Y. Pirson et E. Goffin, HEPATITIS-C INFECTION IN RENAL-TRANSPLANT PATIENTS - NEW INSIGHTS ANDUNANSWERED QUESTIONS, Nephrology, dialysis, transplantation, 11, 1996, pp. 42-45
The prevalence of HCV infection in a population of renal transplantati
on patients is mostly dependent on that preexisting before transplanta
tion, It also has been demonstrated that HCV infection can be transmit
ted by the renal graft. Although grafting an HCV+ kidney does not affe
ct survival 5 years after surgery, the risk incurred by recipients on
the longer term is unclear. A suggestion has been made to reserve HCV kidneys for recipients who are themselves HCV+. However, it has been
established that a given HCV strain has little chance of inducing immu
nity to a different HCV strain. This is why the use of HCV+ kidneys no
longer meets consensus. It could be considered to match the recipient
and the graft with regard to the HCV strain when genotype identificat
ion is routinely available, quick and reliable. Immunosuppressive ther
apy enhances viral replication Its longterm effect on the course of HC
V disease is unclear. In particular, no studies have compared the long
-term outcome of HCV+ patients treated by haemodialysis and transplant
ation. The data available on the 10-year outcome of HCV+ grafted patie
nts are nonetheless reassuring. At least they allow considering renal
transplantation to non-cirrhotic HCV+ patients. Several issues related
to the interaction between HCV and immunosuppressive therapy remain t
o be clarified. Does the viral strain play a role in the course of inf
ection under immunosuppressive treatment? Does immunosuppressive treat
ment promote strain mutagenesis? Does HCV infection require modulation
of the immunosuppressive treatment?