[1] Carbone M, Neuberger JM. Autoimmune liver disease, autoimmunity and liver transplantation. J Hepatol, 2014, 60(1): 210-223. [2] 王燕燕, 周桐桐, 卞兆连. 原发性胆汁性胆管炎和原发性胆汁性胆管炎-自身免疫性肝炎重叠综合征患者临床与肝组织病理学特点分析. 实用肝脏病杂志, 2024, 27(5): 721-724. [3] Yan Y L, Xing X, Wang Y, et al. Clinical utility of two-dimensional shear-wave elastography in monitoring disease course in autoimmune hepatitis-primary biliary cholangitis overlap syndrome.World J Gastroenterol, 2022, 28(18): 2021-2033. [4] Sucher E,Sucher R, Gradistanac T, et al. Autoimmune hepatitis-immunologically triggered liver pathogenesis-diagnostic and therapeutic strategies. J Immunol Res, 2019, 2019:9437043. [5] Graham R P, Smyrk T C, Zhang L. Evaluation of langerhans cell infiltrate by CD1a immunostain in liver biopsy for the diagnosis of primary biliary cirrhosis. Am J Surg Pathol, 2012, 36(5): 732-736. [6] Worbs T, Hammerschmidt S I, Forster R. Dendritic cell migration in health and disease. Nat Rev Immunol, 2017, 17(1): 30-48. [7] Macri C, Pang E S, Patton T, et al. Dendritic cell subsets. Semin Cell Dev Biol, 2018, 84:11-21. [8] Chen K, Wang J M, Yuan R, et al. Tissue-resident dendritic cells and diseases involving dendritic cell malfunction. Int Immunopharmacol, 2016, 34:1-15. [9] Rontogianni D, Gerber H, Zimmermann A. Primary biliary cirrhosis (PBC): antigen-presenting cells differ in their distribution in early and late stage PBC and involve the ductal, but not the ductular compartment. Histol Histopathol, 1994, 9(2): 211-220. [10] Patente T A, Pinho M P, Oliveira A A, et al. Human dendritic cells: their heterogeneity and clinical application potential in cancer immunotherapy. Front Immunol, 2018, 9:3176. [11] 中华医学会肝病学分会、消化病学分会、感染病学分会.胆汁淤积性肝病诊断和治疗共识(2015年).实用肝脏病杂志,2016,19(6):Ⅰ-ⅩⅠ. [12] 中华医学会肝病学分会. 原发性胆汁性胆管炎的诊断和治疗指南(2021). 中华肝脏病杂志,2022,30(3):264-275. [13] 中华医学会肝病学分会.自身免疫性肝炎诊断和治疗指南(2021).中华肝脏病杂志,2022,30(5):482-492. [14] European Associationforthe Studyofthe L. Easlclinical practice guidelines: autoimmune hepatitis. J Hepatol, 2015, 63(4): 971-1004. [15] Kowdley K V, Bowlus C L, Levy C, et al. Application of the latest advances in evidence-based medicine in primary biliary cholangitis. Am J Gastroenterol, 2023, 118(2): 232-242. [16] Lleo A, Leung P S C, Hirschfield G M, et al. The pathogenesis of primary biliary cholangitis: acomprehensive review. Semin Liver Dis, 2020, 40(1): 34-48. [17] Tanaka A. Current understanding of primary biliary cholangitis. Clin Mol Hepatol, 2021, 27(1): 1-21. [18] Tanaka A, Leung P S C, Gershwin M E. The genetics of primary biliary cholangitis. Curr Opin Gastroenterol, 2019, 35(2): 93-98. [19] Medford A, Childs J, Little A, et al. Emerging therapeutic strategies in the fight against primary biliary cholangitis. J Clin Transl Hepatol, 2023, 11(4): 949-957. [20] Talwalkar J A, Lindor K D. Primary biliary cirrhosis. Lancet, 2003, 362(9377): 53-61. [21] Sherlock S. Primary biliary cirrhosis, primary sclerosing cholangitis, and autoimmune cholangitis. Clin Liver Dis, 2000, 4(1): 97-113. [22] Ma W T, Chen D K. Immunological abnormalities in patients with primary biliary cholangitis. Clin Sci (Lond), 2019, 133(6): 741-760. [23] Reuveni D, Assi S, Gore Y, et al. Conventional type 1 dendritic cells are essential for the development of primary biliary cholangitis. Liver Int, 2024, 44(8): 2063-2074. |