<?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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Problems of Virology</journal-id><journal-title-group><journal-title xml:lang="en">Problems of Virology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы вирусологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0507-4088</issn><issn publication-format="electronic">2411-2097</issn><publisher><publisher-name xml:lang="en">Central Research Institute for Epidemiology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">16853</article-id><article-id pub-id-type="doi">10.36233/0507-4088-367</article-id><article-id pub-id-type="edn">nmyakh</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</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Adeno-associated viruses: their impact in the human health and role in the modern healthcare</article-title><trans-title-group xml:lang="ru"><trans-title>Аденоассоциированные вирусы: влияние на здоровье человека и роль в современном здравоохранении</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0003-1143-7339</contrib-id><name-alternatives><name xml:lang="en"><surname>Ulanova</surname><given-names>Ekaterina A.</given-names></name><name xml:lang="ru"><surname>Уланова</surname><given-names>Екатерина Анатольевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Junior Research Fellow of Research Department of Viral Hepatitis and Liver Diseases</p></bio><bio xml:lang="ru"><p>младший научный сотрудник научно-исследовательского отдела вирусных гепатитов и заболеваний печени</p></bio><email>chuhnina_ekaterina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4509-5352</contrib-id><contrib-id contrib-id-type="spin">9914-9205</contrib-id><name-alternatives><name xml:lang="en"><surname>Greshnyakova</surname><given-names>Vera A.</given-names></name><name xml:lang="ru"><surname>Грешнякова</surname><given-names>Вера Александровна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, Head of the Research Department of Viral Hepatitis and Liver Diseases; Associate Professor of the Department of Infectious Diseases in Children of Faculty of Postgraduate and Additional Professional Education; Associate Professor of the Department of Infectious Diseases</p></bio><bio xml:lang="ru"><p>канд. мед. наук, руководитель научно-исследовательского отдела вирусных гепатитов и заболеваний печени; доцент кафедры инфекционных заболеваний у детей факультета послевузовского и дополнительного профессионального образования; доцент кафедры инфекционных болезней медицинского института </p></bio><email>veramamayeva@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Federal Research and Clinical Center for Infectious Diseases</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно-клинический центр инфекционных болезней» ФМБА России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">St. Petersburg State Pediatric Medical University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Санкт-Петербургский государственный педиатрический медицинский университет» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">St. Petersburg State University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Санкт-Петербургский государственный университет»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2026-06-30" publication-format="electronic"><day>30</day><month>06</month><year>2026</year></pub-date><volume>71</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>232</fpage><lpage>243</lpage><history><date date-type="received" iso-8601-date="2026-02-03"><day>03</day><month>02</month><year>2026</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2026, Ulanova E.A., Greshnyakova V.A.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2026, Уланова Е.А., Грешнякова В.А.</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="en">Ulanova E.A., Greshnyakova V.A.</copyright-holder><copyright-holder xml:lang="ru">Уланова Е.А., Грешнякова В.А.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://virusjour.crie.ru/jour/article/view/16853">https://virusjour.crie.ru/jour/article/view/16853</self-uri><abstract xml:lang="en"><p>Adeno-associated viruses (AAVs) are microorganisms capable of replicating in host cells only in the presence of a helper virus. Despite their defective nature, they exhibit broad tropism for various organs and have a ubiquitous distribution. There are no definitive data on the effects of these viruses on the human body under conditions of natural infection. For a long time, AAVs were considered nonpathogenic, even in immunocompromised individuals, which led to their use as vectors in gene therapy. Currently, evidence exists for both neutral interactions between AAVs and the human host, as well as for pathogenic and protective roles of these viruses. A growing body of evidence describes the involvement of AAVs in the oncogenesis of hepatocellular carcinoma, the development of hepatitis, including cases associated with gene therapy, and an increased risk of male infertility, adverse pregnancy outcomes, and spontaneous abortions. At the same time, beneficial effects on human health have also been reported, including the prevention of cervical cancer through suppression of human papillomavirus replication.</p> <p><bold>The aim</bold> of this review is to presents data on the diverse effects of AAVs on human health, with a focus on the natural history of AAV infection.</p></abstract><trans-abstract xml:lang="ru"><p>Аденоассоциированные вирусы (ААВ) – это микроорганизмы, способные к размножению в клетках организма-хозяина только в присутствии вируса-помощника. Несмотря на свою «дефектность», они обладают широкой тропностью к разным органам, а их распространенность носит убиквитарный характер. Точных данных о влиянии данных вирусов на организм человека в условиях естественного инфицирования нет. Долгое время ААВ рассматривались как апатогенные даже у лиц с иммунодефицитными состояниями, благодаря чему стали использоваться в качестве вектора в генной терапии. На сегодняшний день имеются свидетельства как нейтрального взаимодействия ААВ и организма человека, так и патогенного влияния и протективной роли вирусов. Накапливается все больше данных, описывающих роль ААВ в онкогенезе гепатоцеллюлярной карциномы, развитии гепатитов, в том числе вследствие генной терапии, в повышении риска мужского бесплодия, неблагоприятного течения беременности и самопроизвольных абортов. В то же время описывается и их положительное влияние на здоровье, предупреждающее развитие рака шейки матки за счет подавления репликации вируса папилломы человека.</p> <p><bold>Цель</bold> обзора – привести данные о разностороннем влиянии ААВ на здоровье человека с фокусом на естественное течение ААВ-инфекции.</p></trans-abstract><kwd-group xml:lang="en"><kwd>adeno-associated viruses</kwd><kwd>hepatitis of unknown etiology</kwd><kwd>hepatocellular carcinoma</kwd><kwd>cervical cancer</kwd><kwd>gene therapy</kwd><kwd>adeno-associated virus-based vectors</kwd><kwd>AAV vector</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>аденоассоциированные вирусы</kwd><kwd>гепатит неясной этиологии</kwd><kwd>гепатоцеллюлярная карцинома</kwd><kwd>рак шейки матки</kwd><kwd>генная терапия</kwd><kwd>векторы на основе аденоассоциированного вируса</kwd><kwd>ААВ-вектор</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">Greshnyakova V.A., Goryacheva L.G. Acute hepatitis of unknown aetiology in children: a new threat? (Short message). Klinicheskaya infektologiya i parazitologiya. 2022; 11(2): 166–76. https://doi.org/10.34883/PI.2022.11.2.028 https://elibrary.ru/irwqcb (in Russian)</mixed-citation><mixed-citation xml:lang="ru">Грешнякова В.А., Горячева Л.Г. Острый гепатит неизвестной этиологии у детей: новая угроза? (Краткое сообщение). Клиническая инфектология и паразитология. 2022; 11(2): 166–76. https://doi.org/10.34883/PI.2022.11.2.028 https://elibrary.ru/irwqcb</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><mixed-citation>Morfopoulou S., Buddle S., Torres Montaguth O.E., Atkinson L., Guerra-Assunção J.A., Moradi Marjaneh M., et al. Genomic investigations of unexplained acute hepatitis in children. Nature. 2023; 617(7961): 564–73. https://doi.org/10.1038/s41586-023-06003-w https://elibrary.ru/kyuuco</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Servellita V., Sotomayor Gonzalez A., Lamson D.M., Foresythe A., Huh H.J., Bazinet A.L. et al. Adeno-associated virus type 2 in US children with acute severe hepatitis. Nature. 2023; 617(7961): 574–80. https://doi.org/10.1038/s41586-023-05949-1 https://elibrary.ru/wlvilh</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Ho A., Orton R., Tayler R., Asamaphan P., Herder V., Davis C., et al. Adeno-associated virus 2 infection in children with non-A-E hepatitis. Nature. 2023; 617(7961): 555–63. https://doi.org/10.1038/s41586-023-05948-2 https://elibrary.ru/gctvak</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Heugel J., Boeckh M., Huang M.L., Dierks B., Hackman R., Fredricks D., et al. Detection of adeno-associated virus viremia in hematopoietic cell transplant recipients. J. Infect. Dis. 2011; 204(11): 1746–9. https://doi.org/10.1093/infdis/jir655</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Moldavskii D., Gilazieva Z., Fattakhova A., Solovyeva V., Issa S., Sufianov A., et al. AAV-based gene therapy: opportunities, risks, and scale-up strategies. Int. J. Mol. Sci. 2025; 26(17): 8282. https://doi.org/10.3390/ijms26178282 https://elibrary.ru/tlhpok</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Meier A.F., Fraefel C., Seyffert M. The interplay between adeno-associated virus and its helper viruses. Viruses. 2020; 12(6): 662. https://doi.org/10.3390/v12060662 https://elibrary.ru/gtinzr</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Atchison R.W., Casto B.C., Hammon W.M. Adenovirus-associated defective virus particles. Science. 1965; 149(3685): 754–6. https://doi.org/10.1126/science.149.3685.754 https://elibrary.ru/idavst</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Issa S.S., Shaimardanova A.A., Solovyeva V.V., Rizvanov A.A. Various AAV serotypes and their applications in Gene Therapy: an overview. Cells. 2023; 12(5): 785. https://doi.org/10.3390/cells12050785 https://elibrary.ru/hnhgkw</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Bowles D.E., Rabinowitz J.E., Samulski R.J. The genus Dependovirus. In: Kerr J.R., Cotmore S.F., Bloom M.E., Linden R.M., Parrish C.R., eds. Parvoviruses. London: Hodder Arnold; 2006: 15–23.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Yalkinoglu A.O., Heilbronn R., Bürkle A., Schlehofer J.R., zur Hausen H. DNA amplification of adeno-associated virus as a response to cellular genotoxic stress. Cancer Res. 1988; 48(11): 3123–9.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Schnepp B.C., Jensen R.L., Chen C.L., Johnson P.R., Clark K.R. Characterization of adeno-associated virus genomes isolated from human tissues. J. Virol. 2005; 79(23): 14793–803. https://doi.org/10.1128/JVI.79.23.14793-14803.2005</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Mehrle S., Rohde V., Schlehofer J.R. Evidence of chromosomal integration of AAV DNA in human testis tissue. Virus Genes. 2004; 28(1): 61–9. https://doi.org/10.1023/B:VIRU.0000012264.54212.f5 https://elibrary.ru/lwfdbh</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Henckaerts E., Linden R.M. Adeno-associated virus: a key to the human genome? Future Virol. 2010; 5(5): 555–74. https://doi.org/10.2217/fvl.10.48 https://elibrary.ru/xxdxmj</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Dalwadi D.A., Calabria A., Tiyaboonchai A., Posey J., Naugler W.E., Montini E., et al. AAV integration in human hepatocytes. Mol. Ther. 2021; 29(10): 2898–909. https://doi.org/10.1016/j.ymthe.2021.08.031 https://elibrary.ru/nobjqk</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Li C., Narkbunnam N., Samulski R.J., Asokan A., Hu G., Jacobson L.J., et al. Neutralizing antibodies against adeno-associated virus examined prospectively in pediatric patients with hemophilia. Gene Ther. 2012; 19(3): 288–94. https://doi.org/10.1038/gt.2011.90</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Liu Q., Huang W., Zhang H., Wang Y., Zhao J., Song A., et al. Neutralizing antibodies against AAV2, AAV5 and AAV8 in healthy and HIV-1-infected subjects in China: implications for gene therapy using AAV vectors. Gene Ther. 2014; 21(8): 732–8. https://doi.org/10.1038/gt.2014.47</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Klamroth R., Hayes G., Andreeva T., Gregg K., Suzuki T., Mitha I.H., et al. Global seroprevalence of pre-existing immunity against AAV5 and other AAV serotypes in people with hemophilia A. Hum. Gene Ther. 2022; 33(7-8): 432–41. https://doi.org/10.1089/hum.2021.287 https://elibrary.ru/oppwxj</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Calcedo R., Vandenberghe L.H., Gao G., Lin J., Wilson J.M. Worldwide epidemiology of neutralizing antibodies to adeno-associated viruses. J. Infect. Dis. 2009; 199(3): 381–90. https://doi.org/10.1086/595830</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Hüser D., Khalid D., Lutter T., Hammer E.M., Weger S., Heßler M., et al. High Prevalence of Infectious Adeno-associated Virus (AAV) in human peripheral blood mononuclear cells indicative of t lymphocytes as sites of AAV persistence. J. Virol. 2017; 91(4): e02137-16. https://doi.org/10.1128/jvi.02137-16</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Schlehofer J.R., Boeke C., Reuland M., Eggert-Kruse W. Presence of DNA of adeno-associated virus in subfertile couples, but no association with fertility factors. Hum. Reprod. 2012; 27(3): 770–8. https://doi.org/10.1093/humrep/der427</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Burguete T., Rabreau M., Fontanges-Darriet M., Roset E., Hager H.D., Köppel A., et al. Evidence for infection of the human embryo with adeno-associated virus in pregnancy. Hum. Reprod. 1999; 14(9): 2396–401. https://doi.org/10.1093/humrep/14.9.2396 https://elibrary.ru/ipfzxn</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Sayyadi-Dehno Z., Seyed Khorrami S.M., Ghavami N., Ghotbi-Zadeh F., Khushideh M., Hosseini M., et al. Molecular detection of adeno-associated virus DNA in cases of spontaneous and therapeutic abortion. Fetal Pediatr. Pathol. 2019; 38(3): 206–14. https://doi.org/10.1080/15513815.2019.1576817 https://elibrary.ru/gesrod</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Gao G., Vandenberghe L.H., Alvira M.R., Lu Y., Calcedo R., Zhou X., et al. Clades of Adeno-associated viruses are widely disseminated in human tissues. J. Virol. 2004; 78(12): 6381–8. https://doi.org/10.1128/JVI.78.12.6381-6388.2004</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Martin N.A., Gonzalez G., Reynolds L.J., Bennett C., Campbell C., Nolan T.M., et al. Adeno-associated virus 2 and human adenovirus F41 in wastewater during outbreak of severe acute hepatitis in children, Ireland. Emerg. Infect. Dis. 2023; 29(4): 751–60. https://doi.org/10.3201/eid2904.221878 https://elibrary.ru/inpzew</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>La Bella T., Imbeaud S., Peneau C., Mami I., Datta S., Bayard Q., et al. Adeno-associated virus in the liver: natural history and consequences in tumour development. Gut. 2020; 69(4): 737–47. https://doi.org/10.1136/gutjnl-2019-318281</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Fujimoto A., Furuta M., Totoki Y., Tsunoda T., Kato M., Shiraishi Y., et al. Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer. Nat. Genet. 2016; 48(5): 500–9. https://doi.org/10.1038/ng.3547 https://elibrary.ru/wpxier</mixed-citation></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Park K.J., Lee J., Park J.H., Joh J.W., Kwon C.H., Kim J.W. Adeno-associated virus 2-mediated hepatocellular carcinoma is very rare in Korean patients. Ann Lab Med. 2016; 36(5): 469–74. https://doi.org/10.3343/alm.2016.36.5.469</mixed-citation><mixed-citation xml:lang="ru">Park K.J., Lee J., Park J.H., Joh J.W., Kwon C.H., Kim J.W. Adeno-associated virus 2-mediated hepatocellular carcinoma is very rare in Korean patients. Ann. Lab. Med. 2016; 36(5): 469–74. https://doi.org/10.3343/alm.2016.36.5.469</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><mixed-citation>Tatsuno K., Midorikawa Y., Takayama T., Yamamoto S., Nagae G., Moriyama M., et al. Impact of AAV2 and hepatitis B virus integration into genome on development of hepatocellular carcinoma in patients with prior hepatitis B virus infection. Clin. Cancer Res. 2019; 25(20): 6217–27. https://doi.org/10.1158/1078-0432.CCR-18-4041</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Bayard Q., Meunier L., Peneau C., Renault V., Shinde J., Nault J.C., et al. Cyclin A2/E1 activation defines a hepatocellular carcinoma subclass with a rearrangement signature of replication stress. Nat. Commun. 2018; 9(1): 5235. https://doi.org/10.1038/s41467-018-07552-9 https://elibrary.ru/uinkfq</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Chand D., Mohr F., McMillan H., Tukov F.F., Montgomery K., Kleyn A., Sun R., et al. Hepatotoxicity following administration of onasemnogene abeparvovec (AVXS-101) for the treatment of spinal muscular atrophy. J. Hepatol. 2021; 74(3): 560–6. https://doi.org/10.1016/j.jhep.2020.11.001 https://elibrary.ru/vxenbi</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Shieh P.B., Bönnemann C.G., Müller-Felber W., Blaschek A., Dowling J.J., Kuntz N.L., et al. Re: “Moving forward after two deaths in a gene therapy trial of myotubular myopathy” by Wilson Flotte. Hum. Gene Ther. 2020; 31(15-16): 787. https://doi.org/10.1089/hum.2020.217 https://elibrary.ru/fqrfes</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Guo Y., Zhou G., Feng Y., Zhang J., Liu Y., Yang X., et al. The association between male viral infections and infertility: a systematic review and meta-analysis. Rev. Med. Virol. 2024; 34(6): e70002. https://doi.org/10.1002/rmv.70002 https://elibrary.ru/zyaeqi</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Tobiasch E., Rabreau M., Geletneky K., Laruë-Charlus S., Severin F., Becker N., et al. Detection of adeno-associated virus DNA in human genital tissue and in material from spontaneous abortion. J. Med. Virol. 1994; 44(2): 215–22. https://doi.org/10.1002/jmv.1890440218</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Pereira C.C., de Freitas L.B., de Vargas P.R., de Azevedo M.L., do Nascimento J.P., Spano L.C. Molecular detection of adeno-associated virus in cases of spontaneous and intentional human abortion. J. Med. Virol. 2010; 82(10): 1689–93. https://doi.org/10.1002/jmv.21841</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Kiehl K., Schlehofer J.R., Schultz R., Zugaib M., Armbruster-Moraes E. Adeno-associated virus DNA in human gestational trophoblastic disease. Placenta. 2002; 23(5): 410–5. https://doi.org/10.1053/plac.2002.0827</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Arechavaleta-Velasco F., Ma Y., Zhang J., McGrath C.M., Parry S. Adeno-associated virus-2 (AAV-2) causes trophoblast dysfunction, and placental AAV-2 infection is associated with preeclampsia. Am. J. Pathol. 2006; 168(6): 1951–9. https://doi.org/10.2353/ajpath.2006.050781</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Arechavaleta-Velasco F., Gomez L., Ma Y., Zhao J., McGrath C.M., Sammel M.D., et al. Adverse reproductive outcomes in urban women with adeno-associated virus-2 infections in early pregnancy. Hum. Reprod. 2008; 23(1): 29–36. https://doi.org/10.1093/humrep/dem360 https://elibrary.ru/ipfwzj</mixed-citation></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Greshnyakova V.A., Bekhtereva M.K., Goryacheva L.G., Karev V.E., Komarova A.M., Konev A.I., et al. A case of severe acute hepatitis of unknown etiology requiring liver transplantation in a child with adenovirus infection. Zhurnal infektologii. 2022; 14(2): 161–70. https://elibrary.ru/bxbbnh (in Russian)</mixed-citation><mixed-citation xml:lang="ru">Грешнякова В.А., Бехтерева М.К., Горячева Л.Г., Карев В.Е., Комарова А.М., Конев А.И. и др. Случай тяжелого течения острого гепатита неясной этиологии, потребовавшего трансплантации печени, у ребенка с аденовирусной инфекцией. Журнал инфектологии. 2022; 14(2): 161–70. https://elibrary.ru/bxbbnh</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><mixed-citation>Gates S., Andreani J., Dewar R., Smith D.B., Templeton K., Child H.T., et al. Postpandemic rebound of adeno-associated virus type 2 (AAV2) infections temporally associated with an outbreak of unexplained severe acute hepatitis in children in the United Kingdom. J. Med. Virol. 2023; 95(7): e28921. https://doi.org/10.1002/jmv.28921 https://elibrary.ru/kfvnun</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Hsu H.L., Brown A., Loveland A.B., Lotun A., Xu M., Luo L., et al. Structural characterization of a novel human adeno-associated virus capsid with neurotropic properties. Nat. Commun. 2020; 30(1): 3279. https://doi.org/10.1038/s41467-020-17047-1 https://elibrary.ru/lhywtn</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>van Gerven N.M., de Boer Y.S., Zwiers A., Verwer B.J., Drenth J.P., van Hoek B., et al. HLA-DRB1*03:01 and HLA-DRB1*04:01 modify the presentation and outcome in autoimmune hepatitis type-1. Genes Immun. 2015; 16(4): 247–52. https://doi.org/10.1038/gene.2014.82</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Lanchbury J.S., Jaeger E.E., Sansom D.M., Hall M.A., Wordsworth P., Stedeford J., et al. Strong primary selection for the Dw4 subtype of DR4 accounts for the HLA-DQw7 association with Felty’s syndrome. Hum. Immunol. 1991; 32(1): 56–64. https://doi.org/10.1016/0198-8859(91)90117-r</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Flotte T.R. Revisiting the “new” inflammatory toxicities of adeno-associated virus vectors. Hum. Gene Ther. 2020; 31(7-8): 398–9. https://doi.org/10.1089/hum.2020.29117.trf https://elibrary.ru/kohsks</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Stone D., Aubert M., Jerome K.R. Adeno-associated virus vectors and neurotoxicity-lessons from preclinical and human studies. Gene Ther. 2025; 32(1): 60–73. https://doi.org/10.1038/s41434-023-00405-1 https://elibrary.ru/pjanzu</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Manno C.S., Pierce G.F., Arruda V.R., Glader B., Ragni M., Rasko J.J., et al. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response. Nat. Med. 2006; 12(3): 342–7. https://doi.org/10.1038/nm1358</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Mingozzi F., Maus M.V., Sabatino D.E., Hui D., Manno C.S., Ragni M.V., et al. T-cell responses to AAV vector capsid limit the duration of transgene expression in human after liver-directed gene therapy. Blood. 2005; 106(11): 3055. https://doi.org/10.1182/blood.V106.11.3055.3055</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Salabarria S.M., Corti M., Coleman K.E., Wichman M.B., Berthy J.A., D’Souza P., et al. Thrombotic microangiopathy following systemic AAV administration is dependent on anti-capsid antibodies. J. Clin. Invest. 2024; 134(1): e173510. https://doi.org/10.1172/JCI173510 https://elibrary.ru/obermr</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Matovina M., Husnjak K., Milutin N., Ciglar S., Grce M. Possible role of bacterial and viral infections in miscarriages. Fertil. Steril. 2004; 81(3): 662–9. https://doi.org/10.1016/j.fertnstert.2003.08.020</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Mayor H.D., Drake S., Stahmann J., Mumford D.M. Antibodies to adeno-associated satellite virus and herpes simplex in sera from cancer patients and normal adults. Am. J. Obstet. Gynecol. 1976; 126(1): 100–4. https://doi.org/10.1016/0002-9378(76)90472-5</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Georg-Fries B., Biederlack S., Wolf J., zur Hausen H. Analysis of proteins, helper dependence, and seroepidemiology of a new human parvovirus. Virology. 1984; 134(1): 64–71. https://doi.org/10.1016/0042-6822(84)90272-1</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Freitas L.B., Tonani de Mattos A., Lima B.M., Miranda A.E., Spano L.C. Adeno-associated virus may play a protective role against human papillomavirus-induced cervical lesions independent of HIV serostatus. Int. J. STD AIDS. 2012; 23(4): 258–61. https://doi.org/10.1258/ijsa.2009.009150</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Zheng B.Y., Li X.D., Wiklund F., Chowdhry S., Angstrom T., Hallmans G., et al. Detection of adeno-associated virus type 2 genome in cervical carcinoma. Br. J. Cancer. 2006; 94(12): 1913–7. https://doi.org/10.1038/sj.bjc.6603179 https://elibrary.ru/uomtnk</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Shafiei-Jandaghi N.Z., Yavarian J., Faghihloo E., Ghavami N., Ghalejoogh Z.Y., Kiani S.J., et al. Prevalence of adeno-associated virus and human papillomavirus DNA in Iranian women with and without cervical cancer. Pathol. Res. Pract. 2017; 213(5): 457–60. https://doi.org/10.1016/j.prp.2017.02.010</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Lopez-Gordo E., Chamberlain K., Riyad J.M., Kohlbrenner E., Weber T. Natural adeno-associated virus serotypes and engineered adeno-associated virus capsid variants: tropism differences and mechanistic insights. Viruses. 2024; 16(3): 442. https://doi.org/10.3390/v16030442 https://elibrary.ru/rxllbw</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Suarez-Amaran L., Song L., Tretiakova A.P., Mikhail S.A., Samulski R.J. AAV vector development, back to the future. Mol. Ther. 2025; 33(5): 1903–36. https://doi.org/10.1016/j.ymthe.2025.03.064 https://elibrary.ru/jpumcg</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Wang J.H., Gessler D.J., Zhan W., Gallagher T.L., Gao G. Adeno-associated virus as a delivery vector for gene therapy of human diseases. Signal Transduct. Target. Ther. 2024; 9(1): 78. https://doi.org/10.1038/s41392-024-01780-w https://elibrary.ru/qqqbfs</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Han Z., Tan C., Ai J., Zhu Y. In vivo adeno-associated virus-mediated LDLR/PCSK9 intervention for familial hypercholesterolemia. Genes Dis. 2025; 12(6): 101632. https://doi.org/10.1016/j.gendis.2025.101632 https://elibrary.ru/bmkgdx</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Shanshan W., Yu Z. Recombinant adeno-associated virus 2-mediated miRNA-199 suppression vector alleviates dextran sulfate sodium-induced ulcerative colitis in mice. Virus Res. 2025; 357: 199588. https://doi.org/10.1016/j.virusres.2025.199588 https://elibrary.ru/vkhmsw</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Fox D., Xie J., Burwinkel J.L., Adams J.M., Chetal K., Keivandarian M., et al. Adeno-associated virus-mediated silencing of Sox4 leads to long-term amelioration of liver phenotypes in mouse models of Alagille syndrome. Gastroenterology. 2025; 169(5): 1000–16. https://doi.org/10.1053/j.gastro.2025.04.033 https://elibrary.ru/dlhrbt</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Martinez-Navio J.M., Fuchs S.P., Pantry S.N., Lauer W.A., Duggan N.N., Keele B.F., et al. Adeno-associated virus delivery of anti-HIV monoclonal antibodies can drive long-term virologic suppression. Immunity. 2019; 50(3): 567–75. https://doi.org/10.1016/j.immuni.2019.02.005</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Xie K., Yuan Y., Jiang M., Chen D., Chen S., Zhou X. Protamine-1 encoded recombinant adeno-associated virus for enhanced brain magnetic resonance imaging. Magn. Reson. Lett. 2025; 6(1): 200222. https://doi.org/10.1016/j.mrl.2025.200222 https://elibrary.ru/olmchl</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Hoption Cann S.A. Paediatric acute hepatitis and therapeutic doses of paracetamol. Acta Paediatr. 2024; 113(1): 19–21. https://doi.org/10.1111/apa.16920 https://elibrary.ru/rdoeds</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Brodin P., Arditi M. Severe acute hepatitis in children: investigate SARS-CoV-2 superantigens. Lancet Gastroenterol. Hepatol. 2022; 7(7): 594–5. https://doi.org/10.1016/s2468-1253(22)00166-2</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Cates J., Baker J.M., Almendares O., Balachandran N., McKeever E.R., Kambhampati A.K., et al. Paediatric acute hepatitis of unknown aetiology: a national surveillance investigation in the USA during 2021 and 2022. Lancet Child Adolesc. Health. 2023; 7(11): 773–85. https://doi.org/10.1016/s2352-4642(23)00192-x https://elibrary.ru/rsofnm</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Maison N., Peck A., Illi S., Meyer-Buehn M., von Mutius E., Hübner J., et al. The rising of old foes: impact of lockdown periods on “non-SARS-CoV-2” viral respiratory and gastrointestinal infections. Infection. 2022; 50(2): 519–24. https://doi.org/10.1007/s15010-022-01756-4 https://elibrary.ru/lllajx</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Wang H., Zheng Y., de Jonge M.I., Wang R., Verhagen L.M., Chen Y., et al. Lockdown measures during the COVID-19 pandemic strongly impacted the circulation of respiratory pathogens in Southern China. Sci. Rep. 2022; 12(1): 16926. https://doi.org/10.1038/s41598-022-21430-x https://elibrary.ru/encnyq</mixed-citation></ref></ref-list></back></article>
