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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">10.20538/1682-0363-2017-4-195-206</article-id><article-id custom-type="elpub" pub-id-type="custom">ssmu-1037</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 PAPERS</subject></subj-group></article-categories><title-group><article-title>Характеристика дендритных клеток у больных ревматоидным артритом с различным типом медикаментозной терапии</article-title><trans-title-group xml:lang="en"><trans-title>Characteristics of dendritic cells from patients with rheumatoid arthritis and different type of drug therapy</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>Курочкина</surname><given-names>Ю. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Kurochkina</surname><given-names>Yu. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>аспирант</p><p>лаборатория клеточной иммунотерапии</p><p>врач-ревматолог</p><p>клиника иммунопатологии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>Postgraduate Student, Laboratory of Cellular Immunotherapy, Doctor-rheumatologist, Clinic of Immunopathology</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</p></bio><email xlink:type="simple">Juli_k@bk.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>Тихонова</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tikhonova</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. биол. наук, ст. науч. сотрудник</p><p>лаборатория клеточной иммунотерапии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>PhD, Superior Researcher, Laboratory of Cellular Immunotherapy</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Тыринова</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tyrinova</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, науч. сотрудник</p><p>лаборатория клеточной иммунотерапии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>PhD, Researcher, Laboratory of Cellular Immunotherapy</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Леплина</surname><given-names>О. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Leplina</surname><given-names>O. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р мед. наук, вед. науч. сотрудник</p><p>лаборатория клеточной иммунотерапии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>DM, Leading Researcher, Laboratory of Cellular Immunotherapy</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Сизиков</surname><given-names>А. Э.</given-names></name><name name-style="western" xml:lang="en"><surname>Sizikov</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, зав. отделением</p><p>отделение ревматологии клиники иммунопатологии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>PhD, Head of Rheumatology Department, Clinic of Immunopathology</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Сулутьян</surname><given-names>А. Э.</given-names></name><name name-style="western" xml:lang="en"><surname>Sulutian</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, врач-ревматолог</p><p>отделение ревматологии клиники иммунопатологии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>PhD, Doctor-rheumatologist of the Rheumatology Department, Clinic of Immunopathology</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Коненкова</surname><given-names>Л. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Konenkova</surname><given-names>L. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>врач-ревматолог</p><p>отделение ревматологии клиники иммунопатологии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>PhD, Doctor-rheumatologist of the Rheumatology Department, Clinic of Immunopathology</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Чумасова</surname><given-names>О. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Chumasova</surname><given-names>O. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, врач-ревматолог</p><p>отделение ревматологии клиники иммунопатологии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>PhD, Doctor-rheumatologist of the Rheumatology Department, Clinic of Immunopathology</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Останин</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ostanin</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р мед. наук, профессор, гл. науч. сотрудник</p><p>лаборатория клеточной иммунотерапии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>DM, Professor, Main Researcher, Laboratory of Cellular Immunotherapy</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</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>Черных</surname><given-names>Е. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Chernykh</surname><given-names>E. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р мед. наук, профессор, член-корреспондент РАН, зав. лабораторией</p><p>лаборатория клеточной иммунотерапии</p><p>630099, г. Новосибирск, ул. Ядринцевская, 14 </p></bio><bio xml:lang="en"><p>DM, Рrofessor, Corresponding Member of the Russian Academy of Sciences, Head of the Laboratory of Cellular Immunotherapy</p><p>14, Yadrintsevskaya Str., Novosibirsk, 630099</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт фундаментальной и клинической иммунологии (НИИФиКИ)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Scientific Institution Research Institute of Fundamental and Clinical Immunology</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>02</day><month>01</month><year>2018</year></pub-date><volume>16</volume><issue>4</issue><fpage>195</fpage><lpage>206</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Курочкина Ю.Д., Тихонова М.А., Тыринова Т.В., Леплина О.Ю., Сизиков А.Э., Сулутьян А.Э., Коненкова Л.П., Чумасова О.А., Останин А.А., Черных Е.Р., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Курочкина Ю.Д., Тихонова М.А., Тыринова Т.В., Леплина О.Ю., Сизиков А.Э., Сулутьян А.Э., Коненкова Л.П., Чумасова О.А., Останин А.А., Черных Е.Р.</copyright-holder><copyright-holder xml:lang="en">Kurochkina Y.D., Tikhonova M.A., Tyrinova T.V., Leplina O.Y., Sizikov A.E., Sulutian A.E., Konenkova L.P., Chumasova O.A., Ostanin A.A., Chernykh E.R.</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/1037">https://bulletin.ssmu.ru/jour/article/view/1037</self-uri><abstract><sec><title>Цель исследования</title><p>Цель исследования. Сравнительное исследование фенотипических и функциональных свойств дендритных клеток (ДК) в группах больных ревматоидным артритом (РА), получающих болезнь-модифицирующие препараты, либо биологические препараты и (или) пульс-терапию высокими дозами глюкокортикоидов.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. В исследование включены 39 пациентов с РА и 20 сопоставимых по возрасту и полу здоровых доноров. Девятнадцать больных на момент обследования получали терапию стандартными болезнь-модифицирующими препаратами (БМП) в виде монотерапии или в комбинации (группа РА1), 20 – биологические препараты либо пульс-терапию глюкокортикоидами (группа РА2). В последнем случае обследование проводилось на 2–7-е сут после последнего введения метилпреднизолона.</p></sec><sec><title>Результаты</title><p>Результаты. В настоящем исследовании впервые описаны свойства ДК, генерируемых из моноцитов под действием IFN-α (IFN-ДК), при РА. Установлено, что общей особенностью ДК в группах РА1 и РА2 являются признаки незрелости ДК, проявляющиеся усилением экспрессии CD14 и снижением доли зрелых (CD14-CD83+) ДК. Несмотря на различия ДК в группах РА1 и РА2, оба типа клеток сохраняют in vitro чувствительность к действию дексаметазона, обработка которым приводит к значительному угнетению продукции TNF-α и снижению аллостимуляторной активности ДК. Таким образом, IFN-ДК у больных РА, получающих медикаментозную терапию, характеризуются наличием толерогенных свойств, которые наиболее выражены при использовании в программе лечения биологических препаратов или пульс-терапии кортикостероидами. </p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Purpose of the study</title><p>Purpose of the study. Comparative study of the phenotypic and functional properties of dendritic cells (DC) in groups of patients with rheumatoid arthritis (RA) receiving disease-modifying drugs, or biological drugs and (or) pulse therapy with high doses of glucocorticoids.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. The study included 39 patients with RA and 20 age-appropriate and semihealthy donors. Nineteen patients were treated with standard disease-modifying drugs (BMP) in the form of monotherapy or in combination (group PA1) at the time of the examination, 20 – biological preparations or pulse-therapy with glucocorticoids (group PA2). In the latter case, the examination was carried out for 2–7 days after the last injection of methylprednisolone.</p></sec><sec><title>Results</title><p>Results. In this study, the properties of DC generated from monocytes under the action of IFN-α (IFN-DK) for RA are described for the first time. It has been established that the general feature of DC in the PA1 and PA2 groups are signs of immaturity of the DC, manifested by increased CD14 expression and a decrease in the proportion of mature (CD14-CD83 +) DC. Despite the differences in DC in the PA1 and PA2 groups, both cell types retain in vitro sensitivity to dexamethasone, the treatment of which leads to a significant inhibition of TNF-α production and a decrease in allostimulant activity of the DC. Thus, IFN-DK in RA patients receiving medical therapy is characterized by the presence of tolerogenic properties, which are most pronounced when used in a program of treatment of biological agents or pulse therapy with corticosteroids. </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ревматоидный артрит</kwd><kwd>дендритные клетки</kwd><kwd>дексаметазон</kwd><kwd>интерферон альфа</kwd></kwd-group><kwd-group xml:lang="en"><kwd>rheumatoid arthritis</kwd><kwd>dendritic cells</kwd><kwd>dexamethasone</kwd><kwd>interferon α</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">Tsark E.C., Wang W., Teng Y.C., Arkfeld D., Dodge G.R., Kovats S. Differential MHC class II-mediated presentation of rheumatoid arthritis autoantigens by human dendritic cells and macrophages // J. Immunol. 2002; 169 (11): 6625–6633. DOI: 10.4049/jimmunol.169.11.6625.</mixed-citation><mixed-citation xml:lang="en">Tsark E.C., Wang W., Teng Y.C., Arkfeld D., Dodge G.R., Kovats S. Differential MHC class II-mediated presentation of rheumatoid arthritis autoantigens by human dendritic cells and macrophages // J. Immunol. 2002; 169 (11): 6625–6633. DOI: 10.4049/jimmunol.169.11.6625.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Wenink M.H., Han W., Toes R.E., Radstake T.R. Dendritic cells and their potential implication in pathology and treatment of rheumatoid arthritis // Handb. Exp. Pharmacol. 2009; 188: 81–98. DOI: 10.1007/978-3-540- 71029-5_4.</mixed-citation><mixed-citation xml:lang="en">Wenink M.H., Han W., Toes R.E., Radstake T.R. Dendritic cells and their potential implication in pathology and treatment of rheumatoid arthritis // Handb. Exp. Pharmacol. 2009; 188: 81–98. DOI: 10.1007/978-3-540- 71029-5_4.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Khan S., Greenberg J.D., Bhardwaj N. Dendritic cells as targets for therapy in rheumatoid arthritis. Nat. Rev.Rheumatol. 2009; 5 (10): 566–571. DOI: 10.1038/ nrrheum.2009.185.</mixed-citation><mixed-citation xml:lang="en">Khan S., Greenberg J.D., Bhardwaj N. Dendritic cells as targets for therapy in rheumatoid arthritis. Nat. Rev.Rheumatol. 2009; 5 (10): 566–571. DOI: 10.1038/ nrrheum.2009.185.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Liu J., Cao X. Regulatory dendritic cells in autoimmunity: a comprehensive review // J. Autoimmun. 2015; 63: 1–12. DOI: 10.1016/j.jaut.2015.07.011.</mixed-citation><mixed-citation xml:lang="en">Liu J., Cao X. Regulatory dendritic cells in autoimmunity: a comprehensive review // J. Autoimmun. 2015; 63: 1–12. DOI: 10.1016/j.jaut.2015.07.011.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Thomas R., MacDonald K.P., Pettit A.R., Cavanagh L.L., Padmanabha J., Zehntner S. Dendritic cells and the pathogenesis of rheumatoid arthritis // J. Leukoc. Biol. 1999; 66 (2): 286–292. PMID: 10449169.</mixed-citation><mixed-citation xml:lang="en">Thomas R., MacDonald K.P., Pettit A.R., Cavanagh L.L., Padmanabha J., Zehntner S. Dendritic cells and the pathogenesis of rheumatoid arthritis // J. Leukoc. Biol. 1999; 66 (2): 286–292. PMID: 10449169.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Santiago-Schwarz F., Anand P., Liu S., Carsons S.E. Dendritic cells (DCs) in rheumatoid arthritis (RA): progenitor cells and soluble factors contained in RA synovial fluid yield a subset of myeloid DCs that preferentially activate Th1 inflammatory-type responses // J. Immunol. 2001; 167 (3): 1758–1768. DOI: 10.4049/jimmunol.167.3.1758.</mixed-citation><mixed-citation xml:lang="en">Santiago-Schwarz F., Anand P., Liu S., Carsons S.E. Dendritic cells (DCs) in rheumatoid arthritis (RA): progenitor cells and soluble factors contained in RA synovial fluid yield a subset of myeloid DCs that preferentially activate Th1 inflammatory-type responses // J. Immunol. 2001; 167 (3): 1758–1768. DOI: 10.4049/jimmunol.167.3.1758.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Chen K., Wang J.M., Yuan R., Yi X., Li L., Gong W., Yang T., Li L., Su S. Tissue-resident dendritic cells and diseases involving dendritic cell malfunction // Int. Immunopharmacol. 2016; 34: 1–15. DOI: 10.1016/j.intimp.2016.02.007.</mixed-citation><mixed-citation xml:lang="en">Chen K., Wang J.M., Yuan R., Yi X., Li L., Gong W., Yang T., Li L., Su S. Tissue-resident dendritic cells and diseases involving dendritic cell malfunction // Int. Immunopharmacol. 2016; 34: 1–15. DOI: 10.1016/j.intimp.2016.02.007.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Hilkens C.M.U., Isaacs J.D. Tolerogenic dendritic cells in clinical practice // Open Arthritis Journal. 2010; 3: 8–12. DOI: 10.2174/1876539401003010008.</mixed-citation><mixed-citation xml:lang="en">Hilkens C.M.U., Isaacs J.D. Tolerogenic dendritic cells in clinical practice // Open Arthritis Journal. 2010; 3: 8–12. DOI: 10.2174/1876539401003010008.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Torres-Aguilar H., Aguilar-Ruiz S.R., Gonzalez-Perez G., Munguia R., Bajaсa S., Meraz-Rios M.A., Sanchez-Torres C. Tolerogenic dendritic cells generated with different immunosuppressive cytokines induce antigen-specific anergy and regulatory properties in memory CD4+ T cells // J. Immunol. 2010; 184 (4): 1765–1775. DOI: 10.4049/jimmunol.0902133.</mixed-citation><mixed-citation xml:lang="en">Torres-Aguilar H., Aguilar-Ruiz S.R., Gonzalez-Perez G., Munguia R., Bajaсa S., Meraz-Rios M.A., Sanchez-Torres C. Tolerogenic dendritic cells generated with different immunosuppressive cytokines induce antigen-specific anergy and regulatory properties in memory CD4+ T cells // J. Immunol. 2010; 184 (4): 1765–1775. DOI: 10.4049/jimmunol.0902133.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Yu X., Wang C., Luo J, Zhao X., Wang L., Li X. Combination with methotrexate and cyclophosphamide attenuated maturation of dendritic cells: inducing Treg skewing and Th17 suppression in vivo // Clin. Dev. Immunol. 2013; 2013: 238035. DOI: 10.1155/2013/238035.</mixed-citation><mixed-citation xml:lang="en">Yu X., Wang C., Luo J, Zhao X., Wang L., Li X. Combination with methotrexate and cyclophosphamide attenuated maturation of dendritic cells: inducing Treg skewing and Th17 suppression in vivo // Clin. Dev. Immunol. 2013; 2013: 238035. DOI: 10.1155/2013/238035.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Piemonti L., Monti P., Allavena P., Sironi M., Soldini L., Leone B.E., Socci C.,Di Carlo V.. Glucocorticoids affect human dendritic cell differentiation and maturation // J. Immunol. 1999; 162 (11): 6473–6481.</mixed-citation><mixed-citation xml:lang="en">Piemonti L., Monti P., Allavena P., Sironi M., Soldini L., Leone B.E., Socci C.,Di Carlo V.. Glucocorticoids affect human dendritic cell differentiation and maturation // J. Immunol. 1999; 162 (11): 6473–6481.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Xia C.Q., Peng R., Beato F., Clare-Salzler M.J. Dexamethasone induces IL-10-producing monocyte-derived dendritic cells with durable immaturity // Scand. J. Immunol. 2005; 62 (1): 45–54. DOI: 10.1111/j.1365- 3083.2005.01640.x.</mixed-citation><mixed-citation xml:lang="en">Xia C.Q., Peng R., Beato F., Clare-Salzler M.J. Dexamethasone induces IL-10-producing monocyte-derived dendritic cells with durable immaturity // Scand. J. Immunol. 2005; 62 (1): 45–54. DOI: 10.1111/j.1365- 3083.2005.01640.x.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">León B., Ardavín C. Monocyte-derived dendritic cells in innate and adaptive immunity // Immunol. Cell. Biol. 2008; 86 (4): 320–324. DOI: 10.1038/icb.2008.</mixed-citation><mixed-citation xml:lang="en">León B., Ardavín C. Monocyte-derived dendritic cells in innate and adaptive immunity // Immunol. Cell. Biol. 2008; 86 (4): 320–324. DOI: 10.1038/icb.2008.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Epub 2008 Mar 25. 14. Gessani S., Conti L., Del Cornò M., Belardelli F. Type I interferons as regulators of human antigen presenting cell functions // Toxins (Basel). 2014; 6 (6): 1696–1723. DOI: 10.3390/toxins6061696.</mixed-citation><mixed-citation xml:lang="en">Epub 2008 Mar 25. 14. Gessani S., Conti L., Del Cornò M., Belardelli F. Type I interferons as regulators of human antigen presenting cell functions // Toxins (Basel). 2014; 6 (6): 1696–1723. DOI: 10.3390/toxins6061696.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Runnblom L., Eloranta M.L. The interferon signature in autoimmune diseases // Curr. Opin. Rheumatol. 2013; 25 ( 2): 248–253. DOI: 10.1097/BOR.0b013e32835c7e32.</mixed-citation><mixed-citation xml:lang="en">Runnblom L., Eloranta M.L. The interferon signature in autoimmune diseases // Curr. Opin. Rheumatol. 2013; 25 ( 2): 248–253. DOI: 10.1097/BOR.0b013e32835c7e32.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Rodriguez-Carrio J., de Paz B., Lуpez P., Prado C., Alperi-Lуpez M., Ballina-Garcнa F.J., Suarez A. IFNα serum levels are associated with endothelial progenitor cells imbalance and disease features in rheumatoid arthritis patients // PLoS One. 2014; 9 (1): e86069. DOI: 10.1371/journal.pone.0086069.</mixed-citation><mixed-citation xml:lang="en">Rodriguez-Carrio J., de Paz B., Lуpez P., Prado C., Alperi-Lуpez M., Ballina-Garcнa F.J., Suarez A. IFNα serum levels are associated with endothelial progenitor cells imbalance and disease features in rheumatoid arthritis patients // PLoS One. 2014; 9 (1): e86069. DOI: 10.1371/journal.pone.0086069.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Miossec P., Naviliat A., Duput-dAngeac A., Sany J., Banchereau J. Low levels of interleukin-4 and high levels of transforming growth factor beta in rheumatoid synovitis // Arthr. Rheum. 1999; 33: 1180–1187. DOI: 10.1002/art.1780330819.</mixed-citation><mixed-citation xml:lang="en">Miossec P., Naviliat A., Duput-dAngeac A., Sany J., Banchereau J. Low levels of interleukin-4 and high levels of transforming growth factor beta in rheumatoid synovitis // Arthr. Rheum. 1999; 33: 1180–1187. DOI: 10.1002/art.1780330819.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Chen E., Keystone E.C., Fish E.N. Restricted cytokine expression in rheumatoid arthritis // Arthritis Rheum. 1993; 36 (7): 901–910. PMID:8318038.</mixed-citation><mixed-citation xml:lang="en">Chen E., Keystone E.C., Fish E.N. Restricted cytokine expression in rheumatoid arthritis // Arthritis Rheum. 1993; 36 (7): 901–910. PMID:8318038.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Prevoo M.L., van ‘t Hof M.A., Kuper H.H., van Leeuwen M.A., van de Putte L.B., van Riel P.L. Modified disease activity scores that include twenty-eight-joint counts.Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis // Arthritis Rheum. 1995;38 (1):44–8. DOI: http://dx.doi. org/10.1002/art.1780380107.</mixed-citation><mixed-citation xml:lang="en">Prevoo M.L., van ‘t Hof M.A., Kuper H.H., van Leeuwen M.A., van de Putte L.B., van Riel P.L. Modified disease activity scores that include twenty-eight-joint counts.Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis // Arthritis Rheum. 1995;38 (1):44–8. DOI: http://dx.doi. org/10.1002/art.1780380107.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Курочкина Ю.Д., Леплина О.Ю., Тихонова М.А., Тыринова Т.В., Баторов Е.В., Сизиков А.Э., Оста- нин А.А., Черных Е.Р. Влияние дексаметазона на интерферон-α- индуцированную дифференцировку моноцитов в дендритные клетки // Медицинская им- мунология. 2016; 18 (4): 347–356. DOI: 10.15789/1563- 0625-2016-4-347-356. Kurochkina Y.D., Leplina O.Y., Tikhonova M.A., Tyrinova T.V., Batorov E.V., Sizikov A.E., Ostanin A.A., Chernykh E.R. Effect of dexamethasone on interferon-α-induced differentiation of monocytes to dendritic cells // Medical Immunology (Russia). 2016; 18 (4): 347–356 (in Russian). DOI: 10.15789/1563-0625-2016-4-347-356.</mixed-citation><mixed-citation xml:lang="en">Курочкина Ю.Д., Леплина О.Ю., Тихонова М.А., Тыринова Т.В., Баторов Е.В., Сизиков А.Э., Оста- нин А.А., Черных Е.Р. Влияние дексаметазона на интерферон-α- индуцированную дифференцировку моноцитов в дендритные клетки // Медицинская им- мунология. 2016; 18 (4): 347–356. DOI: 10.15789/1563- 0625-2016-4-347-356. Kurochkina Y.D., Leplina O.Y., Tikhonova M.A., Tyrinova T.V., Batorov E.V., Sizikov A.E., Ostanin A.A., Chernykh E.R. Effect of dexamethasone on interferon-α-induced differentiation of monocytes to dendritic cells // Medical Immunology (Russia). 2016; 18 (4): 347–356 (in Russian). DOI: 10.15789/1563-0625-2016-4-347-356.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Rutella S., De Cristofaro R., Ferraccioli G. Function and dysfunction of dendritic cells in autoimmune rheumatic diseases // Hum. Immunol. 2009; 70: 360–373. PMID: 19405176.</mixed-citation><mixed-citation xml:lang="en">Rutella S., De Cristofaro R., Ferraccioli G. Function and dysfunction of dendritic cells in autoimmune rheumatic diseases // Hum. Immunol. 2009; 70: 360–373. PMID: 19405176.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Broder A., Chan J.J., Putterman C. Dendritic cells: an important link between antiphospholipid antibodies, endothelial dysfunction, and atherosclerosis in autoimmune and non-autoimmune diseases // Clin. Immunol. 2013; 146 (3): 197–206. DOI: 10.1016/j.clim.2012.12.002.</mixed-citation><mixed-citation xml:lang="en">Broder A., Chan J.J., Putterman C. Dendritic cells: an important link between antiphospholipid antibodies, endothelial dysfunction, and atherosclerosis in autoimmune and non-autoimmune diseases // Clin. Immunol. 2013; 146 (3): 197–206. DOI: 10.1016/j.clim.2012.12.002.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Wenink M.H., Han W., Toes R.E., Radstake T.R. Dendritic cells and their potential implication in pathology and treatment of rheumatoid arthritis // Handb. Exp Pharmacol. 2009; 188: 81–98. DOI: 10.1007/978-3-540-71029-5_4.</mixed-citation><mixed-citation xml:lang="en">Wenink M.H., Han W., Toes R.E., Radstake T.R. Dendritic cells and their potential implication in pathology and treatment of rheumatoid arthritis // Handb. Exp Pharmacol. 2009; 188: 81–98. DOI: 10.1007/978-3-540-71029-5_4.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">García-González P.A., Schinnerling K., Sepúlveda-Gutiérrez A., Maggi J., Hoyos L., Morales R.A., Mehdi A.M., Nel H.J., Soto L., Pesce B., Molina M.C., Cuchacovich M., Larrondo M.L., Neira Ó., Catalán D.F., Hilkens C.M., Thomas R., Verdugo R.A., Aguillón J.C. Treatment with dexamethasone and monophosphoryl lipid a removes disease-associated transcriptional signatures in monocyte-derived dendritic cells from rheumatoid arthritis patients and confers tolerogenic features // Front. Immunol. 2016; 7: 458. eCollection 2016.</mixed-citation><mixed-citation xml:lang="en">García-González P.A., Schinnerling K., Sepúlveda-Gutiérrez A., Maggi J., Hoyos L., Morales R.A., Mehdi A.M., Nel H.J., Soto L., Pesce B., Molina M.C., Cuchacovich M., Larrondo M.L., Neira Ó., Catalán D.F., Hilkens C.M., Thomas R., Verdugo R.A., Aguillón J.C. Treatment with dexamethasone and monophosphoryl lipid a removes disease-associated transcriptional signatures in monocyte-derived dendritic cells from rheumatoid arthritis patients and confers tolerogenic features // Front. Immunol. 2016; 7: 458. eCollection 2016.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Balanescu A., Radu E., Nat R., Regalia T., Bojinca V., Ionescu R., Balanescu S., Savu C., Predeteanu D. Early and late effect of infliximab on circulating dendritic cells phenotype in rheumatoid arthritis patients // Int. J. Clin. Pharmacol. Res. 2005; 25 (1): 9–18. PMID: 15864873.</mixed-citation><mixed-citation xml:lang="en">Balanescu A., Radu E., Nat R., Regalia T., Bojinca V., Ionescu R., Balanescu S., Savu C., Predeteanu D. Early and late effect of infliximab on circulating dendritic cells phenotype in rheumatoid arthritis patients // Int. J. Clin. Pharmacol. Res. 2005; 25 (1): 9–18. PMID: 15864873.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Wehner R., Bitterlich A., Meyer N., Kloß A., Schäkel K., Bachmann M., Schmitz M. Impact of chemotherapeutic agents on the immunostimulatory properties of human 6-sulfo LacNAc+ (slan) dendritic cells // Int. J. Cancer. 2013; 132 (6): 1351–1359. DOI: 10.1002/ijc.27786.</mixed-citation><mixed-citation xml:lang="en">Wehner R., Bitterlich A., Meyer N., Kloß A., Schäkel K., Bachmann M., Schmitz M. Impact of chemotherapeutic agents on the immunostimulatory properties of human 6-sulfo LacNAc+ (slan) dendritic cells // Int. J. Cancer. 2013; 132 (6): 1351–1359. DOI: 10.1002/ijc.27786.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Raker V.K., Domogalla M.P., Steinbrink K. Tolerogenic dendritic cells for regulatory T cell induction in man // Front. Immunol. 2015; 6: 569. DOI: 10.3389/fimmu.2015.00569.</mixed-citation><mixed-citation xml:lang="en">Raker V.K., Domogalla M.P., Steinbrink K. Tolerogenic dendritic cells for regulatory T cell induction in man // Front. Immunol. 2015; 6: 569. DOI: 10.3389/fimmu.2015.00569.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Chamorro S. TLR triggering on tolerogenic dendritic cells results in TLR2 up-regulation and a reduced proinflammatory immune program // J. Immunol. 2009; 183 (5): 2984–2994. DOI: 10.4049/jimmunol.0801155.</mixed-citation><mixed-citation xml:lang="en">Chamorro S. TLR triggering on tolerogenic dendritic cells results in TLR2 up-regulation and a reduced proinflammatory immune program // J. Immunol. 2009; 183 (5): 2984–2994. DOI: 10.4049/jimmunol.0801155.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Radstake T.R., Nabbe K.C., Wenink M.H., Roelofs M.F., Oosterlaar A., van Lieshout A.W., Barrera P., van Lent P.L., van den Berg W.B. Dendritic cells from patients with rheumatoid arthritis lack the interleukin 13 mediated increase of FcRII expression, which has clear functional consequences // Ann. Rheum. Dis. 2005; 64: 1737–1743. DOI: 10.1136/ard.2004.034405.</mixed-citation><mixed-citation xml:lang="en">Radstake T.R., Nabbe K.C., Wenink M.H., Roelofs M.F., Oosterlaar A., van Lieshout A.W., Barrera P., van Lent P.L., van den Berg W.B. Dendritic cells from patients with rheumatoid arthritis lack the interleukin 13 mediated increase of FcRII expression, which has clear functional consequences // Ann. Rheum. Dis. 2005; 64: 1737–1743. DOI: 10.1136/ard.2004.034405.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Harry R.A., Anderson A.E., Isaacs J.D., Hilkens C.M. Generation and characterization of therapeutic tolerogenic dendritic cells for rheumatoid arthritis // Ann. Rheum. Dis. 2010; 69 (11): 2042–2050. DOI: 10.1136/ ard.2009.126383.</mixed-citation><mixed-citation xml:lang="en">Harry R.A., Anderson A.E., Isaacs J.D., Hilkens C.M. Generation and characterization of therapeutic tolerogenic dendritic cells for rheumatoid arthritis // Ann. Rheum. Dis. 2010; 69 (11): 2042–2050. DOI: 10.1136/ ard.2009.126383.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Estrada-Capetillo L., Hernandez-Castro B., MonsivaisUrenda A., Alvarez-Quiroga C., Layseca-Espinosa E., Abud-Mendoza C., Baranda L., Urzainqui А., Sanchez-Madrid F., Gonzalez-Amaro R. Induction of Th17 lymphocytes and Treg cells by monocyte-derived dendritic cells in patients with rheumatoid arthritis and systemic lupus erythematosus // Clin. Dev. Immunol. 2013; 2013, Article ID 584303, 9. DOI: 10.1155/2013/584303.</mixed-citation><mixed-citation xml:lang="en">Estrada-Capetillo L., Hernandez-Castro B., MonsivaisUrenda A., Alvarez-Quiroga C., Layseca-Espinosa E., Abud-Mendoza C., Baranda L., Urzainqui А., Sanchez-Madrid F., Gonzalez-Amaro R. Induction of Th17 lymphocytes and Treg cells by monocyte-derived dendritic cells in patients with rheumatoid arthritis and systemic lupus erythematosus // Clin. Dev. Immunol. 2013; 2013, Article ID 584303, 9. DOI: 10.1155/2013/584303.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Ziegler-Heitbrock L., Ancuta P., Crowe S., Dalod M., Grau V., Hart D.N., Leenen P.J., Liu Y.J., MacPherson G., Randolph G.J., Scherberich J., Schmitz J., Shortman K., Sozzani S., Strobl H., Zembala M., Austyn J.M., Lutz M.B. Nomenclature of monocytes and dendritic cells in blood // Blood. 2010;116: e74–e80. DOI: 10.1182/blood2010-02-258558.</mixed-citation><mixed-citation xml:lang="en">Ziegler-Heitbrock L., Ancuta P., Crowe S., Dalod M., Grau V., Hart D.N., Leenen P.J., Liu Y.J., MacPherson G., Randolph G.J., Scherberich J., Schmitz J., Shortman K., Sozzani S., Strobl H., Zembala M., Austyn J.M., Lutz M.B. Nomenclature of monocytes and dendritic cells in blood // Blood. 2010;116: e74–e80. DOI: 10.1182/blood2010-02-258558.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Sprangers S., de Vries T.J., Everts V. Monocyte heterogeneity: consequences for monocyte-derived immune cells // Journal of Immunology Research. 2016; Article ID 1475435, 10.</mixed-citation><mixed-citation xml:lang="en">Sprangers S., de Vries T.J., Everts V. Monocyte heterogeneity: consequences for monocyte-derived immune cells // Journal of Immunology Research. 2016; Article ID 1475435, 10.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Balboa L., Romero M.M., Laborde E. et al. Impaired dendritic cell differentiation of CD16-positive monocytes in tuberculosis: role of p38 MAPK // European Journal of Immunology. 2013; 43 (2); 335–347. DOI: 10.1002/eji.201242557.</mixed-citation><mixed-citation xml:lang="en">Balboa L., Romero M.M., Laborde E. et al. Impaired dendritic cell differentiation of CD16-positive monocytes in tuberculosis: role of p38 MAPK // European Journal of Immunology. 2013; 43 (2); 335–347. DOI: 10.1002/eji.201242557.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Rossol M., Kraus S., Pierer M., Baerwald C., Wagner U. The CD14(bright) CD16+ monocyte subset is expanded in rheumatoid arthritis and promotes expansion of the Th17 cell population // Arthritis Rheum. 2012; 64: 671–677. DOI: 10.1002/art.33418.</mixed-citation><mixed-citation xml:lang="en">Rossol M., Kraus S., Pierer M., Baerwald C., Wagner U. The CD14(bright) CD16+ monocyte subset is expanded in rheumatoid arthritis and promotes expansion of the Th17 cell population // Arthritis Rheum. 2012; 64: 671–677. DOI: 10.1002/art.33418.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Radwan W.M. , Khalifa R.A., Esaily H.A., Lashin N.A. CD14++CD16+ monocyte subset expansion in rheumatoid arthritis patients: Relation to disease activity and interleukin-17 // The Egyptian Rheumatologist. 2016; 38 (3): 161–169. http://dx.doi.org/10.1016/j.ejr.2015.12.002.</mixed-citation><mixed-citation xml:lang="en">Radwan W.M. , Khalifa R.A., Esaily H.A., Lashin N.A. CD14++CD16+ monocyte subset expansion in rheumatoid arthritis patients: Relation to disease activity and interleukin-17 // The Egyptian Rheumatologist. 2016; 38 (3): 161–169. http://dx.doi.org/10.1016/j.ejr.2015.12.002.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Cooper D.L., Martin S.G., Robinson J.I., Mackie S.L., Charles C.J., Nam J., Consortium Y., Isaacs J.D., Emery P., Morgan A.W. FcgammaRIIIa expression on monocytes in rheumatoid arthritis: role in immune-complex stimulated TNF production and non-response to methotrexate therapy // PLoS ONE. 2012;7:e28918. DOI: 10.1371/journal.pone.0028918.</mixed-citation><mixed-citation xml:lang="en">Cooper D.L., Martin S.G., Robinson J.I., Mackie S.L., Charles C.J., Nam J., Consortium Y., Isaacs J.D., Emery P., Morgan A.W. FcgammaRIIIa expression on monocytes in rheumatoid arthritis: role in immune-complex stimulated TNF production and non-response to methotrexate therapy // PLoS ONE. 2012;7:e28918. DOI: 10.1371/journal.pone.0028918.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Liu B., Dhanda A., Hirani S., Williams E.L., Sen H.N., Martinez Estrada F., Ling D., Thompson I., Casady M., Li Z., Si H., Tucker W., Wei L., Jawad S., Sura A., Dailey J., Hannes S., Chen P., Chien J.L., Gordon S., Lee R.W., Nussenblatt R.B. CD14++CD16+ Monocytes are enriched by glucocorticoid treatment and are functionally attenuated in driving effector T-cell responses // J. Immunol. 2015; 194 (11): 5150–5160. DOI: 10.4049/jimmunol. 1402409.</mixed-citation><mixed-citation xml:lang="en">Liu B., Dhanda A., Hirani S., Williams E.L., Sen H.N., Martinez Estrada F., Ling D., Thompson I., Casady M., Li Z., Si H., Tucker W., Wei L., Jawad S., Sura A., Dailey J., Hannes S., Chen P., Chien J.L., Gordon S., Lee R.W., Nussenblatt R.B. CD14++CD16+ Monocytes are enriched by glucocorticoid treatment and are functionally attenuated in driving effector T-cell responses // J. Immunol. 2015; 194 (11): 5150–5160. DOI: 10.4049/jimmunol. 1402409.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Chara L., Sánchez-Atrio A., Pérez A., Cuende E., Albarrán F., Turrión A., Chevarria J., Sánchez M.A., Monserrat J., de la Hera A., Prieto A., Sanz I., Diaz D., Alvarez-Mon M. Monocyte populations as markers of response to adalimumab plus MTX in rheumatoid arthritis // Arthritis Res. Ther. 2012; 14 (4): R175. DOI: 10.1186/ar3928.</mixed-citation><mixed-citation xml:lang="en">Chara L., Sánchez-Atrio A., Pérez A., Cuende E., Albarrán F., Turrión A., Chevarria J., Sánchez M.A., Monserrat J., de la Hera A., Prieto A., Sanz I., Diaz D., Alvarez-Mon M. Monocyte populations as markers of response to adalimumab plus MTX in rheumatoid arthritis // Arthritis Res. Ther. 2012; 14 (4): R175. DOI: 10.1186/ar3928.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Randolph G.J., Beaulieu S., Lebecque S., Steinman R.M., Muller W.A. Differentiation of monocytes into dendritic cells in a model of transendothelial trafficking // Science. 1998; 282: 480–483.</mixed-citation><mixed-citation xml:lang="en">Randolph G.J., Beaulieu S., Lebecque S., Steinman R.M., Muller W.A. Differentiation of monocytes into dendritic cells in a model of transendothelial trafficking // Science. 1998; 282: 480–483.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Farkas A., Kemény L. Interferon-α in the generation of monocyte-derived dendritic cells: recent advances and implications for dermatology // Br. J. Dermatol. 2011; 165 (2): 247-54. DOI: 10.1111/j.1365-2133.2011.10301.x.</mixed-citation><mixed-citation xml:lang="en">Farkas A., Kemény L. Interferon-α in the generation of monocyte-derived dendritic cells: recent advances and implications for dermatology // Br. J. Dermatol. 2011; 165 (2): 247-54. DOI: 10.1111/j.1365-2133.2011.10301.x.</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>
