Liver infiltrating mononuclear cells in children with type 1 autoimmune hepatitis
- M B De Biasio1,
- N Periolo1,
- A Avagnina2,
- M T García de Dávila3,
- M Ciocca4,
- J Goñi5,
- E de Matteo6,
- C Galoppo7,
- M C Cañero-Velasco8,
- H Fainboim9,
- A E Muñoz10,
- L Fainboim1,
- A C Cherñavsky1
- 1División inmunogenética, Hospital de Clínicas “José de San Martín”, Universidad de Buenos Aires, Buenos Aires, Argentina
- 2Anatomía patológica, Hospital de Clínicas “José de San Martín”, Universidad de Buenos Aires
- 3Sección Anatomía patológica, Hospital Nacional de Pediatría “J P Garrahan”, Buenos Aires
- 4Hepatología, Hospital Nacional de Pediatría “J P Garrahan”, Buenos Aires
- 5Transplante hepático, Hospital Nacional de Pediatría “J P Garrahan”, Buenos Aires
- 6Unidad de Anatomía patológica, Hospital Nacional de Pediatría “J P Garrahan”, Buenos Aires
- 7Hepatología, Hospital Nacional de Pediatría “J P Garrahan”, Buenos Aires
- 8Unidad de Hepatología, Hospital municipal de niños de San Justo, Buenos Aires, Argentina
- 9Unidad de Hepatología, Hospital general de infecciosas “F J Muñiz”, Buenos Aires
- 10Unidad de Hepatología, Hospital de Gastroenterología “Dr C Bonorino Udaondo”, Buenos Aires
- Correspondence to:
Dr A C Cherñavsky
División Inmunogenética, Hospital de Clínicas “José de San Martín”, Universidad de Buenos Aires, Av Córdoba 2351, (1120) Buenos Aires, Argentina; accher{at}fibertel.com.ar
- Accepted 7 October 2005
- Published Online First 17 February 2006
Abstract
Objective: To investigate infiltrating cells in the liver of children with type 1 autoimmune hepatitis (AH-1).
Methods: liver biopsies from 24 untreated AH-1 patients (14 children, 10 adults), five patients with hepatitis C virus related chronic hepatitis (HCV), and 10 control liver specimens (CL) were processed for immunohistochemical cell characterisation.
Results: Two different cell distribution patterns were detected in the liver of patients with AH-1: (1) CD4+ and CD20+ cells were found in the central areas of the portal tracts (portal distribution); (2) CD8+ cells were observed at the periphery of the portal space (periportal distribution). Some cell subsets, like CD56, CD57, Fas-L, and Bak, showed a non-defined distribution pattern. The presence of two well defined patterns of cell distribution was not observed in HCV and CL (CD4+, CD20+, and CD8+ cells were uniformly distributed in the portal space). In AH-1 and CL, the NK markers CD56 and CD57 were found scattered throughout the liver parenchyma. However, in HCV biopsies, CD56+ cells were also clearly increased in both the portal and the periportal areas. Biopsies of AH-1 and HCV patients showed a uniform distribution of Fas-L and Bak in the portal and periportal areas, with Bak staining also detected in the hepatic parenchyma.
Conclusions: Despite clinical and genetic differences, there was a similar distribution of liver infiltrating mononuclear cells in children and adults with AH-1. These results raise the possibility of reclassifying cryptogenic chronic hepatitis by immunohistochemical analysis of infiltrating liver cells.
- AAH, adult autoimmune hepatitis type 1
- AH-1, type 1 autoimmune hepatitis
- ANA, antinuclear antibodies
- CL, control liver specimen
- HCV, hepatitis C virus related chronic hepatitis
- PAH, paediatric autoimmune hepatitis type 1
- SMA, smooth muscle antibodies









