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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Infection and Immunity</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Infection and Immunity</journal-title><trans-title-group xml:lang="ru"><trans-title>Инфекция и иммунитет</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2220-7619</issn><issn publication-format="electronic">2313-7398</issn><publisher><publisher-name xml:lang="en">SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1855</article-id><article-id pub-id-type="doi">10.15789/2220-7619-ILV-1855</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Intra-laboratory validated “TigraTest® SARS-CoV-2” — test assessing release of interferon gamma in vitro to identify peripheral blood T-lymphocytes specifically responding against SARS-CoV-2 virus antigens</article-title><trans-title-group xml:lang="ru"><trans-title>Внутрилабораторная валидация «ТиграТест® SARS-CoV-2» — теста на высвобождение интерферона гамма in vitro для определения в крови Т-лимфоцитов, специфически отвечающих на антигены вируса SARS-CоV-2</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9058-1106</contrib-id><name-alternatives><name xml:lang="en"><surname>Lyagoskin</surname><given-names>Ivan V.</given-names></name><name xml:lang="ru"><surname>Лягоскин</surname><given-names>Иван Владимирович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD (Biology), Head of the Analytical Methods Division, Department of the Pharmaceutical Analysis</p></bio><bio xml:lang="ru"><p>к.б.н., руководитель отдела аналитических методов департамента фармацевтического анализа</p></bio><email>lyagoskin@ibcgenerium.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4132-5971</contrib-id><name-alternatives><name xml:lang="en"><surname>Kargopolova</surname><given-names>Pauline E.</given-names></name><name xml:lang="ru"><surname>Каргополова</surname><given-names>Полина Евгеньевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Analytical Chemist, Laboratory of Biological Methods, Analytical Methods Division, Department of the Pharmaceutical Analysis</p></bio><bio xml:lang="ru"><p>химик-аналитик лаборатории биологических методов отдела аналитических методов департамента фармацевтического анализа</p></bio><email>peignatieva@ibcgenerium.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8719-7795</contrib-id><name-alternatives><name xml:lang="en"><surname>Obyedkov</surname><given-names>Dmitry A.</given-names></name><name xml:lang="ru"><surname>Объедков</surname><given-names>Дмитрий Анатольевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Researcher, Laboratory of Biological Methods, Analytical Methods Division, Department of the Pharmaceutical Analysis</p></bio><bio xml:lang="ru"><p>научный сотрудник лаборатории биологических методов отдела аналитических методов департамента фармацевтического анализа</p></bio><email>daobedkov@generium.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7996-9321</contrib-id><name-alternatives><name xml:lang="en"><surname>Egorova</surname><given-names>Irina Yu.</given-names></name><name xml:lang="ru"><surname>Егорова</surname><given-names>Ирина Юрьевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, MD (Veterinary), Associate Professor, Head of the Group of Diagnostic Test-Systems, Division of Molecular Diagnostics, Department of the Pharmaceutical Analysis</p></bio><bio xml:lang="ru"><p>д.в.н., доцент, руководитель группы диагностических тест-систем отдела молекулярной диагностики департамента фармацевтического анализа</p></bio><email>iyegorova@generium.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6532-7835</contrib-id><name-alternatives><name xml:lang="en"><surname>Shukurov</surname><given-names>Rahim R.</given-names></name><name xml:lang="ru"><surname>Шукуров</surname><given-names>Рахим Рахманкулыевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD (Biology), Director of the Department of the Pharmaceutical Analysis</p></bio><bio xml:lang="ru"><p>к.б.н., директор департамента фармацевтического анализа</p></bio><email>Shukurov@ibcgenerium.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">JSC “GENERIUM”</institution></aff><aff><institution xml:lang="ru">АО «ГЕНЕРИУМ»</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2022-06-27" publication-format="electronic"><day>27</day><month>06</month><year>2022</year></pub-date><pub-date date-type="pub" iso-8601-date="2022-11-15" publication-format="electronic"><day>15</day><month>11</month><year>2022</year></pub-date><volume>12</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>701</fpage><lpage>713</lpage><history><date date-type="received" iso-8601-date="2021-12-28"><day>28</day><month>12</month><year>2021</year></date><date date-type="accepted" iso-8601-date="2022-06-02"><day>02</day><month>06</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Lyagoskin I.V., Kargopolova P.E., Obyedkov D.A., Egorova I.Y., Shukurov R.R.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Лягоскин И.В., Каргополова П.Е., Объедков Д.А., Егорова И.Ю., Шукуров Р.Р.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Lyagoskin I.V., Kargopolova P.E., Obyedkov D.A., Egorova I.Y., Shukurov R.R.</copyright-holder><copyright-holder xml:lang="ru">Лягоскин И.В., Каргополова П.Е., Объедков Д.А., Егорова И.Ю., Шукуров Р.Р.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://iimmun.ru/iimm/article/view/1855">https://iimmun.ru/iimm/article/view/1855</self-uri><abstract xml:lang="en"><p>SARS-CoV-2 (Severe acute respiratory syndrome coronavirus 2), also known as 2019-nCoV (2019-Novel Coronavirus) is a strain of coronavirus from the genus Betacoronavirus, discovered in China at the end of 2019 in patients with pneumonia. “Coronavirus infection COVID-19” (COrona VIrus Disease 2019) caused by coronavirus 2019 (COVID-19) has spread around the world at a very fast pace, with death toll exceeding more than 5.2 million people worldwide. Limited success in developing new drugs as well as use of existing drugs for the treatment of COVID-19 resulted in situation when the main prevention measures for a long time were based on testing and isolation of sick subjects, which started to reverse due to vaccination. Monitoring the formation of humoral and T-cell population immunity against the SARS-CoV-2 virus during the COVID-19 pandemic is a necessary element for epidemiological surveillance. ELISA-based methods are widely used to assess humoral immunity, and various test systems including ELISPOT (Enzyme-Linked ImmunoSpot) are used to analyze cellular immunity. The ELISPOT assay is a highly sensitive and specific method for quantifying individual cytokine-secreting T cells after being stimulated with a specific antigen. “TigraTest<sup>®</sup> SARS-CoV-2” Test assessing release of interferon gamma <italic>in vitro</italic> to detect peripheral blood T-lymphocytes that specifically respond to the SARS-CoV-2 virus antigens manufactured by GENERIUM JSC, is created on the ELISPOT platform. This study describes the procedure for laboratory validation of this test system to analyze the following parameters: specificity of antibody pair, effect of interfering substances, sensitivity and specificity, precision, stability of blood samples till isolation of target cells. The developed test system showed high diagnostic sensitivity and specificity. The specificity of TigraTest<sup>®</sup> SARS-CoV-2 was 100%, the sensitivity for subjects immunized with the Gam-COVID-Vac vaccine (Sputnik V) was 91.67%, and the sensitivity in convalescent COVID-19 patients was 95.45%. At the same time, the data variability both during within and between series comparison did not exceed 25%, whereas 24-hour storage of peripheral blood samples at (18–25)°С after blood collection followed by isolation of target cells did not affect the test results.</p></abstract><trans-abstract xml:lang="ru"><p>SARS-CoV-2 (Severe acute respiratory syndrome coronavirus 2), он же 2019-nCoV (2019-Novel Coronavirus) — вид коронавируса, из рода бетакоронавирусов <italic>(Betacoronavirus)</italic>, обнаруженный в конце 2019 г. у больных с пневмонией в Китае. «Коронавирусная инфекция COVID-19» (COrona VIrus Disease 2019 — «COVID-19»), вызванная коронавирусом 2019 (COVID-19), распространилась по миру очень быстрыми темпами и унесла уже более 5,2 млн жизней. Ограниченный успех в разработке новых лекарственных средств, а также использование существующих лекарственных препаратов для лечения COVID-19 привел к тому, что долгое время основными мерами профилактики были тестирование и изоляция заболевших, но в настоящий момент ситуацию в лучшую сторону меняет вакцинация. Проведение мониторинга формирования гуморального и Т-клеточного популяционного иммунитета к вирусу SARS-CoV-2 в условиях пандемии COVID-19 является необходимым элементом эпидемиологического надзора. Для оценки гуморального иммунитета широко применяют методы на основе ИФА, а для оценки клеточного иммунитета используют различные тест-системы, в том числе и на основе ELISPOT (Enzyme-Linked ImmunoSpot). Анализ ELISPOT — это высокочувствительный и специфичный метод определения количества отдельных Т-клеток, секретирующих цитокин, после стимуляции определенным антигеном. «ТиграТест<sup>®</sup> SARS-CoV-2» — тест на высвобождение интерферона гамма <italic>in vitro</italic> для определения в крови Т-лимфоцитов, специфически отвечающих на антигены вируса SARS-CoV-2, — производства АО «ГЕНЕРИУМ», изготовлен на платформе ELISPOT. В настоящем исследовании описывается процедура лабораторной валидации тест-системы с определением следующих показателей: специфичность пары антител, влияние интерферирующих веществ, чувствительность и специфичность, прецизионность, стабильность образцов крови до извлечения из нее целевых клеток. Разработанная тест-система показала высокую диагностическую чувствительность и специфичность. Cпецифичность «ТиграТест<sup>®</sup> SARS-CoV-2» составила 100%, чувствительность для иммунизированных вакциной «Гам-КОВИД-Вак» (Спутник V) — 91,67%, а чувствительность при оценке переболевших добровольцев — 95,45%. При этом вариабельность результатов как внутри-, так и межсерийного сравнения теста, не превышала 25%, а хранение крови в условиях (18–25)°С в течение 24 часов после отбора крови от пациента и извлечения из нее целевых клеток не оказывало влияние на результаты теста.</p></trans-abstract><kwd-group xml:lang="en"><kwd>validation</kwd><kwd>TigraTest® SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>T-cell immunity</kwd><kwd>ELISPOT</kwd><kwd>diagnostic sensitivity</kwd><kwd>specificity</kwd><kwd>variability</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>валидация</kwd><kwd>ТиграТест® SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>T-клеточный иммунитет</kwd><kwd>ELISPOT</kwd><kwd>диагностическая чувствительность</kwd><kwd>специфичность</kwd><kwd>вариабельность</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Потеряев Д.А., Аббасова C.Г., Игнатьева П.Е., Стрижакова О.М., Колесник С.В., Хамитов Р.А. 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