Semin Liver Dis 2001; 21(4): 517-524
DOI: 10.1055/s-2001-19032
Copyright © 2001 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

Etiopathogenesis of Biliary Atresia

Ronald J. Sokol1 , Cara Mack2
  • 1Pediatric Liver Center and Liver Transplantation Program and the Pediatric General Clinical Research Center, Department of Pediatrics, University of Colorado School of Medicine and The Children's Hospital, Denver, Colorado
  • 2Department of Pediatric Gastroenterology, Hepatology and Nutrition, Northwestern University School of Medicine and Children's Memorial Hospital, Chicago, Illinois
Further Information

Publication History

Publication Date:
17 December 2001 (online)

ABSTRACT

Biliary atresia, a progressive sclerosis of the extrahepatic biliary tree that occurs only within the first 3 months of life, is one of the most common causes of neonatal cholestasis and accounts for over half of children who undergo liver transplantation. In biliary atresia, a number of prenatal or perinatal insults to the biliary tree appear to culminate in complete obliteration of the lumen of the extrahepatic biliary tree and continued injury and sclerosis of intrahepatic bile ducts, even after portoenterostomy is successful. A minority of cases of biliary atresia may be caused by defects in morphogenesis of the bile ducts. Potential etiologies for the more common perinatal form of biliary atresia include viral infections, immune-mediated bile duct injury, and autoimmune disease involving the bile ducts. Two viruses, reovirus and rotavirus, have received increasing attention as possible inciters of an immune-mediated injury to the biliary tree. Fas ligand upregulation and apoptosis of bile duct epithelia have been demonstrated in human specimens, as well as T-lymphocyte and macrophage activation in portal tracts. An experimental model using rotavirus infection in newborn mice has been useful in characterizing the mechanisms underlying bile duct injury. It is proposed that virally induced neoantigens displayed on biliary epithelium may play a role in initiating the immune processes involved in destruction of the extrahepatic bile duct and ongoing intrahepatic ductal injury in the perinatal form of biliary atresia. The short window of time after birth during which this disease presents suggests that immaturity of the neonatal immune system and genetic susceptibility also may be key factors. Delineation of the mechanisms underlying bile duct injury will be essential to the development of new potential therapies for this important pediatric disorder.

REFERENCES

  • 1 Balistreri W F, Grand R, Hoofnagle J H. Biliary atresia: current concepts and research directions. Summary of a symposium.  Hepatology . 1996;  23 1682-1692
  • 2 Karrer F M, Price M R, Bensard D D. Long-term results with the Kasai operation for biliary atresia.  Arch Surg . 1996;  131 493-496
  • 3 Chardot C, Carton M, Spire-Bendelac N. Epidemiology of biliary atresia in France: a national study 1986-96.  J Hepatol . 1999;  31 1006-1013
  • 4 Davenport M, Kerkar N, Mieli-Vergani G. Biliary atresia: the King's College Hospital experience (1974-1995).  J Pediatr Surg . 1997;  32 479-485
  • 5 Mazziotti M V. Anomalous development of the hepatobiliary system in the inv mouse.  Hepatology . 1999;  30 372-378
  • 6 Mazziotti M V, Willis L K, Heuckeroth R O. Anomalous development of the hepatobiliary system in the Inv mouse.  Hepatology . 1999;  30 372-378
  • 7 Landing B H. Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst-the concept of infantile obstructive cholangiopathy.  Prog Pediatr Surg . 1974;  6 113-139
  • 8 Balistreri W F, Tabor E, Gerety R J. Negative serology for hepatitis A and B viruses in 18 cases of neonatal cholestasis.  Pediatrics . 1980;  66 269-271
  • 9 Tanaka M, Ishikawa T, Sakaguchi M. The pathogenesis of biliary atresia in Japan: immunohistochemical study of HBV-associated antigen.  Acta Pathol Jpn . 1993;  43 360-366
  • 10 Scotto J M, Alavarez F. Biliary atresia and non-A, non-B hepatitis?.  Gastroenterology . 1982;  82 393
  • 11 Tarr P I, Haas J E, Christie D L. Biliary atresia, cytomegalovirus, and age at referral.  Pediatrics . 1996;  97 828-831
  • 12 Fischler B, Ehrnst A, Forsgren M. The viral association of neonatal cholestasis in Sweden: a possible link between cytomegalovirus infection and extrahepatic biliary atresia.  J Pediatr Gastroenterol Nutr . 1998;  27 57-64
  • 13 Jevon G P, Dimmick J E. Biliary atresia and cytomegalovirus infection: a DNA study.  Pediatr Dev Pathol . 1999;  2 11-14
  • 14 Bangaru B, Morecki R, Glaser J H. Comparative studies of biliary atresia in the human newborn and reovirus-induced cholangitis in weanling mice.  Lab Invest . 1980;  43 456-462
  • 15 Papadimitriou J M. The biliary tract in acute murine reovirus 3 infection. Light and electron microscopic study.  Am J Pathol . 1968;  52 595-611
  • 16 Wilson G A, Morrision L A, Fields B N. Association of the reovirus S1 gene with serotype 3-induced biliary atresia in mice.  J Virol . 1994;  68 6458-6465
  • 17 Rosenberg D P, Morecki R, Lollini L O. Extrahepatic biliary atresia in a rhesus monkey (Macaca mulatta).  Hepatology . 1983;  3 577-580
  • 18 Morecki R, Glaser J H, Cho S. Biliary atresia and reovirus type 3 infection.  N Engl J Med . 1982;  307 48l-484
  • 19 Morecki R, Glaser J H, Johnson A B. Detection of reovirus type 3 in the porta hepatis of an infant with extrahepatic biliary atresia: ultrastructural and immunocytochemical study.  Hepatology . 1984;  4 1137-1142
  • 20 Brown W R, Sokol R J, Levin M J. Lack of correlation between infection with reovirus 3 and extrahepatic biliary atresia or neonatal hepatitis.  J Pediatr . 1988;  113 670-676
  • 21 Glaser J H, Balistreri W F, Morecki R. Role of reovirus type 3 in persistent infantile cholestasis.  J Pediatr . 1984;  105 912-915
  • 22 Richardson S C, Bishop R F, Smith A L. Reovirus serotype 3 infection in infants with extrahepatic biliary atresia or neonatal hepatitis.  J Gastroenterol Hepatol . 1994;  9 264-268
  • 23 Dussaix E, Hadchouel M, Tardieu M. Biliary atresia and reovirus type 3 infection.  N Engl J Med . 1984;  310 658
  • 24 Richardson S C, Bishop R F, Smith A L. Reovirus serotype 3 infection in infants with extrahepatic biliary atresia or neonatal hepatitis.  J Gastroenterol Hepatol . 1994;  9 264-268
  • 25 Steele M I, Marshall C M, Lloyd R E. Reovirus 3 not detected by reverse transcriptase-mediated polymerase chain reaction analysis of preserved tissue from infants with cholestatic liver disease.  Hepatology . 1995;  21 697-702
  • 26 Tyler K L, Sokol R J, Oberhaus S M. Detection of reovirus RNA in hepatobiliary tissues from patients with extrahepatic biliary atresia and choledochal cysts.  Hepatology . 1998;  27 1475-1482
  • 27 Riepenhoff-Talty M, Schaekel K, Clark H F. Group A rotaviruses produce extrahepatic biliary obstruction in orally inoculated newborn mice.  Pediatr Res . 1993;  33 394-399
  • 28 Petersen C, Biermanns D, Kuske M. New aspects in a murine model for extrahepatic biliary atresia.  J Pediatr Surg . 1997;  32 1190-1195
  • 29 Petersen C, Grasshoff S, Luciano L. Diverse morphology of biliary atresia in an animal model.  J Hepatol . 1998;  28 603-607
  • 30 Petersen C, Bruns E, Kuske M. Treatment of extrahepatic biliary atresia with interferon-alpha in a murine infectious model.  Pediatr Res . 1997;  42 623-628
  • 31 Qiao H, DeVincentes A, Alashari M. Pathogenesis of rotavirus-induced bile duct obstruction (a model for biliary atresia) in normal Balb/c and CB17 scid mice with severe combined immunodeficiency.  Pediatr Res . 1999;  45 116A
  • 32 Riepenhoff-Talty M, Gouvea V, Evans M J. Detection of group C rotavirus in infants with extrahepatic biliary atresia.  J Infect Dis . 1996;  174 8-15
  • 33 Bobo L, Ojeh C, Chiu D. Lack of evidence for rotavirus by polymerase chain reaction/enzyme immunoassay of hepatobiliary samples from children with biliary atresia.  Pediatr Res . 1997;  41 229-234
  • 34 Drut R, Drut R M, Gomez M A. Presence of human papillomavirus in extrahepatic biliary atresia.  J Pediatr Gastroenterol Nutr . 1998;  27 530-535
  • 35 Drut R, Gomez M A, Drut R M. Human papillomavirus, neonatal giant cell hepatitis and biliary duct atresia.  Acta Gastroenterol Latinoam . 1998;  28 27-31
  • 36 Domiati-Saad R, Dawson D B, Margraf L R. Cytomegalovirus and human herpesvirus 6, but not human papillomavirus, are present in neonatal giant cell hepatitis and extrahepatic biliary atresia.  Pediatr Dev Pathol . 2000;  3 367-373
  • 37 Mason A L, Xu L, Guo L. Detection of retroviral antibodies in primary biliary cirrhosis and other idiopathic biliary disorders.  Lancet . 1998;  351 1620-1624
  • 38 Schreiber R A, Kleinman R E. Genetics, immunology, and biliary atresia: an opening or a diversion?.  J Pediatr Gastroenterol Nutr . 1993;  16 111-113
  • 39 Silveira T R, Salzano F M, Donaldson P T. Association between HLA and extrahepatic biliary atresia.  J Pediatr Gastroenterol Nutr . 1993;  16 114-117
  • 40 Jurado A, Jara P, Camarena C. Is extrahepatic biliary atresia an HLA-associated disease?.  J Pediatr Gastroenterol Nutr . 1997;  25 557-558
  • 41 Broome U, Nemeth A, Hultcrantz R. Different expression of HLA-DR and ICAM-1 in livers from patients with biliary atresia and Byler's disease.  J Hepatol . 1997;  26 857-862
  • 42 Kobayashi H, Puri P, O'Brian D S. Hepatic overexpression of MHC class II antigens and macrophage-associated antigens (CD68) in patients with biliary atresia of poor prognosis.  J Pediatr Surg . 1997;  32 590-593
  • 43 Gosseye S, Otte J B, De Meyer R. A histological study of extrahepatic biliary atresia.  Acta Paediatr Belg . 1977;  30 85-90
  • 44 Bill A H, Haas J E, Foster G L. Biliary atresia: histopathologic observations and reflections upon its natural history.  J Pediatr Surg . 1977;  12 977-982
  • 45 Ohya T, Fujimoto T, Shimomura H, Miyano T. Degeneration of intrahepatic bile duct with lymphocyte infiltration into biliary epithelial cells in biliary atresia.  J Pediatr Surg . 1995;  30 515-518
  • 46 Abbas A K, Lichtman A H, Pober J S. Cellular and Molecular Immunology.  Philadelphia: WB Saunders 2000
  • 47 Van den Oord J J, Sciot R, Desmet V J. Expression of MHC products by normal and abnormal bile duct epithelium.  J Hepatol . 1986;  3 310-317
  • 48 Nakada M, Nakada K, Kawaguchi F. Immunologic reaction and genetic factors in biliary atresia.  Tohoku J Exp Med . 1997;  181 41-47
  • 49 Davenport M, Gonde C, Redkar R. Immunohistochemistry of the liver and biliary tree in extrahepatic biliary atresia.  J Pediatr Surg . 2001;  36 1017-1025
  • 50 Urushihara N, Iwagaki H, Yagi T. Elevation of serum interleukin-18 levels and activation of Kupffer cells in biliary atresia.  J Pediatr Surg . 2000;  35 446-449
  • 51 Tracy Jr F T, Dillon P, Fox E S. The inflammatory response in pediatric biliary disease: macrophage phenotype and distribution.  J Pediatr Surg . 1996;  31 121-125
  • 52 Funaki N, Sasano H, Shizawa S. Apoptosis and cell proliferation in biliary atresia.  J Pathol . 1998;  186 429-433
  • 53 Liu C, Chiu J-H, Chin T, Wang L-S. Expression of Fas ligand on bile ductule epithelium in biliary atresia-a poor prognostic marker.  J Pediatr Surg . 2000;  35 1591-1596
  • 54 Vasiliauskas E A, Targan S R, Cobb L. Biliary atresia-an autoimmune mediated disorder [Abstract]?.  Hepatology . 1995;  22 128A
  • 55 Burch J M, Sokol R J, Narkewicz M. The role of maternal antibodies in cholestatic liver disease in infants: a new isolated finding in neonatal lupus [Abstract]?.  J Pediatr Gastroenterol Nutr . 2000;  31(Suppl 2) S108
  • 56 Bernal W, Moloney M, Underhill J. Association of tumor necrosis factor polymorphism with primary sclerosing cholangitis.  J Hepatol . 1999;  30 237-241
  • 57 Mitchell S A, Grove J, Spurkland A. Association of the tumour necrosis factor alpha-308 but not the interleukin 10-627 promoter polymorphism with genetic susceptibility to primary sclerosing cholangitis.  Gut . 2001;  49 288-294
  • 58 Dillon P W, Owings E, Cilley R. Immunosuppression as adjuvant therapy for biliary atresia.  J Pediatr Surg . 2001;  36 80-85
    >