Lobular damage caused by cellular and humoral immunity in liver allograft rejection
Article first published online: 16 DEC 2004
Volume 19, Issue 1, pages 110–114, February 2005
How to Cite
Sawada, T., Shimizu, A., Kubota, K., Fuchinoue, S. and Teraoka, S. (2005), Lobular damage caused by cellular and humoral immunity in liver allograft rejection. Clinical Transplantation, 19: 110–114. doi: 10.1111/j.1399-0012.2004.00310.x
- Issue published online: 16 DEC 2004
- Article first published online: 16 DEC 2004
- Accepted for publication 24 September 2004
- cellular rejection;
- humoral rejection;
- liver transplantation;
- lobular damage
Abstract: Backgrounds: Diagnosis of acute liver allograft rejection (ALAR) is usually performed by the estimation of changes in portal areas. In this study, changes in the hepatic lobules were investigated retrospectively by immunohistochemistry, and compared with changes in the portal areas. Humoral immunity in ALAR was also studied by C4d-staining.
Materials and methods: In total, 35 biopsy specimens from 20 patients who had undergone living-related liver transplantation were included. Specimens had been graded as mild, moderate-to-severe acute rejection based on the Banff Schema. Changes in hepatic lobules were investigated by hematoxylin-eosin (H & E) staining, an immunohistochemical study using anti-CD3 (T cells), anti-GMP-17 (cytotoxic cells), anti-CD68 (macrophages) and C4d, and the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end-labeling (TUNEL) method.
Results: Changes in hepatic lobules consisted of the infiltration of mononuclear cells, swelling and necrosis of hepatocytes, and hemorrhages. The degree of these changes increased with the severity of ALAR. Immunohistochemical analysis revealed that infiltrating cells included CD3+ T cells, GMP-17+ cytotoxic cells and CD68+ macrophages. The number of infiltrating cells increased with the severity of the ALAR. The TUNEL assay demonstrated apoptotic cells in ALAR and the number of apoptotic cells increased with the severity of the ALAR. In moderate-to-severe rejection, C4d depositions were observed in the hepatic sinusoids as well as the portal veins and hepatic arteries.
Conclusions: Changes in the hepatic lobules were observed in ALAR and the severity increased with the severity of ALAR. Apoptosis was involved in the mechanism of cell death and humoral immunity plays a role in the mechanism of ALAR.