Cytomegalovirus viremia: Risk factor for allograft cirrhosis after liver transplantation for hepatitis C

Hugo R. Rosen, Sunwen Chou, Christopher L. Corless, David R. Gretch, Kenneth D. Flora, Alan Boudousquie, Susan L. Orloff, John M. Rabkin, Kent G. Benner

Research output: Contribution to journalArticlepeer-review

137 Scopus citations

Abstract

Background. Despite recent advances in diagnosis and treatment, cytomegalovirus (CMV) infection continues to be a common cause of morbidity in liver transplant (LT) recipients. Because CMV infection suppresses cell- mediated immunity, which seems to be important in neutralizing hepatitis C virus (HCV) infection, we assessed the impact of CMV infection on histopathological HCV recurrence after LT. Methods. The study group was comprised of 43 consecutive LT recipients with at least 6 months of histologic follow-up. Group 1 consisted of the 8 patients who developed CMV viremia after LT; group 2 comprised the 35 patients without CMV viremia. There was no significant difference with regard to age, initial immunosuppression, incidence of rejection, distribution of HCV genotypes, or mean follow-up between the groups. Semiquantitative histopathologic assessment of allograft hepatitis was performed using the Knodell's score. Results. The mean total Knodell score of the final allograft biopsy was significantly greater in group 1 patients (P=0.016), with most of the difference due to periportal/bridging necrosis (P=0.009) and lobular activity subitem (P=0.01) scores. Half of the CMV viremic patients eventually developed allograft cirrhosis as compared with 11% of the CMV-negative patients (P=0.027). Accordingly, the cirrhosis-free actuarial survival by Kaplan-Meier estimates was significantly diminished in the CMV viremic patients. Glycoprotein B genotype analysis of CMV isolates revealed no significant differences between patients who did and those who did not develop allograft cirrhosis. Conclusions. After LT for chronic HCV, patients who develop CMV viremia incur a significantly greater risk of severe HCV recurrence.

Original languageEnglish (US)
Pages (from-to)721-726
Number of pages6
JournalTransplantation
Volume64
Issue number5
DOIs
StatePublished - Sep 15 1997
Externally publishedYes

ASJC Scopus subject areas

  • Transplantation

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