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<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">veterinary</journal-id><journal-title-group><journal-title xml:lang="ru">Ветеринария сегодня</journal-title><trans-title-group xml:lang="en"><trans-title>Veterinary Science Today</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2304-196X</issn><issn pub-type="epub">2658-6959</issn><publisher><publisher-name>"Veinard"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29326/2304-196X-2026-15-2-123-130</article-id><article-id custom-type="elpub" pub-id-type="custom">veterinary-1011</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 | БОЛЕЗНИ ПТИЦ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS | AVIAN DISEASES</subject></subj-group></article-categories><title-group><article-title>Совершенствование иммунопрофилактики: потенциал и ограничения биотехнологических решений в борьбе с ньюкаслской болезнью</article-title><trans-title-group xml:lang="en"><trans-title>Improving immunoprophylaxis: potential and limitations of biotechnological solutions in Newcastle disease control</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-5673-1535</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Байрашев</surname><given-names>Т. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Bairashev</surname><given-names>T. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Байрашев Тимур Альбертович, аспирант, младший научный сотрудник лаборатории вирусных антропозоонозов</p><p>Научный городок-2, г. Казань, 420075, Республика Татарстан</p></bio><bio xml:lang="en"><p>Timur A. Bairashev, Postgraduate Student, Junior Researcher, Laboratory for Viral Anthropozoonoses</p><p>Nauchnyi gorodok-2, Kazan 420075, Republic of Tatarstan</p></bio><email xlink:type="simple">timurkin2011timur@mail.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/0000-0003-2650-6459</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Галеева</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Galeeva</surname><given-names>A. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Галеева Антонина Глебовна, канд. вет. наук, ведущий научный сотрудник лаборатории вирусных антропозоонозов</p><p>Научный городок-2, г. Казань, 420075, Республика Татарстан</p><p>ул. Сибирский тракт, 35, г. Казань, 420029, Республика Татарстан</p></bio><bio xml:lang="en"><p>Antonina G. Galeeva, Cand. Sci. (Veterinary Medicine), Leading Researcher, Laboratory for Viral Anthropozoonoses</p><p>Nauchnyi gorodok-2, Kazan 420075, Republic of Tatarstan</p><p>ul. Sibirskii Tract 35, Kazan 420029, Republic of Tatarstan</p></bio><email xlink:type="simple">antonina-95@yandex.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/0000-0001-8786-1310</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ефимова</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Efimova</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ефимова Марина Анатольевна, д-р биол. наук, ведущий научный сотрудник лаборатории вирусных антропозоонозов</p><p>Научный городок-2, г. Казань, 420075, Республика Татарстан</p><p>ул. Сибирский тракт, 35, г. Казань, 420029, Республика Татарстан</p></bio><bio xml:lang="en"><p>Marina A. Efimova, Dr. Sci. (Biology), Leading Researcher, Laboratory for Viral Anthropozoonoses</p><p>Nauchnyi gorodok-2, Kazan 420075, Republic of Tatarstan</p><p>ul. Sibirskii Tract 35, Kazan 420029, Republic of Tatarstan</p></bio><email xlink:type="simple">marina-2004r@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Федеральный центр токсикологической, радиационной и биологической безопасности» (ФГБНУ «ФЦТРБ-ВНИВИ»)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Center for Toxicological, Radiation and Biological Safety</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Федеральный центр токсикологической, радиационной и биологической безопасности» (ФГБНУ «ФЦТРБ-ВНИВИ»); ФГБОУ ВО «Казанский государственный аграрный университет», Институт «Казанская академия ветеринарной медицины им. Н. Э. Баумана»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Center for Toxicological, Radiation and Biological Safety; Kazan State Agrarian University, Kazan State Academy of Veterinary Medicine named after N. E. Bauman</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>21</day><month>06</month><year>2026</year></pub-date><volume>15</volume><issue>2</issue><fpage>123</fpage><lpage>130</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Байрашев Т.А., Галеева А.Г., Ефимова М.А., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Байрашев Т.А., Галеева А.Г., Ефимова М.А.</copyright-holder><copyright-holder xml:lang="en">Bairashev T.A., Galeeva A.G., Efimova M.A.</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://veterinary.arriah.ru/jour/article/view/1011">https://veterinary.arriah.ru/jour/article/view/1011</self-uri><abstract><sec><title>Введение</title><p>Введение. Ньюкаслская болезнь продолжает наносить значительный экономический ущерб мировому птицеводству, что диктует необходимость пересмотра традиционных стратегий вакцинации. Классические живые вакцины, несмотря на широкое применение, обладают рядом ограничений, включая интерференцию с материнскими антителами и неспособность полностью предотвратить выделение полевого вируса из-за несоответствия современным генотипам. Настоящая работа представляет собой аналитический обзор современного ландшафта генно-инженерных вакцин против ньюкаслской болезни. Систематизированы данные о ключевых технологических платформах: рекомбинантных векторных вакцинах, препаратах, созданных методами обратной генетики, а также субъединичных, VLP- и ДНК-вакцинах. Проведен сравнительный анализ иммуногенности, безопасности и удобства применения данных платформ; особое внимание уделено возможностям реализации стратегии DIVA. Показано, что, хотя векторные вакцины стали отраслевым стандартом, технологии обратной генетики обладают уникальным потенциалом для контроля вирусной изменчивости и снижения циркуляции вируса в стаде. В заключении обосновывается необходимость интеграции различных технологических подходов для создания эффективных программ элиминации заболевания.</p></sec><sec><title>Цель исследования</title><p>Цель исследования. Формирование объективной картины текущего состояния проблемы вакцинопрофилактики, что необходимо для определения дальнейших путей совершенствования стратегий биозащиты в промышленном птицеводстве.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Аналитическое исследование проводилось на базе отечественных и зарубежных научных публикаций, посвященных иммунопрофилактике ньюкаслской болезни.</p></sec><sec><title>Результаты</title><p>Результаты. Проведен анализ и обзор существующих вакцин против вируса ньюкаслской болезни, описаны их иммуногенность, способность преодолевать материнские антитела, совместимость со стратегией DIVA, контроль вирусовыделения, безопасность и технологичность применения, приведена историческая ремарка. Обоснована необходимость перехода от традиционных вакцин к генно-инженерным профилактическим препаратам.</p></sec><sec><title>Заключение</title><p>Заключение. Разработка и внедрение субъединичных и нуклеиновых вакцин являются важнейшими технологическими этапами в области иммунопрофилактики ньюкаслской болезни, которые позволят на практике применить стратегию элиминации вируса в стаде птиц.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Newcastle disease continues to inflict significant economic damage on the global poultry industry, dictating the need to revise traditional vaccina tion strategies. Classical live vaccines, despite their widespread use, have a number of limitations, including interference with maternal antibodies and inability to completely prevent the field virus shedding due mismatch with current genotypes. This paper constitutes an analytical review of the current landscape of genetically engineered vaccines against Newcastle disease. It systematizes the data on key technological platforms: recombinant vector vaccines, reverse genetics-based prod ucts, as well as subunit, VLP-, and DNA-vaccines. A comparative analysis of the immunogenicity, safety, and ease of use of these platforms is conducted; particular attention is paid to the possibilities of implementing the DIVA strategy. It is demonstrated that, although vector vaccines have become the industry standard, reverse genetics technologies offer unique potential for controlling viral variability and reducing virus circulation in flocks. The conclusion substantiates the need to integrate various technological approaches to create effective disease eradication programs.</p></sec><sec><title>Objective</title><p>Objective. Formation of an objective picture of the current state of the problem, which is necessary for determining further avenues for improving biosecurity strategies in commercial poultry farming.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. The analytical study was conducted on the basis of domestic and foreign scientific publications on Newcastle disease immunoprophylaxis</p></sec><sec><title>Results</title><p>Results. The existing vaccines against Newcastle disease virus have been analyzed and reviewed. Their immunogenicity, ability to overcome maternal antibodies, compatibility with the DIVA strategy, virus shedding control, safety and ease of use have been described. Historical background is also provided. The necessity of transitioning from traditional vaccines to genetically engineered prophylactic products is substantiated.</p></sec><sec><title>Conclusion</title><p>Conclusion. The development and implementation of subunit and nucleic acid vaccines are the most important evolutionary steps in the field of Newcastle disease immunoprophylaxis, thus enabling the implementation of the virus eradication strategy in poultry flocks.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>обзор</kwd><kwd>ньюкаслская болезнь</kwd><kwd>генно-инженерные вакцины</kwd><kwd>векторные вакцины</kwd><kwd>обратная генетика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>review</kwd><kwd>Newcastle disease</kwd><kwd>genetically engineered vaccines</kwd><kwd>vector vaccines</kwd><kwd>reverse genetics</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">Ariyama N., Tapia R., Godoy C., Agüero B., Valdés V., Berrios F., et al. Avian orthoavulavirus 1 (Newcastle disease virus) antibodies in five penguin species, Antarctic peninsula and Southern Patagonia. 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