<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">vtio</journal-id><journal-title-group><journal-title xml:lang="ru">Вестник трансплантологии и искусственных органов</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Transplantology and Artificial Organs</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-1191</issn><publisher><publisher-name>Academician V.I.Shumakov National Medical Research Center of Transplantology and Artificial Organs", Ministry of Health of the Russian Federation</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15825/1995-1191-2022-1-15-22</article-id><article-id custom-type="elpub" pub-id-type="custom">vtio-1469</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 трансплантология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Clinical Transplantology</subject></subj-group></article-categories><title-group><article-title>Трансплантация печени пациентам с первичным билиарным холангитом (обзор литературы)</article-title><trans-title-group xml:lang="en"><trans-title>Liver transplantation for primary biliary cholangitis (review)</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>Ильинский</surname><given-names>И. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Iljinsky</surname><given-names>I. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ильинский Игорь Михайлович</p><p>123182, Москва, ул. Щукинская, д. 1</p><p>Тел. (999) 877-60-95</p><p> </p></bio><bio xml:lang="en"><p>Igor Iljinsky.</p><p>1, Shchukinskaya str., Moscow, 123182</p><p>Phone: (999) 877-60-95</p><p> </p></bio><email xlink:type="simple">iiljinsky@mail.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>Цирульникова</surname><given-names>О. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsirulnikova</surname><given-names>O. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">tsiroulnikova@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр трансплантологии и искусственных органов имени академика В.И. Шумакова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Shumakov National Medical Research Center of Transplantology and Artificial Organs</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр трансплантологии и искусственных органов имени академика В.И. Шумакова» Минздрава России; ФГАОУ ВО Первый Московский государственный медицинский университет имени И.М. Сеченова Минздрава России (Сеченовский университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Shumakov National Medical Research Center of Transplantology and Artificial Organs; Sechenov University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>10</day><month>02</month><year>2022</year></pub-date><volume>24</volume><issue>1</issue><fpage>15</fpage><lpage>22</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ильинский И.М., Цирульникова О.М., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Ильинский И.М., Цирульникова О.М.</copyright-holder><copyright-holder xml:lang="en">Iljinsky I.M., Tsirulnikova O.M.</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://journal.transpl.ru/vtio/article/view/1469">https://journal.transpl.ru/vtio/article/view/1469</self-uri><abstract><p>Первичный билиарный холангит (ПБХ) – аутоиммунное заболевание печени, при котором происходит разрушение и воспаление внутрипеченочных желчных протоков. Ранее это заболевание в терминальной стадии было наиболее частой причиной трансплантации печени. Использование при лечении в качестве препарата первой линии урсодезоксихолевой кислоты и препарата второй линии – обетихоловой кислоты замедляет прогрессирование заболевания. Однако примерно у 40% пациентов с ПБХ лечение оказывается неэффективным, и заболевание может прогрессировать до цирроза и терминальной стадии заболевания печени. Этим пациентам для сохранения жизни проводят трансплантацию печени. После операции возможно развитие рекуррентного ПБХ, которое протекает в более легкой форме и редко вызывает необходимость в ретрансплантации печени.</p></abstract><trans-abstract xml:lang="en"><p>Primary biliary cholangitis (PBC) is an autoimmune liver disease resulting from the destruction and inflammation of intrahepatic bile ducts. This end-stage disease was once the most common cause of liver transplantation. The use of ursodeoxycholic and obeticholic acids as a first-line and second-line treatment, respectively, slows down the disease. However, treatment is not effective in about 40% of PBC patients, and the disease may progress to cirrhosis and end-stage liver disease. These patients undergo liver transplantation to save their lives. After surgery, recurrent PBC can develop in a milder form and rarely requires liver retransplantation.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>первичный билиарный холангит</kwd><kwd>ПБХ</kwd><kwd>трансплантация печени</kwd><kwd>возвратный ПБХ</kwd><kwd>факторы риска</kwd></kwd-group><kwd-group xml:lang="en"><kwd>primary biliary cholangitis</kwd><kwd>PBC</kwd><kwd>Liver transplantation</kwd><kwd>recurrence PBC</kwd><kwd>risk factors</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">Milkiewicz P. Liver transplantation in primary biliary cirrhosis. Clin Liver Dis. 2008; 12 (2): 461–472. doi: 10.1016/j.cld.2008.02.015.</mixed-citation><mixed-citation xml:lang="en">Milkiewicz P. Liver transplantation in primary biliary cirrhosis. Clin Liver Dis. 2008; 12 (2): 461–472. doi: 10.1016/j.cld.2008.02.015.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Boonstra K, Beuers U, Ponsioen CY. Epidemiology of primary sclerosing cholangitis and primary biliary cirrhosis: a systematic review. J Hepatol. 2012 May; 56 (5): 1181–1188. doi: 10.1016/j.jhep.2011.10.025.</mixed-citation><mixed-citation xml:lang="en">Boonstra K, Beuers U, Ponsioen CY. Epidemiology of primary sclerosing cholangitis and primary biliary cirrhosis: a systematic review. J Hepatol. 2012 May; 56 (5): 1181–1188. doi: 10.1016/j.jhep.2011.10.025.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Griffiths L, Dyson JK, Jones DE. The new epidemiology of primary biliary cirrhosis. Semin Liver Dis. 2014 Aug; 34 (3): 318–328. doi: 10.1055/s-0034-1383730.</mixed-citation><mixed-citation xml:lang="en">Griffiths L, Dyson JK, Jones DE. The new epidemiology of primary biliary cirrhosis. Semin Liver Dis. 2014 Aug; 34 (3): 318–328. doi: 10.1055/s-0034-1383730.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Kuiper EM, Hansen BE, de Vries RA, den Ouden-Muller JW, van Ditzhuijsen TJ et al. Im-proved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acid. Gastroenterology. 2009; 136: 1281–1287.</mixed-citation><mixed-citation xml:lang="en">Kuiper EM, Hansen BE, de Vries RA, den Ouden-Muller JW, van Ditzhuijsen TJ et al. Im-proved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acid. Gastroenterology. 2009; 136: 1281–1287.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Schoning W, Schmeding M, Ulmer F, Andert A, Neumann U. Liver transplantation for patients with cholestatic liver diseases. Viszeralmedizin. 2015; 31: 194–198. doi: 10.1159/000431017.</mixed-citation><mixed-citation xml:lang="en">Schoning W, Schmeding M, Ulmer F, Andert A, Neumann U. Liver transplantation for patients with cholestatic liver diseases. Viszeralmedizin. 2015; 31: 194–198. doi: 10.1159/000431017.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Sun CK, Chen CL, Concejero AM, Wang CC, Wang SH, Liu YW et al. Liver transplantation for primary biliary cirrhosis in a hepatitis endemic region: a single-center Asian experience. Clinical Transplantation. 2011; 25: 47–53. doi: 10.1111/j.1399-0012.2010.01288.x.</mixed-citation><mixed-citation xml:lang="en">Sun CK, Chen CL, Concejero AM, Wang CC, Wang SH, Liu YW et al. Liver transplantation for primary biliary cirrhosis in a hepatitis endemic region: a single-center Asian experience. Clinical Transplantation. 2011; 25: 47–53. doi: 10.1111/j.1399-0012.2010.01288.x.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Harms MH, Janssen QP, Adam R, Duvoux C, Mirza D, Hidalgo E et al. European Liver and Intestine Transplant Association (ELITA). Trends in liver transplantation for primary biliary cholangitis in Europe over the past three decades. Aliment Pharmacol Ther. 2019 Feb; 49 (3): 285–295. doi: 10.1111/apt.15060.</mixed-citation><mixed-citation xml:lang="en">Harms MH, Janssen QP, Adam R, Duvoux C, Mirza D, Hidalgo E et al. European Liver and Intestine Transplant Association (ELITA). Trends in liver transplantation for primary biliary cholangitis in Europe over the past three decades. Aliment Pharmacol Ther. 2019 Feb; 49 (3): 285–295. doi: 10.1111/apt.15060.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Lee J, Belanger A, Doucette JT, Stanca C, Friedman S, Bach N. Transplantation trends in primary biliary cirrhosis. Clin Gastroenterol Hepatol. 2007 Nov; 5 (11): 1313–1315. doi: 10.1016/j.cgh.2007.07.015.</mixed-citation><mixed-citation xml:lang="en">Lee J, Belanger A, Doucette JT, Stanca C, Friedman S, Bach N. Transplantation trends in primary biliary cirrhosis. Clin Gastroenterol Hepatol. 2007 Nov; 5 (11): 1313–1315. doi: 10.1016/j.cgh.2007.07.015.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Pares A, Caballeria L, Rodes J. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic Acid. Gastroenterology. 2006; 130 (3): 715–720. doi: 10.1053/j.gastro.2005.12.029.</mixed-citation><mixed-citation xml:lang="en">Pares A, Caballeria L, Rodes J. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic Acid. Gastroenterology. 2006; 130 (3): 715–720. doi: 10.1053/j.gastro.2005.12.029.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Corpechot C, Abenavoli L, Rabahi N, Chretien Y, Andreani T, Johanet C et al. Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis. Hepatology. 2008; 48 (3): 871–877. doi: 10.1002/hep.22428.</mixed-citation><mixed-citation xml:lang="en">Corpechot C, Abenavoli L, Rabahi N, Chretien Y, Andreani T, Johanet C et al. Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis. Hepatology. 2008; 48 (3): 871–877. doi: 10.1002/hep.22428.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Lammers WJ, van Buuren HR, Hirschfield GM, Janssen HL, Invernizzi P, Mason AL et al. Global PBC Study Group. Levels of alkaline phosphatase and bilirubin are surrogate end points of outcomes of patients with primary biliary cirrhosis: an international follow-up study. Gastroenterology. 2014 Dec; 147 (6): 1338–1349.e5; quiz e15. doi: 10.1053/j.gastro.2014.08.029.</mixed-citation><mixed-citation xml:lang="en">Lammers WJ, van Buuren HR, Hirschfield GM, Janssen HL, Invernizzi P, Mason AL et al. Global PBC Study Group. Levels of alkaline phosphatase and bilirubin are surrogate end points of outcomes of patients with primary biliary cirrhosis: an international follow-up study. Gastroenterology. 2014 Dec; 147 (6): 1338–1349.e5; quiz e15. doi: 10.1053/j.gastro.2014.08.029.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Poupon R, Ping C, Chretien Y, Corpechot C, Chazouilleres O, Simon T et al. Genetic factors of susceptibility and of severity in primary biliary cirrhosis. J Hepatol. 2008; 49: 1038–1045.</mixed-citation><mixed-citation xml:lang="en">Poupon R, Ping C, Chretien Y, Corpechot C, Chazouilleres O, Simon T et al. Genetic factors of susceptibility and of severity in primary biliary cirrhosis. J Hepatol. 2008; 49: 1038–1045.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Hohenester S, Oude-Elferink RP, Beuers U. Primary biliary cirrhosis. Semin Immunopathol. 2009; 31: 283–307.</mixed-citation><mixed-citation xml:lang="en">Hohenester S, Oude-Elferink RP, Beuers U. Primary biliary cirrhosis. Semin Immunopathol. 2009; 31: 283–307.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Akamatsu N, Sugawara Y. Primary biliary cirrhosis and liver transplantation. Intractable &amp; Rare Diseases Research. 2012; 1: 66–80. doi: 10.5582/irdr.2012.v1.2.66.</mixed-citation><mixed-citation xml:lang="en">Akamatsu N, Sugawara Y. Primary biliary cirrhosis and liver transplantation. Intractable &amp; Rare Diseases Research. 2012; 1: 66–80. doi: 10.5582/irdr.2012.v1.2.66.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Aguilar MT, Carey EJ. Current Status of Liver Transplantation for Primary Biliary Cholangitis. Clin Liver Dis. 2018 Aug; 22 (3): 613–624. doi: 10.1016/j. cld.2018.03.011.</mixed-citation><mixed-citation xml:lang="en">Aguilar MT, Carey EJ. Current Status of Liver Transplantation for Primary Biliary Cholangitis. Clin Liver Dis. 2018 Aug; 22 (3): 613–624. doi: 10.1016/j. cld.2018.03.011.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Ter Borg PC, Schalm SW, Hansen BE, van Buuren HR. Dutch PBC Study Group. Prognosis of ursodeoxycholic Acid-treated patients with primary biliary cirrhosis. Results of a 10-yr cohort study involving 297 patients. Am J Gastroenterol. 2006 Sep; 101 (9): 2044–2050. doi: 10.1111/j.1572-0241.2006.00699.x.</mixed-citation><mixed-citation xml:lang="en">Ter Borg PC, Schalm SW, Hansen BE, van Buuren HR. Dutch PBC Study Group. Prognosis of ursodeoxycholic Acid-treated patients with primary biliary cirrhosis. Results of a 10-yr cohort study involving 297 patients. Am J Gastroenterol. 2006 Sep; 101 (9): 2044–2050. doi: 10.1111/j.1572-0241.2006.00699.x.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Hirschfield GM, Dyson JK, Alexander GJM, Chapman MH, Collier J, Hübscher S et al. The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines. Gut. 2018 Sep; 67 (9): 1568–1594. doi: 10.1136/gutjnl-2017-315259.</mixed-citation><mixed-citation xml:lang="en">Hirschfield GM, Dyson JK, Alexander GJM, Chapman MH, Collier J, Hübscher S et al. The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines. Gut. 2018 Sep; 67 (9): 1568–1594. doi: 10.1136/gutjnl-2017-315259.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Chen L, Shi X, Lv G, Sun X, Sun C et al. The long-term outcomes of deceased-donor liver transplantation for primary biliary cirrhosis: a two-center study in China. PeerJ. 2020; 8: e9563. Published 2020 Aug 19. doi: 10.7717/peerj.9563.</mixed-citation><mixed-citation xml:lang="en">Hirschfield GM, Dyson JK, Alexander GJM, Chapman MH, Collier J, Hübscher S et al. The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines. Gut. 2018 Sep; 67 (9): 1568–1594. doi: 10.1136/gutjnl-2017-315259.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Singal AK, Fang X, Kaif M, Hasanin M, Mcguire BM, Kuo YF, Wiesner RH. Primary biliary cirrhosis has high wait-list mortality among patients listed for liver trans plantation. Transpl Int. 2017 May; 30 (5): 454–462. doi: 10.1111/tri.12877.</mixed-citation><mixed-citation xml:lang="en">Chen L, Shi X, Lv G, Sun X, Sun C et al. The long-term outcomes of deceased-donor liver transplantation for primary biliary cirrhosis: a two-center study in China. PeerJ. 2020; 8: e9563. Published 2020 Aug 19. doi: 10.7717/peerj.9563.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Murillo Perez CF, Goet JC, Lammers WJ, Gulamhusein A, van Buuren HR, Ponsioen CY et al. GLOBAL PBC Study Group. Milder disease stage in patients with primary biliary cholangitis over a 44-year period: A changing natural history. Hepatology. 2018 May; 67 (5): 1920–1930. doi: 10.1002/hep.29717.</mixed-citation><mixed-citation xml:lang="en">Singal AK, Fang X, Kaif M, Hasanin M, Mcguire BM, Kuo YF, Wiesner RH. Primary biliary cirrhosis has high wait-list mortality among patients listed for liver trans plantation. Transpl Int. 2017 May; 30 (5): 454–462. doi: 10.1111/tri.12877.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Webb GJ, Rana A, Hodson J, Akhtar MZ, Ferguson JW, Neuberger JM et al. Twenty-Year Comparative Analysis of Patients With Autoimmune Liver Diseases on Transplant Waitlists. Clin Gastroenterol Hepatol. 2018 Feb; 16 (2): 278–287.e7. doi: 10.1016/j.cgh.2017.09.062.</mixed-citation><mixed-citation xml:lang="en">Murillo Perez CF, Goet JC, Lammers WJ, Gulamhusein A, van Buuren HR, Ponsioen CY et al. GLOBAL PBC Study Group. Milder disease stage in patients with primary biliary cholangitis over a 44-year period: A changing natural history. Hepatology. 2018 May; 67 (5): 1920–1930. doi: 10.1002/hep.29717.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Lleo A, Jepsen P, Morenghi E, Carbone M, Moroni L, Battezzati PM et al. Evolving Trends in Female to Male Incidence and Male Mortality of Primary Biliary Cholangitis. Sci Rep. 2016 May 19; 6: 25906. doi: 10.1038/ srep25906.</mixed-citation><mixed-citation xml:lang="en">Webb GJ, Rana A, Hodson J, Akhtar MZ, Ferguson JW, Neuberger JM et al. Twenty-Year Comparative Analysis of Patients With Autoimmune Liver Diseases on Transplant Waitlists. Clin Gastroenterol Hepatol. 2018 Feb; 16 (2): 278–287.e7. doi: 10.1016/j.cgh.2017.09.062.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Silveira MG, Talwalkar JA, Lindor KD, Wiesner RH. Recurrent primary biliary cirrhosis after liver transplantation. Am J Transplant. 2010; 10: 720–726.</mixed-citation><mixed-citation xml:lang="en">Lleo A, Jepsen P, Morenghi E, Carbone M, Moroni L, Battezzati PM et al. Evolving Trends in Female to Male Incidence and Male Mortality of Primary Biliary Cholangitis. Sci Rep. 2016 May 19; 6: 25906. doi: 10.1038/ srep25906.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Mac Quillan GC, Neuberger J. Liver transplantation for primary biliary cirrhosis. Clin Liver Dis. 2003; 7: 941– 956.</mixed-citation><mixed-citation xml:lang="en">Silveira MG, Talwalkar JA, Lindor KD, Wiesner RH. Recurrent primary biliary cirrhosis after liver transplantation. Am J Transplant. 2010; 10: 720–726.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Naik P, Sritharan V, Bandi P, Madhavarapu M. A single centre prospective study of liver function tests in post liver transplant patients. Indian Journal of Clinical Biochemistry. 2013; 28: 38–45. doi: 10.1007/s12291-012- 0245-4.</mixed-citation><mixed-citation xml:lang="en">Mac Quillan GC, Neuberger J. Liver transplantation for primary biliary cirrhosis. Clin Liver Dis. 2003; 7: 941– 956.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang W, Wang M, Xie HY, Zhou L, Meng XQ, Shi J, Zheng S. Role of reactive oxygen species in mediating hepatic ischemia-reperfusion injury and its therapeutic applications in liver transplantation. Transplantation Proceedings. 2007; 39: 1332–1337. doi: 10.1016/j.transproceed.2006.11.021.</mixed-citation><mixed-citation xml:lang="en">Naik P, Sritharan V, Bandi P, Madhavarapu M. A single centre prospective study of liver function tests in post liver transplant patients. Indian Journal of Clinical Biochemistry. 2013; 28: 38–45. doi: 10.1007/s12291-012- 0245-4.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Li C, Wen TF, Mi K, Wang C, Yan LN, Li B. Analysis of infections in the first 3-month after living donor liver transplantation. World Journal of Gastroenterology. 2012; 18: 1975–1980. doi: 10.3748/wjg.v18.i16.1975.</mixed-citation><mixed-citation xml:lang="en">Zhang W, Wang M, Xie HY, Zhou L, Meng XQ, Shi J, Zheng S. Role of reactive oxygen species in mediating hepatic ischemia-reperfusion injury and its therapeutic applications in liver transplantation. Transplantation Proceedings. 2007; 39: 1332–1337. doi: 10.1016/j.transproceed.2006.11.021.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Vera A, Contreras F, Guevara F. Incidence and risk factors for infections after liver transplant: single-center experience at the University Hospital Fundacion Santa Fe de Bogota, Colombia. Transplant Infectious Disease. 2011; 130: 608–615. doi: 10.1111/j.1399-3062.2011.00640.x.</mixed-citation><mixed-citation xml:lang="en">Li C, Wen TF, Mi K, Wang C, Yan LN, Li B. Analysis of infections in the first 3-month after living donor liver transplantation. World Journal of Gastroenterology. 2012; 18: 1975–1980. doi: 10.3748/wjg.v18.i16.1975.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Wojcicki M, Milkiewicz P, Silva M. Biliary tract complications after liver transplantation: a review. Digestive Surgery. 2008; 25: 245–257. doi: 10.1159/000144653.</mixed-citation><mixed-citation xml:lang="en">Vera A, Contreras F, Guevara F. Incidence and risk factors for infections after liver transplant: single-center experience at the University Hospital Fundacion Santa Fe de Bogota, Colombia. Transplant Infectious Disease. 2011; 130: 608–615. doi: 10.1111/j.1399-3062.2011.00640.x.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Khalaf H. Vascular complications after deceased and living donor liver transplantation: a single-center experience. Transplantation Proceedings. 2010; 42: 865–870. doi: 10.1016/j.transproceed.2010.02.037.</mixed-citation><mixed-citation xml:lang="en">Wojcicki M, Milkiewicz P, Silva M. Biliary tract complications after liver transplantation: a review. Digestive Surgery. 2008; 25: 245–257. doi: 10.1159/000144653.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Mejia GA, Olarte-Parra C, Pedraza A, Rivera JB, Benavides CA. Biliary complications after liver transplantation: incidence. Risk factors and impact on patient and graft survival. Transplantation Proceedings. 2016; 48: 665–668. doi: 10.1016/j.transproceed.2016.02.033.</mixed-citation><mixed-citation xml:lang="en">Khalaf H. Vascular complications after deceased and living donor liver transplantation: a single-center experience. Transplantation Proceedings. 2010; 42: 865–870. doi: 10.1016/j.transproceed.2010.02.037.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Ma L, Lu Q, Luo Y. Vascular complications after adult living donor liver transplantation: evaluation with ultrasonography. World Journal of Gastroenterology. 2016; 22: 1617–1626. doi: 10.3748/wjg.v22.i4.1617.</mixed-citation><mixed-citation xml:lang="en">Mejia GA, Olarte-Parra C, Pedraza A, Rivera JB, Benavides CA. Biliary complications after liver transplantation: incidence. Risk factors and impact on patient and graft survival. Transplantation Proceedings. 2016; 48: 665–668. doi: 10.1016/j.transproceed.2016.02.033.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Kashyap R, Safadjou S, Chen R, Mantry P, Sharma R, Patil V et al. Living donor and deceased donor liver transplantation for autoimmune and cholestatic liver diseases – an analysis of the UNOS database. Journal of Gastrointestinal Surgery. 2010; 14: 1362–1369. doi: 10.1007/s11605-010-1256-1.</mixed-citation><mixed-citation xml:lang="en">Ma L, Lu Q, Luo Y. Vascular complications after adult living donor liver transplantation: evaluation with ultrasonography. World Journal of Gastroenterology. 2016; 22: 1617–1626. doi: 10.3748/wjg.v22.i4.1617.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Liberal R, Zen Y, Mieli-Vergani G, Vergani D. Liver transplantation and autoimmune liver diseases. Liver Transplantation. 2013; 19: 1065–1077. doi: 10.1002/ lt.23704.</mixed-citation><mixed-citation xml:lang="en">Kashyap R, Safadjou S, Chen R, Mantry P, Sharma R, Patil V et al. Living donor and deceased donor liver transplantation for autoimmune and cholestatic liver diseases – an analysis of the UNOS database. Journal of Gastrointestinal Surgery. 2010; 14: 1362–1369. doi: 10.1007/s11605-010-1256-1.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Maheshwari A, Yoo HY, Thuluvath PJ. Long-term outcome of liver transplantation in patients with PSC: a comparative analysis with PBC. Am J Gastroenterol. 2004; 99: 538–542.</mixed-citation><mixed-citation xml:lang="en">Liberal R, Zen Y, Mieli-Vergani G, Vergani D. Liver transplantation and autoimmune liver diseases. Liver Transplantation. 2013; 19: 1065–1077. doi: 10.1002/ lt.23704.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Jacob DA, Neumann UP, Bahra M et al. Liver transplantation for primary biliary cirrhosis: influence of primary immunosuppression on survival. Transplant Proc. 2005; 37: 1691–1692.</mixed-citation><mixed-citation xml:lang="en">Maheshwari A, Yoo HY, Thuluvath PJ. Long-term outcome of liver transplantation in patients with PSC: a comparative analysis with PBC. Am J Gastroenterol. 2004; 99: 538–542.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Jacob DA, Neumann UP, Bahra M et al. Long-term follow-up after recurrence of primary biliary cirrhosis after liver transplantation in 100 patients. Clin Transpl. 2006; 20: 211–220.</mixed-citation><mixed-citation xml:lang="en">Jacob DA, Neumann UP, Bahra M et al. Liver transplantation for primary biliary cirrhosis: influence of primary immunosuppression on survival. Transplant Proc. 2005; 37: 1691–1692.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Neuberger J, Gunson B, Hubscher S, Nightingale P. Immunosuppression affects the rate of recurrent primary biliary cirrhosis after liver transplantation. Liver Transpl. 2004; 10: 488–491.</mixed-citation><mixed-citation xml:lang="en">Jacob DA, Neumann UP, Bahra M et al. Long-term follow-up after recurrence of primary biliary cirrhosis after liver transplantation in 100 patients. Clin Transpl. 2006; 20: 211–220.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Ziarkiewlcz-Wrobiewska B, Wroblewskl T, Wasiutynski A. Morphological features and differential diagnosis of hepatitis C recurrence after liver transplantation – literature review and results of single transplantation center. Ann Transplant. 2008; 13 (2): 12–20.</mixed-citation><mixed-citation xml:lang="en">Neuberger J, Gunson B, Hubscher S, Nightingale P. Immunosuppression affects the rate of recurrent primary biliary cirrhosis after liver transplantation. Liver Transpl. 2004; 10: 488–491.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Charatcharoenwitthaya P, Pimentel S, Talwalkar JA et al. Long-term survival and impact of ursodeoxycholic acid treatment for recurrent primary biliary cirrhosis after liver transplantation. Liver Transpl. 2007; 13: 1236– 1245.</mixed-citation><mixed-citation xml:lang="en">Ziarkiewlcz-Wrobiewska B, Wroblewskl T, Wasiutynski A. Morphological features and differential diagnosis of hepatitis C recurrence after liver transplantation – literature review and results of single transplantation center. Ann Transplant. 2008; 13 (2): 12–20.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Haga H, Miyagawa-Hayashino A, Taira K et al. Histological recurrence of autoimmune liver diseases after living-donor liver transplantation. Hepatol Res. 2007; 37: 463–469.</mixed-citation><mixed-citation xml:lang="en">Charatcharoenwitthaya P, Pimentel S, Talwalkar JA et al. Long-term survival and impact of ursodeoxycholic acid treatment for recurrent primary biliary cirrhosis after liver transplantation. Liver Transpl. 2007; 13: 1236– 1245.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Hashimoto E, Taniai M, Yatsuji S et al. Long-term clinical outcome of living-donor liver transplantation for primary biliary cirrhosis. Hepatol Res. 2007; 37: 455–461. 43. Yamagiwa S, Ichida T. Recurrence of primary biliary cirrhosis and primary sclerosing cholangitis after liver transplantation in Japan. Hepatol Res. 2007; 37: 449– 454.</mixed-citation><mixed-citation xml:lang="en">Haga H, Miyagawa-Hayashino A, Taira K et al. Histological recurrence of autoimmune liver diseases after living-donor liver transplantation. Hepatol Res. 2007; 37: 463–469.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Duclos-Vallee JC, Sebagh M. Recurrence of autoimmune disease, primary sclerosing cholangitis, primary biliary cirrhosis, and autoimmune hepatitis after liver transplantation. Liver Transpl. 2009; 15 (Suppl 2): S25–34. doi: 10.1002/lt.21916.</mixed-citation><mixed-citation xml:lang="en">Hashimoto E, Taniai M, Yatsuji S et al. Long-term clinical outcome of living-donor liver transplantation for primary biliary cirrhosis. Hepatol Res. 2007; 37: 455–461. 43. Yamagiwa S, Ichida T. Recurrence of primary biliary cirrhosis and primary sclerosing cholangitis after liver transplantation in Japan. Hepatol Res. 2007; 37: 449– 454.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Neuberger J. Liver transplantation for primary biliary cirrhosis: indications and risk of recurrence. J Hepatol. 2003; 39: 142–148.</mixed-citation><mixed-citation xml:lang="en">Duclos-Vallee JC, Sebagh M. Recurrence of autoimmune disease, primary sclerosing cholangitis, primary biliary cirrhosis, and autoimmune hepatitis after liver transplantation. Liver Transpl. 2009; 15 (Suppl 2): S25–34. doi: 10.1002/lt.21916.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Hytiroglou P, Gutierrez JA, Freni M et al. Recurrence of primary biliary cirrhosis and development of autoimmune hepatitis after liver transplant: A blind histologic study. Hepatol Res. 2009; 39 (6): 577–584.</mixed-citation><mixed-citation xml:lang="en">Neuberger J. Liver transplantation for primary biliary cirrhosis: indications and risk of recurrence. J Hepatol. 2003; 39: 142–148.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Mendes F, Couto CA, Levy C. Recurrent and de novo autoimmune liver diseases. Clin Liver Dis. 2011; 15 (4): 859–878. doi: 10.1016/j.cld.2011.08.008.</mixed-citation><mixed-citation xml:lang="en">Hytiroglou P, Gutierrez JA, Freni M et al. Recurrence of primary biliary cirrhosis and development of autoimmune hepatitis after liver transplant: A blind histologic study. Hepatol Res. 2009; 39 (6): 577–584.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Carbone M, Neuberger J. Liver transplantation in PBC and PSC: Indications and disease recurrence. Clin Res Hepatol Gastroenterol. 2011; 35: 446–454. doi: 10.1016/j.clinre.2011.02.007.</mixed-citation><mixed-citation xml:lang="en">Mendes F, Couto CA, Levy C. Recurrent and de novo autoimmune liver diseases. Clin Liver Dis. 2011; 15 (4): 859–878. doi: 10.1016/j.cld.2011.08.008.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Liermann Garcia RF, Evangelista Garcia C, McMaster P, Neuberger J. Transplantation for primary biliary cirrhosis: Retrospective analysis of 400 patients in a single center. Hepatology. 2001; 33: 22–27.</mixed-citation><mixed-citation xml:lang="en">Carbone M, Neuberger J. Liver transplantation in PBC and PSC: Indications and disease recurrence. Clin Res Hepatol Gastroenterol. 2011; 35: 446–454. doi: 10.1016/j.clinre.2011.02.007.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Kurdow R, Marks HG, Kraemer-Hansen H et al. Recurrence of primary biliary cirrhosis after orthotopic liver transplantation. Hepatogastroenterology. 2003; 50: 322– 325.</mixed-citation><mixed-citation xml:lang="en">Liermann Garcia RF, Evangelista Garcia C, McMaster P, Neuberger J. Transplantation for primary biliary cirrhosis: Retrospective analysis of 400 patients in a single center. Hepatology. 2001; 33: 22–27.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Levitsky J, Hart J, Cohen SM, Te HS. The effect of immunosuppressive regimens on the recurrence of primary biliary cirrhosis after liver transplantation. Liver Transpl. 2003; 9: 733–736.</mixed-citation><mixed-citation xml:lang="en">Kurdow R, Marks HG, Kraemer-Hansen H et al. Recurrence of primary biliary cirrhosis after orthotopic liver transplantation. Hepatogastroenterology. 2003; 50: 322– 325.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Guy JE, Qian P, Lowell JA, Peters MG. Recurrent primary biliary cirrhosis: peritransplant factors and ursodeoxycholic acid treatment post-liver transplant. Liver Transpl. 2005; 11: 1252–1257.</mixed-citation><mixed-citation xml:lang="en">Levitsky J, Hart J, Cohen SM, Te HS. The effect of immunosuppressive regimens on the recurrence of primary biliary cirrhosis after liver transplantation. Liver Transpl. 2003; 9: 733–736.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Gautam M, Cheruvattath R, Balan V. Recurrence of autoimmune liver disease after liver transplantation: a systematic review. Liver Transpl. 2006; 12 (12): 1813– 1824.</mixed-citation><mixed-citation xml:lang="en">Guy JE, Qian P, Lowell JA, Peters MG. Recurrent primary biliary cirrhosis: peritransplant factors and ursodeoxycholic acid treatment post-liver transplant. Liver Transpl. 2005; 11: 1252–1257.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Kogiso T, Egawa H, Teramukai S, Taniai M, Hashimoto E et al. Risk factors for recurrence of primary biliary cholangitis after liver transplantation in female patients: A Japanese multicenter retrospective study. Hepatol Commun. 2017 May 16; 1 (5): 394–405. doi: 10.1002/ hep4.1037.</mixed-citation><mixed-citation xml:lang="en">Gautam M, Cheruvattath R, Balan V. Recurrence of autoimmune liver disease after liver transplantation: a systematic review. Liver Transpl. 2006; 12 (12): 1813– 1824.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Yamashiki N, Haga H, Ueda Y, Ito T, Yagi S et al. Use of Nakanuma staging and cytokeratin 7 staining for diagnosing recurrent primary biliary cholangitis after livingdonor liver transplantation. Hepatol Res. 2020 Apr; 50 (4): 478–487. doi: 10.1111/hepr.13476.</mixed-citation><mixed-citation xml:lang="en">Kogiso T, Egawa H, Teramukai S, Taniai M, Hashimoto E et al. Risk factors for recurrence of primary biliary cholangitis after liver transplantation in female patients: A Japanese multicenter retrospective study. Hepatol Commun. 2017 May 16; 1 (5): 394–405. doi: 10.1002/ hep4.1037.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Sylvestre PB, Batts KP, Burgart LJ et al. Recurrence of primary biliary cirrhosis after liver transplantation: histologic estimate of incidence and natural history. Liver Transpl. 2003; 9: 1086–1093.</mixed-citation><mixed-citation xml:lang="en">Yamashiki N, Haga H, Ueda Y, Ito T, Yagi S et al. Use of Nakanuma staging and cytokeratin 7 staining for diagnosing recurrent primary biliary cholangitis after livingdonor liver transplantation. Hepatol Res. 2020 Apr; 50 (4): 478–487. doi: 10.1111/hepr.13476.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Egawa H, Sakisaka S, Teramukai S, Sakabayashi S, Yamamoto M, Umeshita K et al. Long-term outcomes of living-donor liver transplantation for primary biliary cirrhosis: a Japanese multi-center study. Am J Transplant. 2016; 16: 1248–1257.</mixed-citation><mixed-citation xml:lang="en">Sylvestre PB, Batts KP, Burgart LJ et al. Recurrence of primary biliary cirrhosis after liver transplantation: histologic estimate of incidence and natural history. Liver Transpl. 2003; 9: 1086–1093.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Bosch A, Dumortier J, Maucort-Boulch D, Scoazec JY, Wendum D, Conti F et al. Preventive administration of UDCA after liver transplantation for primary biliary cirrhosis is associated with a lower risk of disease recurrence. Journal of Hepatology. 2015; 63: 1449–1458. doi: 10.1016/j.jhep.2015.07.038.</mixed-citation><mixed-citation xml:lang="en">Egawa H, Sakisaka S, Teramukai S, Sakabayashi S, Yamamoto M, Umeshita K et al. Long-term outcomes of living-donor liver transplantation for primary biliary cirrhosis: a Japanese multi-center study. Am J Transplant. 2016; 16: 1248–1257.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Schreuder TC, Hubscher SG, Neuberger J. Autoimmune liver diseases and recurrence after orthotopic liver transplantation: what have we learned so far? Transpl Int. 2009; 22: 144–152.</mixed-citation><mixed-citation xml:lang="en">Bosch A, Dumortier J, Maucort-Boulch D, Scoazec JY, Wendum D, Conti F et al. Preventive administration of UDCA after liver transplantation for primary biliary cirrhosis is associated with a lower risk of disease recurrence. Journal of Hepatology. 2015; 63: 1449–1458. doi: 10.1016/j.jhep.2015.07.038.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Kotlyar DS, Campbell MS, Reddy KR. Recurrence of diseases following orthotopic liver transplantation. Am J Gastroenterol. 2006; 101: 1370–1378.</mixed-citation><mixed-citation xml:lang="en">Schreuder TC, Hubscher SG, Neuberger J. Autoimmune liver diseases and recurrence after orthotopic liver transplantation: what have we learned so far? Transpl Int. 2009; 22: 144–152.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Sanchez EQ, Levy MF, Goldstein RM et al. The changing clinical presentation of recurrent primary biliary cirrhosis after liver transplantation. Transplantation. 2003; 76: 1583–1588.</mixed-citation><mixed-citation xml:lang="en">Kotlyar DS, Campbell MS, Reddy KR. Recurrence of diseases following orthotopic liver transplantation. Am J Gastroenterol. 2006; 101: 1370–1378.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Khettry U, Anand N, Faul PN, Lewis WD, Pomfret EA, Pomposelli J et al. Liver transplantation for primary biliary cirrhosis: a long-term pathologic study. Liver Transpl. 2003; 9: 87–96.</mixed-citation><mixed-citation xml:lang="en">Sanchez EQ, Levy MF, Goldstein RM et al. The changing clinical presentation of recurrent primary biliary cirrhosis after liver transplantation. Transplantation. 2003; 76: 1583–1588.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Montano-Loza AJ, Hansen BE, Corpechot C, Roccarina D, Thorburn D, Trivedi P et al. Global PBC Study Group. Factors Associated With Recurrence of Primary Biliary Cholangitis After Liver Transplantation and Effects on Graft and Patient Survival. Gastroenterology. 2019 Jan; 156 (1): 96–107.e1. doi: 10.1053/j.gastro.2018.10.001.</mixed-citation><mixed-citation xml:lang="en">Khettry U, Anand N, Faul PN, Lewis WD, Pomfret EA, Pomposelli J et al. Liver transplantation for primary biliary cirrhosis: a long-term pathologic study. Liver Transpl. 2003; 9: 87–96.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Grąt M, Lewandowski Z, Patkowski W, Wronka KM, Grąt K, Krasnodębski M et al. Relevance of male-tofemale sex mismatch in liver transplantation for primary biliary cirrhosis. Ann Transplant. 2015; 20: 116–123.</mixed-citation><mixed-citation xml:lang="en">Montano-Loza AJ, Hansen BE, Corpechot C, Roccarina D, Thorburn D, Trivedi P et al. Global PBC Study Group. Factors Associated With Recurrence of Primary Biliary Cholangitis After Liver Transplantation and Effects on Graft and Patient Survival. Gastroenterology. 2019 Jan; 156 (1): 96–107.e1. doi: 10.1053/j.gastro.2018.10.001.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Morioka D, Egawa H, Kasahara M, Jo T, Sakamoto S, Ogura Y et al. Impact of human leukocyte antigen mismatching on outcomes of living donor liver transplantation for primary biliary cirrhosis. Liver Transpl. 2007; 13: 80–90.</mixed-citation><mixed-citation xml:lang="en">Grąt M, Lewandowski Z, Patkowski W, Wronka KM, Grąt K, Krasnodębski M et al. Relevance of male-tofemale sex mismatch in liver transplantation for primary biliary cirrhosis. Ann Transplant. 2015; 20: 116–123.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Balan V, Ruppert K, Demetris AJ, Ledneva T, Duquesnoy RJ, Detre KM et al. Long-term outcome of human leukocyte antigen mismatching in liver transplantation: results of the National Institute of Diabetes and Digestive and Kidney Diseases Liver Transplantation Database. Hepatology. 2008; 48: 878–888.</mixed-citation><mixed-citation xml:lang="en">Morioka D, Egawa H, Kasahara M, Jo T, Sakamoto S, Ogura Y et al. Impact of human leukocyte antigen mismatching on outcomes of living donor liver transplantation for primary biliary cirrhosis. Liver Transpl. 2007; 13: 80–90.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Manousou P, Arvaniti V, Tsochatzis E, Isgro G, Jones K, Shirling G et al. Primary biliary cirrhosis after liver transplantation: influence of immunosuppression and human leukocyte antigen locus disparity. Liver Transpl. 2010; 16: 64–73.</mixed-citation><mixed-citation xml:lang="en">Balan V, Ruppert K, Demetris AJ, Ledneva T, Duquesnoy RJ, Detre KM et al. Long-term outcome of human leukocyte antigen mismatching in liver transplantation: results of the National Institute of Diabetes and Digestive and Kidney Diseases Liver Transplantation Database. Hepatology. 2008; 48: 878–888.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Hubscher SG, Portmann BC. Transplantation pathology. In: Burt A.D., Portmann B.C., Ferrell L.D. editors. MacSween’s Pathology of the Liver. 5th edn. London: Churchill Livingstone. 2007: 815–879.</mixed-citation><mixed-citation xml:lang="en">Manousou P, Arvaniti V, Tsochatzis E, Isgro G, Jones K, Shirling G et al. Primary biliary cirrhosis after liver transplantation: influence of immunosuppression and human leukocyte antigen locus disparity. Liver Transpl. 2010; 16: 64–73.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Faust ThW. Recurrent Primary Biliary Cirrhosis, Primary Sclerosing Cholangitis, and Autoimmune Hepatitis After Transplantation. Liver Transplantation. 2001; 7 (11), Suppl 1: 99–108.</mixed-citation><mixed-citation xml:lang="en">Hubscher SG, Portmann BC. Transplantation pathology. In: Burt A.D., Portmann B.C., Ferrell L.D. editors. MacSween’s Pathology of the Liver. 5th edn. London: Churchill Livingstone. 2007: 815–879.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Demetris AJ, Adeyi O, Bellamy CO, Clouston A, Charlotte F et al. Liver biopsy interpretation for causes of late liver allograft dysfunction. Banff Working Group. Hepatology. 2006; 44 (2): 489–501. doi: 10.1002/hep.21280.</mixed-citation><mixed-citation xml:lang="en">Faust ThW. Recurrent Primary Biliary Cirrhosis, Primary Sclerosing Cholangitis, and Autoimmune Hepatitis After Transplantation. Liver Transplantation. 2001; 7 (11), Suppl 1: 99–108.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Demetris AJ, Adeyi O, Bellamy CO, Clouston A, Charlotte F et al. Liver biopsy interpretation for causes of late liver allograft dysfunction. Banff Working Group. Hepatology. 2006; 44 (2): 489–501. doi: 10.1002/hep.21280.</mixed-citation><mixed-citation xml:lang="en">Demetris AJ, Adeyi O, Bellamy CO, Clouston A, Charlotte F et al. Liver biopsy interpretation for causes of late liver allograft dysfunction. Banff Working Group. Hepatology. 2006; 44 (2): 489–501. doi: 10.1002/hep.21280.</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>
