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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">734</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2023-22-2-175-184</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>DIAGNOSTIC GUIDELINES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ДИАГНОСТИЧЕСКИЕ РЕКОМЕНДАЦИИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Guidelines for the flow cytometric minimal residual disease monitoring in B-lineage acute lymphoblastic leukemia after CD19-directed immunotherapy</article-title><trans-title-group xml:lang="ru"><trans-title>Рекомендации по определению минимальной остаточной болезни методом проточной цитометрии при остром В-лимфобластном лейкозе в условиях применения CD19-направленной терапии</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3450-0498</contrib-id><name-alternatives><name xml:lang="en"><surname>Mikhailova</surname><given-names>E. V.</given-names></name><name xml:lang="ru"><surname>Михайлова</surname><given-names>Е. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Ekaterina V. Mikhailova, MD</p><p>Leukemia Immunophenotyping Laboratory</p><p>117997</p><p>1 Samory Mashela St.</p><p>Moscow</p></bio><bio xml:lang="ru"><p>Екатерина Валерьевна Михайлова, врач клинической лабораторной диагностики</p><p>лаборатория иммунофенотипирования гемобластозов</p><p>117997</p><p>ул. Саморы Машела, 1</p><p>Москва</p></bio><email>katmikhailova1805@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2685-674X</contrib-id><name-alternatives><name xml:lang="en"><surname>Illarionova</surname><given-names>O. I.</given-names></name><name xml:lang="ru"><surname>Илларионова</surname><given-names>О. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1735-0093</contrib-id><name-alternatives><name xml:lang="en"><surname>Maschan</surname><given-names>M. A.</given-names></name><name xml:lang="ru"><surname>Масчан</surname><given-names>М. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2322-5734</contrib-id><name-alternatives><name xml:lang="en"><surname>Novichkova</surname><given-names>G. A.</given-names></name><name xml:lang="ru"><surname>Новичкова</surname><given-names>Г. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Karachunskiy</surname><given-names>A. I.</given-names></name><name xml:lang="ru"><surname>Карачунский</surname><given-names>А. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0889-6986</contrib-id><name-alternatives><name xml:lang="en"><surname>Popov</surname><given-names>A. M.</given-names></name><name xml:lang="ru"><surname>Попов</surname><given-names>А. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-07-08" publication-format="electronic"><day>08</day><month>07</month><year>2023</year></pub-date><volume>22</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>175</fpage><lpage>184</lpage><history><date date-type="received" iso-8601-date="2023-04-06"><day>06</day><month>04</month><year>2023</year></date><date date-type="accepted" iso-8601-date="2023-05-25"><day>25</day><month>05</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</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://hemoncim.com/jour/article/view/734">https://hemoncim.com/jour/article/view/734</self-uri><abstract xml:lang="en"><p>   Multicolor flow cytometry is now routinely used in laboratory practice for the minimal residual disease (MRD) monitoring in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Wide application of CD19-directed immunotherapy leads to frequent loss of CD19 expression, that hampers significantly the flow cytometric MRD detection methodology. We developed an antibody panel and data analysis algorithm for multicolor flow cytometry, which is a reliable method for MRD detection in patients with BCP-ALL treated with CD19-directed therapy. We recommend a single-tube 11-color panel for MRD detection, which is adapted for the case of possible CD19 loss. Based on patterns of antigen expression changes and the relative expansion of normal CD19-negative BCPs, guidelines for multicolored flow cytometry data analysis and interpretation are established. The recommended approach is reliable tool for therapy response monitoring displaying the same effectiveness with the more laborious and costly molecular techniques.</p></abstract><trans-abstract xml:lang="ru"><p>   Многоцветная проточная цитометрия широко используется в современной лабораторной практике для определения минимальной остаточной болезни (МОБ) у пациентов с острым лимфобластным лейкозом из В-клеточных предшественников (ВП-ОЛЛ). Активное внедрение в лечебную практику таргетных препаратов, приводя к частичной или полной потере CD19 на поверхности опухолевых клеток, существенно осложняет мониторинг МОБ. В данной работе представлен рекомендованный подход к поиску МОБ при ВП-ОЛЛ после таргетной  терапии. Данный подход учитывает возможную потерю основного таргетируемого антигена CD19, изменения в антигенном профиле опухоли и особенности нормальных клеточных популяций костного мозга при применении иммунотерапии. Разработанная панель антител и алгоритм анализа позволяют проводить мониторинг результатов терапии с высокой эффективностью, не уступающей значительно менее воспроизводимым и более дорогостоящим молекулярным методам.</p></trans-abstract><kwd-group xml:lang="en"><kwd>acute B-lymphoblastic leukemia</kwd><kwd>minimal residual disease</kwd><kwd>flow cytometry</kwd><kwd>CD19-directed therapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>острый В-лимфобластный лейкоз</kwd><kwd>минимальная остаточная болезнь</kwd><kwd>проточная цитометрия</kwd><kwd>CD19-направленная терапия</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Not specified</funding-statement><funding-statement xml:lang="ru">Не указано</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Di Giuseppe J. A., Wood B. L. 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