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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">clinicaloncology</journal-id><journal-title-group><journal-title xml:lang="ru">Клинический случай в онкологии</journal-title><trans-title-group xml:lang="en"><trans-title>Clinical Case in Oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">3034-1477</issn><issn pub-type="epub">3034-4018</issn><publisher><publisher-name>ОНКОПРАКТИК</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.62546/3034-1477-2024-2-3-62-69</article-id><article-id custom-type="elpub" pub-id-type="custom">clinicaloncology-27</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>КЛИНИЧЕСКИЕ СЛУЧАИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CASE REPORTS</subject></subj-group></article-categories><title-group><article-title>Редкое осложнение, ассоциированное c использованием современных иммуноонкологических препаратов, - поражение почек</article-title><trans-title-group xml:lang="en"><trans-title>А rare complication, associated with the use of modern immunooncology drugs - kidney injury</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>Орлова</surname><given-names>Р. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Orlova</surname><given-names>R. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>199106, Санкт-Петербург, 21-линия В.О., д. 8а; 198255, Санкт-Петербург, пр. Ветеранов, д. 56</p></bio><bio xml:lang="en"><p>7/9 Universitetskaya Emb., 199034; 56 Veteranov Ave., St. Petersburg 193318</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>Беляк</surname><given-names>Н. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Belyak</surname><given-names>N. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>199106, Санкт-Петербург, 21-линия В.О., д. 8а; 198255, Санкт-Петербург, пр. Ветеранов, д. 56</p></bio><bio xml:lang="en"><p>7/9 Universitetskaya Emb., 199034; 56 Veteranov Ave., St. Petersburg 193318</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>Мгарь</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Mgar</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мгарь Екатерина Андреевна</p><p>199106, Санкт-Петербург, 21-линия В.О., д. 8а</p></bio><bio xml:lang="en"><p>Mgar Ekaterina Andreevna</p><p>7/9 Universitetskaya Emb., 199034</p></bio><email xlink:type="simple">caterina.odinets@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Санкт-Петербургский государственный университет»; СПб ГБУЗ «Городской клинический онкологический диспансер»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>St. Petersburg State University; St. Petersburg City Clinical Oncology Dispensary</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБОУ ВО «Санкт-Петербургский государственный университет»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>St. Petersburg State University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>27</day><month>01</month><year>2025</year></pub-date><volume>2</volume><issue>3</issue><fpage>62</fpage><lpage>69</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Орлова Р.В., Беляк Н.П., Мгарь Е.А., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Орлова Р.В., Беляк Н.П., Мгарь Е.А.</copyright-holder><copyright-holder xml:lang="en">Orlova R.V., Belyak N.P., Mgar E.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://www.oncocase.ru/jour/article/view/27">https://www.oncocase.ru/jour/article/view/27</self-uri><abstract><p>Ингибиторы иммунных контрольных точек (ИКТ), в том числе антиген цитотоксических Т-лимфоцитов 4 (cytotoxic T-lymphocyte antigen 4 – CTLA-4), рецептор запрограммированной гибели 1 (programmed death 1 – PD-1) и его лиганд 1 (PD-ligand-1 – PD-L1), представляют собой современные иммуноонкологические препараты, которые на сегодняшний день продемонстрировали эффективность лечения при ряде злокачественных новообразований. Механизм действия ингибиторов ИКТ заключается в потенцировании иммунного отчета за счет устранения тормозящего влияния опухолевых клеток на активацию Т-лимфоцитов. Однако чрезмерная активация иммунной системы может стать причиной развития иммуноопосредованных нежелательных явлений (иоНЯ) со стороны ряда органов и систем, в том числе и почек. Несмотря на то, что иммуноопосредованное поражение почек на фоне терапии ингибиторами ИКТ развивается относительно редко, оно может быть достаточно серьезным и определять прогноз пациента, что обусловливает необходимость ранней диагностики и своевременного начала лечения. В связи с этим приобретает особую актуальность информированность о проявлениях иоНЯ со стороны почек на фоне иммунотерапии не только онкологов и нефрологов, но и врачей других специальностей</p></abstract><trans-abstract xml:lang="en"><p>Immune checkpoint inhibitors (ICIs), including cytotoxic T-lymphocyte associated antigen 4 (CTLA-4) and programmed death protein 1 (PD-1) or its ligand (PD-L1), are a new generation of immuno-oncological drugs that to date have demonstrated efficacy in a number of malignancies. The mechanism of ICIs action consist in the potentiation of the immune response by eliminating the tumor cells inhibitory effect on the T-lymphocytes activation. However, excessive immune system activation can cause the development of a special class of immune-related adverse events (irAEs) involved a wide variety of organs and systems, including the kidneys. Despite the fact that immunomediated kidney injury caused by ICI therapy develops quite rarely (2–15%), it can be serious and determine the patient’s prognosis, which necessitates early diagnosis and timely start of treatment. In this regard, awareness of the manifestations of ICI-associated renal irAEs is particularly relevant not only for oncologists and for nephrologists, but for doctors of other specialties.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>иммунотерапия</kwd><kwd>ингибиторы иммунных контрольных точек</kwd><kwd>редкие иммуноопосредованные нежелательные явления</kwd><kwd>иммуноопосредованные нежелательные явления со стороны почек</kwd><kwd>острое почечное повреждение</kwd></kwd-group><kwd-group xml:lang="en"><kwd>immunotherapy</kwd><kwd>immune checkpoint inhibitors</kwd><kwd>rare immune-mediated adverse events</kwd><kwd>renal&#13;
immune-related adverse events</kwd><kwd>acute kidney injury</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Статья подготовлена без спонсорской поддержки.</funding-statement><funding-statement xml:lang="en">The article was prepared without sponsorship.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Hodi F.S., O’Day S.J., McDermott D.F. et al. Improved survival with ipilimumab in patients with metastatic melanoma // N. Engl. J. Med. 2010. Vol. 363, No 8. P. 711–723. https: //doi.org/10.1056/NEJMoa1003466.</mixed-citation><mixed-citation xml:lang="en">Hodi F.S., O’Day S.J., McDermott D.F. et al. Improved survival with ipilimumab in patients with metastatic melanoma // N. Engl. J. Med. 2010. Vol. 363, No 8. 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