell receptor for Epstein-Barr virus entry. Nat Microbiol 2018; 3 (2): 1–8. DOI: 10.1038/s41564-017-0080-8</mixed-citation><mixed-citation xml:lang="ru">Zhang H., Li Y., Wang H. B., Zhang A., Chen M. L., Fang Z. X., et al. Ephrin receptor A2 is an epithelialcell receptor for Epstein-Barr virus entry. Nat Microbiol 2018; 3 (2): 1–8. DOI: 10.1038/s41564-017-0080-8</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Hutt-Fletcher L. M. Epstein–Barr virus entry. J Virol 2007; 81 (15): 7825–32. DOI: 10.1128/jvi.00445-07</mixed-citation><mixed-citation xml:lang="ru">Hutt-Fletcher L. M. Epstein–Barr virus entry. J Virol 2007; 81 (15): 7825–32. DOI: 10.1128/jvi.00445-07</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Morgan S. M., Tanizawa H., Caruso L. B., Hulse M., Kossenkov A., Madzo J., et al. The three-dimensional structure of Epstein-Barr virus genome varies by latency type and is regulated by PARP1 enzymatic activity. Nat Commun 2022; 13: 187. DOI: 10.1038/S41467-021-27894-1</mixed-citation><mixed-citation xml:lang="ru">Morgan S. M., Tanizawa H., Caruso L. B., Hulse M., Kossenkov A., Madzo J., et al. The three-dimensional structure of Epstein-Barr virus genome varies by latency type and is regulated by PARP1 enzymatic activity. Nat Commun 2022; 13: 187. DOI: 10.1038/S41467-021-27894-1</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Tse E., Kwong Y. L. Epstein–Barr Virus-associated lymphoproliferative diseases: the virus as a therapeutic target. Exp Mol Med 2015; 47: el36. DOI: 10.1038/emm.2014.102</mixed-citation><mixed-citation xml:lang="ru">Tse E., Kwong Y. L. Epstein–Barr Virus-associated lymphoproliferative diseases: the virus as a therapeutic target. Exp Mol Med 2015; 47: el36. DOI: 10.1038/emm.2014.102</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Thorley-Lawson D. A., Gross A. Persistence of the Epstein-Barr virus and the forigins of associated lymphomas. N Engl J Med 2004; 350: 1328–37. DOI: 10.1056/NEJMra032015</mixed-citation><mixed-citation xml:lang="ru">Thorley-Lawson D. A., Gross A. Persistence of the Epstein-Barr virus and the forigins of associated lymphomas. N Engl J Med 2004; 350: 1328–37. DOI: 10.1056/NEJMra032015</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Dugan J. P., Coleman C. B., Haverkos B. Opportunities to target the life cycle of Epstein-Barr virus (EBV) in EBV-associated lymphoproliferative disorders. Front Oncol 2019; 9: 127. DOI: 10.3389/fonc.2019.00127</mixed-citation><mixed-citation xml:lang="ru">Dugan J. P., Coleman C. B., Haverkos B. Opportunities to target the life cycle of Epstein-Barr virus (EBV) in EBV-associated lymphoproliferative disorders. Front Oncol 2019; 9: 127. DOI: 10.3389/fonc.2019.00127</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Heslop H. E. Sensitizing burkitt lymphoma to EBV-Cl'Ls. Blood 2020; 135 (21): 1822–3. DOI: 10.1182/blood.2020005492</mixed-citation><mixed-citation xml:lang="ru">Heslop H. E. Sensitizing burkitt lymphoma to EBV-Cl'Ls. Blood 2020; 135 (21): 1822–3. DOI: 10.1182/blood.2020005492</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Kenney S. C. Reactivation and lytic replication of EBV. In: Arvin A., Campadelli-Fiume G., Mocarski E., Moore P. S., Roizman B., Whitley R., Yamanishi K. (eds.). Human herpes-viruses: Biology, therapy, and immunoprophylaxis. Cambridge: Cambridge University Press; 2007.</mixed-citation><mixed-citation xml:lang="ru">Kenney S. C. Reactivation and lytic replication of EBV. In: Arvin A., Campadelli-Fiume G., Mocarski E., Moore P. S., Roizman B., Whitley R., Yamanishi K. (eds.). Human herpes-viruses: Biology, therapy, and immunoprophylaxis. Cambridge: Cambridge University Press; 2007.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Kim W. Y., Montes-Mojarro I. A., Fend F., Quintanilla-Martinez L. Epstein–Barr Virus-associated T-and NK-cell lymphoproliferative diseases. Front Pediatr 2019; 7: 71. DOI: 10.3389/fped.2019.00071</mixed-citation><mixed-citation xml:lang="ru">Kim W. Y., Montes-Mojarro I. A., Fend F., Quintanilla-Martinez L. Epstein–Barr Virus-associated T-and NK-cell lymphoproliferative diseases. Front Pediatr 2019; 7: 71. DOI: 10.3389/fped.2019.00071</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Sakai Y., Ohga S., Tonegawa Y., Takada H., Nakao F., Nakayama H., et al. Interferon-alpha therapy for chronic active Epstein–Barr virus infection: potential effect on the development of T-lymphoproliferative disease. Pediatr Нematol Oncol 1998; 20: 342–6. DOI: 10.1097/00043426-199807000-00013</mixed-citation><mixed-citation xml:lang="ru">Sakai Y., Ohga S., Tonegawa Y., Takada H., Nakao F., Nakayama H., et al. Interferon-alpha therapy for chronic active Epstein–Barr virus infection: potential effect on the development of T-lymphoproliferative disease. Pediatr Нematol Oncol 1998; 20: 342–6. DOI: 10.1097/00043426-199807000-00013</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Zhang Q., Zhao Y. Z., Ma H. H., Wang D., Cui L., Li W. J., et al. A study of ruxolitinib response-based stratified treatment for pediatric hеmophagocytic lymphohistiocytosis. Blood 2022; 139: 3493–504. DOI: 10.1182/blood.2021014860</mixed-citation><mixed-citation xml:lang="ru">Zhang Q., Zhao Y. Z., Ma H. H., Wang D., Cui L., Li W. J., et al. A study of ruxolitinib response-based stratified treatment for pediatric hеmophagocytic lymphohistiocytosis. Blood 2022; 139: 3493–504. DOI: 10.1182/blood.2021014860</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Kim H. J., Ko Y. H., Kim J. E., Lee S. S., Lee H., Park G., et al. Epstein–Barr Virus-associated lymphoproliferative disorders: Review and update on 2016 WHO classification. J Pathol Transl Med 2017; 51: 352–8. DOI: 10.4132/jptm.2017.03.15</mixed-citation><mixed-citation xml:lang="ru">Kim H. J., Ko Y. H., Kim J. E., Lee S. S., Lee H., Park G., et al. Epstein–Barr Virus-associated lymphoproliferative disorders: Review and update on 2016 WHO classification. J Pathol Transl Med 2017; 51: 352–8. DOI: 10.4132/jptm.2017.03.15</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Pietersma F., Piriou E., van Baarle D. Immune surveillance of EBV-infected cells and the development of non-Hodgkin lymphomas in immunocompromised patients. Leuk Lymphoma 2008; 49: 1028–41. DOI: 10.1080/10428190801911662</mixed-citation><mixed-citation xml:lang="ru">Pietersma F., Piriou E., van Baarle D. Immune surveillance of EBV-infected cells and the development of non-Hodgkin lymphomas in immunocompromised patients. Leuk Lymphoma 2008; 49: 1028–41. DOI: 10.1080/10428190801911662</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Burkitt D. A sarcoma involving the jaws in African children. Br J Surg 1958; 46: 218–23. DOI: 10.1002/bjs.18004619704</mixed-citation><mixed-citation xml:lang="ru">Burkitt D. A sarcoma involving the jaws in African children. Br J Surg 1958; 46: 218–23. DOI: 10.1002/bjs.18004619704</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Zheng X., Huang Y., Li K., Luo R., Cai M., Yun J. Immunosuppressive tumor 'microenvironment and immunotherapy of Epstein–Barr virus-associated malignancies. Viruses 2022; 14 (5): 1017. DOI: 10.3390/v14051017</mixed-citation><mixed-citation xml:lang="ru">Zheng X., Huang Y., Li K., Luo R., Cai M., Yun J. Immunosuppressive tumor 'microenvironment and immunotherapy of Epstein–Barr virus-associated malignancies. Viruses 2022; 14 (5): 1017. DOI: 10.3390/v14051017</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Joko-Fru W. Y., Parkin D. M., Borok M., Chokunonga E., Korir A., Nambooze S., et al. Survival from childhood cancers in Eastern Africa: A population-based registry study. Int J Chancer 2018; 143: 2409–15. DOI: 10.1002/ijc.31723</mixed-citation><mixed-citation xml:lang="ru">Joko-Fru W. Y., Parkin D. M., Borok M., Chokunonga E., Korir A., Nambooze S., et al. Survival from childhood cancers in Eastern Africa: A population-based registry study. Int J Chancer 2018; 143: 2409–15. DOI: 10.1002/ijc.31723</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Ikeda M., Hayes C. K., Schaller S. J., Longncckcr R. Latent membrane proteins from EBV differentially target cellular pathways to accelerate MYC-induccd lymphomagenesis. Blood Adv 2022; 6: 4283–96. DOI: 10.1182/bloodadvances.2022007695</mixed-citation><mixed-citation xml:lang="ru">Ikeda M., Hayes C. K., Schaller S. J., Longncckcr R. Latent membrane proteins from EBV differentially target cellular pathways to accelerate MYC-induccd lymphomagenesis. Blood Adv 2022; 6: 4283–96. DOI: 10.1182/bloodadvances.2022007695</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Takizawa M., Tolarova H., Li Z., Dubois W., Lim S., Callen E., et al. AID expression levels determine the extent of cMyc oncogenic translocations and the incidence of b cell tumor development. Exp Med 2008; 205: 1949–57. DOI: 10.1084/jem.20081007</mixed-citation><mixed-citation xml:lang="ru">Takizawa M., Tolarova H., Li Z., Dubois W., Lim S., Callen E., et al. AID expression levels determine the extent of cMyc oncogenic translocations and the incidence of b cell tumor development. Exp Med 2008; 205: 1949–57. DOI: 10.1084/jem.20081007</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Moody C. A., Scott R. S., Amirghahari N., Nathan C. O., Young L. S., Dawson I. W., et al. Modulation of the cell growth regulator mTOR by Epstein–Barr virus-encoded LMP2A. J Virol 2005; 79 (9): 5499–06. DOI: 10.1128/jVI.79.9.5499-5506.2005</mixed-citation><mixed-citation xml:lang="ru">Moody C. A., Scott R. S., Amirghahari N., Nathan C. O., Young L. S., Dawson I. W., et al. Modulation of the cell growth regulator mTOR by Epstein–Barr virus-encoded LMP2A. J Virol 2005; 79 (9): 5499–06. DOI: 10.1128/jVI.79.9.5499-5506.2005</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Thompson L. World health organization classification of tumours: patholog and genetics of head and neck tumours. Ear Nose Throat J 2006; 85: 74. DOI: 10.1177/014556130608500201</mixed-citation><mixed-citation xml:lang="ru">Thompson L. World health organization classification of tumours: patholog and genetics of head and neck tumours. Ear Nose Throat J 2006; 85: 74. DOI: 10.1177/014556130608500201</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Lo A. K., Dawson C. W., Lung H. L., Wong K. L., Young L. S. The role of EBV-encoded LMP1 in the NPC tumor microenvironment: From function to therapy. Front Oncol 2021; 11: 640207. DOI: 10.3389/fonc.2021.640207</mixed-citation><mixed-citation xml:lang="ru">Lo A. K., Dawson C. W., Lung H. L., Wong K. L., Young L. S. The role of EBV-encoded LMP1 in the NPC tumor microenvironment: From function to therapy. Front Oncol 2021; 11: 640207. DOI: 10.3389/fonc.2021.640207</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Sun K., Jia K., Lv H., Wang S. Q., Wu Y., Lei H., et al. EBV-Positive Gastric Cancer: Current knowledge and future perspectives. Front Oncol 2020; 10: 583463. DOI: 10.3389/fonc.2020.583463</mixed-citation><mixed-citation xml:lang="ru">Sun K., Jia K., Lv H., Wang S. Q., Wu Y., Lei H., et al. EBV-Positive Gastric Cancer: Current knowledge and future perspectives. Front Oncol 2020; 10: 583463. DOI: 10.3389/fonc.2020.583463</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Ribeiro J., Oliveira C., Malta M., Sousa H. Epstein–Barr virus gene expression and latency pattern in gastric carcinomas: a systematic review. Future Oncol 2017; 13: 567–79. DOI: 10.2217/fon-2016-0475</mixed-citation><mixed-citation xml:lang="ru">Ribeiro J., Oliveira C., Malta M., Sousa H. Epstein–Barr virus gene expression and latency pattern in gastric carcinomas: a systematic review. Future Oncol 2017; 13: 567–79. DOI: 10.2217/fon-2016-0475</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Lanz T. V., Brewer R. C., Ho P. P., Moon J. S., Jude K. M., Fernandez D., et al. Сlonally expanded В cells in multiple sclerosis bind EBV EBNA1 and GlialCAM. Nature 2022; 603: 321–7. DOI: 10.1038/s41586-022-04432-7</mixed-citation><mixed-citation xml:lang="ru">Lanz T. V., Brewer R. C., Ho P. P., Moon J. S., Jude K. M., Fernandez D., et al. Сlonally expanded В cells in multiple sclerosis bind EBV EBNA1 and GlialCAM. Nature 2022; 603: 321–7. DOI: 10.1038/s41586-022-04432-7</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Bar-Or A., Pender M. P., Khanna R., Steinman L., Hartung H. P., Maniar T., et al. Epstein–Barr Virus in multiple sclerosis: Theory and emerging immunotherapies. Trends Mol Med 2020; 26: 296–310. DOI: 10.1016/j.molmed.2019.11.003</mixed-citation><mixed-citation xml:lang="ru">Bar-Or A., Pender M. P., Khanna R., Steinman L., Hartung H. P., Maniar T., et al. Epstein–Barr Virus in multiple sclerosis: Theory and emerging immunotherapies. Trends Mol Med 2020; 26: 296–310. DOI: 10.1016/j.molmed.2019.11.003</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Biggi A. F. B., Elgui de Oliveira D. The Epstein–Barr virus hacks immune checkpoints: Evidence and consequences for lymphoproliferative disorders and cancers. Biomolecules 2022; 12 (3): 397. DOI: 10.3390/biom12030397</mixed-citation><mixed-citation xml:lang="ru">Biggi A. F. B., Elgui de Oliveira D. The Epstein–Barr virus hacks immune checkpoints: Evidence and consequences for lymphoproliferative disorders and cancers. Biomolecules 2022; 12 (3): 397. DOI: 10.3390/biom12030397</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Jangra S., Yuen K. S., Botelho M. G., Jin D. Y. Epstein–Barr Virus and innate immunity: Friends or foes? Microorganisms 2019; 7 (6): 183. DOI: 10.3390/microorganisms7060183</mixed-citation><mixed-citation xml:lang="ru">Jangra S., Yuen K. S., Botelho M. G., Jin D. Y. Epstein–Barr Virus and innate immunity: Friends or foes? Microorganisms 2019; 7 (6): 183. DOI: 10.3390/microorganisms7060183</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Ressing M. E., van Gent M., Gram A. M., Hooykaas M. J., Piersma S. J., Wiertz E. J. Immune evasion by Epstein–Barr virus. Curr Top Microbiol Immunol 2015; 391: 355–81. DOI: 10.1007/978-3-319-22834-1_12</mixed-citation><mixed-citation xml:lang="ru">Ressing M. E., van Gent M., Gram A. M., Hooykaas M. J., Piersma S. J., Wiertz E. J. Immune evasion by Epstein–Barr virus. Curr Top Microbiol Immunol 2015; 391: 355–81. DOI: 10.1007/978-3-319-22834-1_12</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Keir M. E., Butte M. J., Freeman G. J., Sharpe A. H. PD-1 and its ligands in tolerance and immunity. Ann Rev Immunol 2008; 26: 677–704. DOI: 10.1146/annurev.immunol.26.021607.090331</mixed-citation><mixed-citation xml:lang="ru">Keir M. E., Butte M. J., Freeman G. J., Sharpe A. H. PD-1 and its ligands in tolerance and immunity. Ann Rev Immunol 2008; 26: 677–704. DOI: 10.1146/annurev.immunol.26.021607.090331</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Maschan M., Caimi P. F., Reese-Koc J., Sanchez G. P., Sharma A. A., Molostova O., et al. Multiple site place-of-care manufactured anti-CD19 CAR-T cells induce high remission rates in B-cell malignancy patients. Nat Commun 2021; 12 (1): 7200. DOI: 10.1038/s41467-021-27312-6</mixed-citation><mixed-citation xml:lang="ru">Maschan M., Caimi P. F., Reese-Koc J., Sanchez G. P., Sharma A. A., Molostova O., et al. Multiple site place-of-care manufactured anti-CD19 CAR-T cells induce high remission rates in B-cell malignancy patients. Nat Commun 2021; 12 (1): 7200. DOI: 10.1038/s41467-021-27312-6</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Liu E., Marin D., Banerjee P., Macapinlac H. A., Thompson P., Basar R., et al. Use of CAR-transduced natural killer cells in CD 19-positive lymphoid tumors. N Engl f Med 2020; 382: 545–53. DOI: 10.1056/nejmoa1910607</mixed-citation><mixed-citation xml:lang="ru">Liu E., Marin D., Banerjee P., Macapinlac H. A., Thompson P., Basar R., et al. Use of CAR-transduced natural killer cells in CD 19-positive lymphoid tumors. N Engl f Med 2020; 382: 545–53. DOI: 10.1056/nejmoa1910607</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Poole C. L., James S. H. Antiviral therapies for herpesviruses: Current agents fand new directions. Clin Ther 2018; 40: 1282–98. DOI: 10.1016/j.clinthera.2018.07.006</mixed-citation><mixed-citation xml:lang="ru">Poole C. L., James S. H. Antiviral therapies for herpesviruses: Current agents fand new directions. Clin Ther 2018; 40: 1282–98. DOI: 10.1016/j.clinthera.2018.07.006</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Hocker B., Bohm S., Fickcnscher H., Kusters U., Schnitzler P., Pohl M., et al. (Val-)Ganciclovir prophylaxis reduces Epstein–Barr virus primary infection in pediatric renal transplantation. Transpl Int 2012; 25: 723–31. DOI: 10.1111/j.1432-2277.2012.01485.x</mixed-citation><mixed-citation xml:lang="ru">Hocker B., Bohm S., Fickcnscher H., Kusters U., Schnitzler P., Pohl M., et al. (Val-)Ganciclovir prophylaxis reduces Epstein–Barr virus primary infection in pediatric renal transplantation. Transpl Int 2012; 25: 723–31. DOI: 10.1111/j.1432-2277.2012.01485.x</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Yoshizaki T., Wakisaka N., Kondo S., Murono S., Shimizu Y., Nakashima M., et al. Treatment of locally recurrent Epstein–Barr virus-associated nasopharyngeal carcinoma using die anti-viral agent cidofovir. J Med Virol 2008; 80: 879–82. DOI: 10.1002/jmv.21165</mixed-citation><mixed-citation xml:lang="ru">Yoshizaki T., Wakisaka N., Kondo S., Murono S., Shimizu Y., Nakashima M., et al. Treatment of locally recurrent Epstein–Barr virus-associated nasopharyngeal carcinoma using die anti-viral agent cidofovir. J Med Virol 2008; 80: 879–82. DOI: 10.1002/jmv.21165</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Gallant J. E., Daar E. S., Raffi F., Brinson C., Ruane P., Dejesus E., et al. Efficacy ind safety of tenofovir alafenamide versus tenofovir disoproxil fumarate given as fixed-dose combinations containing emtricitabine as backbones for treatment of HIV-1 infection in virologically suppressed adults: a randomised, double-blind, active-controlled phase 3 trial. Lancet HIV 2016; 3: el58–65. DOI: 10.1016/S2352-3018(16)00024-2</mixed-citation><mixed-citation xml:lang="ru">Gallant J. E., Daar E. S., Raffi F., Brinson C., Ruane P., Dejesus E., et al. Efficacy ind safety of tenofovir alafenamide versus tenofovir disoproxil fumarate given as fixed-dose combinations containing emtricitabine as backbones for treatment of HIV-1 infection in virologically suppressed adults: a randomised, double-blind, active-controlled phase 3 trial. Lancet HIV 2016; 3: el58–65. DOI: 10.1016/S2352-3018(16)00024-2</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Afshar K., Rao A. P., Patel V., Forrester K., Ganesh S. Use of foscarnet therapy for EBV infection following control of PTLD with enhancement of cellular immunity in a lung-transplant recipient. Transplant 2011; 2011: 919651. DOI: 10.1155/2011/919651</mixed-citation><mixed-citation xml:lang="ru">Afshar K., Rao A. P., Patel V., Forrester K., Ganesh S. Use of foscarnet therapy for EBV infection following control of PTLD with enhancement of cellular immunity in a lung-transplant recipient. Transplant 2011; 2011: 919651. DOI: 10.1155/2011/919651</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Kenney S. C., Mertz J. E. Regulation of the latent-lytic switch in Epstein-Barr virus. Semm Cancer Biol 2014; 26: 60–8. DOI: 10.1016/j.semcancer.2014.01.002</mixed-citation><mixed-citation xml:lang="ru">Kenney S. C., Mertz J. E. Regulation of the latent-lytic switch in Epstein-Barr virus. Semm Cancer Biol 2014; 26: 60–8. DOI: 10.1016/j.semcancer.2014.01.002</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Yiu S. P. T., Dorothea M., Hui K. F., Chiang A. K. S. Lytic induction therapy Against Epstein–Barr virus-associated malignancies: Past, present, and future. Cancers (Basel) 2020; 12 (8): 2142. DOI: 10.3390/cancers12082142</mixed-citation><mixed-citation xml:lang="ru">Yiu S. P. T., Dorothea M., Hui K. F., Chiang A. K. S. Lytic induction therapy Against Epstein–Barr virus-associated malignancies: Past, present, and future. Cancers (Basel) 2020; 12 (8): 2142. DOI: 10.3390/cancers12082142</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Ghosh S. K., Perrine S. P., Williams R. M., Faller D. V. Histone deacetylase inhibitors are potent inducers of gene expression in latent EBV and sensitize lymphoma cells to nucleosidc antiviral agents. Blood 2012; 119: 1008–17. DOI: 10.1182/blood-2011-06-362434</mixed-citation><mixed-citation xml:lang="ru">Ghosh S. K., Perrine S. P., Williams R. M., Faller D. V. Histone deacetylase inhibitors are potent inducers of gene expression in latent EBV and sensitize lymphoma cells to nucleosidc antiviral agents. Blood 2012; 119: 1008–17. DOI: 10.1182/blood-2011-06-362434</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Kraus R. J., Yu X., Cordes B. A., Sathiamoorthi S., Iempridee T., Nawandar D. M., еt al. Hypoxia-inducible factor-1a plays roles in Epstein–Barr virus’s natural life cycle and tumorigenesis by inducing lytic infection through direct binding to the immediate-early BZLF1 gene promoter. PloS Pathog 2017; 13: el006404. DOI: 10.1371/journal.ppat.1006404</mixed-citation><mixed-citation xml:lang="ru">Kraus R. J., Yu X., Cordes B. A., Sathiamoorthi S., Iempridee T., Nawandar D. M., еt al. Hypoxia-inducible factor-1a plays roles in Epstein–Barr virus’s natural life cycle and tumorigenesis by inducing lytic infection through direct binding to the immediate-early BZLF1 gene promoter. PloS Pathog 2017; 13: el006404. DOI: 10.1371/journal.ppat.1006404</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Sokal E. M., Hoppenbrouwers K., Vandermeulen C., Moutschen M., Leonard P., Moreels A., еt al. Recombinant gp350 vaccine for infectious mononucleosis: a phase 2, randomized, double-blind, placebo-controlled trial to evaluate the safety, immunogenicity, and efficacy of an Epstein–Barr virus vaccine in healthy young adults. Infect Dis 2007; 196: 1749–53. DOI: 10.1086/523813</mixed-citation><mixed-citation xml:lang="ru">Sokal E. M., Hoppenbrouwers K., Vandermeulen C., Moutschen M., Leonard P., Moreels A., еt al. Recombinant gp350 vaccine for infectious mononucleosis: a phase 2, randomized, double-blind, placebo-controlled trial to evaluate the safety, immunogenicity, and efficacy of an Epstein–Barr virus vaccine in healthy young adults. Infect Dis 2007; 196: 1749–53. DOI: 10.1086/523813</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Cohen J. I. Vaccine development for Epstein–Barr virus. Adv Exp Med Biol 2018; 1045: 477–93. DOI: 10.1007/978-981-10-7230-7_22</mixed-citation><mixed-citation xml:lang="ru">Cohen J. I. Vaccine development for Epstein–Barr virus. Adv Exp Med Biol 2018; 1045: 477–93. DOI: 10.1007/978-981-10-7230-7_22</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Gu S. Y., Huang T. M., Ruan L., Miao Y. H., Lu H., Chu C. M., et al. First EBV vaccine trial in humans using recombinant vaccinia virus expressing the major membrane antigen. Dev Biol Stand 1995; 84: 171–7.</mixed-citation><mixed-citation xml:lang="ru">Gu S. Y., Huang T. M., Ruan L., Miao Y. H., Lu H., Chu C. M., et al. First EBV vaccine trial in humans using recombinant vaccinia virus expressing the major membrane antigen. Dev Biol Stand 1995; 84: 171–7.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Taylor G. S., Jia H., Harrington K., Lee L. W., Turner J., Ladell K., et al. A recombinant modified vaccinia ankara vaccine encoding Epstein–Barr virus (EBV) target antigens: a phase 1 trial in UK patients with EBV-positivc cancer. Clin Chancer Res 2014; 20: 5009–22. DOI: 10.1158/1078-0432.CCR-14-1122-T</mixed-citation><mixed-citation xml:lang="ru">Taylor G. S., Jia H., Harrington K., Lee L. W., Turner J., Ladell K., et al. A recombinant modified vaccinia ankara vaccine encoding Epstein–Barr virus (EBV) target antigens: a phase 1 trial in UK patients with EBV-positivc cancer. Clin Chancer Res 2014; 20: 5009–22. DOI: 10.1158/1078-0432.CCR-14-1122-T</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Smith C., Tsang J., Beagley L., Chua D., Lee V., Li V., et al. Effective treatment of metastatic forms of Epstein–Barr virus-associated nasopharyngeal carcinoma with a novel adenovirus-based adoptive immunotherapy. Cancer Res 2012; 72: 1116–25. DOI: 10.1158/0008-5472.CAN-11-3399</mixed-citation><mixed-citation xml:lang="ru">Smith C., Tsang J., Beagley L., Chua D., Lee V., Li V., et al. Effective treatment of metastatic forms of Epstein–Barr virus-associated nasopharyngeal carcinoma with a novel adenovirus-based adoptive immunotherapy. Cancer Res 2012; 72: 1116–25. DOI: 10.1158/0008-5472.CAN-11-3399</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Ruhl J., Leung C. S., Munz C. Vaccination against the Epstein–Barr virus. Cell Mol Life Sci 2020; 77: 4315–24. DOI: 10.1007/s00018-020-03538-3</mixed-citation><mixed-citation xml:lang="ru">Ruhl J., Leung C. S., Munz C. Vaccination against the Epstein–Barr virus. Cell Mol Life Sci 2020; 77: 4315–24. DOI: 10.1007/s00018-020-03538-3</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Ogembo J. G., Muraswki M. R., McGinnes L. W., Parcharidou A., Sutiwisesak R., Tison T., et al. A chimeric EBV gp350/220-based VLP replicates the virion В-cell attachment mcchanism and elicits long-lasting neutralizing antibodies in mice. Transl Med 2015; 13: 50. DOI: 10.1186%2Fs12967-015-0415-2</mixed-citation><mixed-citation xml:lang="ru">Ogembo J. G., Muraswki M. R., McGinnes L. W., Parcharidou A., Sutiwisesak R., Tison T., et al. A chimeric EBV gp350/220-based VLP replicates the virion В-cell attachment mcchanism and elicits long-lasting neutralizing antibodies in mice. Transl Med 2015; 13: 50. DOI: 10.1186%2Fs12967-015-0415-2</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Cui X., Snapper C. M. Epstein–Barr Virus: Development of vaccines and immune cell therapy for EBV-associated diseases. Front Immunol 2021; 12: 734471. DOI: 10.3389/fimmu.2021.734471</mixed-citation><mixed-citation xml:lang="ru">Cui X., Snapper C. M. Epstein–Barr Virus: Development of vaccines and immune cell therapy for EBV-associated diseases. Front Immunol 2021; 12: 734471. DOI: 10.3389/fimmu.2021.734471</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54. Панкратьева Л. Л. Клиническое значение материнского микрохимеризма и возможности его количественной оценки / Л. Л. Панкратьева [и др.] // Вопросы практической педиатрии. – 2015. – 10 (2): 47–51.</mixed-citation><mixed-citation xml:lang="ru">Панкратьева Л. Л. Клиническое значение материнского микрохимеризма и возможности его количественной оценки / Л. Л. Панкратьева [и др.] // Вопросы практической педиатрии. – 2015. – 10 (2): 47–51.</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55. Jiang S., Zhou H., Liang J., Gerdt C., Wang C., Ke L., et al. The Epstein–Barr virus rcgulome in lymphoblastoid cells. Cell Host Microbe 2017; 22: 561–73.e4. DOI: 10.1016/j.chom.2017.09.001</mixed-citation><mixed-citation xml:lang="ru">Jiang S., Zhou H., Liang J., Gerdt C., Wang C., Ke L., et al. The Epstein–Barr virus rcgulome in lymphoblastoid cells. Cell Host Microbe 2017; 22: 561–73.e4. DOI: 10.1016/j.chom.2017.09.001</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56. Wen Y., Xu H., Han J., Jin R., Chen H. How does Epstein–Barr virus interact with other microbiomes in EBV-driven cancers? Front Cell Infect Microbiol 2022; 12: 852066. DOI: 10.3389/fcimb.2022.852066</mixed-citation><mixed-citation xml:lang="ru">Wen Y., Xu H., Han J., Jin R., Chen H. How does Epstein–Barr virus interact with other microbiomes in EBV-driven cancers? Front Cell Infect Microbiol 2022; 12: 852066. DOI: 10.3389/fcimb.2022.852066</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57. Исаков В. А. Герпесвирусные инфекции человека: руководство для врачей / В, А. Исаков, Е. И. Архипова, Д. В. Исаков. – СПб., 2013. – 670 с.</mixed-citation><mixed-citation xml:lang="ru">Исаков В. А. Герпесвирусные инфекции человека: руководство для врачей / В, А. Исаков, Е. И. Архипова, Д. В. Исаков. – СПб., 2013. – 670 с.</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">58. Алимбарова Л. М. Эффективность герпетической поливакцины в лечении часто рецидивирующей герпес-вирусной инфекции / Л. М. Алимбарова, Н. Д. Львов, М. В. Мезенцева // Современная медицина. – 2018. – (3): 26–32.</mixed-citation><mixed-citation xml:lang="ru">Алимбарова Л. М. Эффективность герпетической поливакцины в лечении часто рецидивирующей герпес-вирусной инфекции / Л. М. Алимбарова, Н. Д. Львов, М. В. Мезенцева // Современная медицина. – 2018. – (3): 26–32.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
