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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">tumors</journal-id><journal-title-group><journal-title xml:lang="ru">Malignant tumours</journal-title><trans-title-group xml:lang="en"><trans-title>Malignant tumours</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2224-5057</issn><issn pub-type="epub">2587-6813</issn><publisher><publisher-name>Rosoncoweb</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18027/2224-5057-2015-2-22-39</article-id><article-id custom-type="elpub" pub-id-type="custom">tumors-132</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</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL REPORTS</subject></subj-group></article-categories><title-group><article-title>Иммунотерапия злокачественных глиом: современное состояние проблемы и перспективные направления</article-title><trans-title-group xml:lang="en"><trans-title>Immunotherapy for malignant gliomas: current status and perspective</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>Борисов</surname><given-names>Константин Евгеньевич</given-names></name><name name-style="western" xml:lang="en"><surname>Borisov</surname><given-names>K. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к. м.н., врач-онколог, г. Уфа</p></bio><bio xml:lang="en"><p>к. м.н., врач-онколог, </p><p>Ufa</p></bio><email xlink:type="simple">konstantin9671@rambler.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>Сакаева</surname><given-names>Дина Дамировна</given-names></name><name name-style="western" xml:lang="en"><surname>SAKAEVA</surname><given-names>DINA</given-names></name></name-alternatives><bio xml:lang="ru"><p>д. м.н., заместитель главного врача по химиотерапии, г. Уфа</p></bio><bio xml:lang="en"><p>д. м.н., заместитель главного врача по химиотерапии, г. Уфа</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГУЗ Республиканский клинический онкологический диспансер Минздрава Республики Башкортостан</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Republican Clinical Dispensary, Ministry of Health of the Republic of Bashkortostan</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ГУЗ Республиканский клинический онкологический диспансер Минздрава Республики Башкортостан</institution><country>Россия</country></aff><aff xml:lang="en"><institution>ГУЗ Республиканский клинический онкологический диспансер Минздрава Республики Башкортостан</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2015</year></pub-date><pub-date pub-type="epub"><day>01</day><month>07</month><year>2015</year></pub-date><volume>0</volume><issue>2</issue><fpage>22</fpage><lpage>39</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Борисов К.Е., Сакаева Д.Д., 2015</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="ru">Борисов К.Е., Сакаева Д.Д.</copyright-holder><copyright-holder xml:lang="en">Borisov K.E., SAKAEVA D.</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.malignanttumors.org/jour/article/view/132">https://www.malignanttumors.org/jour/article/view/132</self-uri><abstract><p>Несмотря на агрессивное мультимодальное лечение прогноз при злокачественных глиомах остается плохим. Низкая эффективность традиционной цитостатической терапии вынуждает искать альтернативные подходы к лечению. В данном обзоре рассматриваются вопросы активной иммунотерапии с помощью противоопухолевых вакцин и адоптивной клеточной терапии. Вакцинотерапия может осуществляться с использованием опухолевых лизатов или отдельных пептидов или мРНК. Для улучшения иммуногенности вакцины используются дендритные клетки и различные иммуноадъюванты. При использовании лизатной вакцины при вновь выявленной мультиформной глиобластоме медиана выживаемости без прогрессирования составляет 9,5–18 месяцев, а медиана общей выживаемости 16,25–35,9 месяца, что значительно выше, чем в историческом контроле. Среди пептидных вакцин изучаются вакцины к WT-1, сурвивину, мутированному варианту изоцитратдегидрогеназы (IDHR132H), мутированному варианту рецептора эпидермального фактора роста (EGFRvIII). Перспективными представляются методы вакцинотерапии против антигенов стволовых клеток глиом, цитомегаловирусных антигенов. Активно изучается возможность интеграции иммунотерапии в существующие стандарты лечения, а также комбинация нескольких иммунотерапевтических стратегий.</p></abstract><trans-abstract xml:lang="en"><p>Despite aggressive multimodal treatment prognosis for malignant gliomas remains poor. The low efficiency of conventional cytostatic therapy forced to look for alternative approaches to treatment. This review deals with active immunotherapy using tumor vaccines and adoptive cell therapy. Vaccinotherapy may be carried out using tumor lysates or individual peptides, or mRNA. To improve the immunogenicity of vaccines dendritic cells and various immunoadjuvants are widely used. When using lysate vaccine in patients with newly diagnosed glioblastoma multiforme median progression-free survival is 9,5–18 months, and median overall survival is 16,25–35,9 months, significantly more than the historical control. Peptide vaccines to WT-1, survivin, mutated isocitrate dehydrogenase (IDHR132H), mutated epidermal growth factor receptor (EGFRvIII) are under investigation. Promising are the methods of vaccinotherapy against glioma stem cells antigens, cytomegalovirus antigens. The possibility of integration of immunotherapy in the existing treatment standards, as well as a combination of several immunotherapeutic strategies, has been studied extensively.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>злокачественные глиомы</kwd><kwd>иммунотерапия</kwd><kwd>вакцины</kwd><kwd>дендритные клетки</kwd></kwd-group><kwd-group xml:lang="en"><kwd>malignant gliomas</kwd><kwd>immunotherapy</kwd><kwd>vaccines</kwd><kwd>dendritic 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">Stupp R., Hegi M. E., Mason W. P., van den Bent M. J., Taphoorn M. J., Janzer R. C., et al. Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. 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PLoS One. 2014; 9 (9): e107173.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
