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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">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/2079-701X-2018-10-128-133</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-2543</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>Обзоры</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Reviews</subject></subj-group></article-categories><title-group><article-title>Роль кишечной микробиоты в формировании ответа на иммунотерапию злокачественных новообразований: состояние проблемы</article-title><trans-title-group xml:lang="en"><trans-title>The role of gut microbiota in forming a response to immunotherapy of malignant neoplasms: problem state</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>Семиглазова</surname><given-names>Т. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Semiglazova</surname><given-names>T. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Доктор медицинских наук </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бриш</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Brish</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"/><bio xml:lang="en"/><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Галунова</surname><given-names>Т. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Galunova</surname><given-names>T. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"/><bio xml:lang="en"/><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бернацкий</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Bernatskiy</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"/><bio xml:lang="en"/><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Семиглазов</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Semiglazov</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Доктор медицинских наук </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"/><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Петрова» Минздрава России; &#13;
ФГБОУ ВО «Северо-Западный государственный медицинский университет им. И.И. Мечникова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>N.N.Petrov National Medical Research Centre of Oncology the Ministry of Health of Russia;&#13;
I.I. Mechnikov North-Western State Medical University of the Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Петрова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>N.N.Petrov National Medical Research Centre of Oncology the Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Петрова» Минздрава России;&#13;
ФГБОУ ВО «Первый Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>N.N.Petrov National Medical Research Centre of Oncology the Ministry of Health of Russia;&#13;
I.P. Pavlov First Saint Petersburg State Medical University of the Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>18</day><month>07</month><year>2018</year></pub-date><volume>0</volume><issue>10</issue><fpage>128</fpage><lpage>133</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Семиглазова Т.Ю., Бриш Н.А., Галунова Т.Ю., Бернацкий А.С., Семиглазов В.В., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Семиглазова Т.Ю., Бриш Н.А., Галунова Т.Ю., Бернацкий А.С., Семиглазов В.В.</copyright-holder><copyright-holder xml:lang="en">Semiglazova T.Y., Brish N.A., Galunova T.Y., Bernatskiy A.S., Semiglazov V.V.</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.med-sovet.pro/jour/article/view/2543">https://www.med-sovet.pro/jour/article/view/2543</self-uri><abstract><p>Современная концепция симбиотических взаимоотношений между макроорганизмом и микробиотой кишечника не вызывает сомнений. На состав микробиоты прежде всего влияют факторы окружающей среды, генетические и иммунные факторы организма хозяина. Дисбиоз кишечника может привести к доминированию некоторых видов бактерий, способствующих активации механизмов канцерогенеза и развитию злокачественных опухолей толстой кишки за счет хронического воспаления или местной иммуносупрессии. В эру иммуноонкологии роль кишечной микробиоты в формировании ответа на иммунотерапию злокачественных новообразований представляет большой интерес для медицинского сообщества. Учитывая, что состав кишечной микробиоты является индивидуальным для каждого человека, ее исследование как нельзя лучше вписывается в набирающую силу концепцию персонализированного медицинского подхода.</p></abstract><trans-abstract xml:lang="en"><p>The modern concept of symbiotic relationship between the macroorganism and the gut microbiota is practically assured. The microbiota composition is primarily influenced by environmental factors, genetic and immune factors of the host organism. The gut dysbiosis can lead to the dominance of certain types of bacteria that promote the activation of carcinogenesis mechanisms and the development of malignant tumours of the colon due to chronic inflammation or local immunosuppression. The role of the intestinal microbiota in forming a response to the immunotherapy of malignant neoplasms is of great interest to the medical community in the era of immunooncology. Given that the gut microbiota composition is individual for each person, its examination fits nicely into the up-and-coming concept of a personalized medical approach.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>кишечная микробиота</kwd><kwd>иммунотерапия</kwd><kwd>checkpoint-ингибиторы</kwd><kwd>антибиотикотерапия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>intestinal microbiota</kwd><kwd>immunotherapy</kwd><kwd>checkpoint-inhibitors</kwd><kwd>antibiotic therapy</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">Hawrelak JA, Myers SP. The causes of intestinal dysbiosis: a review Altern Med Rev, 2004, 9: 180-197.</mixed-citation><mixed-citation xml:lang="en">Hawrelak JA, Myers SP. The causes of intestinal dysbiosis: a review Altern Med Rev, 2004, 9: 180-197.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Stark PL, Lee А. The microbial ecology of the large bowel of breast–fed and formula–fed infants during the first year of life. J Med Microbiol, 1982 May, 5(2): 189–203, Walker &amp; Duffy, 1998.</mixed-citation><mixed-citation xml:lang="en">Stark PL, Lee А. The microbial ecology of the large bowel of breast–fed and formula–fed infants during the first year of life. J Med Microbiol, 1982 May, 5(2): 189–203, Walker &amp; Duffy, 1998.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Tuohy K, Del Rio D. Diet-microbe interactions in the gut. Elsevier Science, 2014: 268.</mixed-citation><mixed-citation xml:lang="en">Tuohy K, Del Rio D. Diet-microbe interactions in the gut. Elsevier Science, 2014: 268.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Кожевников А.А., Раскина К.В., Мартынова Е.Ю., Тяхт А.В., Перфильев А.В., Драпкина О.М. и др. Кишечная микробиота: современные представления о видовом составе, функциях и методах исследования. РМЖ, 2017, 17: 1244–1247.</mixed-citation><mixed-citation xml:lang="en">Kozhevnikov AA, Raskina KV, Martynova EYu, Tahht AV, Perfiliev AV, Drapkina OM et al. Gut microbiota: modern concepts of the species composition, functions and methods of investigation. RMJ, 2017, 17: 1244-1247.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Arora T, Bäckhed F. The gut microbiota and metabolic disease: current understanding and future perspectives. J Intern Med, 2016, 280(4): 339–349.</mixed-citation><mixed-citation xml:lang="en">Arora T, Bäckhed F. The gut microbiota and metabolic disease: current understanding and future perspectives. J Intern Med, 2016, 280(4): 339–349.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Salminen S, Bouley C, Boutron-Ruault M-C, Cummings JH, Franck A, Gibson GR, et al. Functional food science and gastrointestinal physiology and function. Br J Nutr, 1998, 80(suppl1).</mixed-citation><mixed-citation xml:lang="en">Salminen S, Bouley C, Boutron-Ruault M-C, Cummings JH, Franck A, Gibson GR, et al. Functional food science and gastrointestinal physiology and function. Br J Nutr, 1998, 80(suppl1).</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Хавкин А.И. Микробиоценоз кишечника и иммунитет. РМЖ, 2003, 3(11): 122-125.</mixed-citation><mixed-citation xml:lang="en">Khavkin AI. Microbiocenosis of the intestine and immunity. RMJ, 2003, 3 (11): 122-125</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Dominguez-Bello MG, Blaser MJ, Ley RE, Knight R. Development of the human gastrointestinal microbiota and insights from high-throughput sequencing. Gastroenterology, 2011, 140: 17131719.</mixed-citation><mixed-citation xml:lang="en">Dominguez-Bello MG, Blaser MJ, Ley RE, Knight R. Development of the human gastrointestinal microbiota and insights from high-throughput sequencing. Gastroenterology, 2011, 140: 17131719.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Sekirov I, Russell SL, Antunes LC, et al. Gut microbiota in health and disease. Physiol Rev, 2010. 90.</mixed-citation><mixed-citation xml:lang="en">Sekirov I, Russell SL, Antunes LC, et al. Gut microbiota in health and disease. Physiol Rev, 2010. 90.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Arumugam M, Raes J, Pelletier E, Le Paslier D, Yamada T, Mende DR et al. Enterotypes of the human gut microbiome. Nature, 2011, 473(7346): 174–180.</mixed-citation><mixed-citation xml:lang="en">Arumugam M, Raes J, Pelletier E, Le Paslier D, Yamada T, Mende DR et al. Enterotypes of the human gut microbiome. Nature, 2011, 473(7346): 174–180.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Iizumi T, Battaglia T, Ruiz V, Perez Perez GI. Gut Microbiome and Antibiotics. Arch Med Res, 2017 Nov, 48(8): 727-734</mixed-citation><mixed-citation xml:lang="en">Iizumi T, Battaglia T, Ruiz V, Perez Perez GI. Gut Microbiome and Antibiotics. Arch Med Res, 2017 Nov, 48(8): 727-734</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Koenig JE, Spor A, Scalfone N, Fricker AD, Stombaugh J, Knight R, Angenent LT et al. Succession of microbial consortia in the developing infant gut microbiome. Proc Natl AcadSci U S A, 2011 Mar 15, 108(Suppl 1): 4578-85.</mixed-citation><mixed-citation xml:lang="en">Koenig JE, Spor A, Scalfone N, Fricker AD, Stombaugh J, Knight R, Angenent LT et al. Succession of microbial consortia in the developing infant gut microbiome. Proc Natl AcadSci U S A, 2011 Mar 15, 108(Suppl 1): 4578-85.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Qin J, Li R, Raes J, Arumugam M, Burgdorf KS, Manichanh C. et al. A human gut microbial gene catalogue established by metagenomic sequencing. Nature, 2010 Mar 4, 464(7285): 59-65.</mixed-citation><mixed-citation xml:lang="en">Qin J, Li R, Raes J, Arumugam M, Burgdorf KS, Manichanh C. et al. A human gut microbial gene catalogue established by metagenomic sequencing. Nature, 2010 Mar 4, 464(7285): 59-65.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Yatsunenko T, Rey FE, Manary MJ, Trehan I, Dominguez-Bello MG, Contreras M. et al. Human gut microbiome viewed across age and geography. Nature, 2012 May 9, 486(7402): 222-227.</mixed-citation><mixed-citation xml:lang="en">Yatsunenko T, Rey FE, Manary MJ, Trehan I, Dominguez-Bello MG, Contreras M. et al. Human gut microbiome viewed across age and geography. Nature, 2012 May 9, 486(7402): 222-227.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Bager P, Melbye M, Rostgaard K, Benn CS, Westergaard T. Mode of delivery and risk of allergic rhinitis and asthma. J Allergy ClinImmunol, 2003 Jan, 111(1): 51-56.</mixed-citation><mixed-citation xml:lang="en">Bager P, Melbye M, Rostgaard K, Benn CS, Westergaard T. Mode of delivery and risk of allergic rhinitis and asthma. J Allergy ClinImmunol, 2003 Jan, 111(1): 51-56.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Cardwell CR, Stene LC, Joner G, Cinek O, Svensson J, Goldacre MJ. Caesarean section is associated with an increased risk of childhoodonset type 1 diabetes mellitus: a meta-analysis of observational studies. Diabetologia, 2008 May, 51(5): 726-735.</mixed-citation><mixed-citation xml:lang="en">Cardwell CR, Stene LC, Joner G, Cinek O, Svensson J, Goldacre MJ. Caesarean section is associated with an increased risk of childhoodonset type 1 diabetes mellitus: a meta-analysis of observational studies. Diabetologia, 2008 May, 51(5): 726-735.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Debley JS, Smith JM, Redding GJ, Critchlow CW. Childhood asthma hospitalization risk after cesarean delivery in former term and premature infants. Ann Allergy Asthma Immunol, 2005 Feb, 94(2): 228-233.</mixed-citation><mixed-citation xml:lang="en">Debley JS, Smith JM, Redding GJ, Critchlow CW. Childhood asthma hospitalization risk after cesarean delivery in former term and premature infants. Ann Allergy Asthma Immunol, 2005 Feb, 94(2): 228-233.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Phillips J, Gill N, Sikdar K, Penney S, Newhook LA. History of cesarean section associated with childhood onset of T1DM in Newfoundland and Labrador, Canada. J Environ Public Health, 2012, 2012: 635097.</mixed-citation><mixed-citation xml:lang="en">Phillips J, Gill N, Sikdar K, Penney S, Newhook LA. History of cesarean section associated with childhood onset of T1DM in Newfoundland and Labrador, Canada. J Environ Public Health, 2012, 2012: 635097.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Zeissig S, Blumberg R.S. Life at the beginning: perturbation of the microbiota by antibiotics in early life and its role in health and disease. Nat Immuno, 2014 Apr, 15(4): 307-310.</mixed-citation><mixed-citation xml:lang="en">Zeissig S, Blumberg R.S. Life at the beginning: perturbation of the microbiota by antibiotics in early life and its role in health and disease. Nat Immuno, 2014 Apr, 15(4): 307-310.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Бельмер С.В. Антибиотик-ассоциированный дисбактериоз кишечника. РМЖ, 2004, 3(12): 148–151.</mixed-citation><mixed-citation xml:lang="en">Belmer SV. Antibiotic-associated intestinal dysbacteriosis. RMJ, 2004, 3 (12): 148-151.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Янковский Д.С. Микробная экология человека: современные возможности ее поддержания и восстановления. К.: Эксперт ЛТД, 2005. С. 362.</mixed-citation><mixed-citation xml:lang="en">Yankovsky DS. Microbial human ecology: modern possibilities of its maintenance and restoration. К.: Expert of LTD., 2005. С. 362.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Burns AJ, Rowland IR. Anti-carcinogenicity of probiotics and prebiotics. Curr Issues Intest Microbiol, 2000 Mar, 1(1): 13-24.</mixed-citation><mixed-citation xml:lang="en">Burns AJ, Rowland IR. Anti-carcinogenicity of probiotics and prebiotics. Curr Issues Intest Microbiol, 2000 Mar, 1(1): 13-24.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Grivennikov SI, Wang K, Mucida D, Stewart CA, Schnabl B, Jauch D et al. Adenoma-linked barrier defects and microbial products drive IL-23/ IL-17-mediated tumour growth. Nature. 2012 Nov 8, 491(7423): 254-258.</mixed-citation><mixed-citation xml:lang="en">Grivennikov SI, Wang K, Mucida D, Stewart CA, Schnabl B, Jauch D et al. Adenoma-linked barrier defects and microbial products drive IL-23/ IL-17-mediated tumour growth. Nature. 2012 Nov 8, 491(7423): 254-258.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Wu S, Rhee KJ, Albesiano E, Rabizadeh S, Wu X, Yen HR. et al. A human colonic commensal promotes colon tumorigenesis via activation of T helper type 17 T cell responses. Nat Med, 2009 Sep, 15(9): 1016-1022.</mixed-citation><mixed-citation xml:lang="en">Wu S, Rhee KJ, Albesiano E, Rabizadeh S, Wu X, Yen HR. et al. A human colonic commensal promotes colon tumorigenesis via activation of T helper type 17 T cell responses. Nat Med, 2009 Sep, 15(9): 1016-1022.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Ghiringhelli F, Larmonier N, Schmitt E, Parcellier A, Cathelin D, Garrido C. et al. CD4+CD25+ regulatory T cells suppress tumor immunity but are sensitive to cyclophosphamide which allows immunotherapy of established tumors to be curative. Eur J Immunol, 2004 Feb, 34(2): 336-344.</mixed-citation><mixed-citation xml:lang="en">Ghiringhelli F, Larmonier N, Schmitt E, Parcellier A, Cathelin D, Garrido C. et al. CD4+CD25+ regulatory T cells suppress tumor immunity but are sensitive to cyclophosphamide which allows immunotherapy of established tumors to be curative. Eur J Immunol, 2004 Feb, 34(2): 336-344.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Noriho Iida, AmiranDzutsev, C. Andrew Stewart, Loretta Smith, Nicolas Bouladoux, Rebecca A. W. et al. Commensal Bacteria Control Cancer Response to Therapy by Modulating the Tumor Microenvironment. Science, 2013 Nov 22, 342(Issue 6161): 967-970.</mixed-citation><mixed-citation xml:lang="en">Noriho Iida, AmiranDzutsev, C. Andrew Stewart, Loretta Smith, Nicolas Bouladoux, Rebecca A. W. et al. Commensal Bacteria Control Cancer Response to Therapy by Modulating the Tumor Microenvironment. Science, 2013 Nov 22, 342(Issue 6161): 967-970.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Pochard P, Gosset P, Grangette C, Andre C, Tonnel AB, Pestel J. et al. Lactic acid bacteria inhibit TH2 cytokine production by mononuclear cells from allergic patients. J Allergy Clin Immunol, 2002 Oct, 110(4): 617-623.</mixed-citation><mixed-citation xml:lang="en">Pochard P, Gosset P, Grangette C, Andre C, Tonnel AB, Pestel J. et al. Lactic acid bacteria inhibit TH2 cytokine production by mononuclear cells from allergic patients. J Allergy Clin Immunol, 2002 Oct, 110(4): 617-623.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Viaud S, Flament C, Zoubir M, Pautier P, LeCesne A, Ribrag V. et al. Cyclophosphamide induces differentiation of Th17 cells in cancer patients. Cancer Res, 2011 Feb 1, 71(3): 661-665.</mixed-citation><mixed-citation xml:lang="en">Viaud S, Flament C, Zoubir M, Pautier P, LeCesne A, Ribrag V. et al. Cyclophosphamide induces differentiation of Th17 cells in cancer patients. Cancer Res, 2011 Feb 1, 71(3): 661-665.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Viaud S, Saccheri F, Mignot G, Yamazaki T, Daillère R, Dalil H et al. The Intestinal Microbiota Modulates the Anticancer Immune Effects of Cyclophosphamide. Science, 2013 Nov22, 342(Issue 6161): 971-976.</mixed-citation><mixed-citation xml:lang="en">Viaud S, Saccheri F, Mignot G, Yamazaki T, Daillère R, Dalil H et al. The Intestinal Microbiota Modulates the Anticancer Immune Effects of Cyclophosphamide. Science, 2013 Nov22, 342(Issue 6161): 971-976.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Vicari AP, Chiodoni C, Vaure C, Aït-Yahia S, Dercamp C, Matsos F et al. Reversal of tumorinduced dendritic cell paralysis by CpGimmunostimulatory oligonucleotide and anti-interleukin 10 receptor antibody. J Exp Med, 2002 Aug 19, 196(4): 541-549.</mixed-citation><mixed-citation xml:lang="en">Vicari AP, Chiodoni C, Vaure C, Aït-Yahia S, Dercamp C, Matsos F et al. Reversal of tumorinduced dendritic cell paralysis by CpGimmunostimulatory oligonucleotide and anti-interleukin 10 receptor antibody. J Exp Med, 2002 Aug 19, 196(4): 541-549.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Yamamoto ML, Maier I, Dang AT, Berry D, Liu J, Ruegger PM et al. Intestinal bacteria modify lymphoma incidence and latency by affecting systemic inflammatory state, oxidative stress, and leukocyte genotoxicity. Cancer Research, 2013, 73: 4222-4232.</mixed-citation><mixed-citation xml:lang="en">Yamamoto ML, Maier I, Dang AT, Berry D, Liu J, Ruegger PM et al. Intestinal bacteria modify lymphoma incidence and latency by affecting systemic inflammatory state, oxidative stress, and leukocyte genotoxicity. Cancer Research, 2013, 73: 4222-4232.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Joo HM, Hyun YJ, Myoung KS, Ahn YT, Lee JH, Huh CS et al. Lactobacillus johnsonii HY7042 ameliorates Gardnerella vaginalis-induced vaginosis by killing Gardnerella vaginalis and inhibiting NF-κB activation. Int Immunopharmacol, 2011 Nov, 11(11): 1758-1765.</mixed-citation><mixed-citation xml:lang="en">Joo HM, Hyun YJ, Myoung KS, Ahn YT, Lee JH, Huh CS et al. Lactobacillus johnsonii HY7042 ameliorates Gardnerella vaginalis-induced vaginosis by killing Gardnerella vaginalis and inhibiting NF-κB activation. Int Immunopharmacol, 2011 Nov, 11(11): 1758-1765.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Valladares R, Sankar D, Li N, Williams E, Lai K, Abdelgelie A et al. Lactobacillus johnsonii N6.2 Mitigates the Development of Type 1 Diabetes in BB-DP Rats. PLoS One, 2010, 5: e10507.</mixed-citation><mixed-citation xml:lang="en">Valladares R, Sankar D, Li N, Williams E, Lai K, Abdelgelie A et al. Lactobacillus johnsonii N6.2 Mitigates the Development of Type 1 Diabetes in BB-DP Rats. PLoS One, 2010, 5: e10507.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Pardoll D. Cancer and the Immune System: Basic Concepts and Targets for Intervention. Semin Oncol, 2015 Aug, 42(4): 523-538.</mixed-citation><mixed-citation xml:lang="en">Pardoll D. Cancer and the Immune System: Basic Concepts and Targets for Intervention. Semin Oncol, 2015 Aug, 42(4): 523-538.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Peled JU, Devlin SM, Staffas A, Lumish M, Khanin R, Littmann ER et al. Intestinal Microbiota and Relapse After HematopoieticCell Transplantation. J Clin Oncol, 2017 May 20, 35(15): 1650-1659.</mixed-citation><mixed-citation xml:lang="en">Peled JU, Devlin SM, Staffas A, Lumish M, Khanin R, Littmann ER et al. Intestinal Microbiota and Relapse After HematopoieticCell Transplantation. J Clin Oncol, 2017 May 20, 35(15): 1650-1659.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Routy B, Chatelier E, Derosa L, Duong C, Tidjani Alou M, Daillère R et al. Gut microbiome influences efficacy of PD-1–based immunotherapy against epithelial tumors. Science, 2017, Nov 02, pii: eaan3706. doi: 10.1126/science.aan3706.</mixed-citation><mixed-citation xml:lang="en">Routy B, Chatelier E, Derosa L, Duong C, Tidjani Alou M, Daillère R et al. Gut microbiome influences efficacy of PD-1–based immunotherapy against epithelial tumors. Science, 2017, Nov 02, pii: eaan3706. doi: 10.1126/science.aan3706.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Sivan A, Corrales L, Hubert N, Williams JB, Keston Aquino-Michaels, Zachary M Earley et al. Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy. Science, 2015 Nov 27, 350(6264): 1084–1089.</mixed-citation><mixed-citation xml:lang="en">Sivan A, Corrales L, Hubert N, Williams JB, Keston Aquino-Michaels, Zachary M Earley et al. Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy. Science, 2015 Nov 27, 350(6264): 1084–1089.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Vétizou M, Pitt JM, Daillère R, Lepage P, Waldschmitt N, Flament C et al. Anticancer immunotherapy by CTLA-4 blockade relies on the gut microbiota. Science, 2015 Nov 27, 350(6264): 1079–1084.</mixed-citation><mixed-citation xml:lang="en">Vétizou M, Pitt JM, Daillère R, Lepage P, Waldschmitt N, Flament C et al. Anticancer immunotherapy by CTLA-4 blockade relies on the gut microbiota. Science, 2015 Nov 27, 350(6264): 1079–1084.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Dong P, Yang Y, Wang WP. The role of intestinal bifidobacteria on immune system development in young rats. Early Hum Dev, 2010 Jan, 86(1): 51-58.</mixed-citation><mixed-citation xml:lang="en">Dong P, Yang Y, Wang WP. The role of intestinal bifidobacteria on immune system development in young rats. Early Hum Dev, 2010 Jan, 86(1): 51-58.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">López P, Gueimonde M, Margolles A, Suárez A: Distinct Bifidobacterium strains drive different immune responses in vitro. Int J Food Microbiol, 2010, 138: 157-165.</mixed-citation><mixed-citation xml:lang="en">López P, Gueimonde M, Margolles A, Suárez A: Distinct Bifidobacterium strains drive different immune responses in vitro. Int J Food Microbiol, 2010, 138: 157-165.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Ménard O, Butel M.J, Gaboriau-Routhiau V, Waligora-Dupriet AJ. Gnotobiotic mouse immune response induced by Bifidobacterium sp. strains isolated from infants. Appl Environ Microbiol, 2008, 74: 660–666.</mixed-citation><mixed-citation xml:lang="en">Ménard O, Butel M.J, Gaboriau-Routhiau V, Waligora-Dupriet AJ. Gnotobiotic mouse immune response induced by Bifidobacterium sp. strains isolated from infants. Appl Environ Microbiol, 2008, 74: 660–666.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Spranger S, Spaapen RM, Zha Y, Williams J, Meng Y, Ha TT, Gajewski TF. Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells. Sci Transl Med, 2013 Aug 28, 5(200): 200ra116.</mixed-citation><mixed-citation xml:lang="en">Spranger S, Spaapen RM, Zha Y, Williams J, Meng Y, Ha TT, Gajewski TF. Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells. Sci Transl Med, 2013 Aug 28, 5(200): 200ra116.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Gopalakrishnan V, Spencer CN, Nezi L, Reuben A, Andrews MC, Karpinets TV, Prieto PA et al. Gut microbiome modulates response to anti– PD-1 immunotherapy in melanoma patients. Science, 2018 Jan 05, 359(Issue 6371): 97-103.</mixed-citation><mixed-citation xml:lang="en">Gopalakrishnan V, Spencer CN, Nezi L, Reuben A, Andrews MC, Karpinets TV, Prieto PA et al. Gut microbiome modulates response to anti– PD-1 immunotherapy in melanoma patients. Science, 2018 Jan 05, 359(Issue 6371): 97-103.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Chaput N, Lepage P, Coutzac C, Soularue E, Le Roux K, Monot C et al. Baseline gut microbiota predicts clinical response and colitis in metastatic melanoma patients treated with ipilimumab. Ann Oncol, 2017 Jun 1, 28(6): 1368-1379.</mixed-citation><mixed-citation xml:lang="en">Chaput N, Lepage P, Coutzac C, Soularue E, Le Roux K, Monot C et al. Baseline gut microbiota predicts clinical response and colitis in metastatic melanoma patients treated with ipilimumab. Ann Oncol, 2017 Jun 1, 28(6): 1368-1379.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Xu H, Yang J, Gao W, Li L, Li P, Zhang L. et al. Innate immune sensing of bacterial modifications of Rho GTPases by the Pyrin inflammasome. Nature, 2014 Sep 11, 513(7517): 237-241.</mixed-citation><mixed-citation xml:lang="en">Xu H, Yang J, Gao W, Li L, Li P, Zhang L. et al. Innate immune sensing of bacterial modifications of Rho GTPases by the Pyrin inflammasome. Nature, 2014 Sep 11, 513(7517): 237-241.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Huang JY, Lee SM, Mazmanian SK. The human commensal Bacteroidesfragilis binds intestinal mucin. Anaerobe, 2011 Aug, 17(4): 137-141.</mixed-citation><mixed-citation xml:lang="en">Huang JY, Lee SM, Mazmanian SK. The human commensal Bacteroidesfragilis binds intestinal mucin. Anaerobe, 2011 Aug, 17(4): 137-141.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Dethlefsen L, Huse S, Sogin ML, Relman DA. The pervasive effects of an antibiotic on the human gut microbiota, as revealed by deep 16S rRNA sequencing. PLoS Biol, 2008 Nov 18, 6(11): e280.</mixed-citation><mixed-citation xml:lang="en">Dethlefsen L, Huse S, Sogin ML, Relman DA. The pervasive effects of an antibiotic on the human gut microbiota, as revealed by deep 16S rRNA sequencing. PLoS Biol, 2008 Nov 18, 6(11): e280.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Dethlefsen L, Relman DA. Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation. Proc Natl AcadSci U S A, 2011 Mar 15, 108(Suppl 1): 4554-61.</mixed-citation><mixed-citation xml:lang="en">Dethlefsen L, Relman DA. Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation. Proc Natl AcadSci U S A, 2011 Mar 15, 108(Suppl 1): 4554-61.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Jernberg C, Löfmark S, Edlund C, Jansson JK. Long-term ecological impacts of antibiotic administration on the human intestinal microbiota. ISME J, 2007 May, 1(1): 56-66.</mixed-citation><mixed-citation xml:lang="en">Jernberg C, Löfmark S, Edlund C, Jansson JK. Long-term ecological impacts of antibiotic administration on the human intestinal microbiota. ISME J, 2007 May, 1(1): 56-66.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Bartosch S, Fite A, Macfarlane GT, McMurdo ME. Characterization of bacterial communities in feces from healthy elderly volunteers and hospitalized elderly patients by using real-time PCR and effects of antibiotic treatment on the fecal microbiota. Appl Environ Microbiol, 2004 Jun, 70(6): 3575-81.</mixed-citation><mixed-citation xml:lang="en">Bartosch S, Fite A, Macfarlane GT, McMurdo ME. Characterization of bacterial communities in feces from healthy elderly volunteers and hospitalized elderly patients by using real-time PCR and effects of antibiotic treatment on the fecal microbiota. Appl Environ Microbiol, 2004 Jun, 70(6): 3575-81.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Palmer C, Bik EM, DiGiulio DB, Relman DA, Brown PO. Development of the human infant intestinal microbiota. PLoS Biol, 2007 Jul, 5(7): e177.</mixed-citation><mixed-citation xml:lang="en">Palmer C, Bik EM, DiGiulio DB, Relman DA, Brown PO. Development of the human infant intestinal microbiota. PLoS Biol, 2007 Jul, 5(7): e177.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">http: //www.ascopost.com/News/48357.</mixed-citation><mixed-citation xml:lang="en">http: //www.ascopost.com/News/48357.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Kamada N, Núñez G. Regulation of the immune system by the resident intestinal bacteria. Gastroenterology, 2014 May, 146(6): 1477-1488.</mixed-citation><mixed-citation xml:lang="en">Kamada N, Núñez G. Regulation of the immune system by the resident intestinal bacteria. Gastroenterology, 2014 May, 146(6): 1477-1488.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Kamada N, Seo SU, Chen GY, Núñez G. Role of the gut microbiota in immunity and inflammatory disease. Nat Rev Immunol. 2013 May, 13(5): 321-335</mixed-citation><mixed-citation xml:lang="en">Kamada N, Seo SU, Chen GY, Núñez G. Role of the gut microbiota in immunity and inflammatory disease. Nat Rev Immunol. 2013 May, 13(5): 321-335</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Derosa L, Routy B, Enot D, Baciarello G, Massard C, Loriot Y et al. Impact of antibiotics on outcome in patients with metastatic renal cell carcinoma treated with immune checkpoint inhibitors. J Clin Oncol, 2017, 35(suppl 6S, abstract 462).</mixed-citation><mixed-citation xml:lang="en">Derosa L, Routy B, Enot D, Baciarello G, Massard C, Loriot Y et al. Impact of antibiotics on outcome in patients with metastatic renal cell carcinoma treated with immune checkpoint inhibitors. J Clin Oncol, 2017, 35(suppl 6S, abstract 462).</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">https:www.ncbi.nlm.nih.gov/pmc/articles/ PMC44896221/.</mixed-citation><mixed-citation xml:lang="en">https:www.ncbi.nlm.nih.gov/pmc/articles/ PMC44896221/.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Derosa L, Hellmann MD, Spaziano M, Halpenny D, Fidelle M, Rizvi H et al. Negative association of antibiotics on clinical activity of immune checkpoint inhibitors in patients with advanced renal cell and non-small cell lung cancer. Ann Oncol, 2018 Mar 30, pii: 4956695. doi: 10.1093.</mixed-citation><mixed-citation xml:lang="en">Derosa L, Hellmann MD, Spaziano M, Halpenny D, Fidelle M, Rizvi H et al. Negative association of antibiotics on clinical activity of immune checkpoint inhibitors in patients with advanced renal cell and non-small cell lung cancer. Ann Oncol, 2018 Mar 30, pii: 4956695. doi: 10.1093.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Полуэктова Е.А., Ляшенко О.С., Шифрин О.С. и др. Современные методы изучения микрофлоры желудочно-кишечного тракта человека. РЖГГК, 2014, 2: 85-91./ Poluektova EA, Lyashenko OS, Shifrin OS. Modern methods for studying the microflora of the human gastrointestinal tract. RZHGGK, 2014, 2: 85-91.</mixed-citation><mixed-citation xml:lang="en">Полуэктова Е.А., Ляшенко О.С., Шифрин О.С. и др. Современные методы изучения микрофлоры желудочно-кишечного тракта человека. РЖГГК, 2014, 2: 85-91./ Poluektova EA, Lyashenko OS, Shifrin OS. Modern methods for studying the microflora of the human gastrointestinal tract. RZHGGK, 2014, 2: 85-91.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Blaut M, Collins MD, Welling GW et al. Molecular biological methods for studying the gut microbiota: The EU human gut flora project. Br J Nutr, 2002, 87(suppl. 2): 203–211.</mixed-citation><mixed-citation xml:lang="en">Blaut M, Collins MD, Welling GW et al. Molecular biological methods for studying the gut microbiota: The EU human gut flora project. Br J Nutr, 2002, 87(suppl. 2): 203–211.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Dennemont J, Roupas A, Heitz M. Differentiation of Campylobacter jejuni, C. coli, C. lary and C. fetus fatty acid profiles obtained by gas chromatography – mass spectrometry and by their hippurate hydrolysis. Mitt Geb Lebensmittelunters Hyg, 1992, 83(2): 142–150.</mixed-citation><mixed-citation xml:lang="en">Dennemont J, Roupas A, Heitz M. Differentiation of Campylobacter jejuni, C. coli, C. lary and C. fetus fatty acid profiles obtained by gas chromatography – mass spectrometry and by their hippurate hydrolysis. Mitt Geb Lebensmittelunters Hyg, 1992, 83(2): 142–150.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Morgan XC, Huttenhower C. Chapter: Human microbiome analysis. PLoS Comput Biol, 2012, 8(suppl. 12).</mixed-citation><mixed-citation xml:lang="en">Morgan XC, Huttenhower C. Chapter: Human microbiome analysis. PLoS Comput Biol, 2012, 8(suppl. 12).</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Prakash S et al. Gut microbiota: next frontier in understanding human health and development of biotherapeutics. Biologics, 2011, 5: 71–86.</mixed-citation><mixed-citation xml:lang="en">Prakash S et al. Gut microbiota: next frontier in understanding human health and development of biotherapeutics. Biologics, 2011, 5: 71–86.</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>
