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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">ssmu</journal-id><journal-title-group><journal-title xml:lang="ru">Бюллетень сибирской медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Bulletin of Siberian Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-0363</issn><issn pub-type="epub">1819-3684</issn><publisher><publisher-name>Siberian State Medical University, the Ministry of Healthcare of the Russian Federation</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20538/1682-0363-2008-5-1-13-18</article-id><article-id custom-type="elpub" pub-id-type="custom">ssmu-3430</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>МАТЕРИАЛЫ 5-й МЕЖРЕГИОНАЛЬНОЙ НАУЧНО-ПРАКТИЧЕСКОЙ КОНФЕРЕНЦИИ «АКТУАЛЬНЫЕ ВОПРОСЫ НЕВРОЛОГИИ»</subject></subj-group></article-categories><title-group><article-title>Полиморфизм гена интерлейкина-12 (IL12B) у больных рассеянным склерозом и здоровых лиц</article-title><trans-title-group xml:lang="en"><trans-title>Polymorphism of a gene IL12B in patients with multiple sclerosis and healthy persons</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>Алифирова</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Alifirova</surname><given-names>V. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>г. Томск</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>Орлова</surname><given-names>Ю. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Orlova</surname><given-names>Yu. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>г. Томск</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>Титова</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Titova</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>г. Томск</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>Чердынцева</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Cherdyntseva</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>г. Томск</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Николаева</surname><given-names>Т. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikolayeva</surname><given-names>T. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>г. Томск</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Сибирский государственный медицинский университет</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>НИИ онкологии ТНЦ СО РАМН</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2008</year></pub-date><pub-date pub-type="epub"><day>30</day><month>12</month><year>2008</year></pub-date><volume>7</volume><issue>5-1</issue><fpage>13</fpage><lpage>18</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Алифирова В.М., Орлова Ю.Ю., Титова М.А., Чердынцева Н.В., Николаева Т.Н., 2008</copyright-statement><copyright-year>2008</copyright-year><copyright-holder xml:lang="ru">Алифирова В.М., Орлова Ю.Ю., Титова М.А., Чердынцева Н.В., Николаева Т.Н.</copyright-holder><copyright-holder xml:lang="en">Alifirova V.M., Orlova Y.Y., Titova M.A., Cherdyntseva N.V., Nikolayeva T.N.</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://bulletin.ssmu.ru/jour/article/view/3430">https://bulletin.ssmu.ru/jour/article/view/3430</self-uri><abstract><p>Обследовано 62 пациента с различными типами течения рассеянного склероза, средний возраст которых составил (31,8 ± 1,2) года. Проведено генотипирование с помощью полимеразной цепной реакции по полиморфному варианту 1188А/С гена IL12B в 3'-нетранслируемой области и обнаружена не только более высокая частота аллеля С гена IL12B у больных РС по сравнению со здоровыми лицами, но также выявлена ассоциация с более активным течением болезни. При анализе иммунологических показателей больных в зависимости от генотипа IL12B у носителей аллеля С отмечена тенденция к уменьшению абсолютного содержания зрелых Т-лимфоцитов (CD3+-клеток) наряду с увеличением процентного содержания клеток CD25+ и CD95+.</p></abstract><trans-abstract xml:lang="en"><p>We examined of 62 patients with various types of multiple sclerosis current, which middle age has made (31,8 ± 1,2) years. It has been lead genotyping by means of PCR by a polymorphic variant 1188A/С gene IL12B in 3`-not broadcast area and has been found out not only higher frequency of alleles C of a gene IL12B in comparison with healthy persons, but also the association with more active of MS current is revealed. At the analysis of immunological parameters of patients depending on a genotype IL12B, it has been found at carriers alleles C the tendency to reduction absolute maintenance of mature T-lymphocytes and increase CD25+ and CD95+.</p></trans-abstract></article-meta></front><back><ref-list><title>References</title></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>
