<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Journal of microbiology, epidemiology and immunobiology</journal-id><journal-title-group><journal-title xml:lang="en">Journal of microbiology, epidemiology and immunobiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Журнал микробиологии, эпидемиологии и иммунобиологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0372-9311</issn><issn publication-format="electronic">2686-7613</issn><publisher><publisher-name xml:lang="en">Central Research Institute for Epidemiology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">13917</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">INTESTINE INFECTIONS, INFLAMMATION AND AUTOIMMUNITY. LYMPHOID APPARATUS OF INTESTINE IN INTERACTION WITH INTESTINE MICROFLORA</article-title><trans-title-group xml:lang="ru"><trans-title>КИШЕЧНЫЕ ИНФЕКЦИИ, ВОСПАЛЕНИЕ И АУТОИММУНИТЕТ. ЛИМФОИДНЫЙ АППАРАТ КИШЕЧНИКА ВО ВЗАИМОДЕЙСТВИИ С КИШЕЧНОЙ МИКРОФЛОРОЙ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Balmasova</surname><given-names>I. P</given-names></name><name xml:lang="ru"><surname>Балмасова</surname><given-names>И. П</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sepiashvili</surname><given-names>R. I</given-names></name><name xml:lang="ru"><surname>Сепиашвили</surname><given-names>Р. И</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Russian University of Peoples’ Friendship, Moscow, Russia</institution></aff><aff><institution xml:lang="ru">Российский университет дружбы народов, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-02-15" publication-format="electronic"><day>15</day><month>02</month><year>2013</year></pub-date><volume>90</volume><issue>1</issue><issue-title xml:lang="en">NO1 (2013)</issue-title><issue-title xml:lang="ru">№1 (2013)</issue-title><fpage>113</fpage><lpage>120</lpage><history><date date-type="received" iso-8601-date="2023-06-09"><day>09</day><month>06</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2013, Balmasova I.P., Sepiashvili R.I.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2013, Балмасова И.П., Сепиашвили Р.И.</copyright-statement><copyright-year>2013</copyright-year><copyright-holder xml:lang="en">Balmasova I.P., Sepiashvili R.I.</copyright-holder><copyright-holder xml:lang="ru">Балмасова И.П., Сепиашвили Р.И.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://microbiol.crie.ru/jour/article/view/13917">https://microbiol.crie.ru/jour/article/view/13917</self-uri><abstract xml:lang="en"><p>Topicality of interrelation between intestine infections, inflammation diseases of intestine and autoimmune processes is widely discussed in scientific literature of recent years. Thereby a review of literature on the designated aspect of the problem is dedicated to the analysis of interconnection between structural-functional features of lymphoid apparatus of intestine and its ability to react to antigen load from both commensal and pathogenic intestine microflora. During description of structure and functions of lymphoid formation of intestine a particular attention is paid to difference of subpopulation characteristics of lymphocytes and antigen-presenting cells composing intra-epithelial lymphocytes, elements of immune system lamina propria , Peyer’s patches, mesenteric lymphatic nodes. The role of normal microflora and infectious agents in trigger mechanisms of reaction of immunocompetent cells is underscored; key aspects of cellular-molecular mechanisms of mucous membrane immune system functions are discussed.</p></abstract><trans-abstract xml:lang="ru"><p>Актуальность взаимосвязи между кишечными инфекциями, воспалительными заболеваниями кишечника и аутоиммунными процессами широко обсуждается в научной литературе последних лет. Обзор литературы по обозначенному аспекту проблемы посвящен анализу взаимосвязи между структурно-функциональными особенностями лимфоидного аппарата кишечника и его способностью реагировать на антигенную нагрузку со стороны как комменсальной, так и патогенной кишечной микрофлоры. При описании структуры и функций лимфоидных образований кишечника особое внимание уделяется различию субпопуляционных характеристик лимфоцитов и антигенпрезентирующих клеток в составе интраэпителиальных лимфоцитов, элементов иммунной системы lamina propria, пейеровых бляшек, мезентериальных лимфатических узлов. Подчеркивается роль нормальной микрофлоры и инфекционных агентов в пусковых механизмах реагирования иммунокомпетентных клеток, обсуждаются ключевые аспекты клеточно-молекулярных механизмов функционирования иммунной системы слизистых оболочек кишечника.</p></trans-abstract><kwd-group xml:lang="en"><kwd>intestine infections</kwd><kwd>autoimmune diseases</kwd><kwd>intestine lymphoid formations</kwd><kwd>lymphocyte subpopu- lations</kwd><kwd>antigen-presenting cells</kwd><kwd>commensal microflora</kwd><kwd>infectious agents</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>кишечные инфекции</kwd><kwd>аутоиммунные заболевания</kwd><kwd>лимфоидные образования кишечника</kwd><kwd>субпопуляции лимфоцитов</kwd><kwd>антигенпрезентирующие клетки</kwd><kwd>комменсальная микро- флора</kwd><kwd>инфекционные агенты</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Мазанкова Л.Н., Захарова И.Н. Инфекционные аспекты соматической патологии у детей. Российский вестник перинатологии и педиатрии. 2010, 55: 82-85.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Онищенко Г.Г., Жебрун А.Б. О санитарно-эпидемиологической обстановке в Российской Федерации в 2008 году. М., Федеральный центр гигиены и эпидемиологии Роспотребнадзора, 2009.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Abraham C., Cho J.H. IL-23 and autoimmunity: new insights into the pathogenesis of inflammatory bowel disease. Annu. Rev. Med. 2009, 60: 97-110.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Abraham C., Cho J. Interleukin-23/Th17 pathways and inflammatory bowel disease. Inflamm. Bowel Dis. 2009, 15: 1090-1100.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Acheson D.W., Luccioli S. Microbial-gut interactions in health and disease. Mucosal immune responses. Best Pract. Res. Clin. Gastroenterol. 2004, 18: 387-404.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Bach J.F. Protective role of infections and vaccinations on autoimmune diseases. J. Autoimmun. 2001, 16: 347-353.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Bach J.F. Infections and autoimmune diseases. J. Autoimmun. 2005, 25: 74-80.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Bargen J.A., Jackman R.J., Kerr J.G. Complications and sequelae of chronic ulcerative colitis. Ann. Intern. Med. 1929, 3: 335-352.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Biancone L., Monteleone I., Del Vecchio Blanco G. et al. Resident bacterial flora and immune system. Dig. Liver Dis. 2002, 34: 37-43.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Chong V.V.W., Simpson N., Ciofani M. et al. Epigenetic propagation of CD4 expression is established by the Cd4 proximal enhancer in helper T cells. Immunity. 2003, 19: 71-82.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Christen U., von Herrath M.G. Infections and Autoimmunity – Good or Bad? J. Immunol. 2005, 174: 7481-7486.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Finch W. Arthritis and the gut. Postgrad. Med. 1989, 86 (229—230): 233-234.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Gaisford W., Cooke A. Can infections protect against autoimmunity? Curr. Opin. Rheumatol. 2009, 21: 391-396.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Garrett W.S., Gordon J.I., Glimcher L.H. Homeostasis and inflammation in the intestine. Cell. 2010, 140: 859-870.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Gelman A.E., Zhang J., Choi Y., Turka L.A. Toll-like receptor ligands directly promote activated CD4+ T cell survival. J. Immunol. 2004, 172: 6065-6073.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Inman R.D. Arthritis and enteritis an interface of protean manifestations. J. Rheumatol. 1987, 14: 406-410.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Ivanov I.I., McKenzie B.S., Zhou L. et al. The orphan nuclear receptor RORgamma directs the differentiation program of proinflammatory IL-17(+) T helper cells. Nat. Neurosci. 2005, 8: 752-758.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Kannan S. Free radical theory of autoimmunity. Theor. Biol. Med. Model. 2006, 3: 22.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Le Bourhis L., Guerri L., Dusseaux M. et al. Mucosal-associated invariant T cells: unconventional development and function. Trends Immunol. 2011, 32: 212-218.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Leskovek N.V., Mackay I.R., Rose N.R. Cell damage and autoimmunity: a critical appraisal. J. Autoimmun. 2008, 30: 5-11.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Martin F., Oliver A.M., Kearney J.F. Marginal zone and B1 B cells unite in the early response against T-independent blood-borne particulate antigens. Immunity. 2001, 14: 617-629.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Mazmanian S.K., Liu C.H., Tzianabos A.O. et al. An immunomodulatory molecule of symbiotic bacteria directs maturation of the host immune system. Cell. 2005, 122: 107-118.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Mazmanian S.K., Round J.L., Kasper D.L. A microbial symbiosis factor prevents intestinal inflammatory disease. Nature. 2008, 453: 620-625.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Milner E.C.B., Anolik J., Cappione A. et al. Human innate B cells: a link between host defense and autoimmunity? Springer Semin. Immunopathol. 2005, 26: 433-452.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Mowat A.M., Bain C.C. Mucosal macrophages in intestinal homeostasis and inflammation. J. Innate Immun. 2011, 3: 550-564.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Münz С., Lünemann J.D., Getts M.T. et al. Antiviral immune responses: triggers of or triggered by autoimmunity? Nat. Rev. Immunol. 2009, 9: 246-258.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Niess J.H. Role of mucosal dendritic cells in inflammatory bowel disease. World J. Gastroenterol. 2008, 14: 5138-5148.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Niess J.H., Brand S., Gu X. et al. CX3CR1-mediated dendritic cell access to the intestinal lumen and bacterial clearance. Cell. 2006, 126: 1121-1133.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Orlando A., Renna S., Perricone G. et al. Gastro-intestinal lesions associated with spondyloarthropathies. World J. Gastroenterol. 2009, 15: 2443-2448.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Peaudecerf L., Rocha B. Role of the gut as a primary lymphoid organ. Immunol. Lett. 2011, 140: 1-6.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Peterson D.A., McNulty N.P., Guruge J.L. et al. IgA response to symbiotic bacteria as a mediator of gut homeostasis. Cell Host and Microbe. 2007, 2: 328-339.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Pordeus V., Szyper-Kravitz M., Levy R.A. et al. Infections and autoimmunity: a panorama. Clin. Rev. Allergy Immunol. 2008, 34: 283-299.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Ramiro-Puig E., Pérez-Cano F.J., Castellote C. et al. The bowel: A key component of the immune system. Rev. Esp. Enferm. Dig. (Madrid). 2008, 100: 29-34.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Rodríguez-Reyna T.S., Martínez-Reyes C., Yamamoto-Furusho J.K. Rheumatic manifestations of inflammatory bowel disease. World J. Gastroenterol. 2009, 15: 5517-5524.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Rutella S., Locatelli F. Intestinal dendritic cells in the pathogenesis of inflammatory bowel disease. World J. Gastroenterol. 2011, 17: 3761-3775.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Sahly H., Podschun R., Kekow J. et al. Humoral immune response to Klebsiella capsular polysaccharides in HLA-B27-positive patients with acute anterior uveitis and ankylosing spondylitis. Autoim- munity. 1998, 28: 209-215.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Suzuki K., Kawamoto S., Maruya M. et al. GALT: organization and dynamics leading to IgA synthesis. Adv. Immunol. 2010, 107: 153-185.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Suzuki K., Meek B., Doi Y. et al. Aberrant expansion of segmented filamentous bacteria in IgA-deficient gut. Proc. Natl. Acad. Sci. USA. 2004, 101: 1981-1986.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Tiwana H., Wilson C., Walmsley R.S. et al. Antibody responses to gut bacteria in ankylosing spondylitis, rheumatoid arthritis, Crohn's disease and ulcerative colitis. Rheumatol. Int. 1997, 17: 11-16.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Tlaskalová-Hogenová H., Stepánková R., Hudcovic T. et al. Commensal bacteria (normal microflora), mucosal immunity and chronic inflammatory and autoimmune diseases. Immunol. Lett. 2004, 93: 97-108.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Van der Kleij D., Yazdanbakhsh M. Control of inflammatory diseases by pathogens: lipids and the immune system. Eur. J. Immunol. 2003, 33: 2953-2963.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Van Wijk F., Cheroutre H. Intestinal T cells: Facing the mucosal immune dilemma with synergy and diversity. Semin. Immunol. 2009, 21: 130-138.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Wenzel B. E., Heesemann J., Heufelder A. et al. Enteropathogenic Yersinia enterocolitica and organ- specific autoimmune diseases in man. In: Une Т., Maruyama Т., Tsubokura M. (ed.). Current investi- gation of the microbiology of Yersinia. Basel, Karger. 1991, p. 80-88.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Wu H.-J., Ivanov I.I., Darce J. et al. Gut-residing segmented filamentous bacteria drive autoimmune arthritis via T helper 17 cells. Immunity. 2010, 32: 815-827.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Zhou L., Ivanov I.I., Spolski R. et al. IL-6 programs T(H)-17 cell differentiation by promoting sequential engagement of the IL-21 and IL-23 pathways. Development. 2002, 129: 4249-4260.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Zhou L., Lopes J.E., Chong M.M.W. et al. TGF-beta-induced Foxp3 inhibits T(H)17 cell differentiation by antagonizing RORgammat function. J. Exp. Med. 2002, 196: 65-75.</mixed-citation></ref></ref-list></back></article>
