Intragraft localization of activated nuclear factor kappa B in recurrent hepatitis C virus disease following liver transplantation

Nuclear factor kappa B (NF-kappa B) is activated during viral infection and is central to the regulation of host immune responses. The NF-kappa B acti vation status and its morphological sources were assessed by immunohistoche mistry in allograft biopsy specimens of orthotopic liver transplantation pa tients with recurrent hepatitis C virus (HCV). Hepatocellular NF-kappa B im munostaining was detected in HCV cases compared with controls (nontransplan t: P < .001; transplant: P = .006), which correlated with the number of NF- kappa B positive hepatocytes (P = .007) and contrasted to the absent to wea k staining of controls (nontransplant: P = .001; transplant: P = .009). Enh anced NF-kappa B staining of cytokeratin 19-positive bile ducts and prolife rating ductules in the HCV group was in contrast to controls. Intense NF-ka ppa B immunoreactivity was detected in CD68-positive Kupffer cells and macr ophages of all HCV specimens compared with a few controls (nontransplant: P < .001; transplant: P = .001) and contrasted to the weak staining of contr ols (nontransplant: P < .001; transplant: P = .001), NF-kappa B-positive im munoreactivity correlated with the number of T cell receptor (TCR) alpha/be ta-positive lymphocytes (P < .001), which was not observed in controls. In those HCV cases showing evidence of necroinflammatory activity (grade) and individual features of portal inflammation, periportal inflammation/pieceme al necrosis, lobular inflammation, and fibrosis (stage), higher NF-kappa B staining intensity scores within bile ducts, proliferating ductules, hepato cytes (piecemeal necrosis: P = .016; stage: P = .030), and lymphocytes (sta ge: P = .044) and increased number of NF-kappa B-positive cells within bile ducts, proliferating ductules (grade, lobular inflammation, piecemeal necr osis, stage: P = .022), hepatocytes, and lymphocytes were observed. Increas ed staining intensity and frequency of NF-kappa B-positive cells were simil arly observed in HCV-positive allografts obtained from patients under tacro limus- compared with cyclosporine-based immunosuppression. These data impli cate an immunoregulatory role of intragraft NF-kappa B activation in the pa thogenesis and progression of posttransplantation HCV disease recurrence.