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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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Genes &amp; Cells</journal-id><journal-title-group><journal-title xml:lang="en">Genes &amp; Cells</journal-title><trans-title-group xml:lang="ru"><trans-title>Гены и Клетки</trans-title></trans-title-group><trans-title-group xml:lang="zh"><trans-title>Genes and Cells</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-1829</issn><issn publication-format="electronic">2500-2562</issn><publisher><publisher-name xml:lang="en">Human Stem Cells Institute</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">121954</article-id><article-id pub-id-type="doi">10.23868/202110003</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Next-generation immunotherapy: regulatory T-cells</article-title><trans-title-group xml:lang="ru"><trans-title>Иммунотерапия нового поколения: регуляторные Т-клетки</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Churov</surname><given-names>A. V</given-names></name><name xml:lang="ru"><surname>Чуров</surname><given-names>А. В</given-names></name></name-alternatives><email>achurou@yandex.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Novitskaya</surname><given-names>A. V</given-names></name><name xml:lang="ru"><surname>Новицкая</surname><given-names>А. В</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zhulai</surname><given-names>G. A</given-names></name><name xml:lang="ru"><surname>Жулай</surname><given-names>Г. А</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Karelian Research Center of the RAS</institution></aff><aff><institution xml:lang="ru">Карельский научный центр Российской академии наук</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Center for Biomedical Research, KarRC RAS</institution></aff><aff><institution xml:lang="ru">Центр медико-биологических исследований КарНЦ РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2021-09-15" publication-format="electronic"><day>15</day><month>09</month><year>2021</year></pub-date><volume>16</volume><issue>3</issue><issue-title xml:lang="en">VOL 16, NO3 (2021)</issue-title><issue-title xml:lang="ru">ТОМ 16, №3 (2021)</issue-title><fpage>16</fpage><lpage>32</lpage><history><date date-type="received" iso-8601-date="2023-01-16"><day>16</day><month>01</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2021, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2021, Эко-Вектор</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">Эко-Вектор</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2024-09-15"/></permissions><self-uri xlink:href="https://genescells.ru/2313-1829/article/view/121954">https://genescells.ru/2313-1829/article/view/121954</self-uri><abstract xml:lang="en"><p>Regulatory T lymphocytes (Treg) control the activity of immune cells and suppress the development of inflammation, maintaining the immune balance necessary for the body. Dysfunctions of Tregs are associated with the pathogenesis of autoimmune and oncological diseases. With systemic and organ-specific autoimmune reactions, as well as organ transplantation, a decrease in the function of Tregs is observed. While in the course of oncogenesis, the activity of Tregs prevents the development of an adequate immune response to tumor antigens, promotes the processes of angiogenesis and uncontrolled growth of transformed cells. Taking into account the important function of Tregs in the control of autoimmunity and oncogenesis, approaches to immunotherapy of inflammatory pathologies based on autologous and donor Tregs, as well as methods of activating an antitumor immune response as a result of selective blockade of the functional activity of Tregs, are being actively developed. The review provides an overview of technologies for modulating the activity of Tregs for the treatment of cancer, autoimmunity and adverse reactions after transplantation.</p></abstract><trans-abstract xml:lang="ru"><p>Регуляторные T-лимфоциты контролируют активность клеток иммунной системы и подавляют развитие воспаления, поддерживая необходимый для организма баланс. Нарушения функций Treg связаны с патогенезом аутоиммунных и онкологических заболеваний. При системных и органоспецифических аутоиммунных заболеваниях, а также трансплантации органов наблюдается снижение функции Treg. тогда как в ходе опухолевого роста активность Treg повышена, что препятствует развитию адекватного иммунного ответа на антигены опухолей, способствует процессам ангиогенеза и неконтролируемого роста трансформированных клеток. с учетом важной функции Treg в контроле аутоиммунитета и онкогенеза, сегодня активно развиваются подходы к иммунотерапии иммуновоспалительных патологий на основе собственных и донорских Treg, а также методы активации противоопухолевого иммунного ответа в результате селективной блокады функциональной активности Treg. В статье приведен обзор технологий для модуляции активности Treg в целях терапии рака, аутоиммунных заболеваний и нежелательных реакций после трансплантации.</p></trans-abstract><kwd-group xml:lang="en"><kwd>FOXP3</kwd><kwd>CAR-Treg</kwd><kwd>regulatory T-cells (Treg)</kwd><kwd>FOXP3</kwd><kwd>immunotherapy</kwd><kwd>adoptive cell therapy</kwd><kwd>CAR-Treg</kwd><kwd>immuno-oncology</kwd><kwd>autoimmunity</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>регуляторные T-клетки (Treg)</kwd><kwd>иммунотерапия</kwd><kwd>адоптивная клеточная терапия</kwd><kwd>иммуноонкология</kwd><kwd>аутоиммунитет</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Nishizuka Y., Sakakura T. Thymus and reproduction: sex-linked dysgenesia of the gonad after neonatal thymectomy in mice. Science 1969; 166 (3906): 753-5.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Gershon R.K., Kondo K. 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