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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">mimmun</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская иммунология</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Immunology (Russia)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1563-0625</issn><issn pub-type="epub">2313-741X</issn><publisher><publisher-name>SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15789/1563-0625-DSC-2782</article-id><article-id custom-type="elpub" pub-id-type="custom">mimmun-2782</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>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SHORT COMMUNICATIONS</subject></subj-group></article-categories><title-group><article-title>Диагностически значимые изменения субпопуляций CD11b+CD64-CD32+CD16+, CD11b+CD64+CD32+CD16+ нейтрофильных гранулоцитов иммунокомпрометированных женщин с хроническими инфекционно-воспалительными заболеваниями генитального тракта различной этиологии</article-title><trans-title-group xml:lang="en"><trans-title>Diagnostically significant changes in subsets CD11b+CD64-CD32+CD16+, CD11b+CD64+CD32+CD16+ neutrophilic granulocytes of immunocompromised women with chronic infectious and inflammatory diseases of the genital tract of various etiologies</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9604-5806</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ковалева</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kovaleva</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ковалева С.В. – д.м.н., доцент, старший научный сотрудник отдела клинико-экспериментальной иммунологии и молекулярной биологии центральной научно-исследовательской лаборатории, доцент кафедры клинической иммунологии, аллергологии и лабораторной диагностики ФПК и ППС </p><p>г. Краснодар</p></bio><bio xml:lang="en"><p>Kovaleva S.V., PhD, MD (Medicine), Associate Professor, Research Associate, Department of Clinical and Experimental Immunology and Molecular Biology, Central Research Laboratory, Associate Professor, Department of Clinical Immunology, Allergology and Laboratory Diagnostics of FAT and PRS </p><p>Krasnodar</p></bio><email xlink:type="simple">3483335@mail.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/0000-0001-6071-4409</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нестерова</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Nesterova</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Нестерова И.В. – д.м.н., профессор, главный научный сотрудник отдела клинико-экспериментальной иммунологии и молекулярной биологии центральной научно-исследовательской лаборатории; профессор кафедры клинической иммунологии, аллергологии и адаптологии факультета непрерывного медицинского образования Медицинского института </p><p>г. Краснодар;г. Москва</p></bio><bio xml:lang="en"><p>Nesterova I.V., PhD, MD (Medicine), Professor, Chief Research Associate, Department of Clinical and Experimental Immunology and Molecular Biology, Central Research Laboratory; Professor, Department of Clinical Immunology, Allergology and Adaptology Faculty of Continuing Medical Education, Medical Institute </p><p>Krasnodar;Moscow</p></bio><email xlink:type="simple">inesterova1@yandex.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9376-3397</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пиктурно</surname><given-names>С. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Pikturno</surname><given-names>S. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Пиктурно С.Н. – аспирант кафедры клинической иммунологии, аллергологии и лабораторной диагностики ФПК и ППС </p><p>г. Краснодар</p></bio><bio xml:lang="en"><p>Pikturno S.N., Postgraduate Student, Department of Clinical Immunology, Allergology and Laboratory Diagnostics of FAT and PRS </p><p>Krasnodar</p></bio><email xlink:type="simple">spikturno@yandex.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>Дыдышко</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Dydyshko</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дыдышко Е.И. – к.м.н., доцент кафедры клинической иммунологии, аллергологии и лабораторной диагностики ФПК и ППС </p><p>г. Краснодар</p></bio><bio xml:lang="en"><p>Dydyshko E.I., PhD (Medicine), Associate Professor, Department of Clinical Immunology, Allergology and Laboratory Diagnostics of FAT and PRS </p><p>Krasnodar</p></bio><email xlink:type="simple">vochka@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>Просолупова</surname><given-names>Н. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Prosolypova</surname><given-names>N. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Просолупова Н.С. – заведующая консультативнодиагностическим отделением клиники </p><p>г. Краснодар</p></bio><bio xml:lang="en"><p>Prosolypova N.S., Head, Consultative and Diagnostic Department of the Clinic </p><p>Krasnodar</p></bio><email xlink:type="simple">NatalyPro87@yandex.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>Чулкова</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Chulkova</surname><given-names>А. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Чулкова А.М. – к.м.н., заведующая дневным стационаром клиники </p><p>г. Краснодар</p></bio><bio xml:lang="en"><p>Chulkova А.M., PhD (Medicine), Head, Day Hospital Clinic </p><p>Krasnodar</p></bio><email xlink:type="simple">achulkova@bagk-med.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">ФГБОУ ВО «Кубанский государственный медицинский университет» Министерства здравоохранения РФ<country>Россия</country></aff><aff xml:lang="en">Kuban State Medical University<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">ФГБОУ ВО «Кубанский государственный медицинский университет» Министерства здравоохранения РФ;&#13;
ФГАОУ ВО «Российский университет дружбы народов»<country>Россия</country></aff><aff xml:lang="en">Kuban State Medical University;&#13;
Peoples’ Friendship University of Russia<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>01</day><month>06</month><year>2023</year></pub-date><volume>25</volume><issue>4</issue><fpage>855</fpage><lpage>862</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ковалева С.В., Нестерова И.В., Пиктурно С.Н., Дыдышко Е.И., Просолупова Н.С., Чулкова А.М., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Ковалева С.В., Нестерова И.В., Пиктурно С.Н., Дыдышко Е.И., Просолупова Н.С., Чулкова А.М.</copyright-holder><copyright-holder xml:lang="en">Kovaleva S.V., Nesterova I.V., Pikturno S.N., Dydyshko E.I., Prosolypova N.S., Chulkova А.M.</copyright-holder><license 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.mimmun.ru/mimmun/article/view/2782">https://www.mimmun.ru/mimmun/article/view/2782</self-uri><abstract><p>Хронические воспалительные заболевания органов малого таза (ХВЗОМТ) у женщин остаются основной проблемой в структуре гинекологических заболеваний ввиду значимости медицинских и социально-экономических последствий. Течение и исход ХВЗОМТ зависят от состояния иммунной системы. Актуальным представляется изучение рецепторного аппарата нейтрофильных гранулоцитов (НГ), участвующих в противоинфекционной защите при заболеваниях различной этиологии. Цель: уточнить особенности вариантов количественных и фенотипических изменений субпопуляций НГ CD11b+CD64-CD32+CD16+, CD11b+CD64+CD32+CD16+  иммунокомпрометированных женщин в период обострения ХВЗОМТ различной этиологии. Тестировали НГ периферической крови 70 женщин 20-40 лет: группа исследования 1 (ГИ1) – 20 иммунокомпрометированных женщин в период обострения ХВЗОМТ с моно- или микст-латентными или рецидивирующими различными вирусными инфекциями (хронические герпес-вирусные инфекции, папилломавирусная инфекция, рекуррентные ОРВИ); группа исследования 2 (ГИ2) – 30 иммунокомпрометированных женщин с ХВЗОМТ бактериальной этиологии; группа сравнения – 20 условно-здоровых женщин. Методом проточной цитометрии (CYTOMICS FC500, США) определяли количество НГ и уровень экспрессии рецепторов субпопуляций CD11b+CD64-CD32+CD16+НГ (мажорной) и CD11b+CD64+CD32+CD16+НГ (минорной). Установлено, что у иммунокомпрометированных женщин с ХВЗОМТ в период обострения выявлены диагностически значимые различия в субпопуляционном составе НГ. При ХВЗОМТ бактериальной этиологии (ГИ2) снижение субпопуляции CD11b+СD64-СD32+СD16+НГ и увеличение в 7,6 раз субпопуляции CD11b+CD64+CD32+CD16+НГ в отличие от ХВЗОМТ, протекающих в сочетании с рецидивирующей или персистирующей вирусной инфекцией (ГИ1). Негативная трансформация субпопуляций НГ связана с преимущественным снижением уровня экспрессии активационного CD16. Выявлено отсутствие адекватного ответа на воспаление – отсутствие повышения экспрессии активационного CD11b в мажорной субпопуляции в ГИ1, а также в минорной субпопуляции в ГИ1 и ГИ2. В мажорной субпопуляции ГИ2 выявлено нарушение – снижение экспрессии активационного маркера CD11b в период обострения ХВЗОМТ. Также при наличии различной вирусной инфекции и ХВЗОМТ (ГИ1) в негативно измененной минорной субпопуляции выявлено снижение уровня экспрессии CD16, повышение уровня экспрессии CD64 и CD32. Определение субпопуляционного состава CD11b+СD64-СD32+СD16+ и CD11b+CD64+CD32+CD16+ НГ и их фенотипа можно использовать как в качестве диагностических маркеров для дифференциальной диагностики ХВЗОМТ вирусной и бактериальной этиологии, так и для последующей разработки новых методов таргетной иммуномодулирующей терапии.</p></abstract><trans-abstract xml:lang="en"><p>Chronic pelvic inflammatory disease (PID) in women remains a problem due to the importance of medical consequences. The study of the receptor apparatus of neutrophilic granulocytes (NG) involved in anti-infective protection in diseases of various etiologies seems to be relevant. Aim: to clarify the features of variants of quantitative and phenotypic changes in subsets of NG CD11b+CD64-CD32+CD16+, CD11b+CD64+CD32+CD16+ of immunocompromised women during exacerbation of chronic PID of various etiologies. We were tested women 20-40 years: Study Group 1 (SG1, n = 20) – chronic PID during the exacerbation with mono- or mixed latent/recurrent various viral infections (chronic herpes-virus infections, papillomavirus infection, recurrent ARVI); Study Group 2 (SG2, n = 30) – chronic PID of bacterial etiologies; Comparison Group (CG)– 20 healthy women. The number of subsets CD11b+CD64-CD32+CD16+NG (major) and CD11b+CD64+CD32+CD16+NG (minor), receptor expression density (MFI) was determined (FC500, USA). It was found that in PID during the period of exacerbation, diagnostically significant differences in the subset composition of NG were revealed. We got a decrease in the CD11b+СD64-СD32+СD16+NG subset and in 7,6 times increase in the CD11b+CD64+CD32+CD16+NG subset in SG2 with chronic PID of bacterial etiology, in contrast to chronic PID occurring in combination with recurrent/persistent viral infection SG1. Negative transformation of NG subsets is associated with a predominant decrease in the level of expression of the activation CD16. The absence of an adequate response to the infectious and inflammatory process was revealed – the absence of an increase in the expression of the activation CD11b in the major subset in SG1, as well as in the minor subset in groups SG1 and SG2. In the major subset of NG in groups SG2 a decrease in the expression of the activation marker CD11b. In the various viral infections and PID (SG1), in the negatively altered minor subset of NG we got a decrease of expression of CD16, an increase of expression of CD64 and CD32. Determination of subsets of CD11b+СD64-СD32+СD16+, CD11b+CD64+CD32+CD16+NG and their phenotype can be used as diagnostic markers for the differential diagnosis of PID of viral and bacterial etiology, and for the development of new methods of targeted immunomodulatory therapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>нейтрофильные гранулоциты</kwd><kwd>субпопуляции</kwd><kwd>фенотип</kwd><kwd>диагностический маркер</kwd><kwd>хронические воспалительные заболевания органов малого таза</kwd><kwd>иммунокомпрометированность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>neutrophilic granulocytes</kwd><kwd>subsets</kwd><kwd>phenotype</kwd><kwd>diagnostic marker</kwd><kwd>chronic pelvic inflammatory disease</kwd><kwd>immunocompromised</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">Abakumova T.V, Gening T.P., Dolgova D.R., Antoneeva I.I., Peskov A.B., Gening S.O. 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(In Russ.)</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>
