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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">10.15789/1563-0625-2016-3-279-286</article-id><article-id custom-type="elpub" pub-id-type="custom">mimmun-1041</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 СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>ДИНАМИЧЕСКИЕ ИЗМЕНЕНИЯ ХЕМОКИНА CXCL-10 (IP-10) У ДЕТЕЙ И ПОДРОСТКОВ, БОЛЬНЫХ РАЗЛИЧНЫМИ ФОРМАМИ ТУБЕРКУЛЕЗА ОРГАНОВ ДЫХАНИЯ</article-title><trans-title-group xml:lang="en"><trans-title>DYNAMIC CHANGES OF CHEMOKINE CXCL-10 (IP-10) IN CHILDREN AND ADOLESCENTS WITH DIFFERENT FORMS OF PULMONARY TUBERCULOSIS</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>Авербах (мл.)</surname><given-names>М. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Averbakh (Jr)</surname><given-names>M. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>107564, Россия, Москва, Яузская аллея, 2. Тел.: 8 (499) 785-90-72. Факс: 8 (499) 785-91-08 д.м.н., профессор, главный научный сотрудник, отдел иммунологии</p></bio><bio xml:lang="en"><p>107564, Russian Federation, Moscow, Yausa Allee, 2. Phone: 7 (499) 785-90-72. Fax: 7 (499) 785-91-08 PhD, MD (Medicine), Professor, Main Research Associate, Department of Immunology</p></bio><email xlink:type="simple">amm50@mail.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>Панова</surname><given-names>Л. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Panova</surname><given-names>L. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., ведущий научный сотрудник, детско-подростковый отдел</p></bio><bio xml:lang="en"><p>PhD, MD (Medicine), Professor, Leading Research Associate, Pediatric Department</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>Губкина</surname><given-names>М. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Gubkina</surname><given-names>M. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., ведущий научный сотрудник, детско-подростковый отдел</p></bio><bio xml:lang="en"><p>PhD, MD (Medicine), Professor, Leading Research Associate</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Центральный научно-исследовательский институт туберкулеза», Москва, Россия</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Central Research Institute for Tuberculosis, Moscow, Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>13</day><month>07</month><year>2016</year></pub-date><volume>18</volume><issue>3</issue><fpage>279</fpage><lpage>286</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Авербах (мл.) М.М., Панова Л.В., Губкина М.Ф., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Авербах (мл.) М.М., Панова Л.В., Губкина М.Ф.</copyright-holder><copyright-holder xml:lang="en">Averbakh (Jr) M.M., Panova L.V., Gubkina M.F.</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.mimmun.ru/mimmun/article/view/1041">https://www.mimmun.ru/mimmun/article/view/1041</self-uri><abstract><p>Хемокин CXCL-10 (IP-10) является одним из дополнительных гуморальных маркеров, применяемых наряду с определением антиген-индуцированного IFNγ для диагностики латентной туберкулезной инфекции человека. Динамика изменения IP-10 и его прогностическое значение в процессе лечения различных форм туберкулеза, особенно детско-подросткового возраста, является малоизученной проблемой. В настоящем исследовании выявлено увеличение спонтанной и антиген-индуцируемой продукции IP-10 у детей и подростков, больных туберкулезом, по сравнению с латентным формой туберкулеза с последующим ее значительным снижением в случаях успешной противотуберкулезной химиотерапии. При деструктивных формах туберкулеза, имеющих торпидное и прогрессирующее течение, подобная динамика отсутствовала.</p></abstract><trans-abstract xml:lang="en"><p>CXCL10 (IP-10) chemokine is one of additional humoral markers applied along with determination of antigen-induced IFNγ for diagnosis of latent tuberculosis infection in humans. Dynamics of the IP-10 changes and its prognostic value in planning treatment for various forms of tuberculosis is a scarcely studied problem, especially, in children and adolescents. Present study has revealed an increase in spontaneous and antigen-induced IP-10 production in children and adolescents with overt tuberculosis, when compared with latent course of tuberculosis, followed by its significant reduction in cases of successful chemotherapy of tuberculosis. Such dynamics was not evident in destructive forms of tuberculosis manifesting as torpid and progressive infection.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>туберкулез</kwd><kwd>дети</kwd><kwd>подростки</kwd><kwd>хемокины</kwd></kwd-group><kwd-group xml:lang="en"><kwd>tuberculosis</kwd><kwd>children</kwd><kwd>adolescents</kwd><kwd>chemokines</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">Al-Attyan R., Mustafa A.S. Characterization of Human Cellular Immune Responses to Novel Mycobacterium tuberculosis Antigens Encoded by Genomic Regions Absent in Mycobacterium bovis BCG. Infect Immun., 2008, Vol. 76, pp. 4190-4198.</mixed-citation><mixed-citation xml:lang="en">Al-Attyan R., Mustafa A.S. Characterization of Human Cellular Immune Responses to Novel Mycobacterium tuberculosis Antigens Encoded by Genomic Regions Absent in Mycobacterium bovis BCG. Infect Immun., 2008, Vol. 76, pp. 4190-4198.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Alsleben N., Ruhwald M., Rüssmann H., Marx F.M., Wahn U., Magdorf K. Interferon-gamma inducible protein 10 as a biomarker for active tuberculosis and latent tuberculosis infection in children: a case-control study. Scand. J. Infect. Dis., 2012, Vol. 44, no. 4, pp. 256-262.</mixed-citation><mixed-citation xml:lang="en">Alsleben N., Ruhwald M., Rüssmann H., Marx F.M., Wahn U., Magdorf K. Interferon-gamma inducible protein 10 as a biomarker for active tuberculosis and latent tuberculosis infection in children: a case-control study. Scand. J. Infect. Dis., 2012, Vol. 44, no. 4, pp. 256-262.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Djoba Siawaya J.F., Beyers N., van Helden P., Walzl G. Differential cytokine secretion and early treatment response in patients with pulmonary tuberculosis. Clinical and Experimental Immunology, 2009, Vol. 156, pp. 69-77.</mixed-citation><mixed-citation xml:lang="en">Djoba Siawaya J.F., Beyers N., van Helden P., Walzl G. Differential cytokine secretion and early treatment response in patients with pulmonary tuberculosis. Clinical and Experimental Immunology, 2009, Vol. 156, pp. 69-77.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Farber J.M. Mig and IP-10: CXC chemokines that target lymphocytes. J. Leukoc. Biol., 1997, Vol. 61, pp. 246-257.</mixed-citation><mixed-citation xml:lang="en">Farber J.M. Mig and IP-10: CXC chemokines that target lymphocytes. J. Leukoc. Biol., 1997, Vol. 61, pp. 246-257.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Groom J.R., Luster A.D. CXCR3 ligands: redundant, collaborative and antagonistic functions. Immunol. Cell Biol., 2011, Vol. 89, pp. 207-215.</mixed-citation><mixed-citation xml:lang="en">Groom J.R., Luster A.D. CXCR3 ligands: redundant, collaborative and antagonistic functions. Immunol. Cell Biol., 2011, Vol. 89, pp. 207-215.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Hong J.Y., Jung G.S., Kim H., Kim Y.M., Lee H.J., Cho S.N., Kim S.K., Chang J., Kang Y.A. Efficacy of inducible protein 10 as a biomarker for the diagnosis of tuberculosis. Int. J. Infect. Dis., 2012, Vol. 16, no. 12, e855-859.</mixed-citation><mixed-citation xml:lang="en">Hong J.Y., Jung G.S., Kim H., Kim Y.M., Lee H.J., Cho S.N., Kim S.K., Chang J., Kang Y.A. Efficacy of inducible protein 10 as a biomarker for the diagnosis of tuberculosis. Int. J. Infect. Dis., 2012, Vol. 16, no. 12, e855-859.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Hong J.Y., Lee H.J., Kim S.Y., Chung K.S., Kim E.Y., Jung J.Y., Park M. S., Kim Y.S., Kim S.K., Chang J., Cho S.N., Kang Y.A. Efficacy of IP-10 as a biomarker for monitoring tuberculosis treatment. Journal of Infection, 2014, Vol. 68, pp. 252-258.</mixed-citation><mixed-citation xml:lang="en">Hong J.Y., Lee H.J., Kim S.Y., Chung K.S., Kim E.Y., Jung J.Y., Park M. S., Kim Y.S., Kim S.K., Chang J., Cho S.N., Kang Y.A. Efficacy of IP-10 as a biomarker for monitoring tuberculosis treatment. Journal of Infection, 2014, Vol. 68, pp. 252-258.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Lighter J., Rigaud M., Huie M., Peng C.H., Pollack H. Chemokine IP-10: an adjunct marker for latent tuberculosis infection in children. Int. J. Tuberc. Lung Dis., 2009, Vol. 13, pp. 731-736.</mixed-citation><mixed-citation xml:lang="en">Lighter J., Rigaud M., Huie M., Peng C.H., Pollack H. Chemokine IP-10: an adjunct marker for latent tuberculosis infection in children. Int. J. Tuberc. Lung Dis., 2009, Vol. 13, pp. 731-736.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ruhwald M., Bjerregaard-Andersen M., Rabna P., Kofoed K., Eugen-Olsen J., Ravn P. IP-10/CXCL10 release is induced by incubation of whole blood from tuberculosis patients with ESAT-6, CFP10 and TB77. Microbes Infect., 2007, Vol. 9, pp. 806-812.</mixed-citation><mixed-citation xml:lang="en">Ruhwald M., Bjerregaard-Andersen M., Rabna P., Kofoed K., Eugen-Olsen J., Ravn P. IP-10/CXCL10 release is induced by incubation of whole blood from tuberculosis patients with ESAT-6, CFP10 and TB77. Microbes Infect., 2007, Vol. 9, pp. 806-812.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Ruhwald M., Bodmer T., Maier C., JepsenM., HaalandM.B., Eugen-Olsen J., Ravn P. Evaluating the potential of IP-10 and MCP-2 as biomarkers for the diagnosis of tuberculosis. Eur. Respir. J., 2008, Vol. 32, pp. 1607-1615.</mixed-citation><mixed-citation xml:lang="en">Ruhwald M., Bodmer T., Maier C., JepsenM., HaalandM.B., Eugen-Olsen J., Ravn P. Evaluating the potential of IP-10 and MCP-2 as biomarkers for the diagnosis of tuberculosis. Eur. Respir. J., 2008, Vol. 32, pp. 1607-1615.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ruhwald M., Aabye M.G., Ravn P. IP-10 release assays in the diagnosis of tuberculosis infection: current status and future directions. Expert Rev. Mol. Diagn., 2012, Vol. 12, pp. 175-187.</mixed-citation><mixed-citation xml:lang="en">Ruhwald M., Aabye M.G., Ravn P. IP-10 release assays in the diagnosis of tuberculosis infection: current status and future directions. Expert Rev. Mol. Diagn., 2012, Vol. 12, pp. 175-187.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Tang N.L., Fan H.P., Chang K.C., Ching J.K., Kong K.P., Yew W.W., Kam K.M., Leung C.C., Tam C.M., Blackwell J., Chan C.Y. Genetic association between a chemokine gene CXCL-10 (IP-10, interferon gamma inducible protein 10) and susceptibility to tuberculosis. Clin. Chim. Acta, 2009, Vol. 406, pp. 98-102.</mixed-citation><mixed-citation xml:lang="en">Tang N.L., Fan H.P., Chang K.C., Ching J.K., Kong K.P., Yew W.W., Kam K.M., Leung C.C., Tam C.M., Blackwell J., Chan C.Y. Genetic association between a chemokine gene CXCL-10 (IP-10, interferon gamma inducible protein 10) and susceptibility to tuberculosis. Clin. Chim. Acta, 2009, Vol. 406, pp. 98-102.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Yassin M.A., Petrucci R., Garie K.T. Can interferon-g or interferon-g-inducedprotein-10 differentiate tuberculosis infection and disease in children of high endemic areas. PLoS One, 2011, Vol. 6, e23733.</mixed-citation><mixed-citation xml:lang="en">Yassin M.A., Petrucci R., Garie K.T. Can interferon-g or interferon-g-inducedprotein-10 differentiate tuberculosis infection and disease in children of high endemic areas. PLoS One, 2011, Vol. 6, e23733.</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>
