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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">diaendo</journal-id><journal-title-group><journal-title xml:lang="ru">Сахарный диабет</journal-title><trans-title-group xml:lang="en"><trans-title>Diabetes mellitus</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2072-0351</issn><issn pub-type="epub">2072-0378</issn><publisher><publisher-name>Endocrinology research centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/DM12988</article-id><article-id custom-type="elpub" pub-id-type="custom">diaendo-12988</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>Новости</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>News</subject></subj-group></article-categories><title-group><article-title>На пути к профилактике сахарного диабета 1 типа: зарегистрирован первый в истории препарат, замедляющий развитие аутоиммунного процесса</article-title><trans-title-group xml:lang="en"><trans-title>Towards prevention of type 1 diabetes: FDA approved first drug with potential to delay clinical stage of disease</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4316-8546</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лаптев</surname><given-names>Д. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Laptev</surname><given-names>D. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лаптев Дмитрий Никитич, д.м.н.</p><p>Researcher ID: O-1826-2013; Scopus Author ID: 24341083800; eLibrary SPIN: 2419-4019</p><p>117036, Москва, ул. Дмитрия Ульянова, д. 11</p></bio><bio xml:lang="en"><p>Dmitry N. Laptev, MD, PhD</p><p>Researcher ID: O-1826-2013; Scopus Author ID: 24341083800; eLibrary SPIN: 2419-4019</p><p>11, Dm. Ul’yanova street, 117036 Moscow</p></bio><email xlink:type="simple">laptevdn@ya.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8175-7886</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дедов</surname><given-names>И. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Dedov</surname><given-names>I. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дедов Иван Иванович, профессор, д.м.н., академик РАН</p><p>Researcher ID: D-3729-2014; Scopus Author ID: 7101843976; eLibrary SPIN: 5873-2280</p><p>Москва</p></bio><bio xml:lang="en"><p>Ivan I. Dedov, MD, PhD, Professor, Academician of the Russian Academy of Sciences</p><p>Researcher ID: D-3729-2014; Scopus Author ID: 7101843976; eLibrary SPIN: 5873-2280</p><p>Moscow</p></bio><email xlink:type="simple">dedov@endocrincentr.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Национальный медицинский исследовательский центр эндокринологии</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Endocrinology Research Centre</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>28</day><month>12</month><year>2022</year></pub-date><volume>25</volume><issue>6</issue><fpage>576</fpage><lpage>579</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Лаптев Д.Н., Дедов И.И., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Лаптев Д.Н., Дедов И.И.</copyright-holder><copyright-holder xml:lang="en">Laptev D.N., Dedov I.I.</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://www.dia-endojournals.ru/jour/article/view/12988">https://www.dia-endojournals.ru/jour/article/view/12988</self-uri><abstract><p>Принимая во внимание высокую вероятность неблагоприятных исходов у пациентов с сахарным диабетом 1 типа (СД1), а также бремя, создаваемое болезнью, поиск методов, предупреждающих разрушение бета-клеток, имеет первостепенное значение. До недавнего времени все попытки иммунотерапевтических вмешательств не достигали существенных успехов, позволяя в лучшем случае уменьшить скорость разрушения бета-клеток, не останавливая иммунный процесс и не позволяя нормализовать гликемию. В ноябре 2022 г. Управление по санитарному надзору за качеством пищевых продуктов и медикаментов США (FDA) одобрило препарат теплизумаб для замедления развития клинической стадии СД1. Целью публикации является оценка результатов применения препарата теплизумаб у людей на второй (доклинической) стадии СД1, а также рассмотрение дальнейших перспектив данного лечения.</p></abstract><trans-abstract xml:lang="en"><p>Given the increased morbidity and mortality in patients with type 1 diabetes mellitus (T1DM), as well as the burden posed by the disease, the search for methods to prevent the destruction of beta cells is of paramount importance. Until recently, no attempts of immunotherapeutic interventions have achieved significant success, allowing at best reducing the rate of destruction of beta cells without stopping the immune process and not allowing normalization of glycemia. In November 2022, the U.S. Food and Drug Administration (FDA) approved the drug teplizumab to delay clinical diagnosis of T1DM. The purpose of the publication is to evaluate the results of teplizumab treatment in high-risk participants with the second (preclinical) stage of T1DM, as well as to consider further prospects for this treatment.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>сахарный диабет 1 типа</kwd><kwd>иммунотерапия</kwd><kwd>профилактика</kwd><kwd>Т-клетки</kwd></kwd-group><kwd-group xml:lang="en"><kwd>type 1 diabetes mellitus</kwd><kwd>immunotherapy</kwd><kwd>prevention</kwd><kwd>T-cells</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">FDA Approves First Drug That Can Delay Onset of Type 1 Diabetes. Available at: https://www.fda.gov/news-events/press-announcements/fda-approves-first-drug-can-delay-onset-type-1-diabetes Accessed November 18, 2022.</mixed-citation><mixed-citation xml:lang="en">FDA Approves First Drug That Can Delay Onset of Type 1 Diabetes. 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