<?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">biopreparat</journal-id><journal-title-group><journal-title xml:lang="ru">БИОпрепараты. Профилактика, диагностика, лечение</journal-title><trans-title-group xml:lang="en"><trans-title>Biological Products. Prevention, Diagnosis, Treatment</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2221-996X</issn><issn pub-type="epub">2619-1156</issn><publisher><publisher-name>Scientific Centre for Expert Evaluation of Medicinal Products</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.30895/2221-996X-2021-21-4-225-233</article-id><article-id custom-type="elpub" pub-id-type="custom">biopreparat-355</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Сравнительная характеристика существующих платформ для создания вакцин против опасных и особо опасных вирусных инфекций, обладающих пандемическим потенциалом</article-title><trans-title-group xml:lang="en"><trans-title>Comparative analysis of existing platforms for the development of vaccines against dangerous and extremely dangerous viral infections with pandemic potential</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0135-7258</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Онищенко</surname><given-names>Г. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Onishchenko</surname><given-names>G. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Онищенко Геннадий Григорьевич, доктор медицинских наук, профессор, академик РАН</p><p>Трубецкая ул., д. 8, стр. 2, Москва, 119991</p></bio><bio xml:lang="en"><p>Gennadiy G. Onishchenko, Dr. Sci. (Med.), Professor, Academician of RAS</p><p>8/2 Trubetskaya St., Moscow 119991</p></bio><email xlink:type="simple">48cnii@mil.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1817-0126</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сизикова</surname><given-names>Т. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Sizikova</surname><given-names>T. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сизикова Татьяна Евгеньевна, кандидат биологических наук</p><p>ул. Октябрьская, д. 11, Сергиев Посад-6, Московская область, 141306</p></bio><bio xml:lang="en"><p>Tatyana E. Sizikova, Cand. Sci. (Biol.)</p><p>11 Oktyabr’skaya St., Sergiev Posad-6, Moscow Region 141306</p></bio><email xlink:type="simple">48cnii@mil.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6552-4599</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лебедев</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Lebedev</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лебедев Виталий Николаевич, доктор биологических наук, профессор</p><p>ул. Октябрьская, д. 11, Сергиев Посад-6, Московская область, 141306</p></bio><bio xml:lang="en"><p>Vitaliy N. Lebedev, Dr. Sci. (Biol.), Professor</p><p>11 Oktyabr’skaya St., Sergiev Posad-6, Moscow Region 141306</p></bio><email xlink:type="simple">48cnii@mil.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6742-3919</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Борисевич</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Borisevich</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Борисевич Сергей Владимирович, доктор биологических наук, профессор, член-корреспондент РАН</p><p>ул. Октябрьская, д. 11, Сергиев Посад-6, Московская область, 141306</p></bio><bio xml:lang="en"><p>Sergey V. Borisevich, Dr. Sci. (Biol.), Professor, Corr. Member of RAS</p><p>11 Oktyabr’skaya St., Sergiev Posad-6, Moscow Region 141306</p></bio><email xlink:type="simple">48cnii@mil.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное автономное образовательное учреждение высшего образования «Первый Московский государственный медицинский университет им. И. М. Сеченова» (Сеченовский университет) Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I. M. Sechenov First Moscow State Medical University (Sechenov University)</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «48 Центральный научно-исследовательский институт» Министерства обороны Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>48 Central Scientific Research Institute</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>19</day><month>10</month><year>2021</year></pub-date><volume>21</volume><issue>4</issue><fpage>225</fpage><lpage>233</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Онищенко Г.Г., Сизикова Т.Е., Лебедев В.Н., Борисевич С.В., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Онищенко Г.Г., Сизикова Т.Е., Лебедев В.Н., Борисевич С.В.</copyright-holder><copyright-holder xml:lang="en">Onishchenko G.G., Sizikova T.E., Lebedev V.N., Borisevich S.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.biopreparations.ru/jour/article/view/355">https://www.biopreparations.ru/jour/article/view/355</self-uri><abstract><p>Спонтанное появление более вирулентных для человека штаммов возбудителей инфекционных заболеваний, способствующих трансмиссии патогенных микроорганизмов изменения окружающей среды, социально-экономические факторы, возрастание уровня контактов между различными регионами являются основными причинами возникновения новых инфекционных заболеваний, в том числе обладающих пандемическим потенциалом. Для успешной борьбы с пандемией необходимо проведение массовой вакцинации против соответствующей нозологической формы инфекции, направленной на активное формирование коллективного иммунитета, в основе которого лежит непрямая защита человеческой популяции в целом, при иммунизации определенной ее части. Обоснованный выбор платформы для разработки вакцины является важным звеном решения данной задачи. Цель работы — сравнительная характеристика платформ для создания вакцин (аттенуированных, инактивированных, субъединичных, векторных рекомбинантных вакцин, ДНК- и РНК-вакцин), предназначенных для проведения массовой иммунизации против опасных и особо опасных вирусных инфекций, обладающих пандемическим потенциалом. В качестве возможных возбудителей таких инфекций рассмотрены представители семейств Poxviridae, Orthomyxoviridae и Coronaviridae. Проведено сравнение платформ для создания вакцин по следующим показателям: возможность формирования полноценного иммунного ответа; защитная эффективность; время, необходимое для проведения разработки и испытания вакцин; возможность производства объемов вакцины, необходимых для проведения массовой иммунизации; возможные препятствия при использовании вакцин по целевому назначению. Предполагается, что в ближайшие десятилетия приоритетными вакцинными платформами для создания защитных препаратов против опасных и особо опасных вирусных инфекций с пандемическим потенциалом, независимо от таксономической принадлежности их возбудителей, станут ДНК- или РНК-вакцины.</p></abstract><trans-abstract xml:lang="en"><p>The main triggers of new infectious diseases, including those with pandemic potential, are: spontaneous emergence of infectious strains which are more virulent for humans and contribute to transmission of pathogenic microorganisms, environmental changes, social and economic factors, increased contact rates between different regions. A successful pandemic response requires mass immunisation against a specific disease, aimed at the development of herd immunity which is based on the concept of indirect protection of the whole of the population by immunising a part of it. A well-grounded choice of the vaccine platform is central to dealing with this problem. The aim of the study was to compare characteristics of vaccine platforms (attenuated, inactivated, subunit, recombinant vector, DNA, and RNA vaccines) intended for mass immunisation against dangerous and extremely dangerous viral infections with pandemic potential. The study focused on the members of Poxviridae, Orthomyxoviridae and Coronaviridae families as potential pathogens. The vaccine platforms were compared in terms of the following parameters: capability of producing a robust immune response; protective efficacy; time required for vaccine development and testing; ability to produce vaccine in volumes required for mass immunisation; potential obstacles associated with the intended use of the vaccine. It is expected that in the next few decades DNA and RNA vaccine platforms will be most widely used for development of products against dangerous and extremely dangerous viral infections with pandemic potential, regardless of taxonomic groups of pathogens.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>поксвирусы</kwd><kwd>ортомиксовирусы</kwd><kwd>коронавирусы</kwd><kwd>вирус SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>массовая иммунизация</kwd><kwd>инактивированные вакцины</kwd><kwd>субъединичные вакцины</kwd><kwd>векторные рекомбинантные вакцины</kwd><kwd>РНК-вакцины</kwd><kwd>ДНК-вакцины</kwd></kwd-group><kwd-group xml:lang="en"><kwd>poxviruses</kwd><kwd>orthomyxoviruses</kwd><kwd>coronaviruses</kwd><kwd>SARS-CoV-2 virus</kwd><kwd>COVID-19</kwd><kwd>mass immunisation</kwd><kwd>inactivated vaccines</kwd><kwd>subunit vaccines</kwd><kwd>recombinant vector vaccines</kwd><kwd>RNA vaccines</kwd><kwd>DNA vaccines</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование проводилось без спонсорской поддержки.</funding-statement><funding-statement xml:lang="en">The study was performed without external funding.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Львов ДК, Альховский СВ, Колобухина ЛВ, Бурцева ЕИ. Этиология эпидемической вспышки COVID-19 в г. Ухань (провинция Хубэй, Китайская Народная Республика), ассоциированной с вирусом 2019-nCoV (Nidivirales, Coronaviridae, Coronavirinae, Betacoronavirus, подрод Sarbecoronavirus): уроки эпидемии SARS-CoV. Вопросы вирусологии. 2020;65(1):6–15. https://doi.org/10.36233/0507-4088-2020-65-1-6-15</mixed-citation><mixed-citation xml:lang="en">Lvov DK, Alkhovsky SV, Kolobukhina LV, Burtseva EI. Etiology of epidemic outbreaks COVID-19 in Wuhan, Hubei province, Chinese People Republic associated with 2019-nCoV (Nidovirales, Coronaviridae, Coronavirinae, Betacoronavirus, Subgenus Sarbecovirus): lessons of SARS-CoV outbreak. Voprosy virusologii = Problems of Virology. 2020;65(1):6–15 (In Russ.) https://doi.org/10.36233/0507-4088-2020-65-1-6-15</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Taubenberger JK, Kash JC, Morens DM. The 1918 influenza pandemic: 100 years of questions answered and unanswered. Sci Transl Med. 2019;11(502);eaau5485. https://doi.org/10.1126/scitranslmed.aau5485</mixed-citation><mixed-citation xml:lang="en">Taubenberger JK, Kash JC, Morens DM. The 1918 influenza pandemic: 100 years of questions answered and unanswered. Sci Transl Med. 2019;11(502);eaau5485. https://doi.org/10.1126/scitranslmed.aau5485</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Ижуткин ВС, Семин ПН. Программная реализация математических моделей распространения эпидемий. Международный журнал экспериментального образования. 2015;(2-1):32–3.</mixed-citation><mixed-citation xml:lang="en">Izhutkin VS, Semin PN. Software implementation of mathematical models of the spread of epidemics. Mezhdunarodnyi zhurnal eksperimental’nogo obrazovaniya = International Journal of Experimental Education. 2015;(2-1):32–3 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Holme P, Masuda N. The basic reproductive number as a predictor for epidemic outbreaks in temporal networks. PloS One. 2015;10(3):e0120567. https://doi.org/10.1371/journal.pone.0120567</mixed-citation><mixed-citation xml:lang="en">Holme P, Masuda N. The basic reproductive number as a predictor for epidemic outbreaks in temporal networks. PloS One. 2015;10(3):e0120567. https://doi.org/10.1371/journal.pone.0120567</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Gouglas D, Christodoulou M, Plotkin SA, Hatchett R. CEPI: Driving progress toward epidemic preparedness and response. Epidemiol Rev. 2019;41(1):28–33. https://doi.org/10.1093/epirev/mxz012</mixed-citation><mixed-citation xml:lang="en">Gouglas D, Christodoulou M, Plotkin SA, Hatchett R. CEPI: Driving progress toward epidemic preparedness and response. Epidemiol Rev. 2019;41(1):28–33. https://doi.org/10.1093/epirev/mxz012</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Щелкунов СН, Щелкунова ГА. Нужно быть готовыми к возврату оспы. Вопросы вирусологии. 2019;64(5):206–14. https://doi.org/10.36233/0507-4088-2019-64-5-206-214</mixed-citation><mixed-citation xml:lang="en">Shchelkunov SN, Shchelkunova GA. We should be prepared to smallpox re-emergence. Voprosy virusologii = Problems of Virology, Russian journal. 2019;64(5):206–14 (In Russ.) . https://doi.org/10.36233/0507-4088-2019-64-5-206-214</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Iwasaki A, Omer SB. Why and how vaccines work. Cell. 2020;183(2):290–5. https://doi.org/10.1016/j.cell.2020.09.040</mixed-citation><mixed-citation xml:lang="en">Iwasaki A, Omer SB. Why and how vaccines work. Cell. 2020;183(2):290–5. https://doi.org/10.1016/j.cell.2020.09.040</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Calina D, Docea AO, Petrakis D, Egorov AM, Ishmukhame tov AA, Gabibov AG, et al. Towards effective COVID-19 vaccines: updates, perspectives and challenges (review). Int J Mol Med. 2020;46:3–16. https://doi.org/10.3892/ijmm.2020.4596</mixed-citation><mixed-citation xml:lang="en">Calina D, Docea AO, Petrakis D, Egorov AM, Ishmukhame tov AA, Gabibov AG, et al. Towards effective COVID-19 vaccines: updates, perspectives and challenges (review). Int J Mol Med. 2020;46:3–16. https://doi.org/10.3892/ijmm.2020.4596</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ройт А, Бростофф Дж, Мейл Д. Иммунология. Пер с англ. М.: Мир; 2000.</mixed-citation><mixed-citation xml:lang="en">Roit A, Brostoff J, Mail D. Immunology. Moscow: Mir; 2000 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Лашкевич ВА. История создания в 1959 г. живой вакцины из аттенуированных штаммов А. Сэбина и идея искоренения полиомиелита. Вопросы вирусологии. 2013;58(1):4–10.</mixed-citation><mixed-citation xml:lang="en">Lashkevich VA. History of development of the live poliomyelitis vaccine from Sabin attenuated strains in 1959 and idea of poliomyelitis eradication. Voprosy virusologii = Problems of Virology. 2013;58(1):4–10 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Behbehani AM. The smallpox story: life and death of an old disease. Microbiol Rev. 1983;47(4):455–509. https://doi.org/10.1128/mr.47.4.455-509.1983</mixed-citation><mixed-citation xml:lang="en">Behbehani AM. The smallpox story: life and death of an old disease. Microbiol Rev. 1983;47(4):455–509. https://doi.org/10.1128/mr.47.4.455-509.1983</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Ou X, Liu Y, Lei X, Li P, Mi D, Ren L, et al. Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV. Nat Commun. 2020;11:1620. https://doi.org/10.1038/s41467-020-15562-9</mixed-citation><mixed-citation xml:lang="en">Ou X, Liu Y, Lei X, Li P, Mi D, Ren L, et al. Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV. Nat Commun. 2020;11:1620. https://doi.org/10.1038/s41467-020-15562-9</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Coutard B, Valle C, de Lamballerie X, Canard B, Seidah NG, Decroly E. The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade. Antiviral Res. 2020;176:104742. https://doi.org/10.1016/j.antiviral.2020.104742</mixed-citation><mixed-citation xml:lang="en">Coutard B, Valle C, de Lamballerie X, Canard B, Seidah NG, Decroly E. The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade. Antiviral Res. 2020;176:104742. https://doi.org/10.1016/j.antiviral.2020.104742</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Wan Y, Shang J, Graham R, Baric RS, Li F. Receptor recognition by the novel coronavirus from Wuhan: an analysis based on decade-long structural studies of SARS coronavirus. J Virol. 2020;94(7):e00127-20. https://doi.org/10.1128/JVI.00127-20</mixed-citation><mixed-citation xml:lang="en">Wan Y, Shang J, Graham R, Baric RS, Li F. Receptor recognition by the novel coronavirus from Wuhan: an analysis based on decade-long structural studies of SARS coronavirus. J Virol. 2020;94(7):e00127-20. https://doi.org/10.1128/JVI.00127-20</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Tai W, He L, Zhang X, Pu J, Voronin D, Jiang S, et al. Characterization of the receptor-binding domain (RBD) of 2019 novel coronavirus: implication for development of RBD protein as a viral attachment inhibitor and vaccine. Cell Mol Immunol. 2020;17(6):613–20. https://doi.org/10.1038/s41423-020-0400-4</mixed-citation><mixed-citation xml:lang="en">Tai W, He L, Zhang X, Pu J, Voronin D, Jiang S, et al. Characterization of the receptor-binding domain (RBD) of 2019 novel coronavirus: implication for development of RBD protein as a viral attachment inhibitor and vaccine. Cell Mol Immunol. 2020;17(6):613–20. https://doi.org/10.1038/s41423-020-0400-4</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Masters PS. The molecular biology of coronaviruses. Adv Virus Res. 2006;66:193–292. https://doi.org/10.1016/S0065-3527(06)66005-3</mixed-citation><mixed-citation xml:lang="en">Masters PS. The molecular biology of coronaviruses. Adv Virus Res. 2006;66:193–292. https://doi.org/10.1016/S0065-3527(06)66005-3</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Khattari Z, Brotons G, Akkawi M, Arbely E, Arkin IT, Salditt T. SARS coronavirus E protein in phospholipid bilayers: an X-ray study. Biophys J. 2006;90(6):2038–50. https://doi.org/10.1529/biophysj.105.072892</mixed-citation><mixed-citation xml:lang="en">Khattari Z, Brotons G, Akkawi M, Arbely E, Arkin IT, Salditt T. SARS coronavirus E protein in phospholipid bilayers: an X-ray study. Biophys J. 2006;90(6):2038–50. https://doi.org/10.1529/biophysj.105.072892</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Kuo L, Hurst KR, Masters PS. Exceptional flexibility in the sequence requirements for coronavirus small envelope protein function. J Virol. 2007;81(5):2249–62. https://doi.org/10.1128/JVI.01577-06</mixed-citation><mixed-citation xml:lang="en">Kuo L, Hurst KR, Masters PS. Exceptional flexibility in the sequence requirements for coronavirus small envelope protein function. J Virol. 2007;81(5):2249–62. https://doi.org/10.1128/JVI.01577-06</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Forster P, Forster L, Renfrew C, Forster M. Phylogenetic network analysis of SARS-CoV-2 genomes. Proc Natl Acad Sci USA. 2020;117(17):9241–3. https://doi.org/10.1073/pnas.2004999117</mixed-citation><mixed-citation xml:lang="en">Forster P, Forster L, Renfrew C, Forster M. Phylogenetic network analysis of SARS-CoV-2 genomes. Proc Natl Acad Sci USA. 2020;117(17):9241–3. https://doi.org/10.1073/pnas.2004999117</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Siu YL, Teoh KT, Lo J, Chan CM, Kien F, Escriou N, et al. The M, E, and N structural proteins of the severe acute respiratory syndrome coronavirus are required for efficient assembly, trafficking, and release of virus-like particles. J Virol. 2008;82(22):11318–30. https://doi.org/10.1128/JVI.01052-08</mixed-citation><mixed-citation xml:lang="en">Siu YL, Teoh KT, Lo J, Chan CM, Kien F, Escriou N, et al. The M, E, and N structural proteins of the severe acute respiratory syndrome coronavirus are required for efficient assembly, trafficking, and release of virus-like particles. J Virol. 2008;82(22):11318–30. https://doi.org/10.1128/JVI.01052-08</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Fan K, Wei P, Feng Q, Chen S, Huang C, Ma L, et al. Biosynthesis, purification, and substrate specificity of severe acute respiratory syndrome coronavirus 3C-like proteinase. J Biol Chem. 2004;279(3):1637–42. https://doi.org/10.1074/jbc.M310875200</mixed-citation><mixed-citation xml:lang="en">Fan K, Wei P, Feng Q, Chen S, Huang C, Ma L, et al. Biosynthesis, purification, and substrate specificity of severe acute respiratory syndrome coronavirus 3C-like proteinase. J Biol Chem. 2004;279(3):1637–42. https://doi.org/10.1074/jbc.M310875200</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Calisher C, Carroll D, Colwell R, Corley RB, Daszak P, Drosten C, et al. Statement in support of the scientists, public health professionals, and medical professionals of China combatting COVID-19. Lancet. 2020;395(10226):е42–3. https://doi.org/10.1016/S0140-6736(20)30418-9</mixed-citation><mixed-citation xml:lang="en">Calisher C, Carroll D, Colwell R, Corley RB, Daszak P, Drosten C, et al. Statement in support of the scientists, public health professionals, and medical professionals of China combatting COVID-19. Lancet. 2020;395(10226):е42–3. https://doi.org/10.1016/S0140-6736(20)30418-9</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Khoury DS, Cromer D, Reynaldi A, Schlub TE, Wheatley AK, Juno JA, et al. Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection. Nat Med. 2021;27(7):1205–11. https://doi.org/10.1038/s41591-021-01377-8</mixed-citation><mixed-citation xml:lang="en">Khoury DS, Cromer D, Reynaldi A, Schlub TE, Wheatley AK, Juno JA, et al. Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection. Nat Med. 2021;27(7):1205–11. https://doi.org/10.1038/s41591-021-01377-8</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Heath PT, Galiza EP, Baxter DN, Boffito M, Browne D, Burns F, et al. Safety and efficacy of NVX-CoV2373 Covid-19 vaccine. N Engl J Med. 2021;385:1172–83. https://doi.org/10.1056/NEJMoa2107659</mixed-citation><mixed-citation xml:lang="en">Heath PT, Galiza EP, Baxter DN, Boffito M, Browne D, Burns F, et al. Safety and efficacy of NVX-CoV2373 Covid-19 vaccine. N Engl J Med. 2021;385:1172–83. https://doi.org/10.1056/NEJMoa2107659</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Callaway E, Mallapaty S. Novavax offers first evidence that COVID vaccines protect people against variants. Nature. 2021;590(7844):17. https://doi.org/10.1038/d41586-021-00268-9</mixed-citation><mixed-citation xml:lang="en">Callaway E, Mallapaty S. Novavax offers first evidence that COVID vaccines protect people against variants. Nature. 2021;590(7844):17. https://doi.org/10.1038/d41586-021-00268-9</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Pollet J, Chen WH, Strych U. Recombinant protein vaccines, a proven approach against coronavirus pandemics. Adv Drug Deliv Rev. 2021;170:71–82. https://doi.org/10.1016/j.addr.2021.01.001</mixed-citation><mixed-citation xml:lang="en">Pollet J, Chen WH, Strych U. Recombinant protein vaccines, a proven approach against coronavirus pandemics. Adv Drug Deliv Rev. 2021;170:71–82. https://doi.org/10.1016/j.addr.2021.01.001</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Kaur SP, Gupta V. COVID-19 vaccine: a comprehensive status report. Virus Res. 2020;288:198114. https://doi.org/10.1016/j.virusres.2020.198114</mixed-citation><mixed-citation xml:lang="en">Kaur SP, Gupta V. COVID-19 vaccine: a comprehensive status report. Virus Res. 2020;288:198114. https://doi.org/10.1016/j.virusres.2020.198114</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Callaway E. The race for coronavirus vaccines: a graphical guide. Nature. 2020;580: 576–7. https://doi.org/10.1038/d41586-020-01221-y</mixed-citation><mixed-citation xml:lang="en">Callaway E. The race for coronavirus vaccines: a graphical guide. Nature. 2020;580: 576–7. https://doi.org/10.1038/d41586-020-01221-y</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Bull JJ, Nuismer SL, Antia R. Recombinant vector vaccine evolution. PLoS Comput Biol. 2019;15(7):e1006857. https://doi.org/10.1371/journal.pcbi.1006857</mixed-citation><mixed-citation xml:lang="en">Bull JJ, Nuismer SL, Antia R. Recombinant vector vaccine evolution. PLoS Comput Biol. 2019;15(7):e1006857. https://doi.org/10.1371/journal.pcbi.1006857</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Triggle CR, Bansal D, Ding H, Islam MM, Farag EABA, Hadi HA, Sultan AA. A comprehensive review of viral characteristics, transmission, pathophysiology, immune response, and management of SARS-CoV-2 and COVID-19 as a basis for controlling the pandemic. Front Immunol. 2021;12:631139. https://doi.org/10.3389/fimmu.2021.631139</mixed-citation><mixed-citation xml:lang="en">Triggle CR, Bansal D, Ding H, Islam MM, Farag EABA, Hadi HA, Sultan AA. A comprehensive review of viral characteristics, transmission, pathophysiology, immune response, and management of SARS-CoV-2 and COVID-19 as a basis for controlling the pandemic. Front Immunol. 2021;12:631139. https://doi.org/10.3389/fimmu.2021.631139</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Volpers C, Kochanek S. Adenoviral vectors for gene transfer and therapy. J Gene Med. 2004;6(Suppl 1):S164–71. https://doi.org/10.1002/jgm.496</mixed-citation><mixed-citation xml:lang="en">Volpers C, Kochanek S. Adenoviral vectors for gene transfer and therapy. J Gene Med. 2004;6(Suppl 1):S164–71. https://doi.org/10.1002/jgm.496</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Tatsis N, Ertl HCJ. Adenoviruses as vaccine vectors. Mol Ther. 2004;10(4):616–29. https://doi.org/10.1016/j.ymthe.2004.07.013</mixed-citation><mixed-citation xml:lang="en">Tatsis N, Ertl HCJ. Adenoviruses as vaccine vectors. Mol Ther. 2004;10(4):616–29. https://doi.org/10.1016/j.ymthe.2004.07.013</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Afkhami S, Yao Y, Xing Z. Methods and clinical development of adenovirus-vectored vaccines against mucosal pathogens. Mol Ther Methods Clin Dev. 2016;3:16030. https://doi.org/10.1038/mtm.2016.30</mixed-citation><mixed-citation xml:lang="en">Afkhami S, Yao Y, Xing Z. Methods and clinical development of adenovirus-vectored vaccines against mucosal pathogens. Mol Ther Methods Clin Dev. 2016;3:16030. https://doi.org/10.1038/mtm.2016.30</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Logunov DY, Dolzhikova IV, Zubkova OV, Tukhvatulin AI, Shcheblyakov DV, Dzharullaeva AS, et al. Safety and immunogenicity of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine in two formulations: two open, non-randomised phase 1/2 studies from Russia. Lancet. 2020;396(10255):887–97. https://doi.org/10.1016/S0140-6736(20)31866-3</mixed-citation><mixed-citation xml:lang="en">Logunov DY, Dolzhikova IV, Zubkova OV, Tukhvatulin AI, Shcheblyakov DV, Dzharullaeva AS, et al. Safety and immunogenicity of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine in two formulations: two open, non-randomised phase 1/2 studies from Russia. Lancet. 2020;396(10255):887–97. https://doi.org/10.1016/S0140-6736(20)31866-3</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Должикова ИВ, Токарская ЕА, Джаруллаева АШ, Тухватулин АИ, Щебляков ДВ, Воронина ОЛ и др. Векторные вакцины против болезни, вызванной вирусом Эбола. Acta Naturae. 2017;9(3):4–12.</mixed-citation><mixed-citation xml:lang="en">Dolzhikova IV, Tokarskaya EA, Dzharullaeva AS, Tukhvatulin AI, Shcheblyakov DV, Voronina OL, et al. Virus-vectored Ebola vaccines. Acta Naturae. 2017;9(3):4–12 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Ковыршина АВ, Должикова ИВ, Гроусова ДМ, Балясин МВ, Ботиков АГ, Панина ЛВ и др. Комбинированная векторная вакцина для профилактики ближневосточного респираторного синдрома индуцирует формирование длительного протективного иммунного ответа к коронавирусу БВРС-КоВ. Иммунология. 2020;41(2):135–43. https://doi.org/10.33029/0206-4952-2020-41-2-135-143</mixed-citation><mixed-citation xml:lang="en">Kovyrshina AV, Dolzhikova IV, Grousova DM, Balyasin MV, Botikov AG, Panina LV, et al. A heterologous virus-vectored vaccine for prevention of Middle East respiratory syndrome induces long protective immune response against MERS-CoV. Immunologiya = Immunology. 2020;41(2):135–43 (In Russ.) https://doi.org/10.33029/0206-4952-2020-41-2-135-143</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Logunov DY, Dolzhikova IV, Shcheblyakov DV, Tukhvatulin AI, Zubkova OV, Dzharullaeva AS, et al. Safety and efficacy of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine: an interim analysis of a randomised controlled phase 3 trial in Russia. Lancet. 2021;397(10275):671–81. https://doi.org/10.1016/S0140-6736(21)00234-8</mixed-citation><mixed-citation xml:lang="en">Logunov DY, Dolzhikova IV, Shcheblyakov DV, Tukhvatulin AI, Zubkova OV, Dzharullaeva AS, et al. Safety and efficacy of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine: an interim analysis of a randomised controlled phase 3 trial in Russia. Lancet. 2021;397(10275):671–81. https://doi.org/10.1016/S0140-6736(21)00234-8</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Voysey M, Clemens SAC, Madhi SA, Weckx LY, Folegatti PM, Aley PK, et al. Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK. Lancet. 2021;397(10269):99–111. https://doi.org/10.1016/S0140-6736(20)32661-1</mixed-citation><mixed-citation xml:lang="en">Voysey M, Clemens SAC, Madhi SA, Weckx LY, Folegatti PM, Aley PK, et al. Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK. Lancet. 2021;397(10269):99–111. https://doi.org/10.1016/S0140-6736(20)32661-1</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Thompson MG, Burgess JL, Naleway AL, Tyner HL, Yoon SK, Meece J, et al. Interim estimates of vaccine effectiveness of BNT162b2 and mRNA-1273 COVID-19 vaccines in preventing SARS-CoV-2 infection among health care personnel, first responders, and other essential and frontline workers — eight U.S. Locations, December 2020–March 2021. MMWR Morb Mortal Wkly Rep 2021;70(13):495–500. https://doi.org/10.15585/mmwr.mm7013e3</mixed-citation><mixed-citation xml:lang="en">Thompson MG, Burgess JL, Naleway AL, Tyner HL, Yoon SK, Meece J, et al. Interim estimates of vaccine effectiveness of BNT162b2 and mRNA-1273 COVID-19 vaccines in preventing SARS-CoV-2 infection among health care personnel, first responders, and other essential and frontline workers — eight U.S. Locations, December 2020–March 2021. MMWR Morb Mortal Wkly Rep 2021;70(13):495–500. https://doi.org/10.15585/mmwr.mm7013e3</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Cui Z. DNA vaccine. Adv Genet. 2005;54:257–89. https://doi.org/10.1016/S0065-2660(05)54011-2</mixed-citation><mixed-citation xml:lang="en">Cui Z. DNA vaccine. Adv Genet. 2005;54:257–89. https://doi.org/10.1016/S0065-2660(05)54011-2</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Liu MA. A comparison of plasmid DNA and mRNA as vaccine technologies. Vaccines. 2019;7(2):37. https://doi.org/10.3390/vaccines7020037</mixed-citation><mixed-citation xml:lang="en">Liu MA. A comparison of plasmid DNA and mRNA as vaccine technologies. Vaccines. 2019;7(2):37. https://doi.org/10.3390/vaccines7020037</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>
