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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">vestim</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной  академии наук Беларуси. Серия медицинских наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Medical series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1814-6023</issn><issn pub-type="epub">2524-2350</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29235/1814-6023-2018-15-1-40-54</article-id><article-id custom-type="elpub" pub-id-type="custom">vestim-413</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>КЛИНИЧЕСКАЯ И ЭКСПЕРИМЕНТАЛЬНАЯ МЕДИЦИНА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL AND EXPERIMENTAL MEDICINE</subject></subj-group></article-categories><title-group><article-title>РЕЗУЛЬТАТЫ ЛЕЧЕНИЯ МУЛЬТИРЕЗИСТЕНТНОГО ТУБЕРКУЛЕЗА С ИСПОЛЬЗОВАНИЕМ НОВЫХ ЛЕКАРСТВЕННЫХ СРЕДСТВ И КЛЕТОЧНЫХ ТЕХНОЛОГИЙ</article-title><trans-title-group xml:lang="en"><trans-title>RESULTS OF MULTIDRUG-RESISTANT TUBERCULOSIS TREATMENT USING NEW DRUGS AND CELLULAR TECHNOLOGIES</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>Гуревич</surname><given-names>Г. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Hurevich</surname><given-names>Gennady L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р мед. наук, профессор, директор </p><p>Долгиновский тракт, 157, 220053, г. Минск</p></bio><bio xml:lang="en"><p>D. Sc. (Med.), Professor, Director</p><p>157, Dolginovskii Tract, 220053, Minsk</p></bio><email xlink:type="simple">ge.gurev@gmail.com</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>Скрягина</surname><given-names>Е. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Skryahina</surname><given-names>Elena M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р мед. наук, профессор, заместитель директора по научной работе</p><p>Долгиновский тракт, 157, 220053, г. Минск</p></bio><bio xml:lang="en"><p>D. Sc. (Med.), Deputy Director for Research</p><p>157, Dolginovskii Tract, 220053, Minsk</p></bio><email xlink:type="simple">alena.skrahina@gmail.com</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>Дюсьмикеева</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Dziusmikeyeva</surname><given-names>Marina I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, заведующий отделением</p><p>Долгиновский тракт, 157, 220053, г. Минск</p></bio><bio xml:lang="en"><p>Ph. D. (Med.), Head of the Department</p><p>157, Dolginovskii Tract, 220053, Minsk</p></bio><email xlink:type="simple">trimige@inbox.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>Исайкина</surname><given-names>Я. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Isaykina</surname><given-names>Janina I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. биол. наук, заведующий лабораторией</p><p>ул. Фрунзенская, 43, 223053, Минский р-н, д. Боровляны</p></bio><bio xml:lang="en"><p>Ph. D. (Biol.), Head of the Laboratory</p><p>43, Frunzenskaya Str., v. Borovliany, 223053, Minsk Region</p></bio><email xlink:type="simple">yaninai@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Республиканский научно-практический центр пульмонологии и фтизиатрии</institution></aff><aff xml:lang="en"><institution>Republican Research and Practical Center for Pulmonology and Tuberculosis</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Республиканский научно-практический центр детской онкологии, гематологии и иммунологии</institution></aff><aff xml:lang="en"><institution>Republican Research and Practical Center for Pediatric Oncology, Hematology and Immunology</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>03</day><month>03</month><year>2018</year></pub-date><volume>15</volume><issue>1</issue><fpage>40</fpage><lpage>54</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Гуревич Г.Л., Скрягина Е.М., Дюсьмикеева М.И., Исайкина Я.И., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Гуревич Г.Л., Скрягина Е.М., Дюсьмикеева М.И., Исайкина Я.И.</copyright-holder><copyright-holder xml:lang="en">Hurevich G.L., Skryahina E.M., Dziusmikeyeva M.I., Isaykina J.I.</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://vestimed.belnauka.by/jour/article/view/413">https://vestimed.belnauka.by/jour/article/view/413</self-uri><abstract><p>Мультирезистетный туберкулез является одной из актуальных проблем здравоохранения в Республике Беларусь.</p><p>Цель исследования – оценка эффективности новых лекарственных средств и схем химиотерапии, а также клеточных технологий как метода аддитивной терапии при лечении пациентов с туберкулезом с множественной и широкой лекарственной устойчивостью возбудителя (М/ШЛУ-ТБ).</p><p>Для оценки эффективности лечения на основании когортного анализа было отобрано 416 человек, которым были назначены новые схемы химиотерапии. Мультирезистентный туберкулез у пациентов выявляли с помощью оптимизированного алгоритма микробиологической диагностики с применением молекулярно-генетических методов. Разработана методика аутологичной трансплантации мультипотентных мезенхимальных стромальных клеток, входящая в комплексную схему лечения пациентов с М/ШЛУ-ТБ.</p><p>Предварительные результаты исследования свидетельствуют о высокой эффективности новых противотуберкулезных схем, а также клеточной технологии на фоне индивидуализированной химиотерапии в лечении лекарственно-устойчивого туберкулеза. При этом установлено, что бедаквилин и деламанид эффективны в сочетании с оптимизированными фоновыми схемами лечения, состоящими в том числе из перепрофилированных противотуберкулезных лекарственных средств, и вызывают незначительное количество побочных явлений. </p></abstract><trans-abstract xml:lang="en"><p>The detection of multidrug-resistant and extensively drug-resistant tuberculosis cases has become a major public health problem and an obstacle to effective global tuberculosis control.</p><p>We have set the task to improve the effectiveness of treatment of patients with multidrug-resistant and extensively drugresistant tuberculosis using new drugs and developed chemotherapy regimens, as well as cellular technologies as a method of additive therapy. Based on the cohort analysis, the effectiveness of treatment was assessed using new and re-profiled antituberculosis drugs, including Bedaquiline and Delamanid. A method of autologous transplantation of multipotent mesenchymal stromal cells was developed, which was included into the complex therapy of patients. Preliminary results of the conducted studies testify to the high effectiveness of new antituberculosis treatment regimens. Autologous transplantation of multipotent mesenchymal stromal cells against the background of individualized chemotherapy speeds up the conversion of sputum and ultimately significantly improves the final results of treatment of patient. Despite the fact that cellular technologies in the treatment of tuberculosis are not widely used at present, these methods aimed at eliminating the causative agent of tuberculosis and the regeneration of damaged lung tissue will be in great demand in the future, primarily because of the significant advantage compared with the use of antituberculosis drugs means – the absence of development of resistance of mycobacteria tuberculosis. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>туберкулез</kwd><kwd>множественная и широкая лекарственная устойчивость</kwd><kwd>противотуберкулезная терапия</kwd><kwd>аутологичная трансплантация</kwd><kwd>мультипотентные мезенхимальные стромальные клетки</kwd><kwd>эффективность лечения</kwd></kwd-group><kwd-group xml:lang="en"><kwd>tuberculosis</kwd><kwd>multiple and extensively drug-resistance</kwd><kwd>anti-tuberculosis drugs</kwd><kwd>new chemotherapy regimens</kwd><kwd>autologous transplantation</kwd><kwd>multipotent mesenchymal stromal cells</kwd><kwd>treatment effectiveness</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">Global tuberculosis report 2016 / World Health Organization. – Geneva : World Health Organization Publ., 2016. – 214 p.</mixed-citation><mixed-citation xml:lang="en">Global tuberculosis report 2016. Geneva, World Health Organization Publ., 2016. 214 p.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Гуревич, Г. Л. Туберкулез: возбудитель, патогенез, риск заболевания, эпидемиология / Г. Л. Гуревич, О. М. Калечиц // Мир медицины. – 2012. – № 5. – С. 3–4.</mixed-citation><mixed-citation xml:lang="en">Gurevich G. L., Kalechits O. M. Tuberculosis: pathogen, pathogenesis, risk of disease, epidemiology. Mir meditsiny [World of Medicine], 2012, no. 5, pp. 3–4 (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">World Health Organization, the HWO/IUATLD Anti-tuberculosis drug resistance in the world: The WHO/IUATLD Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Anti-tuberculosis Drug Resistance in the World: Forth Global Report. WHO/HTM/TB/2008.394. – Geneva : World Health Organization Publ., 2008. – 64 p.</mixed-citation><mixed-citation xml:lang="en">World Health Organization, the HWO/IUATLD Anti-tuberculosis drug resistance in the world: The WHO/IUATLD Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Anti-tuberculosis Drug Resistance in the World: Forth Global Report. WHO/HTM/TB/2008.394. Geneva, World Health Organization Publ., 2008. 64 p.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Влияние множественной лекарственной устойчивости на эффективность лечения больных туберкулезом / Е. М. Скрягина [и др.] // Рецепт. – 2010. – № 1. – С. 61–66.</mixed-citation><mixed-citation xml:lang="en">Skryagina E. M., Astrovko A. P., Gurevich G. L., Dyus’mikeeva M. I., Skryagin A. E., Zalutskaya O. M., Solodovnikova V. V. The effect of multiple drug resistance on the effectiveness of treatment of patients with tuberculosis. Retsept = Recipe, 2010, no. 1, pp. 61–66 (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Multidrug-resistant tuberculosis in Belarus: the size of the problem and associated risk factors / A. Skrahina [et al.] // Bull. of the World Health Organization. – 2013. – Vol. 91, N 1. – P. 36–45.</mixed-citation><mixed-citation xml:lang="en">Skrahina A., Hurevich H., Zalutskaya A., Sahalchyk E., Astrauko A., Hoffner S., Rusovich V., Dadu A., de Colombani P., Dara M., van Gemert W., Zignol M. Multidrug-resistant tuberculosis in Belarus: the size of the problem and associated risk factors. Bulletin of the World Health Organization, 2013, vol. 91, no. 1, pp. 36–45. DOI: 10.2471/blt.12.104588</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Resistance to fluoroquinolones and second-line injectable drugs: impact on multidrug-resistant TB outcomes / D. Falzon [et al.] // Europ. Respiratory J. – 2013. – Vol. 42, N 1. – P. 156–168.</mixed-citation><mixed-citation xml:lang="en">Falzon D., Gandhi N., Migliori G. B., Sotgiu G., Cox H., Holtz T. H., Hollm-Delgado M. G., Keshavjee S., DeRiemer K., Centis R., D’Ambrosio L., Lange C. G., Bauer M., Menzies D. Resistance to fluoroquinolones and second-line injectable drugs: impact on multidrug-resistant TB outcomes. European Respiratory Journal, 2013, vol. 42, no. 1, pp. 156–168. DOI: 10.1183/09031936.00134712</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Drug resistance beyond extensively drug resistant tuberculosis: individual patient data meta-analysis / G. B. Migliori [et al.] // Europ. Respiratory J. – 2013. – Vol. 42, N 1. – P. 169–179.</mixed-citation><mixed-citation xml:lang="en">Migliori G. B., Sotgiu G., Gandhi N. R., Falzon D., DeRiemer K., Centis R., Hollm-Delgado M. G., Palmero D., Pérez-Guzmán C., Vargas M. H., D’Ambrosio L., Spanevello A., Bauer M., Chan E. D., Schaaf H. S., Keshavjee S., Holtz T. H., Menzies D. Drug resistance beyond extensively drug resistant tuberculosis: individual patient data meta-analysis. European Respiratory Journal, 2013, vol. 42, no. 1, pp. 169–179. DOI: 10.1183/09031936.00136312</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Frequency of recurrence among MDR-TB cases «successfully» treated with standardised short-course chemotherapy / G. B. Migliori [et al.] // Intern. J. of Tuberculosis and Lung Disease. – 2002. – Vol. 6, N 10. – P. 858–864.</mixed-citation><mixed-citation xml:lang="en">Migliori G. B., Espinal M., Danilova I. D., Punga V. V., Grzemska M., Raviglione M. C. Frequency of recurrence among MDR-TB cases «successfully» treated with standardised short-course chemotherapy. International Journal of Tuberculosis and Lung Disease, 2002, vol. 6, no. 10, pp. 858–864.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Costs of tuberculosis disease in the European Union: a systematic analysis and cost calculation / R. Diel [et al.] // Europ. Respiratory J. – 2014. – Vol. 43, N 2. – P. 554–565.</mixed-citation><mixed-citation xml:lang="en">Diel R., Vandeputte J., de Vries G., Stillo J., Wanlin M., Nienhaus A. Costs of tuberculosis disease in the European Union: a systematic analysis and cost calculation. European Respiratory Journal, 2014, vol. 43, no. 2, pp. 554–565. DOI: 10.1183/09031936.00079413</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Caminero, J. A. Classification of antituberculosis drugs: a new proposal based on the most recent evidence / J. A. Caminero, A. Scardigli // European Respiratory J. – 2014. – Vol. 46, N 4. – P. 887–893.</mixed-citation><mixed-citation xml:lang="en">Caminero J. A., Scardigli A. Classification of antituberculosis drugs: a new proposal based on the most recent evidence. European Respiratory Journal, 2015, vol. 46, no. 4, pp. 887–893. DOI: 10.1183/13993003.00432-2015</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Sotgiu, G. Linezolid to treat MDR-/XDR-Tuberculosis: available evidence and future scenarios / G. Sotgiu, E. Pontali, G. B. Migliori // Europ. Respiratory J. – 2015. – Vol. 45, N 1. – P. 25–29.</mixed-citation><mixed-citation xml:lang="en">Sotgiu G., Pontali E., Migliori G. B. Linezolid to treat MDR-/XDR-Tuberculosis: available evidence and future scenarios. European Respiratory Journal, 2015, vol. 45, no. 1, pp. 25–29. DOI: 10.1183/09031936.00145014</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Tuberculosis: cost of illness in Germany / R. Diel [et al.] // Europ. Respiratory J. – 2012. – Vol. 40, N 1. – P. 143–151.</mixed-citation><mixed-citation xml:lang="en">Diel R., Rutz S., Castell S., Schaberg T. Tuberculosis: cost of illness in Germany. European Respiratory Journal, 2012, vol. 40, no. 1, pp. 143–150. DOI: 10.1183/09031936.00204611</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">First tuberculosis cases in Italy resistant to all tested drugs / G. B. Migliori [et al.] // Eurosurveillance (Weekly releases). – 2007. – Vol. 12, N 5. – E070517.1.</mixed-citation><mixed-citation xml:lang="en">Migliori G. B., de Iaco G., Besozzi G., Centis R., Cirillo D. M. First tuberculosis cases in Italy resistant to all tested drugs. Eurosurveillance (Weekly releases), 2007, vol. 12, no. 5, E070517.1.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Bedaquiline and MDR-TB: a systematic and critical analysis of the evidence / E. Pontali [et al.] // Europ. Respiratory J. – 2016. – Vol. 47, N 2. – P. 394–402.</mixed-citation><mixed-citation xml:lang="en">Pontali E., Sotgiu G., D’Ambrosio L., Centis R., Migliori G. B. Bedaquiline and MDR-TB: a systematic and critical analysis of the evidence. European Respiratory Journal, 2016, vol. 47, no. 2, pp. 394–402. DOI: 10.1183/13993003.01891-2015</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">WHO guidelines for the programmatic management of drug-resistant tuberculosis: 2011 update / D. Falzon [et al.] // Europ. Respiratory J. – 2011. – Vol. 38, N 3. – P. 516–528.</mixed-citation><mixed-citation xml:lang="en">Falzon D., Jaramillo E., Schünemann H. J., Arentz M., Bauer M., Bayona J., Blanc L., Caminero J. A., Daley C. L., Duncombe C., Fitzpatrick C., Gebhard A., Getahun H., Henkens M., Holtz T. H., Keravec J., Keshavjee S., Khan A. J., Kulier R., Leimane V., Lienhardt C., Lu C., Mariandyshev A., Migliori G. B., Mirzayev F., Mitnick C. D., Nunn P., Nwagboniwe G., Oxlade O., Palmero D., Pavlinac P., Quelapio M. I., Raviglione M. C., Rich M. L., Royce S., Rüsch-Gerdes S., Salakaia A., Sarin R., Sculier D., Varaine F., Vitoria M., Walson J. L., Wares F., Weyer K., White R. A., Zignol M. WHO guidelines for the programmatic management of drug-resistant tuberculosis: 2011 update. European Respiratory Journal, 2011, vol. 38, no. 3, pp. 516–528. DOI: 10.1183/09031936.00073611</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Caminero, J. A. Classification of antituberculosis drugs: a new proposal based on the most recent evidence / J. A. Caminero, A. Scardigli // Europ. Respiratory J. – 2015. – Vol. 46, N 4. – P. 887–893.</mixed-citation><mixed-citation xml:lang="en">Caminero J. A., Scardigli A. Classification of antituberculosis drugs: a new proposal based on the most recent evidence. European Respiratory Journal, 2015, vol. 46, no. 4, pp. 887–893. DOI: 10.1183/13993003.00432-2015</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Bedaquiline in the treatment of multi- and extensively drug-resistant tuberculosis / A. S. Pym [et al.] // Europ. Respiratory J. – 2016. – Vol. 47, N 2. – P. 564–574.</mixed-citation><mixed-citation xml:lang="en">Pym A. S., Diacon A. H., Tang Sh.-J., Conradie F., Danilovits M., Chuchottaworn C., Vasilyeva I., Andries K., Bakare N., de Marez T., Haxaire-Theeuwes M., Lounis N., Meyvisch P., van Baelen B., van Heeswijk R. P. G., Dannemann B. Bedaquiline in the treatment of multi- and extensively drug-resistant tuberculosis. European Respiratory Journal, 2016, vol. 47, no. 2, pp. 564–574. DOI: 10.1183/13993003.00724-2015</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">The diarylquinoline TMC207 for multidrug-resistant tuberculosis / A. H. Diacon [et al.] // New England J. of Medicine. – 2009. – Vol. 360, N 23. – P. 2397–2405.</mixed-citation><mixed-citation xml:lang="en">Diacon A. H., Pym A., Grobusch M., Patientia R., Rustomjee R., Page-Shipp L., Pistorius C., Krause R., Bogoshi M., Churchyard G., Venter A., Allen J., Palomino J. C., De Marez T., van Heeswijk R. P., Lounis N., Meyvisch P., Verbeeck J., Parys W., de Beule K., Andries K., Mc Neeley D. F. The diarylquinoline TMC207 for multidrug-resistant tuberculosis. New England Journal of Medicine, 2009, vol. 360, no. 23, pp. 2397–2405. DOI: 10.1056/NEJMoa0808427.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Multidrug-resistant tuberculosis and culture conversion with bedaquiline / A. H. Diacon [et al.] // New England J. of Medicine. – 2014. –Vol. 371, N 8. – P. 723–732.</mixed-citation><mixed-citation xml:lang="en">Diacon A. H., Pym A., Grobusch M. P., de los Rios J. M., Gotuzzo E., Vasilyeva I., Leimane V., Andries K., Bakare N., De Marez T., Haxaire-Theeuwes M., Lounis N., Meyvisch P., De Paepe E., van Heeswijk R. P., Dannemann B. Multidrugresistant tuberculosis and culture conversion with bedaquiline. New England Journal of Medicine, 2014, vol. 371, no. 8, pp. 723–732. DOI: 10.1056/NEJMoa1313865</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Compassionate use of bedaquiline for the treatment of multidrug-resistant and extensively drug-resistant tuberculosis: interim analysis of a French cohort / L. Guglielmetti [et al.] // Clinical Infectious Diseases. – 2015. – Vol. 60, N 2. – P. 188–194.</mixed-citation><mixed-citation xml:lang="en">Guglielmetti L., Le Dû D., Jachym M., Henry B., Martin D., Caumes E., Veziris N., Métivier N., Robert J. Compassionate use of bedaquiline for the treatment of multidrug-resistant and extensively drug-resistant tuberculosis: interim analysis of a French cohort. Clinical Infectious Diseases, 2015, vol. 60, no. 2, pp. 188–194. DOI: 10.1093/cid/ciu786</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Treatment of drug-resistant tuberculosis with bedaquiline in a high HIV prevalence setting: an interim cohort analysis / N. Ndjeka [et al.] // Intern. J. of Tuberculosis and Lung Disease. – 2015. – Vol. 19, N 8. – P. 979–985.</mixed-citation><mixed-citation xml:lang="en">Ndjeka N., Conradie F., Schnippel K., Hughes J., Bantubani N., Ferreira H., Maartens G., Mametja D., Meintjes G., Padanilam X., Variava E., Pym A., Pillay Y. Treatment of drug-resistant tuberculosis with bedaquiline in a high HIV prevalence setting: an interim cohort analysis. International Journal of Tuberculosis and Lung Disease, 2015, vol. 19, no. 8, pp. 979–985. DOI: 10.5588/ijtld.14.0944</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Bedaquiline in MDR/XDR-TB cases: first experience on compassionate use / S. Tiberi [et al.] // Europ. Respiratory J. – 2014. – Vol. 43, N 1. – P. 289–292.</mixed-citation><mixed-citation xml:lang="en">Tiberi S., de Lorenzo S., Centis R., Viggiani P., D’Ambrosio L., Migliori G. B. Bedaquiline in MDR/XDR-TB cases: first experience on compassionate use. European Respiratory Journal, 2014, vol. 43, no. 1, pp. 289–292. DOI: 10.1183/09031936.00122313</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">First case of extensively drug-resistant tuberculosis treated with both delamanid and bedaquiline / M. Tadolini [et al.] // Europ. Respiratory J. – 2016. – Vol. 48, N 3. – P. 935–938.</mixed-citation><mixed-citation xml:lang="en">Tadolini M., Lingtsang R. D., Tiberi S., Enwerem M., D’Ambrosio L., Sadutshang T. D., Centis R., Migliori G. B. First case of extensively drug-resistant tuberculosis treated with both delamanid and bedaquiline. European Respiratory Journal, 2016, vol. 48, no. 3, pp. 935–938. DOI: 10.1183/13993003.00637-2016</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Wallis, R. S. Cardiac safety of extensively drug-resistant tuberculosis regimens including bedaquiline, delamanid and clofazimine / R. S. Wallis // Europ. Respiratory J. – 2016. – Vol. 48, N 5. – P. 1526–1527.</mixed-citation><mixed-citation xml:lang="en">Wallis R. S. Cardiac safety of extensively drug-resistant tuberculosis regimens including bedaquiline, delamanid and clofazimine. European Respiratory Journal, 2016, vol. 48, no. 5, pp. 1526–1527. DOI: 10.1183/13993003.01207-2016</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Cardiac safety of extensively drug-resistant tuberculosis regimens including bedaquiline, delamanid and clofazimine / M. Tadolini [et al.] // Europ. Respiratory J. – 2016. – Vol. 48, N 5. – P. 1527–1529.</mixed-citation><mixed-citation xml:lang="en">Tadolini M., Lingtsang R. D., Tiberi S., Enwerem M., D’Ambrosio L., Sadutshang T. D., Centis R., Migliori G. B. Cardiac safety of extensively drug-resistant tuberculosis regimens including bedaquiline, delamanid and clofazimine. European Respiratory Journal, 2016, vol. 48, no. 5, pp. 1527–1529. DOI: 10.1183/13993003.01552-2016</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Human but not murine multipotent mesenchymal stromal cells exhibit broad-spectrum antimicrobial effector function mediated by indoleamine 2,3-dioxygenase / R. Meisel [et al.] // Leukemia. – 2011. – Vol. 25, N 4. – P. 648–654.</mixed-citation><mixed-citation xml:lang="en">Meisel R., Brockers S., Heseler K., Degistirici O., Bülle H., Woite C., Stuhlsatz S., Schwippert W., Jäger M., Sorg R., Henschler R., Seissler J., Dilloo D., Däubener W. Human but not murine multipotent mesenchymal stromal cells exhibit broadspectrum antimicrobial effector function mediated by indoleamine 2,3-dioxygenase. Leukemia, 2011, vol. 25, no. 4, pp. 648–654. DOI: 10.1038/leu.2010.310</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Mesenchymal stem cells improve murine acute coxsackievirus B3-induced myocarditis / S. Van Linthout [et al.] // Europ. Heart J. – 2010. – Vol. 32, N 17. – P. 2168–2178.</mixed-citation><mixed-citation xml:lang="en">Van Linthout S., Savvatis K., Miteva K., Peng J., Ringe J., Warstat K., Schmidt-Lucke C., Sittinger M., Schultheiss H. P., Tschöpe C. Mesenchymal stem cells improve murine acute coxsackievirus B3-induced myocarditis. European Heart Journal, 2010, vol. 32, no. 17, pp. 2168–2178. DOI: 10.1093/eurheartj/ehq467</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Mesenchymal stem cells reduce inflammation while enhancing bacterial clearance and improving survival in sepsis / Sh. H. J. Mei [et al.] // Amer. J. of Respiratory and Critical Care Medicine. – 2010. – Vol. 182, N 8. – P. 1047–1057.</mixed-citation><mixed-citation xml:lang="en">Mei Sh. H. J., Haitsma J. J., Dos Santos C. C., Deng Y., Lai P. F. H., Slutsky A. S., Liles W. C., Stewart D. J. Mesenchymal stem cells reduce inflammation while enhancing bacterial clearance and improving survival in sepsis. American Journal of Respiratory and Critical Care Medicine, 2010, vol. 182, no. 8, pp. 1047–1057. DOI: 10.1164/rccm.201001-0010OC</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Antibacterial effect of human mesenchymal stem cells is mediated in part from secretion of the antimicrobial peptide LL-37 / A. Krasnodembskaya [et al.] // Stem Cells. – 2010. – Vol. 28, N 12. – P. 2229–2238.</mixed-citation><mixed-citation xml:lang="en">Krasnodembskaya A., Song Y., Fang X., Gupta N., Serikov V., Lee J.-W., Matthay M. A. Antibacterial effect of human mesenchymal stem cells is mediated in part from secretion of the antimicrobial peptide LL-37. Stem Cells, 2010, vol. 28, no. 12, pp. 2229–2238. DOI: 10.1002/stem.544</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Stem cell transplantation: the lung barrier / S. Schrepfer [et al.] // Transplantation Proc. – 2007. – Vol. 39, N 2. – P. 573–576.</mixed-citation><mixed-citation xml:lang="en">Schrepfer S., Deuse T., Reichenspurner H., Fischbein M. P., Robbins R. C., Pelletier M. P. Stem cell transplantation: the lung barrier. Transplantation Proceedings, 2007, vol. 39, no. 2, pp. 573–576. DOI: http://dx.doi.org/10.1016/j. transproceed.2006.12.019</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Ex vivo glycan engineering of CD44 programs human multipotent mesenchymal stromal cell trafficking to bone / R. Sackstein [et al.] // Nature Medicine. – 2008. – Vol. 14, N 2. – P. 181–187.</mixed-citation><mixed-citation xml:lang="en">Sackstein R., Merzaban J. S., Cain D. W., Dagia N. M., Spencer J. A., Lin Ch. P., Wohlgemuth R. Ex vivo glycan engineering of CD44 programs human multipotent mesenchymal stromal cell trafficking to bone. Nature Medicine, 2008, vol. 14, no. 2, pp. 181–187. DOI: 10.1038/nm1703</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">The dynamic in vivo distribution of bone marrow-derived mesenchymal stem cells after infusion. / J. Gao [et al.] // Cells Tissues Organs. – 2001. – Vol. 169, N 1. – P. 12–20.</mixed-citation><mixed-citation xml:lang="en">Gao J., Dennis J. E., Muzic R. F., Lundberg M., Caplan A. I. The dynamic in vivo distribution of bone marrow-derived mesenchymal stem cells after infusion. Cells Tissues Organs, 2001, vol. 169, no. 1, pp. 12–20. DOI: 10.1159/000047856</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium: feasibility, cell migration, and body distribution. / I. M. Barbash [et al.] // Circulation. – 2003. – Vol. 108, N 7. – P. 863–868.</mixed-citation><mixed-citation xml:lang="en">Barbash I. M., Chouraqui P., Baron J., Feinberg M. S., Etzion Sh., Tessone A., Miller L., Guetta E., Zipori D., Kedes L. H., Kloner R. A., Leor J. Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium: feasibility, cell migration, and body distribution. Circulation, 2003, vol. 108, no. 7, pp. 863–868. DOI: 10.1161/01. CIR.0000084828.50310.6A</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Intravenous hMSCs improve myocardial infarction in mice because cells embolized in lung are activated to secrete the anti-inflammatory protein TSG-6 / R. H. Lee [et al.] // Cell Stem Cell. – 2009. – Vol. 5, N 1. – P. 54–63.</mixed-citation><mixed-citation xml:lang="en">Lee R. H., Pulin A. A., Seo M. J., Kota D. J., Ylostalo J., Larson B. L., Semprun-Prieto L., Delafontaine P., Prockop D. J. Intravenous hMSCs improve myocardial infarction in mice because cells embolized in lung are activated to secrete the antiinflammatory protein TSG-6. Cell Stem Cell, 2009, vol. 5, no. 1, pp. 54–63. DOI: 10.1016/j.stem.2009.05.003</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Therapeutic potential of mesenchymal stem cells for severe acute lung injury / M. A. Matthay [et al.] // Chest. – 2010. – Vol. 138, N 4. – P. 965–972.</mixed-citation><mixed-citation xml:lang="en">Matthay M. A., Thompson B. T., Read E. J., McKenna D. H., Liu K. D., Calfee C. S., Lee J. W. Therapeutic potential of mesenchymal stem cells for severe acute lung injury. Chest, 2010, vol. 138, no. 4, pp. 965–972. DOI: 10.1378/chest.10-0518</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Intrapulmonary delivery of bone marrow-derived mesenchymal stem cells improves survival and attenuates endotoxininduced acute lung injury in mice / N. Gupta [et al.] // J. of Immunology. – 2007. – Vol. 179, N 3. – P. 1855–1863.</mixed-citation><mixed-citation xml:lang="en">Gupta N., Su X., Popov B., Lee J. W., Serikov V., Matthay M. A. Intrapulmonary delivery of bone marrow-derived mesenchymal stem cells improves survival and attenuates endotoxin-induced acute lung injury in mice. Journal of Immunology, 2007, vol. 179, no. 3, pp. 1855–1863. DOI: 10.4049/jimmunol.179.3.1855</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Therapeutic effects of bone marrow-derived mesenchymal stem cells engraftment on bleomycin-induced lung injury in rats / F. Zhao [et al.] // Transplantation Proc. – 2008. – Vol. 40, N 5. – P. 1700–1705.</mixed-citation><mixed-citation xml:lang="en">Zhao F., Zhang Y. F., Liu Y. G., Zhou J. J., Li Z. K., Wu C. G., Qi H. W. Therapeutic effects of bone marrow-derived mesenchymal stem cells engraftment on bleomycin-induced lung injury in rats. Transplantation Proceedings, 2008, vol. 40, no. 5, pp. 1700–1705. DOI: 10.1016/j.transproceed.2008.01.080</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Mesenchymal stem cell engraftment in lung is enhanced in response to bleomycin exposure and ameliorates its fibrotic effects / L. A. Ortiz [et al.] // Proc. of the Nat. Acad. of Sciences. – 2003. – Vol. 100, N 14. – P. 8407–8411.</mixed-citation><mixed-citation xml:lang="en">Ortiz L. A., Gambelli F., McBride C., Gaupp D., Baddoo M., Kaminski N., Phinney D. G. Mesenchymal stem cell engraftment in lung is enhanced in response to bleomycin exposure and ameliorates its fibrotic effects. Proceedings of the National Academy of Sciences, 2003, vol. 100, no. 14, pp. 8407–8411. DOI: 10.1073/pnas.1432929100</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>
