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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">nodgo</journal-id><journal-title-group><journal-title xml:lang="ru">Российский журнал детской гематологии и онкологии (РЖДГиО)</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Pediatric Hematology and Oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2311-1267</issn><issn pub-type="epub">2413-5496</issn><publisher><publisher-name>LTD “Graphica”</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17650/2311-1267-2016-3-4-60-72</article-id><article-id custom-type="elpub" pub-id-type="custom">nodgo-264</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>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ/ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL INVESTIGATIONS/LITERATURE REVIEWS</subject></subj-group></article-categories><title-group><article-title>Анти-CD19-моноклональные антитела при острой лимфобластной лейкемии у детей</article-title><trans-title-group xml:lang="en"><trans-title>Anti-CD19 monoclonal antibodies in acute lymphoblastic leukemia in children</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Карачунский</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Karachunskiy</surname><given-names>A. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>117997, Москва, ул. Саморы Машела, 1</p></bio><bio xml:lang="en"><p>1 Samory Mashela St., Moscow, 117997</p></bio><email xlink:type="simple">aikarat@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Румянцева</surname><given-names>Ю. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Rumyantseva</surname><given-names>Yu. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>117997, Москва, ул. Саморы Машела, 1</p></bio><bio xml:lang="en"><p>1 Samory Mashela St., Moscow, 117997</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>фон Штакельберг</surname><given-names>А.</given-names></name><name name-style="western" xml:lang="en"><surname>Fon Shtakelberg</surname><given-names>A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Берлин</p></bio><bio xml:lang="en"><p>1 Augustenburger Platz, Berlin, 13353</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «ФНКЦ ДГОИ им. Дмитрия Рогачева» Минздрава России;</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of Russia;</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Университетская клиника педиатрии, специализирующаяся в онкологии и гематологии, Университетского медицинского комплекса Шарите</institution><country>Германия</country></aff><aff xml:lang="en"><institution>Klinik für Pädiatrie mit Schwerpunkt Onkologie und Hämatologie, Charité - Universitätsmedizin Berlin;</institution><country>Germany</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>17</day><month>01</month><year>2017</year></pub-date><volume>3</volume><issue>4</issue><fpage>60</fpage><lpage>72</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Карачунский А.И., Румянцева Ю.В., фон Штакельберг А., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Карачунский А.И., Румянцева Ю.В., фон Штакельберг А.</copyright-holder><copyright-holder xml:lang="en">Karachunskiy A.I., Rumyantseva Y.V., fon Shtakelberg 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://journal.nodgo.org/jour/article/view/264">https://journal.nodgo.org/jour/article/view/264</self-uri><abstract><p>Разработка моноклональных антител для лечения гемобластозов является быстро развивающейся областью науки. Ряд соединений оказался эффективен при лечении острого лимфобластного лейкоза (ОЛЛ) у детей. В то время как неконъюгированные гуманизированные антитела хорошо переносимы и могут быть легко объединены с химиотерапией, иммуноконъюгаты, доставляющие токсические соединения прямо в клетки-мишени, имеют более серьезные побочные эффекты. Антигены с высокой и селективной экспрессией являются идеальными мишенями для использования антител и подходят для исследований фазы I/II и III при ОЛЛ у детей. Антигены, стабильно экспрессирующиеся на поверхности клетки, подходят как для неконъюгированных антител, вызывающих антитело-зависимую клеточную и комплемент-зависимую цитотоксичность, так и для биспецифических антител с участием Т-клеток. Моноклональные антитела обладают совершенно иным механизмом действия по сравнению с таковым обычной химиотерапии и, безусловно, способны существенно изменить стратегию лечения ОЛЛ в будущем.</p></abstract><trans-abstract xml:lang="en"><p>Creation of monoclonal antibodies for leukaemia treatment is rapidly developing area of science. A number of compounds were effective for treatment of acute lymphoblastic leukaemia (ALL) at children. While unconjugated humanized antibodies have good tolerability and can be combined with chemotherapy, immunoconjugates, delivering the toxic compounds directly to the target cells, have more serious adverse effects. Antigens with high and selective expression are the ideal targets for usage with antibodies and suitable for studies of phases I/II and III in case of pediatric ALL. Antigens with stable expression on the cells surfaces, suitable both for unconjugated antibodies, leading to antibodies-dependent cell and complement-dependent cytotoxicity, and for bispecific antibodies with participation of T-cells. Monoclonal antibodies have quite different mechanism of action in comparison with routine chemotherapy and, of course, can change the strategy of ALL treatment in future.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>острый лимфобластный лейкоз</kwd><kwd>иммунотерапия</kwd><kwd>анти-CD19</kwd><kwd>блинатумомаб</kwd><kwd>биспецифические моноклональные антитела</kwd></kwd-group><kwd-group xml:lang="en"><kwd>acute lymphoblastic leukemia</kwd><kwd>immunotherapy</kwd><kwd>anti-СВ19</kwd><kwd>blinatumomab</kwd><kwd>bispecific monoclonal antibody</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">Kohler G., Milstein C. 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