A second generation hepatitis C virus recombinant immunoblot assay (RI
BA) was used to screen stored perioperative serum from 641 renal allog
raft recipients. One hundred and nine (17%) were anti-HCV positive at
the time of transplant. RIBA positivity was found to be an independent
predictor of post-transplant liver disease in a logistic regression m
odel (P < 0.05). Moreover, RIBA positive patients were at greater risk
for infectious events (P = 0.03) and rejection episodes (P = 0.002).
The cumulative dose of antilymphoblast globulin administered as induct
ion therapy was an independent predictor of post-transplant liver dise
ase in a dose response relationship. Qualitative PCR showed that 74% o
f the perioperative RIBA positive patients had detectable HCV RNA in a
current serum sample. Further, quantitative HCV RNA analysis with a c
ompetitive template PCR and HCV strain identification by restriction f
ragment length polymorphism demonstrated a large range of HCV RNA copi
es/ml of serum and three different HCV strains (BK, Hutch and HCV-1).
Neither quantity of HCV RNA nor strain type correlated with abnormal t
ransaminases post-transplant. As yet, there has not been an effect of
anti-HCV status on actuarial patient and graft survival. This study su
ggests that anti-HCV is not a contraindication to renal transplantatio
n; however, we would recommend that the pretransplant evaluation of th
e anti-HCV positive patient include a liver biopsy to properly stage t
he disease. Close post-transplant follow-up is required in view of the
increased risk for infection and rejection.