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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Morphology</journal-id><journal-title-group><journal-title xml:lang="en">Morphology</journal-title><trans-title-group xml:lang="ru"><trans-title>Морфология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1026-3543</issn><issn publication-format="electronic">2949-2556</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">399510</article-id><article-id pub-id-type="doi">10.17816/morph.399510</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></subject></subj-group></article-categories><title-group><article-title xml:lang="en">CELLULAR COMPOSITION OF DECIDUA BASALIS INFILTRATE DURING EARLY PREGNANCY IN UROGENITAL MYCOPLASMA INFECTION</article-title><trans-title-group xml:lang="ru"><trans-title>КЛЕТОЧНЫЙ СОСТАВ ИНФИЛЬТРАТА В БАЗАЛЬНОЙ ДЕЦИДУАЛЬНОЙ ОБОЛОЧКЕ В РАННИЕ СРОКИ БЕРЕМЕННОСТИ ПРИ ИНФИЦИРОВАНИИ УРОГЕНИТАЛЬНЫМИ МИКОПЛАЗМАМИ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mustafina</surname><given-names>L R</given-names></name><name xml:lang="ru"><surname>Мустафина</surname><given-names>Л Р</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра гистологии, эмбриологии и цитологии (зав. - проф. С.В. Логвинов); Сибирский государственный медицинский университет</p></bio><email>mustafinalr@rambler.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Khon</surname><given-names>E V</given-names></name><name xml:lang="ru"><surname>Хон</surname><given-names>Е В</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра гистологии, эмбриологии и цитологии (зав. - проф. С.В. Логвинов); Сибирский государственный медицинский университет</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Logvinov</surname><given-names>S V</given-names></name><name xml:lang="ru"><surname>Логвинов</surname><given-names>С В</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра гистологии, эмбриологии и цитологии (зав. - проф. С.В. Логвинов); Сибирский государственный медицинский университет</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Yur'ev</surname><given-names>S Yu</given-names></name><name xml:lang="ru"><surname>Юрьев</surname><given-names>С Ю</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра гистологии, эмбриологии и цитологии (зав. - проф. С.В. Логвинов); Сибирский государственный медицинский университет</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Mustafina</surname><given-names>L R</given-names></name><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Khon</surname><given-names>E V</given-names></name><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Logvinov</surname><given-names>S V</given-names></name><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Yuriyev</surname><given-names>S Yu</given-names></name><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en"></institution></aff><aff><institution xml:lang="ru">Сибирский государственный медицинский университет</institution></aff></aff-alternatives><aff id="aff2"><institution></institution></aff><pub-date date-type="pub" iso-8601-date="2011-09-15" publication-format="electronic"><day>15</day><month>09</month><year>2011</year></pub-date><volume>139</volume><issue>3</issue><issue-title xml:lang="en">NO3 (2011)</issue-title><issue-title xml:lang="ru">№3 (2011)</issue-title><fpage>72</fpage><lpage>76</lpage><history><date date-type="received" iso-8601-date="2023-05-09"><day>09</day><month>05</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2011, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2011, Эко-Вектор</copyright-statement><copyright-year>2011</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/"/></permissions><self-uri xlink:href="https://j-morphology.com/1026-3543/article/view/399510">https://j-morphology.com/1026-3543/article/view/399510</self-uri><abstract xml:lang="en"><p>The composition and distribution of immunocompetent cells in human decidua basalis at 6-8 weeks of pregnancy was studied immunonohistochemically under normal conditions (control group) and in infection with different mycoplasma species (microbial number&gt; 104 CFU). In all the groups studied, monocytes were most numerous cells; large granular lymphocytes (phenotype: CD56++CD16-CD3-), macrophages (CD68+) and immunonegative lymphocytes were observed in equal proportions; the least numerous populations were those of NK-cells (CD56±CD16+), plasmocytes and granulocytes. No statistically significant differences were found between the content of these cells in all the investigated groups. The data obtained suggest that mycoplasma infection even characterized by high microbial number, does not cause significant changes in the composition of decidua basalis cellular infiltrate.</p></abstract><trans-abstract xml:lang="ru"><p>Проведен иммуногистохимический анализ состава и распределения иммунокомпетентных клеток в базальной децидуальной оболочке человека при беременности 6-8 нед в норме (контроль) и при инфицировании микоплазмами разных видов (микробное число более 104 КОЕ). Во всех исследованных группах выявлено преобладание моноцитов; в равных соотношениях встречались большие гранулярные лимфоциты (с фенотипом CD56++CD16-CD3-), макрофаги (с фенотипом CD68+) и иммунонегативные лимфоциты; в наименьшем количестве были представлены НК-клетки (CD56±CD16+), плазмоциты и гранулоциты. Статистически значимых различий между показателями содержания этих клеток у исследованных групп выявлено не было. Полученные данные показали, что микоплазменная инфекция, даже с высоким микробным числом, не вызывает значимых изменений в составе клеточного инфильтрата децидуальной оболочки.</p></trans-abstract><kwd-group xml:lang="en"><kwd>decidua basalis</kwd><kwd>lymphocytes</kwd><kwd>macrophages</kwd><kwd>myco plasma infection</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>базальная децидуальная оболочка</kwd><kwd>лимфоциты</kwd><kwd>макрофаги</kwd><kwd>микоплазменная инфекция</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Быков В.Л. Функциональная морфология больших гранулярных лимфоцитов эндометрия человека. Морфология, 2001, т. 119, вып. 2, с. 70-76.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Быковская О.В. Иммуномодулирующая терапия при хронических цервицитах, обусловленных уреа-и микоплазменной инфекцией. 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