<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">pharmjournal</journal-id><journal-title-group><journal-title xml:lang="ru">Разработка и регистрация лекарственных средств</journal-title><trans-title-group xml:lang="en"><trans-title>Drug development &amp; registration</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2305-2066</issn><issn pub-type="epub">2658-5049</issn><publisher><publisher-name>LLC «CPHA»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.33380/2305-2066-2022-11-1-51-58</article-id><article-id custom-type="elpub" pub-id-type="custom">pharmjournal-1161</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ПОИСК И РАЗРАБОТКА НОВЫХ ЛЕКАРСТВЕННЫХ СРЕДСТВ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>RESEARCH AND DEVELOPMENT OF NEW DRUG PRODUCTS</subject></subj-group></article-categories><title-group><article-title>Вирус кори как векторная платформа для иммунотерапии опухолей головного мозга (обзор)</article-title><trans-title-group xml:lang="en"><trans-title>Measles Virus as a Vector Platform for Glioblastoma Immunotherapy (Review)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2898-9722</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Николаева</surname><given-names>Е. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikolaeva</surname><given-names>E. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>105064, Россия, г. Москва, Малый Казенный переулок, д. 5а</p></bio><bio xml:lang="en"><p>5а, Malyj Kazennyj lane, Moscow, 105064, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6382-9612</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Щетинина</surname><given-names>Ю. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Shchetinina</surname><given-names>Yu. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>105064, Россия, г. Москва, Малый Казенный переулок, д. 5а</p></bio><bio xml:lang="en"><p>5а, Malyj Kazennyj lane, Moscow, 105064, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1185-8630</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шохин</surname><given-names>И. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Shokhin</surname><given-names>I. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>105064, Россия, г. Москва, Малый Казенный переулок, д. 5а</p></bio><bio xml:lang="en"><p>5а, Malyj Kazennyj lane, Moscow, 105064, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5808-2246</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зверев</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Zverev</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра микробиологии, вирусологии и иммунологии имени академика А. А. Воробьева</p><p>105064, Россия, г. Москва, Малый Казенный переулок, д. 5а</p><p>125009, Россия, Москва, ул. Моховая, д. 11, стр. 10</p></bio><bio xml:lang="en"><p>Department of Microbiology, Virology and Immunology named after Academician A. A. Vorobyov</p><p>5а, Malyj Kazennyj lane, Moscow, 105064, Russia</p><p>11/10, Mokhovaya str., Moscow, 125009, Russia</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1757-8389</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Свитич</surname><given-names>О. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Svitich</surname><given-names>O. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра микробиологии, вирусологии и иммунологии имени академика А. А. Воробьева</p><p>105064, Россия, г. Москва, Малый Казенный переулок, д. 5а</p><p>125009, Россия, Москва, ул. Моховая, д. 11, стр. 10</p></bio><bio xml:lang="en"><p>Department of Microbiology, Virology and Immunology named after Academician A. A. Vorobyov</p><p>5а, Malyj Kazennyj lane, Moscow, 105064, Russia</p><p>11/10, Mokhovaya str., Moscow, 125009, Russia</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8192-7913</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сусова</surname><given-names>О. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Susova</surname><given-names>O. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115478, Россия, г. Москва, Каширское шоссе, д. 23</p></bio><bio xml:lang="en"><p>23, Kashirskoe highway, Moscow, 115478, Russia</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4125-7342</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Митрофанов</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Mitrofanov</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115478, Россия, г. Москва, Каширское шоссе, д. 23</p></bio><bio xml:lang="en"><p>23, Kashirskoe highway, Moscow, 115478, Russia</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0223-5738</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аммур</surname><given-names>Ю. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Ammour</surname><given-names>Yu. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Аммур Юлия Игоревна</p><p>105064, Россия, г. Москва, Малый Казенный переулок, д. 5а</p></bio><bio xml:lang="en"><p>Yulia I. Ammour</p><p>5а, Malyj Kazennyj lane, Moscow, 105064, Russia</p></bio><email xlink:type="simple">yulia.ammour@yahoo.fr</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт вакцин и сывороток им. И. И. Мечникова» (ФГБНУ НИИВС им. И. И. Мечникова)</institution></aff><aff xml:lang="en"><institution>Federal State Budgetary Scientific Institution "I. Mechnikov Research Institute of Vaccines and Sera"</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт вакцин и сывороток им. И. И. Мечникова» (ФГБНУ НИИВС им. И. И. Мечникова); ФГАОУ ВО Первый МГМУ им. И. М. Сеченова Минздрава России</institution></aff><aff xml:lang="en"><institution>Federal State Budgetary Scientific Institution "I. Mechnikov Research Institute of Vaccines and Sera"; I. M. Sechenov First MSMU of the Ministry of Health of the Russian Federation</institution></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр онкологии имени Н. Н. Блохина» Минздрава России (НМИЦ онкологии им. Н. Н. Блохина)</institution></aff><aff xml:lang="en"><institution>FSBI "National Medical Research Center of Oncology. N. N. Blokhin"</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>23</day><month>02</month><year>2022</year></pub-date><volume>11</volume><issue>1</issue><fpage>51</fpage><lpage>58</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Николаева Е.Ю., Щетинина Ю.Р., Шохин И.Е., Зверев В.В., Свитич О.А., Сусова О.Ю., Митрофанов А.А., Аммур Ю.И., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Николаева Е.Ю., Щетинина Ю.Р., Шохин И.Е., Зверев В.В., Свитич О.А., Сусова О.Ю., Митрофанов А.А., Аммур Ю.И.</copyright-holder><copyright-holder xml:lang="en">Nikolaeva E.Y., Shchetinina Y.R., Shokhin I.E., Zverev V.V., Svitich O.A., Susova O.Y., Mitrofanov A.A., Ammour Y.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.pharmjournal.ru/jour/article/view/1161">https://www.pharmjournal.ru/jour/article/view/1161</self-uri><abstract><sec><title>Введение</title><p>Введение. Одним из подходов в иммунотерапии солидных опухолей головного мозга является применение онколитических вирусов. Вакцинные штаммы вируса кори рассматривают в качестве перспективных кандидатов для терапии мезотелиомы, нейробластомы и мультиформной глиобластомы. Гиперэкспрессия рецептора CD46 и других белков на поверхности злокачественных клеток позволяет вирусу кори таргетно инфицировать и лизировать опухоль, индуцируя иммунный ответ. Однако широкая иммунизация населения и устойчивость новообразований к онколизу представляют трудности в клинической практике.</p></sec><sec><title>Текст</title><p>Текст. В настоящем обзоре обсуждаются подходы к модификации генома вируса кори с целью повысить таргетность виротерапии, преодолеть существующий иммунитет и усилить онколитический эффект. Показано, что экспрессия провоспалительных цитокинов на вирусных частицах приводит к регрессии опухоли у мышей и запускает Т-клеточный ответ. Для преодоления вирус-нейтрализирующих антител применяются подходы по экранированию вирусных частиц, использованию клеток-носителей и изменению эпитопа белка, обеспечивающего проникновение вируса в клетку. Кроме того, вставка репортерных генов позволяет отслеживать инфицирование таргентных клеток in vivo. Комбинация с новейшими методами иммунотерапии, такими как ингибиторы иммунных контрольных точек, демонстрирует синергизм эффектов, что позволяет рассчитывать на успешное применение сочетанных подходов в терапии рефрактерных опухолей.</p></sec><sec><title>Заключение</title><p>Заключение. Аттенуированные штаммы вируса кори представляют собой удобную и безопасную платформу для иммунотерапии опухолей головного мозга.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Oncolytic virotherapy is one of the approaches in immunotherapy of solid brain tumors. Measles virus vaccine strains are prospective agents for the therapy of cancers such as neuroblastoma, mesothelioma, and glioblastoma multiforme. The hyperexpression of the CD46 and other receptors on the surface of malignant cells allows the measles virus to infect and lyse the tumor, thus inducing an immune response. However, widespread immunization of the population and the resistance of neoplasms to oncolysis present difficulties in clinical practice.</p></sec><sec><title>Text</title><p>Text. This review covers approaches to modifying the measles virus genome in order to increase specificity of virotherapy, overcome existing immunity, and enhance the oncolytic effect. It was shown that expression of proinflammatory cytokines on viral particles leads to tumor regression in mice and triggers a T-cell response. Several approaches have been used to overcome virus-neutralizing antibodies: shielding viral particles, using host cells, and altering the epitope of the protein that enables entry of the virus into the cell. Furthermore, the insertion of reporter genes allows the infection of target cells to be monitored in vivo. A combination with the latest immunotherapies, such as immune checkpoint inhibitors, demonstrates synergistic effects, which suggests the successful use of combined approaches in the therapy of refractory tumors.</p></sec><sec><title>Conclusion</title><p>Conclusion. Measles virus attenuated strains appear to be an easy-to-modify and reliable platform for the therapy of solid brain tumors.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>онколитические вирусы</kwd><kwd>вирус кори</kwd><kwd>иммунотерапия</kwd><kwd>рецептор CD46</kwd><kwd>виротерапия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>oncolytic viruses</kwd><kwd>measles virus</kwd><kwd>immunotherapy</kwd><kwd>CD46 receptor</kwd><kwd>virotherapy</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Lichty B. D., Breitbach C. J., Stojdl D. F., Bell J. C. Going viral with cancer immunotherapy. Nat Rev Cancer. 2014;14(8):559–567. DOI: 10.1038/nrc3770.</mixed-citation><mixed-citation xml:lang="en">Lichty B. D., Breitbach C. J., Stojdl D. F., Bell J. C. Going viral with cancer immunotherapy. Nat Rev Cancer. 2014;14(8):559–567. DOI: 10.1038/nrc3770.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Pidelaserra-Martí G., Engeland C. E. Mechanisms of measles virus oncolytic immunotherapy. Cytokine &amp; Growth Factor Reviews. 2020;56:28–38. DOI: 10.1016/j.cytogfr.2020.07.009.</mixed-citation><mixed-citation xml:lang="en">Pidelaserra-Martí G., Engeland C. E. Mechanisms of measles virus oncolytic immunotherapy. Cytokine &amp; Growth Factor Reviews. 2020;56:28–38. DOI: 10.1016/j.cytogfr.2020.07.009.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Tribe A. K. W., McConnell M. J., Teesdale-Spittle P. H. The Big Picture of Glioblastoma Malignancy: A Meta-Analysis of Glioblastoma Proteomics to Identify Altered Biological Pathways. ACS Omega. 2021;6(38):24535–24544. DOI: 10.1021/acsomega.1c02991.</mixed-citation><mixed-citation xml:lang="en">Tribe A. K. W., McConnell M. J., Teesdale-Spittle P. H. The Big Picture of Glioblastoma Malignancy: A Meta-Analysis of Glioblastoma Proteomics to Identify Altered Biological Pathways. ACS Omega. 2021;6(38):24535–24544. DOI: 10.1021/acsomega.1c02991.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Estevez-Ordonez D., Chagoya G., Salehani A., Atchley T. J., Laskay N. M. B., Parr M. S., Elsayed G. A., Mahavadi A. K., Rahm S. P., Friedman G. K., Markert J. M. Immunovirotherapy for the Treatment of Glioblastoma and Other Malignant Gliomas, Neurosurgery Clinics of North America. 2021;32(2):265–281. DOI: 10.1016/j.nec.2020.12.008.</mixed-citation><mixed-citation xml:lang="en">Estevez-Ordonez D., Chagoya G., Salehani A., Atchley T. J., Laskay N. M. B., Parr M. S., Elsayed G. A., Mahavadi A. K., Rahm S. P., Friedman G. K., Markert J. M. Immunovirotherapy for the Treatment of Glioblastoma and Other Malignant Gliomas, Neurosurgery Clinics of North America. 2021;32(2):265–281. DOI: 10.1016/j.nec.2020.12.008.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Msaouel P., Opyrchal M., Dispenzieri A., Peng K. W., Federspiel M. J., Russell S. J., Galanis E. Clinical Trials with Oncolytic Measles Virus: Current Status and Future Prospects. Curr Cancer Drug Targets. 2018;18(2):177–187. DOI: 10.2174/1568009617666170222125035.</mixed-citation><mixed-citation xml:lang="en">Msaouel P., Opyrchal M., Dispenzieri A., Peng K. W., Federspiel M. J., Russell S. J., Galanis E. Clinical Trials with Oncolytic Measles Virus: Current Status and Future Prospects. Curr Cancer Drug Targets. 2018;18(2):177–187. DOI: 10.2174/1568009617666170222125035.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Allen C., Opyrchal M., Aderca I., Schroeder M. A., Sarkaria J. N., Domingo E., Federspiel M. J., Galanis E. Oncolytic measles virus strains have significant antitumor activity against glioma stem cells. Gene Ther. 2013;20(4):444–449. DOI: 10.1038/gt.2012.62.</mixed-citation><mixed-citation xml:lang="en">Allen C., Opyrchal M., Aderca I., Schroeder M. A., Sarkaria J. N., Domingo E., Federspiel M. J., Galanis E. Oncolytic measles virus strains have significant antitumor activity against glioma stem cells. Gene Ther. 2013;20(4):444–449. DOI: 10.1038/gt.2012.62.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Lin L. T., Richardson C. D. The host cell receptors for measles virus and their interaction with the viral Hemagglutinin (H) Protein. Viruses. 2016;8(9):250. DOI: 10.3390/v8090250.</mixed-citation><mixed-citation xml:lang="en">Lin L. T., Richardson C. D. The host cell receptors for measles virus and their interaction with the viral Hemagglutinin (H) Protein. Viruses. 2016;8(9):250. DOI: 10.3390/v8090250.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Ammour Y., Ryabaya O., Shchetinina Y., Prokofeva E., Gavrilova M., Khochenkov D., Vorobyev D., Faizuloev E., Shohin I., Zverev V. V., Svitich O., Nasedkina T. The Susceptibility of Human Melanoma Cells to Infection with the Leningrad-16 Vaccine Strain of Measles Virus. Viruses. 2020;12(2):173. DOI: 10.3390/v12020173.</mixed-citation><mixed-citation xml:lang="en">Ammour Y., Ryabaya O., Shchetinina Y., Prokofeva E., Gavrilova M., Khochenkov D., Vorobyev D., Faizuloev E., Shohin I., Zverev V. V., Svitich O., Nasedkina T. The Susceptibility of Human Melanoma Cells to Infection with the Leningrad-16 Vaccine Strain of Measles Virus. Viruses. 2020;12(2):173. DOI: 10.3390/v12020173.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Stavrakaki E., Dirven C. M. F., Lamfers M. L. M. Personalizing Oncolytic Virotherapy for Glioblastoma: In Search of Biomarkers for Response. Cancers. 2021;13(4):614. DOI: 10.3390/cancers13040614.</mixed-citation><mixed-citation xml:lang="en">Stavrakaki E., Dirven C. M. F., Lamfers M. L. M. Personalizing Oncolytic Virotherapy for Glioblastoma: In Search of Biomarkers for Response. Cancers. 2021;13(4):614. DOI: 10.3390/cancers13040614.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Aref S., Castleton A. Z., Bailey K., Burt R., Dey A., Leongamornlert D., Mitchell R. J., Okasha D., Fielding A. K. Type 1 Interferon Responses Underlie Tumor-Selective Replication of Oncolytic Measles Virus. Mol Ther. 2020;28(4):1043–1055. DOI: 10.1016/j.ymthe.2020.01.027.</mixed-citation><mixed-citation xml:lang="en">Aref S., Castleton A. Z., Bailey K., Burt R., Dey A., Leongamornlert D., Mitchell R. J., Okasha D., Fielding A. K. Type 1 Interferon Responses Underlie Tumor-Selective Replication of Oncolytic Measles Virus. Mol Ther. 2020;28(4):1043–1055. DOI: 10.1016/j.ymthe.2020.01.027.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Kurokawa C., Iankov I. D., Anderson S. K., Aderca I., Leontovich A. A., Maurer M. J., Oberg A. L., Schroeder M. A., Giannini C., Greiner S. M., Becker M. A., Thompson E. A., Haluska P., Jentoft M. E., Parney I. F., Weroha S. J., Jen J., Sarkaria J. N., Galanis E. Constitutive interferon pathway activation in tumors as an efficacy determinant following oncolytic virotherapy. J Natl Cancer Inst. 2018;110(10):1123–1132. DOI: 10.1093/jnci/djy033.</mixed-citation><mixed-citation xml:lang="en">Kurokawa C., Iankov I. D., Anderson S. K., Aderca I., Leontovich A. A., Maurer M. J., Oberg A. L., Schroeder M. A., Giannini C., Greiner S. M., Becker M. A., Thompson E. A., Haluska P., Jentoft M. E., Parney I. F., Weroha S. J., Jen J., Sarkaria J. N., Galanis E. Constitutive interferon pathway activation in tumors as an efficacy determinant following oncolytic virotherapy. J Natl Cancer Inst. 2018;110(10):1123–1132. DOI: 10.1093/jnci/djy033.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Radecke F., Spielhofer P., Schneider H., Kaelin K., Huber M., Dotsch C., Christiansen G., Billeter M. A. Rescue of measles viruses from cloned DNA. EMBO J. 1995,14(23):5773–5784. DOI: 10.1002/j.1460-2075.1995.tb00266.x.</mixed-citation><mixed-citation xml:lang="en">Radecke F., Spielhofer P., Schneider H., Kaelin K., Huber M., Dotsch C., Christiansen G., Billeter M. A. Rescue of measles viruses from cloned DNA. EMBO J. 1995,14(23):5773–5784. DOI: 10.1002/j.1460-2075.1995.tb00266.x.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Heidmeier S., Hanauer J. R. H., Friedrich K., Prufer S., Schneider I. C., Buchholz C. J., Cichutek K., Muhlebach M. D. A single amino acid substitution in the measles virus F2 protein reciprocally modulates membrane fusion activity in pathogenic and oncolytic strains. Virus Res. 2014;180:43–48. DOI: 10.1016/j.virusres.2013.12.016.</mixed-citation><mixed-citation xml:lang="en">Heidmeier S., Hanauer J. R. H., Friedrich K., Prufer S., Schneider I. C., Buchholz C. J., Cichutek K., Muhlebach M. D. A single amino acid substitution in the measles virus F2 protein reciprocally modulates membrane fusion activity in pathogenic and oncolytic strains. Virus Res. 2014;180:43–48. DOI: 10.1016/j.virusres.2013.12.016.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Haralambieva I., Iankov I., Hasegawa K., Harvey M., Russell S. J., Peng K.-W. Engineering oncolytic measles virus to circumvent the intracellular innate immune response. Mol Ther. 2007;15(3):588–597. DOI: 10.1038/SJ.MT.6300076.</mixed-citation><mixed-citation xml:lang="en">Haralambieva I., Iankov I., Hasegawa K., Harvey M., Russell S. J., Peng K.-W. Engineering oncolytic measles virus to circumvent the intracellular innate immune response. Mol Ther. 2007;15(3):588–597. DOI: 10.1038/SJ.MT.6300076.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Billeter M. A., Naim H. Y., Udem S. A. Reverse genetics of measles virus and resulting multivalent recombinant vaccines: applications of recombinant measles viruses. Curr Top Microbiol Immunol. 2009;329:129–162. DOI: 10.1007/978-3-540-70523-9_7.</mixed-citation><mixed-citation xml:lang="en">Billeter M. A., Naim H. Y., Udem S. A. Reverse genetics of measles virus and resulting multivalent recombinant vaccines: applications of recombinant measles viruses. Curr Top Microbiol Immunol. 2009;329:129–162. DOI: 10.1007/978-3-540-70523-9_7.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Aref S., Bailey K., Fielding A. Measles to the Rescue: A Review of Oncolytic Measles Virus. Viruses. 2016;8(10):294. DOI: 10.3390/v8100294.</mixed-citation><mixed-citation xml:lang="en">Aref S., Bailey K., Fielding A. Measles to the Rescue: A Review of Oncolytic Measles Virus. Viruses. 2016;8(10):294. DOI: 10.3390/v8100294.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Anderson B. D., Nakamura T., Russell S. J., Peng K.-W. High CD46 receptor density determines preferential killing of tumor cells by oncolytic measles virus. Cancer Res. 2004;64(14):4919–4926. DOI: 10.1158/0008-5472.CAN-04-0884.</mixed-citation><mixed-citation xml:lang="en">Anderson B. D., Nakamura T., Russell S. J., Peng K.-W. High CD46 receptor density determines preferential killing of tumor cells by oncolytic measles virus. Cancer Res. 2004;64(14):4919–4926. DOI: 10.1158/0008-5472.CAN-04-0884.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Muhlebach M. D. Measles virus in Cancer therapy. Current Opinion in Virology. 2020;41:85–97. DOI: 10.1016/j.coviro.2020.07.016.</mixed-citation><mixed-citation xml:lang="en">Muhlebach M. D. Measles virus in Cancer therapy. Current Opinion in Virology. 2020;41:85–97. DOI: 10.1016/j.coviro.2020.07.016.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Friedrich K., Hanauer J. R., Prufer S., Munch R. C., Volker I., Filippis C., Jost C., Hanschmann K.-M., Cattaneo R., Peng K.-W., Pluckthun A., Buchholz C. J., Cichutek K., Muhlebach M. D. DARPin-targeting of measles virus: unique bispecificity, effective oncolysis, and enhanced safety. Mol Ther. 2013;21(4):849–859. DOI: 10.1038/mt.2013.16.</mixed-citation><mixed-citation xml:lang="en">Friedrich K., Hanauer J. R., Prufer S., Munch R. C., Volker I., Filippis C., Jost C., Hanschmann K.-M., Cattaneo R., Peng K.-W., Pluckthun A., Buchholz C. J., Cichutek K., Muhlebach M. D. DARPin-targeting of measles virus: unique bispecificity, effective oncolysis, and enhanced safety. Mol Ther. 2013;21(4):849–859. DOI: 10.1038/mt.2013.16.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Hammond A. L., Plemper R. K., Zhang J., Schneider U., Russell S. J., Cattaneo R. Single-chain antibody displayed on a recombinant measles virus confers entry through the tumor-associated carcinoembryonic antigen. J Virol. 2001;75(5):2087–2096. DOI: 10.1128/JVI.75.5.2087-2096.2001.</mixed-citation><mixed-citation xml:lang="en">Hammond A. L., Plemper R. K., Zhang J., Schneider U., Russell S. J., Cattaneo R. Single-chain antibody displayed on a recombinant measles virus confers entry through the tumor-associated carcinoembryonic antigen. J Virol. 2001;75(5):2087–2096. DOI: 10.1128/JVI.75.5.2087-2096.2001.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Peng K.-W., Holler P. D., Orr B. A., Kranz D. M., Russell S. J. Targeting virus entry and membrane fusion through specific peptide/MHC complexes using a high-affinity T-cell receptor. Gene Ther. 2004;11(15):1234–1239. DOI: 10.1038/sj.gt.3302286.</mixed-citation><mixed-citation xml:lang="en">Peng K.-W., Holler P. D., Orr B. A., Kranz D. M., Russell S. J. Targeting virus entry and membrane fusion through specific peptide/MHC complexes using a high-affinity T-cell receptor. Gene Ther. 2004;11(15):1234–1239. DOI: 10.1038/sj.gt.3302286.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Lal S., Raffel C. Using cystine knot proteins as a novel approach to retarget oncolytic measles virus. Mol Ther Oncolytics. 2017;7:57–66. DOI: 10.1016/j.omto.2017.09.005.</mixed-citation><mixed-citation xml:lang="en">Lal S., Raffel C. Using cystine knot proteins as a novel approach to retarget oncolytic measles virus. Mol Ther Oncolytics. 2017;7:57–66. DOI: 10.1016/j.omto.2017.09.005.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Hanauer J. R., Gottschlich L., Riehl D., Rusch T., Koch V., Friedrich K., Hutzler S., Prufer S., Friedel T., Hanschmann K.-M., Munch R. C., Jost C., Pluckthun A., Cichutek K., Buchholz C. J., Muhlebach M. D. Enhanced lysis by bispecific oncolytic measles viruses simultaneously using HER2/neu or EpCAM as target receptors. Mol Ther Oncolytics. 2016;3:16003. DOI: 10.1038/mto.2016.3.</mixed-citation><mixed-citation xml:lang="en">Hanauer J. R., Gottschlich L., Riehl D., Rusch T., Koch V., Friedrich K., Hutzler S., Prufer S., Friedel T., Hanschmann K.-M., Munch R. C., Jost C., Pluckthun A., Cichutek K., Buchholz C. J., Muhlebach M. D. Enhanced lysis by bispecific oncolytic measles viruses simultaneously using HER2/neu or EpCAM as target receptors. Mol Ther Oncolytics. 2016;3:16003. DOI: 10.1038/mto.2016.3.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Maisner A., Mrkic B., Herrler G., Moll M., Billeter M. A., Cattaneo R., Klenk H. D. Recombinant measles virus requiring an exogenous protease for activation of infectivity. J Gen Virol. 2000;81(Pt 2):441–449. DOI: 10.1099/0022-1317-81-2-441.</mixed-citation><mixed-citation xml:lang="en">Maisner A., Mrkic B., Herrler G., Moll M., Billeter M. A., Cattaneo R., Klenk H. D. Recombinant measles virus requiring an exogenous protease for activation of infectivity. J Gen Virol. 2000;81(Pt 2):441–449. DOI: 10.1099/0022-1317-81-2-441.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Leber M. F., Baertsch M.-A., Anker S. C., Henkel L., Singh H. M., Bossow S., Engeland C. E., Barkley R., Hoyler B., Albert J., Springfeld C., Jager D., von Kalle C., Ungerechts G. Enhanced control of oncolytic measles virus using MicroRNA target sites. Mol Ther Oncolytics. 2018;9:30–40. DOI: 10.1016/j.omto.2018.04.002.</mixed-citation><mixed-citation xml:lang="en">Leber M. F., Baertsch M.-A., Anker S. C., Henkel L., Singh H. M., Bossow S., Engeland C. E., Barkley R., Hoyler B., Albert J., Springfeld C., Jager D., von Kalle C., Ungerechts G. Enhanced control of oncolytic measles virus using MicroRNA target sites. Mol Ther Oncolytics. 2018;9:30–40. DOI: 10.1016/j.omto.2018.04.002.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Grossardt C., Engeland C. E., Bossow S., Halama N., Zaoui K., Leber M. F., Springfeld C., Jaeger D., von Kalle C., Ungerechts G. Granulocyte-macrophage colony-stimulating factor-armed oncolytic measles virus is an effective therapeutic cancer vaccine. Hum Gene Ther. 2013;24(7):644–654. DOI: 10.1089/hum.2012.205.</mixed-citation><mixed-citation xml:lang="en">Grossardt C., Engeland C. E., Bossow S., Halama N., Zaoui K., Leber M. F., Springfeld C., Jaeger D., von Kalle C., Ungerechts G. Granulocyte-macrophage colony-stimulating factor-armed oncolytic measles virus is an effective therapeutic cancer vaccine. Hum Gene Ther. 2013;24(7):644–654. DOI: 10.1089/hum.2012.205.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Achard C., Guillerme J.-B., Bruni D., Boisgerault N., Combredet C., Tangy F., Jouvenet N., Gregoire M., Fonteneau J.-F. Oncolytic measles virus induces tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-mediated cytotoxicity by human myeloid and plasmacytoid dendritic cells. Oncoimmunology. 2016;6(1):e1261240. DOI: 10.1080/2162402X.2016.1261240.</mixed-citation><mixed-citation xml:lang="en">Achard C., Guillerme J.-B., Bruni D., Boisgerault N., Combredet C., Tangy F., Jouvenet N., Gregoire M., Fonteneau J.-F. Oncolytic measles virus induces tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-mediated cytotoxicity by human myeloid and plasmacytoid dendritic cells. Oncoimmunology. 2016;6(1):e1261240. DOI: 10.1080/2162402X.2016.1261240.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Klose C., Berchtold S., Schmidt M., Beil J., Smirnow I., Venturelli S., Burkard M., Handgretinger R., Lauer U. M. Biological treatment of pediatric sarcomas by combined virotherapy and NK cell therapy. BMC Cancer. 2019;19(1):1172. DOI: 10.1186/s12885-019-6387-5.</mixed-citation><mixed-citation xml:lang="en">Klose C., Berchtold S., Schmidt M., Beil J., Smirnow I., Venturelli S., Burkard M., Handgretinger R., Lauer U. M. Biological treatment of pediatric sarcomas by combined virotherapy and NK cell therapy. BMC Cancer. 2019;19(1):1172. DOI: 10.1186/s12885-019-6387-5.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Gauvrit A., Brandler S., Sapede-Peroz C., Boisgerault N., Tangy F., Gregoire M. Measles virus induces oncolysis of mesothelioma cells and allows dendritic cells to cross-prime tumor-specific CD8 response. Cancer Res. 2008;68(12):4882–4892. DOI: 10.1158/0008-5472.CAN-07-6265.</mixed-citation><mixed-citation xml:lang="en">Gauvrit A., Brandler S., Sapede-Peroz C., Boisgerault N., Tangy F., Gregoire M. Measles virus induces oncolysis of mesothelioma cells and allows dendritic cells to cross-prime tumor-specific CD8 response. Cancer Res. 2008;68(12):4882–4892. DOI: 10.1158/0008-5472.CAN-07-6265.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Muhlebach M. D. Vaccine platform recombinant measles virus. Virus Genes. 2017;53(5):733–740. DOI: 10.1007/s11262-017-1486-3.</mixed-citation><mixed-citation xml:lang="en">Muhlebach M. D. Vaccine platform recombinant measles virus. Virus Genes. 2017;53(5):733–740. DOI: 10.1007/s11262-017-1486-3.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Pliquet E., Ruffie C., Escande M., Thalmensi J., Najburg V., Combredet C., Bestetti T., Julithe M., Liard C., Huet T., Wain-Hobson S., Tanguy F., Langlade-Demoyen P. Strong antigen-specific T-cell immunity induced by a recombinant human TERT measles virus vaccine and amplified by a DNA/ viral vector prime boost in IFNAR/CD46 mice. Cancer Immunol Immunother. 2019;68(4):533–544. DOI: 10.1007/s00262-018-2272-3.</mixed-citation><mixed-citation xml:lang="en">Pliquet E., Ruffie C., Escande M., Thalmensi J., Najburg V., Combredet C., Bestetti T., Julithe M., Liard C., Huet T., Wain-Hobson S., Tanguy F., Langlade-Demoyen P. Strong antigen-specific T-cell immunity induced by a recombinant human TERT measles virus vaccine and amplified by a DNA/ viral vector prime boost in IFNAR/CD46 mice. Cancer Immunol Immunother. 2019;68(4):533–544. DOI: 10.1007/s00262-018-2272-3.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Opyrchal M., Allen C., Iankov I., Aderca I., Schroeder M., Sarkaria J., Galanis E. Effective radiovirotherapy for malignant gliomas by using oncolytic measles virus strains encoding the sodium iodide symporter (MV-NIS). Hum Gene Ther. 2012;23(4):419–427. DOI: 10.1089/hum.2011.158.</mixed-citation><mixed-citation xml:lang="en">Opyrchal M., Allen C., Iankov I., Aderca I., Schroeder M., Sarkaria J., Galanis E. Effective radiovirotherapy for malignant gliomas by using oncolytic measles virus strains encoding the sodium iodide symporter (MV-NIS). Hum Gene Ther. 2012;23(4):419–427. DOI: 10.1089/hum.2011.158.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Paraskevakou G., Allen C., Nakamura T., Zollman P., James C. D., Peng K. W., Schroeder M., Russell S. J., Galanis E. Epidermal growth factor receptor (EGFR)-retargeted measles virus strains effectively target EGFR or EGFRvIII expressing gliomas. Mol Ther. 2007;15(4):677–686. DOI: 10.1038/sj.mt.6300105.</mixed-citation><mixed-citation xml:lang="en">Paraskevakou G., Allen C., Nakamura T., Zollman P., James C. D., Peng K. W., Schroeder M., Russell S. J., Galanis E. Epidermal growth factor receptor (EGFR)-retargeted measles virus strains effectively target EGFR or EGFRvIII expressing gliomas. Mol Ther. 2007;15(4):677–686. DOI: 10.1038/sj.mt.6300105.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Bach P., Abel T., Homann C., Gal Z., Braun G., Voelker I., Ball C. R., Johnston I. C. D., Lauer U. M., Herold-Mende C., Mühlebach M. D., Glimm H., Buchholz C. J. Specific elimination of CD133⁺ tumor cells with targeted oncolytic measles virus. Cancer Res. 2013;73(2):865–874. DOI: 10.1158/0008-5472.CAN-12-2221.</mixed-citation><mixed-citation xml:lang="en">Bach P., Abel T., Homann C., Gal Z., Braun G., Voelker I., Ball C. R., Johnston I. C. D., Lauer U. M., Herold-Mende C., Mühlebach M. D., Glimm H., Buchholz C. J. Specific elimination of CD133⁺ tumor cells with targeted oncolytic measles virus. Cancer Res. 2013;73(2):865–874. DOI: 10.1158/0008-5472.CAN-12-2221.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Kleinlützum D., Hanauer J. D. S., Muik A., Hanschmann K.-M., Kays S.-K., Ayala-Breton C., Peng K.-W., Mühlebach M. D., Abel T., Buchholz C. J. Enhancing the Oncolytic Activity of CD133-Targeted Measles Virus: Receptor Extension or Chimerism with Vesicular Stomatitis Virus Are Most Effective. Front Oncol. 2017;7:127. DOI: 10.3389/fonc.2017.00127.</mixed-citation><mixed-citation xml:lang="en">Kleinlützum D., Hanauer J. D. S., Muik A., Hanschmann K.-M., Kays S.-K., Ayala-Breton C., Peng K.-W., Mühlebach M. D., Abel T., Buchholz C. J. Enhancing the Oncolytic Activity of CD133-Targeted Measles Virus: Receptor Extension or Chimerism with Vesicular Stomatitis Virus Are Most Effective. Front Oncol. 2017;7:127. DOI: 10.3389/fonc.2017.00127.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Miest T. S., Yaiw K.-C., Frenzke M., Lampe J., Hudacek A. W., Springfeld C., von Messling V., Ungerechts G., Cattaneo R. Envelope-chimeric entry-targeted measles virus escapes neutralization and achieves oncolysis. Mol Ther. 2011;19(10):1813–1820. DOI: 10.1038/mt.2011.92.</mixed-citation><mixed-citation xml:lang="en">Miest T. S., Yaiw K.-C., Frenzke M., Lampe J., Hudacek A. W., Springfeld C., von Messling V., Ungerechts G., Cattaneo R. Envelope-chimeric entry-targeted measles virus escapes neutralization and achieves oncolysis. Mol Ther. 2011;19(10):1813–1820. DOI: 10.1038/mt.2011.92.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Nosaki K., Hamada K., Takashima Y., Sagara M., Matsumura Y., Miyamoto S., Hijikata Y., Okazaki T., Nakanishi Y., Tani K. A novel, polymer-coated oncolytic measles virus overcomes immune suppression and induces robust antitumor activity. Mol Ther Oncolytics. 2016;3:16022. DOI: 10.1038/mto.2016.22.</mixed-citation><mixed-citation xml:lang="en">Nosaki K., Hamada K., Takashima Y., Sagara M., Matsumura Y., Miyamoto S., Hijikata Y., Okazaki T., Nakanishi Y., Tani K. A novel, polymer-coated oncolytic measles virus overcomes immune suppression and induces robust antitumor activity. Mol Ther Oncolytics. 2016;3:16022. DOI: 10.1038/mto.2016.22.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Xia M., Luo D., Dong J., Zheng M., Meng G., Wu J., Wei J. Graphene oxide arms oncolytic measles virus for improved effectiveness of cancer therapy. J Exp Clin Cancer Res. 2019;38(1):408. DOI: 10.1186/s13046-019-1410-x.</mixed-citation><mixed-citation xml:lang="en">Xia M., Luo D., Dong J., Zheng M., Meng G., Wu J., Wei J. Graphene oxide arms oncolytic measles virus for improved effectiveness of cancer therapy. J Exp Clin Cancer Res. 2019;38(1):408. DOI: 10.1186/s13046-019-1410-x.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Ong H. T., Hasegawa K., Dietz A. B., Russell S. J., Peng K.-W. Evaluation of T cells as carriers for systemic measles virotherapy in the presence of antiviral antibodies. Gene Ther. 2007;14(4):324–333. DOI: 10.1038/sj.gt.3302880.</mixed-citation><mixed-citation xml:lang="en">Ong H. T., Hasegawa K., Dietz A. B., Russell S. J., Peng K.-W. Evaluation of T cells as carriers for systemic measles virotherapy in the presence of antiviral antibodies. Gene Ther. 2007;14(4):324–333. DOI: 10.1038/sj.gt.3302880.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Miest T. S., Frenzke M., Cattaneo R. Measles virus entry through the signaling lymphocyte activation molecule governs efficacy of mantle cell lymphoma radiovirotherapy. Mol Ther. 2013;21(11):2019–2031. DOI: 10.1038/mt.2013.171.</mixed-citation><mixed-citation xml:lang="en">Miest T. S., Frenzke M., Cattaneo R. Measles virus entry through the signaling lymphocyte activation molecule governs efficacy of mantle cell lymphoma radiovirotherapy. Mol Ther. 2013;21(11):2019–2031. DOI: 10.1038/mt.2013.171.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Prins R. M., Wang X., Soto H., Young E., Lisiero D. N., Fong B., Everson R., Yong W. H., Lai A., Li G., Cloughesy T. F., Liau L. M. Comparison of glioma-associated antigen peptide-loaded versus autologous tumor lysate-loaded dendritic cell vaccination in malignant glioma patients. J Immunother. 2013;36(2):152–157. DOI: 10.1097/CJI.0b013e3182811ae4.</mixed-citation><mixed-citation xml:lang="en">Prins R. M., Wang X., Soto H., Young E., Lisiero D. N., Fong B., Everson R., Yong W. H., Lai A., Li G., Cloughesy T. F., Liau L. M. Comparison of glioma-associated antigen peptide-loaded versus autologous tumor lysate-loaded dendritic cell vaccination in malignant glioma patients. J Immunother. 2013;36(2):152–157. DOI: 10.1097/CJI.0b013e3182811ae4.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Steinman R. M. Decisions about dendritic cells: past, present, and future. Annu Rev Immunol. 2012;30:1–22. DOI: 10.1146/annurev-immunol-100311-102839.</mixed-citation><mixed-citation xml:lang="en">Steinman R. M. Decisions about dendritic cells: past, present, and future. Annu Rev Immunol. 2012;30:1–22. DOI: 10.1146/annurev-immunol-100311-102839.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Hardcastle J., Mills L., Malo C. S., Jin F., Kurokawa C., Geekiyanage H., Schroeder M., Sarkaria J., Johnson A. J., Galanis E. Immunovirotherapy with measles virus strains in combination with anti-PD-1 antibody blockade enhances antitumor activity in glioblastoma treatment. Neuro-Oncology. 2017;19(4):493–502. DOI: 10.1093/neuonc/now179.</mixed-citation><mixed-citation xml:lang="en">Hardcastle J., Mills L., Malo C. S., Jin F., Kurokawa C., Geekiyanage H., Schroeder M., Sarkaria J., Johnson A. J., Galanis E. Immunovirotherapy with measles virus strains in combination with anti-PD-1 antibody blockade enhances antitumor activity in glioblastoma treatment. Neuro-Oncology. 2017;19(4):493–502. DOI: 10.1093/neuonc/now179.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Berghoff A. S., Kiesel B., Widhalm G., Rajky O., Ricken G., Wöhrer A., Dieckmann K., Filipits M., Brandstetter A., Weller M., Kurscheid S., Hegi M. E., Zielinski C. C., Marosi C., Hainfellner J. A., Preusser M., Wick W. Programmed death ligand 1 expression and tumor-infiltrating lymphocytes in glioblastoma. Neuro Oncol. 2015;17(8):1064–1075. DOI: 10.1093/neuonc/nou307.</mixed-citation><mixed-citation xml:lang="en">Berghoff A. S., Kiesel B., Widhalm G., Rajky O., Ricken G., Wöhrer A., Dieckmann K., Filipits M., Brandstetter A., Weller M., Kurscheid S., Hegi M. E., Zielinski C. C., Marosi C., Hainfellner J. A., Preusser M., Wick W. Programmed death ligand 1 expression and tumor-infiltrating lymphocytes in glioblastoma. Neuro Oncol. 2015;17(8):1064–1075. DOI: 10.1093/neuonc/nou307.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Nduom E. K., Wei J., Yaghi N. K., Huang N., Kong L. Y., Gabrusiewicz K., Ling X., Zhou S., Ivan C., Chen J. Q., Burks J. K., Fuller G. N., Calin G. A., Conrad C. A., Creasy C., Ritthipichai K., Radvanyi L., Heimberger A. B. PD-L1 expression and prognostic impact in glioblastoma. Neuro Oncol. 2016;18(2):195–205. DOI: 10.1093/neuonc/nov172.</mixed-citation><mixed-citation xml:lang="en">Nduom E. K., Wei J., Yaghi N. K., Huang N., Kong L. Y., Gabrusiewicz K., Ling X., Zhou S., Ivan C., Chen J. Q., Burks J. K., Fuller G. N., Calin G. A., Conrad C. A., Creasy C., Ritthipichai K., Radvanyi L., Heimberger A. B. PD-L1 expression and prognostic impact in glioblastoma. Neuro Oncol. 2016;18(2):195–205. DOI: 10.1093/neuonc/nov172.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Bloch O., Crane C. A., Kaur R., Safaee M., Rutkowski M. J., Parsa A. T. Gliomas promote immunosuppression through induction of B7-H1 expression in tumor-associated macrophages. Clin Cancer Res. 2013;19(12):3165–3175. DOI: 10.1158/1078-0432.CCR-12-3314.</mixed-citation><mixed-citation xml:lang="en">Bloch O., Crane C. A., Kaur R., Safaee M., Rutkowski M. J., Parsa A. T. Gliomas promote immunosuppression through induction of B7-H1 expression in tumor-associated macrophages. Clin Cancer Res. 2013;19(12):3165–3175. DOI: 10.1158/1078-0432.CCR-12-3314.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Engeland C. E., Grossardt C., Veinalde R., Bossow S., Lutz D., Kaufmann J. K., Shevchenko I., Umansky V., Nettelbeck D. M., Weichert W., Jager D., von Kall C., Ungerechts G. CTLA-4 and PD-L1 checkpoint blockade enhances oncolytic measles virus therapy. Mol Ther. 2014;22(11):1949–1959. DOI: 10.1038/mt.2014.160.</mixed-citation><mixed-citation xml:lang="en">Engeland C. E., Grossardt C., Veinalde R., Bossow S., Lutz D., Kaufmann J. K., Shevchenko I., Umansky V., Nettelbeck D. M., Weichert W., Jager D., von Kall C., Ungerechts G. CTLA-4 and PD-L1 checkpoint blockade enhances oncolytic measles virus therapy. Mol Ther. 2014;22(11):1949–1959. DOI: 10.1038/mt.2014.160.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Leber M. F., Neault S., Jirovec E., Barkley R., Said A., Bell J. C., Ungerechts G. Engineering and combining oncolytic measles virus for cancer therapy. Cytokine Growth Factor Rev. 2020;56:39–48. DOI: 10.1016/j.cytogfr.2020.07.005.</mixed-citation><mixed-citation xml:lang="en">Leber M. F., Neault S., Jirovec E., Barkley R., Said A., Bell J. C., Ungerechts G. Engineering and combining oncolytic measles virus for cancer therapy. Cytokine Growth Factor Rev. 2020;56:39–48. DOI: 10.1016/j.cytogfr.2020.07.005.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Klose C., Berchtold S., Schmidt M., Beil J., Smirnow I., Venturelli S., Burkard M., Handgretinger R., Lauer U.M. Biological treatment of pediatric sarcomas by combined virotherapy and NK cell therapy. BMC Cancer. 2019;19(1):1172. DOI: 10.1186/s12885-019-6387-5.</mixed-citation><mixed-citation xml:lang="en">Klose C., Berchtold S., Schmidt M., Beil J., Smirnow I., Venturelli S., Burkard M., Handgretinger R., Lauer U.M. Biological treatment of pediatric sarcomas by combined virotherapy and NK cell therapy. BMC Cancer. 2019;19(1):1172. DOI: 10.1186/s12885-019-6387-5.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Leung E. Y. L., McNeish I. A. Strategies to Optimise Oncolytic Viral Therapies: The Role of Natural Killer Cells. Viruses. 2021;13(8):1450. DOI: org/10.3390/v13081450.</mixed-citation><mixed-citation xml:lang="en">Leung E. Y. L., McNeish I. A. Strategies to Optimise Oncolytic Viral Therapies: The Role of Natural Killer Cells. Viruses. 2021;13(8):1450. DOI: org/10.3390/v13081450.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Backhaus P. S., Veinalde R., Hartmann L., Dunder J. E., Jeworowski L. M., Albert J., Hoyler B., Poth T., Jäger D., Ungerechts G., Engeland C. E. Immunological Effects and Viral Gene Expression Determine the Efficacy of Oncolytic Measles Vaccines Encoding IL-12 or IL-15 Agonists. Viruses. 2019;11(10):914. DOI: 10.3390/v11100914.</mixed-citation><mixed-citation xml:lang="en">Backhaus P. S., Veinalde R., Hartmann L., Dunder J. E., Jeworowski L. M., Albert J., Hoyler B., Poth T., Jäger D., Ungerechts G., Engeland C. E. Immunological Effects and Viral Gene Expression Determine the Efficacy of Oncolytic Measles Vaccines Encoding IL-12 or IL-15 Agonists. Viruses. 2019;11(10):914. DOI: 10.3390/v11100914.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
