We have conducted a controlled trial in 20 haemophilic patients in whi
ch intravenous recombinant interferon alpha-2a, 3 mega units thrice we
ekly, was used to treat chronic hepatitis C infection. The study endpo
ints included complete and partial normalization of serum ALT, and los
s of serum HCV RNA as determined by polymerase chain reaction (PCR). I
nterferon treatment was effective, and resulted in improvement in;ALT
in nine (45%) and a loss of HCV RNA in five patients (26%), but a sust
ained normalization of ALT has been seen in only one case. Responses w
ere poor in those with HIV coinfection or with HCV genotype 1 (Simmond
s classification). Troublesome side-effects were reported in 80%. The
occurrence of a factor VIIIc inhibitor during the study was possibly a
n autoimmune complication of interferon. In conclusion, we have shown
lower response rates than those seen in post-transfusion hepatitis C i
nfection and suspect that current interferon regimes are unlikely to i
nfluence the natural history of HCV infection in haemophilia. Consider
ation should be given to trials of higher dosage interferon, and of lo
ng-term maintenance therapy for those who relapse.