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<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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pharmateca</journal-id><journal-title-group><journal-title xml:lang="en">Pharmateca</journal-title><trans-title-group xml:lang="ru"><trans-title>Фарматека</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2073-4034</issn><issn publication-format="electronic">2414-9128</issn><publisher><publisher-name xml:lang="en">Bionika Media</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">294382</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>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">BIOLOGICAL PREPARATIONS IN THERAPY OF INFLAMMATORY BOWEL DISEASES: REALITY AND PROSPECTS</article-title><trans-title-group xml:lang="ru"><trans-title>Биологические препараты в терапии воспалительных заболеваний кишечника: реальность и перспективы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Skalinskaya</surname><given-names>M. I</given-names></name><name xml:lang="ru"><surname>Скалинская</surname><given-names>М. И</given-names></name></name-alternatives><bio xml:lang="en"><p>PhD in Medical Sciences, Associate Professor at the Department of Propaedeutics of Internal Diseases, Gastroenterology and Dietology</p></bio><bio xml:lang="ru"><p>к.м.н., доцент кафедры пропедевтики внутренних болезней, гастроэнтерологии и диетологии</p></bio><email>mskalinskaya@yahoo.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bakulin</surname><given-names>I. G</given-names></name><name xml:lang="ru"><surname>Бакулин</surname><given-names>И. Г</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Skazyvaeva</surname><given-names>E. V</given-names></name><name xml:lang="ru"><surname>Сказываева</surname><given-names>Е. В</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zhigalova</surname><given-names>T. N</given-names></name><name xml:lang="ru"><surname>Жигалова</surname><given-names>Т. Н</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ryndin</surname><given-names>K. N</given-names></name><name xml:lang="ru"><surname>Рындин</surname><given-names>К. Н</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Solovyev</surname><given-names>M. V</given-names></name><name xml:lang="ru"><surname>Соловьев</surname><given-names>М. В</given-names></name></name-alternatives><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">FSBEI HE NWSMU n.a. I.I. Mechnikov</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО СЗГМУ им. И.И. Мечникова</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">FSBMEI HE «Military Medical Academy n.a. S.M. Kirov» of the Ministry of Defense of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБВОУ ВО «Военно-медицинская академия им. С.М. Кирова» МО РФ</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2017-12-15" publication-format="electronic"><day>15</day><month>12</month><year>2017</year></pub-date><volume>24</volume><issue>5S</issue><issue-title xml:lang="en">NOS5 (2017)</issue-title><issue-title xml:lang="ru">№S5 (2017)</issue-title><fpage>85</fpage><lpage>93</lpage><history><date date-type="received" iso-8601-date="2023-02-27"><day>27</day><month>02</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2017, Bionika Media</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2017, ООО «Бионика Медиа»</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="en">Bionika Media</copyright-holder><copyright-holder xml:lang="ru">ООО «Бионика Медиа»</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/2073-4034/article/view/294382">https://journals.eco-vector.com/2073-4034/article/view/294382</self-uri><abstract xml:lang="en"><p>The etiology of inflammatory bowel diseases (IBDs) is unknown, and pathogenesis is not fully understood. To date, monoclonal antibodies to tumor necrosis factor a and antibodies to α4-β7 are available for patients with IBDs in the Russian Federation. But at present, the direction of targeted therapy is actively developing in the world: the experience of the use of these agents is accumulating; the search for new molecules that are capable of interrupting the inflammatory cascade and simultaneously having a high safety profile is continuing.</p></abstract><trans-abstract xml:lang="ru"><p>Этиология воспалительных заболеваний кишечника (ВЗК) неизвестна, а патогенез понятен не в полном объеме. На сегодняшний день для пациентов с ВЗК в Российской Федерации доступны моноклональные антитела к фактору некроза опухоли а и антитела против α4-β7. Но в настоящее время в мире активно развивается направление таргетной терапии: накапливается опыт применения первых препаратов, продолжается поиск новых молекул, способных прерывать воспалительный каскад и одновременно с этим имеющих высокий профиль безопасности.</p></trans-abstract><kwd-group xml:lang="en"><kwd>inflammatory bowel diseases</kwd><kwd>ulcerative colitis</kwd><kwd>Crohn's disease</kwd><kwd>antibodies to tumor necrosis factor β</kwd><kwd>antibodies to α4-β7</kwd><kwd>targeted therapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>воспалительные заболевания кишечника</kwd><kwd>язвенный колит</kwd><kwd>болезнь Крона</kwd><kwd>антитела к фактору некроза опухоли β</kwd><kwd>антитела к α4-β7</kwd><kwd>таргетная терапия</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Neurath M.F., Fuss I., Kelsall B.L., Presky D.H., Waegell W., Strober W. Experimental granulomatous colitis in mice is abrogated by induction of TGF-beta-mediated oral tolerance. J. Exp. Med. 1996;183(6):2605-16.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Monteleone G., Boirivant M., Pallone F., MacDonald T.T. TGF-β1 and Smad7 in the regulation of IBD. Mucosal. Immunol. 2008;1(1):50-3.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Ito R., Shin-Ya M., Kishida T., Urano A., Takada R., Sakagami J., Imanishi J., Kita M., Ueda Y., Iwakura Y., Kataoka K., Okanoue T., Mazda O. Interferongamma is causatively involved in experimental inflammatory bowel disease in mice. Clin. Exp. Immunol. 2006;146(2):330-38.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Roggenbuck D., Reinhold D., Wex T., Goihl A., von Arnim U., Malfertheiner P., B ttnerT., Porstmann T., Porstmann S., Liedvogel B., Bogdanos D.P., Laass M.W, Conrad K. Autoantibodies to GP2, the major zymogen granule membrane glycoprotein, are new markers in Crohn's disease. Clin. Chim. Acta. 2011;412(9-10):718-24.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Muzes G., Molnár B., Tulassay Z., Sipos F. Changes of the cytokine profile in inflammatory bowel diseases. World J. Gastroenterol. 2012;18(41):5848-61.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Geremia A., Jewell D.P. The IL-23/IL-17 pathway in inflammatory bowel disease. Expert Rev. Gastroenterol. Hepatol. 2012;6:223-37.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Lu Y.C., Yeh W.C., Ohashi P.S. LPS/TLR4 signal transduction pathway. Cytokine. 2008; 42:145-51.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Coskun M., Olsen J., Seidelin J.B., Nielsen O.H. MAP kinases in inflammatory bowel disease. Clin. Chim. Acta. 2011;412:513-20.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Белоусова Е.А., Морозова Н.А., Никитина Н.В. Инфликсимаб (ремикейд) в лечении рефрактерных форм болезни Крона. РМЖ. 2005;7(1):28-32.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Hanauer S.B., Feagan B.G., Lichtenstein G.R., Mayer L.F., Schreiber S., Colombel J.F., Rachmilewitz D., Wolf D.C., Olson A., Bao W., Rutgeerts P. Maintenanse Infliximab for Crohn's Disease: the ACCENT I Randomised Trial. Lancet. 2002;359:1541-49.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Rutgeerts P.A. Critical Assessment of new Therapies in Inflammatory Bovel Diseases. J. Gastroenterol. Hepatol. 2002;17:177.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Rutgeerts P., Feagan B., Olson A., et al. A Randomized Placebo-Controlled Trial of Infliximab Therapy for Active Ulcerative Colitis: Act 1 Trial. Gastroenterol. 2005;128(Suppl. 2).</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Sandborn W., Rachmilewitz D., Hanauer S., et al. Infliximab Induction and Maintenanse Therapy for Ulcerative Colitis: the Act 2 Trial. Gastroenterol. 2005;128(4, Suppl. 2):49.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Argüelles-Arias F., Guerra Veloz M.F., Perea Amarillo R., Vilches-Arenas A., Castro Laria L., Maldonado Pérez B., Chaaro D., Benítez Roldán A., Merino V., Ramírez G., Caunedo Álvarez A., Romero Gómez M. Effectiveness and Safety of CT-P13 (Biosimilar Infliximab) in Patients with Inflammatory Bowel Disease in Real Life at 6 Months. Dig. Dis. Sci. 2017;62(5):1305-12.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Jorgensen K.K., Olsen I.C., Goll G.L., Lorentzen M., Bolstad N., Haavardsholm E.A., Lundin K.E.A., Mork C., Jahnsen J., Kvien T.K. Switching from originator infliximab to biosimilar CT-P13 compared with maintained treatment with originator infliximab (NOR-SWITCH): a 52-week, randomised, double-blind, non-inferiority trial. Lancet. 2017;389(10086):2304-16.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Udata C., Hua S.Y., Yin D., et al. A phase I pharmacokinetics trial comparing PF-06438179 (a potential biosimilar) and infliximab in healthy volunteers (REFLEXTIONS B537-01). Ann. Rheum. Dis. 2014;73:494.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Shin D., Kim Y.H., Kim Y.S., Fuhr R., Körnicke T. A phase I pharmacokinetic study comparing SB2, an infliximab biosimilar, and infliximab reference product (Remicade) in healthy subjects [abstract.]. Ann. Rheum. Dis. 2015; 74(suppl 2):459-60.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Hanauer S.B., Sandborn W.J., Rutgeerts P., Fedorak R.N., Lukas M., MacIntosh D., Panaccione R., Wolf D., Pollack P. Human antitumor necrosis factor monoclonal antibody (adalimumab) in Crohn's disease: the CLASSIC-I trial. Gastroenterology. 2006;130(2):323-33.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Yang Z., Ye X.Q., Zhu Y.Z., Liu Z., Zou Y., Deng Y., Guo C.C., Garg S.K., Feng J.S. Short-term effect and adverse events of adalimumab versus placebo in inducing remission for moderate-to-severe ulcerative colitis: a meta-analysis. Int. J. Clin. Exp. Med. 2015;8(1):86-93.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Papp K., Bachelez H., Costanzo A., Foley P., Gooderham M., Kaur P., Philipp S., Spelman L., Zhang N., Strober B. Clinical similarity of the biosimilar ABP 501 compared with adalimumab after single transition: long-term results from a randomized controlled, double-blind, 52-week, phase III trial in patients with moderate-to-severe plaque psoriasis. Br. J. Dermatol. 2017;76(6):1093.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Kaur P., Chow V., Zhang N., Moxness M., Kaliyaperumal A., Markus R. A randomised, single-blind, single-dose, three-arm, parallel-group study in healthy subjects to demonstrate pharmacokinetic equivalence of ABP 501 and adalimumab. Ann. Rheum. Dis. 2017;76(3):526-33.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Lowenberg M., de Boer N.K., Hoentjen F. Golimumab for the treatment of ulcerative colitis. Clin. Exp. Gastroenterol. 2014;7:53-9.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Tursi A., Allegretta L., Buccianti N., Della Valle N., Elisei W., Forti G., Faggiani R., Gallina S., Hadad Y., Larussa T., Lauria A., Luzza F., Lorenzetti R., Mocci G., Penna A., Polimeni N., Pranzo G., Ricciardelli C., Zampaletta C., Picchio M. Effectiveness and Safety of Golimumab in Treating Outpatient Ulcerative Colitis: A Real-Life Prospective, Multicentre, Observational Study in Primary Inflammatory Bowel Diseases Centers. J Gastrointestin Liver Dis. 2017;26(3): 239-44.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Voulgari P.V. Emerging drugs for rheumatoid arthritis. Expert Opin. Emerging Drugs. 2008;13:175-96.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Ruiz Garcia V., Jobanputra P., Burls A., et al. Certolizumab pegol (CDP870) for rheumatoid arthritis in adults. The Cochrane database of systematic reviews 9. MAbs. 2010; 2(2):137-47.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Lee S.D., Rubin D.T., Sandborn W.J., Randall C., Younes Z., Schreiber S., Schwartz D.A., Burakoff R., Binion D., Dassopoulos T., Arsenescu R., Gutierrez A., Scherl E., Kayhan C., Hasan I., Kosutic G., Spearman M., Sen D., Coarse J., Hanauer S. Reinduction with Certolizumab Pegol in Patients with Crohn's Disease Experiencing Disease Exacerbation: 7-Year Data from the PRECiSE 4 Study. Inflamm Bowel Dis. 2016;22(8):1870-80.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Rutgeerts P., Fedorak R., Rachmilevich D., et al. Onercept (Recombinant Human P55 Tumour Necrosis Factor Receptor) Treatment in Patients with Active Crohn's Disease: Randomized, Placebo-Controlled, Dose-Finding Phase II Study. Gut. 2004;53(Suppl. VI.):12</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Travis S., Yap L.M., Hawkey C., Warren B., Lazarov M., Fong T., Tesi R.J. RDP58 is a novel and potentially effective oral therapy for ulcerative colitis. Inflamm. Bowel. Dis. 2005; 11(8):713-19.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Bloomgren G., Richman S., Hotermans C., Subramanyam M., Goelz S., Natarajan A., Lee S., Plavina T., Scanlon J.V., Sandrock A., Bozic C. Risk of natalizumab-associated progressive multifocal leukoencephalopathy. N. Engl. J. Med. 2012;366:1870-80.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Feagan B.G., Rutgeerts P., Sands B.E., Hanauer S., Colombel J.F., Sandborn W.J., Van Assche G., Axler J., Kim H.J., Danese S., Fox I., Milch C., Sankoh S., Wyant T., Xu J., Parikh A. Vedolizumab as induction and maintenance therapy for ulcerative colitis. N. Engl. J. Med. 2013;369:699-710.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Sandborn W.J., Feagan B.G., Rutgeerts P, Hanauer S., Colombel J.F., Sands B.E., Lukas M., Fedorak R.N., Lee S., Bressler B., Fox I., Rosario M., Sankoh S., Xu J., Stephens K., Milch C., Parikh A. Vedolizumab as induction and maintenance therapy for Crohn's disease. N. Engl. J. Med. 2013;369:711-21.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Sands B.E., Feagan B.G., Rutgeerts P., Colombe lJ.F., Sandborn W.J., Sy R., D'Haens G., Ben-Horin S., Xu J., Rosario M., Fox I., Parikh A., Milch C., Hanauer S. Effects of vedolizumab induction therapy for patients with Crohn's disease in whom tumor necrosis factor antagonist treatment failed. Gastroenterology. 2014;147:618-27.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Jin Y., Lin Y., Lin L.J., Zheng C.Q. Meta-analysis of the effectiveness and safety of vedolizumab for ulcerative colitis. World J. Gastroenterol. 2015;21(20):6352-60.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Amiot A., Grimaud J.C., Peyrin-Biroulet L., et al. Observatory on Efficacy and of Vedolizumab in Patients With Inflammatory Bowel Disease Study Group; Groupe d'Etude Therapeutique des Affections Inflammatoires du tube Digestif. Effectiveness and Safety of Vedolizumab Induction Therapy for Patients With Inflammatory Bowel Disease. Clin. Gastroenterol. Hepatol. 2016;14(11):1593-601.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Vermeire S., O'Byrne S., Keir M., Williams M., Lu T.T., Mansfield J.C., Lamb C.A., Feagan B.G., Panes J., Salas A., Baumgart D.C., Schreiber S., Dotan I., Sandborn W.J., Tew G.W., Luca D., Tang M.T., Diehl L., Eastham-Anderson J., De Hertogh G., Perrier C., Egen J.G., Kirby J.A., van Assche G., Rutgeerts P. Etrolizumab as induction therapy for ulcerative colitis: a randomised, controlled, phase 2 trial. Lancet. 2014;384:309-18.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Lin L., Liu X., Wang D., Zheng C. Efficacy and safety of antiintegrin antibody for inflammatory bowel disease: a systematic review and meta-analysis. Medicine (Baltimore). 2015;94(10):e556.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Vermeire S., Sandborn W.J., Danese S., Hébuterne X., Salzberg B.A., Klopocka M., Tarabar D., Vanasek T., Gregus M., Hellstern P.A., Kim J.S., Sparrow M.P., Gorelick K.J., Hinz M., Ahmad A., Pradhan V., Hassan-Zahraee M., Clare R., Cataldi F., Reinisch W. Anti-MAdCAM antibody (PF-00547659) for ulcerative colitis (TURANDOT): a phase 2, randomised, double-blind, placebo-controlled trial. Lancet. 2017;390(10090):135-44.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Namour F., Galien R., Van Kaem T., Van der Aa A., Vanhoutte F., Beetens J., Van't Klooster G. Safety, pharmacokinetics and pharmacodynamics of GLPG0974, a potent and selective FFA2 antagonist, in healthy male subjects. Br. J. Clin. Pharmacol. 2016;82(1):139-48.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>D'Haens G., Vermeire S., Vogelsang H., Allez M., Desreumaux P., Van Gossum A., Sandborn W.J., Baumgart D.C., Ransohoff R.M., Comer G.M., Ahmad A., Cataldi F., Cheng J., Clare R., Gorelick K.J., Kaminski A., Pradhan V., Rivers S., Sikpi M.O., Zhang Y., Hassan-Zahraee M., Reinisch W., Stuve O. Effect of PF-00547659 on Central Nervous System Immune Surveillance and Circulating β7+ T Cells in Crohn's Disease: Report of the TOSCA Study: MADCAM-1Antibody and CNS Immune Surveillance. J. Crohns Colitis. 2017;1:1-9.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>IBD News Today/ [Электронный ресурс]. IBD News Today, 2013-2017 URL: https:// ibdnewstoday.com/ozanimod-rpc-1063/ (Дата обращения 01.10.2017).</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Keshav S., Vañásek T., Niv Y., Petryka R., Howaldt S., Bafutto M., Rácz I., Hetzel D., Nielsen O.H., Vermeire S., Reinisch W., Karién P., Schreiber S., Schall T.J., Bekker P. A randomized controlled trial of the efficacy and safety of CCX282-B, an orally-administered blocker of chemokine receptor CCR9, for patients with Crohn's disease. PLoS One. 2013;8:e60094.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Feagan B.G., Sandborn W.J., D'Haens G., Lee S.D., Allez M., Fedorak R.N., Seidler U., Vermeire S., Lawrance I.C., Maroney A.C., Jurgensen C.H., Heath A., Chang D.J. Randomised clinical trial: vercirnon, an oral CCR9 antagonist, vs. placebo as induction therapy in active Crohn's disease. Aliment. Pharmacol. Ther. 2015;42(10): 1170-81.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Cătană C.S., Berindan Neagoe I., Cozma V., Magdaş C., Tăbăran F, Dumitraşcu D.L. Contribution of the IL-17/IL-23 axis to the pathogenesis of inflammatory bowel disease. World J. Gastroenterol. 2015;21(19):5823-30. Published online 2015 May 21.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>MacDonald J.K., Nguyen T.M., Khanna R., Timmer A. Anti-IL-12/23p40 antibodies for induction of remission in Crohn's disease. Cochrane Database Syst. Rev. 2016.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Yoshida H., Kimura A., Fukaya T., Sekiya T. Low dose CP-690,550 (tofacitinib), a pan-JAK inhibitor, accelerates the onset of experimental autoimmune encephalomyelitis by potentiating Th17 differentiation. Biochem. Biophys. Res. Commun. 2012;418:234-40.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Sandborn W.J., Su C., Sands B.E., D'Haens G.R., Vermeire S., Schreiber S., Danese S., Feagan B.G., Reinisch W., Niezychowski W., Friedman G., Lawendy N., Yu D., Woodworth D., Mukherjee A., Zhang H., Healey P., Panés J. OCTAVE Induction 1, OCTAVE Induction 2, and OCTAVE Sustain Investigators. Tofacitinib as Induction and Maintenance Therapy for Ulcerative Colitis. N. Engl. J. Med. 2017;376(18):1723-36.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Sandborn W.J., Ghosh S., Panes J., Vranic I., Su C., Rousell S., Niezychowski W. Tofacitinib, an oral Janus kinase inhibitor, in active ulcerative colitis. N. Engl. J. Med. 2012;367:616-24.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Panés J., Sandborn WJ, Schreiber S., Sands B.E., Vermeire S., D'Haens G., Panaccione R., Higgins P.D.R., Colombel J.F, Feagan B.G., Chan G., Moscariello M., Wang W., Niezychowski W., Marren A., Healey P., Maller E. Tofacitinib for induction and maintenance therapy of Crohn's disease: results of two phase IIb randomized placebo-controlled trials. Gut. 2017;66(6):1049-59.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Herrlinger K.R., Diculescu M., Fellermann K., Hartmann H., Howaldt S., Nikolov R., Petrov A., Reindl W., Otte J.M., Stoynov S., Strauch U., Sturm A., Voiosu R., Ammendola A., Dietrich B., Hentsch B., Stange E.F. Efficacy, safety and tolerability of vidofludimus in patients with inflammatory bowel disease: The ENTRANCE study. J. Crohn's Colitis. 2013;7(8): 636-43.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Comi G., Jeffery D., Kappos L., Montalban X., Boyko A., Rocca M.A., Filippi M. Placebocontrolled trial of oral laquinimod for multiple sclerosis. N. Engl. J. Med. 2012;366:1000-9.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>D'Haens G., Sandborn W.J., Colombel J.F., et al. A phase II study of laquinimod in Crohn's disease. The small molecule laquinimod was analyzed in a dose escalation induction study in CD showing clinically efficacy versus placebo. Gut. 2015 Aug;64(8):1227-35.</mixed-citation></ref></ref-list></back></article>
