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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">10.17650/2311-1267-2016-3-2-18-30</article-id><article-id custom-type="elpub" pub-id-type="custom">nodgo-208</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>ПРОБЛЕМЫ XXI ВЕКА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>THE PROBLEMS OF THE 21 ST CENTURY</subject></subj-group></article-categories><title-group><article-title>Клинический обзор анти-CD19 BiTE® и ex vivo данных об анти-CD33 BiTE® в качестве примеров ретаргетирования Т-клеток при гематологических опухолях</article-title><trans-title-group xml:lang="en"><trans-title>Clinical overview of anti-CD19 BiTE® and ex vivo data from anti-CD33 BiTE® as examples for retargeting T cells in hematologic malignancies</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>Зугмайер</surname><given-names>Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Zugmaier</surname><given-names>G.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Клингер</surname><given-names>М.</given-names></name><name name-style="western" xml:lang="en"><surname>Klinger</surname><given-names>M.</given-names></name></name-alternatives><email xlink:type="simple">matthias.klinger@amgen.com</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>Шмидт</surname><given-names>М.</given-names></name><name name-style="western" xml:lang="en"><surname>Schmidt</surname><given-names>M.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Субклеве</surname><given-names>М.</given-names></name><name name-style="western" xml:lang="en"><surname>Subklewe</surname><given-names>M.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Киргизов</surname><given-names>К. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kirgizov</surname><given-names>K. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Автор перевода</p></bio><bio xml:lang="en"><p>translator</p></bio></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шаманская</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Shamanskaya</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Автор перевода</p></bio><bio xml:lang="en"><p>translator</p></bio></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт исследований Amgen, Мюнхен</institution><country>Германия</country></aff><aff xml:lang="en"><institution>Amgen Research (Munich) GmbH, Munich</institution><country>Germany</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Департамент внутренней медицины III, Мюнхенский университет, Мюнхен; &#13;
Клиническое сотрудничество Группа иммунотерапии, Институт им. Гельмгольца, Мюнхен, Германия</institution><country>Германия</country></aff><aff xml:lang="en"><institution>Department of Internal Medicine III, Klinikum der Universität München, Munich; &#13;
Clinical Cooperation Group Immunotherapy, Helmholtz Institute Munich, Munich</institution><country>Germany</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>01</day><month>06</month><year>2016</year></pub-date><volume>3</volume><issue>2</issue><fpage>18</fpage><lpage>30</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Зугмайер Г., Клингер М., Шмидт М., Субклеве М., Киргизов К.И., Шаманская Т.В., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Зугмайер Г., Клингер М., Шмидт М., Субклеве М., Киргизов К.И., Шаманская Т.В.</copyright-holder><copyright-holder xml:lang="en">Zugmaier G., Klinger M., Schmidt M., Subklewe M., Kirgizov K.I., Shamanskaya T.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://journal.nodgo.org/jour/article/view/208">https://journal.nodgo.org/jour/article/view/208</self-uri><abstract><p>Блинатумомаб – биспецифичное антитело, созданное для воздействия на CD-19 клетки, является наиболее продвинутой частью биспецифических молекул, рекрутеров Т-клеток (BiTE®). Программа клинических исследований препарата включает такие нозологии, как В-клеточный острый лимфобластный лейкоз (ОЛЛ) и В-клеточную неходжкинскую лимфому (НХЛ). Достижения ремиссии удалось достичь как у взрослых, так и у детей с рефрактерным/рецидивирующим течением В-клеточного ОЛЛ, что позволило успешно выполнить аллогенную трансплантацию гемопоэтических стволовых клеток. Также блинатумомаб обладал стойким ответом к В-клеточной вялотекущей НХЛ. Блинатумомаб недавно получил одобрение FDA (США) для лечения рефрактерного/рецидивирующего ОЛЛ из клеток предшественников В-лимфоцитов, отрицательного по филадельфийской хромосоме. AMG 330 является исследовательским анти-CD33 BiTE®-антителом. Тестирование в режиме ex vivo на первичных образцах CD33-позитивных пациентов с острым миелоидным лейкозом показало экспансию и цитотоксический эффект против злокачественных клеток у AMG 330. </p><p>Оригинальная статья “Clinical overview of anti-CD19 BiTE® and ex vivo data from anti-CD33 BiTE® as examples for retargeting T cells in hematologic malignancies” опубликована в журнале Mol Immunol 2015;67(2 Pt A):58–66. doi: 10.1016/j.molimm.2015.02.033. Epub 2015 Apr 13. Стиль и оформле- ние статьи сохранены. Все права защищены. © 2015 Elsevier Ltd.</p></abstract><trans-abstract xml:lang="en"><p>Blinatumomab, a bispecific antibody construct targeting CD19, is the most advanced member of bis-pecific T-cell engager (BiTE®) molecules. The clinical development program includes B-precursor acute lymphoblastic leukemia (ALL) and B-cell non-Hodgkin lymphoma (NHL). Remissions induced in pediatric and adult patients with relapsed/refractory B-precursor ALL have allowed for successful allogeneic hematopoietic stem cell transplantation in this setting. Blinatumomab has also induced durable responses in low-grade B-cell NHL. Blinatumomab recently gained approval in the United States by the U.S. Food and Drug Administration for treatment of Philadelphia chromosome-negative B-precursor relapsed/refractory acute lymphoblastic leukemia. AMG 330 is an investigational anti-CD33 BiTE® antibody construct. Targeting CD33 ex vivo in primary samples from patients with acute myeloid leukemia (AML) has shown AMG 330-mediated T-cell expansion and T-cell cytotoxicity against AML cells.</p><p>“Clinical overview of anti-CD19 BiTE® and ex vivo data from anti-CD33 BiTE® as examples for retargeting T cells in hematologic malignancies” опубликована в журнале Mol Immunol 2015;67(2 Pt A):58–66. doi: 10.1016/j.molimm.2015.02.033. Epub 2015 Apr 13. Стиль и оформле- ние статьи сохранены. Все права защищены. © 2015 Elsevier Ltd.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>BiTE</kwd><kwd>иммунотерапия</kwd><kwd>НХЛ</kwd><kwd>ОЛЛ</kwd><kwd>ОМЛ</kwd><kwd>блинатумомаб</kwd><kwd>AMG 330</kwd></kwd-group><kwd-group xml:lang="en"><kwd>BiTE</kwd><kwd>immunotherapy</kwd><kwd>NHL</kwd><kwd>ALL</kwd><kwd>AML</kwd><kwd>blinatumomab</kwd><kwd>AMG 330</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">Aigner, M., Feulner, J., Schaffer, S., Kischel, R., Kufer, P., Schneider, K., Henn, A., Rattel, B., Friedrich, M., Baeuerle, P.A., Mackensen, A., Krause, S.W., 2013. T lymphocytes can be effectively recruited for ex vivo and in vivo lysis of AML blasts by a novel CD33/CD3-bispecific BiTE antibody construct. 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