C. Corbi et al., PREVALENCE AND CLINICAL-FEATURES OF HEPATITIS-G VIRUS-INFECTION IN BONE-MARROW ALLOGRAFT RECIPIENTS, Bone marrow transplantation, 20(11), 1997, pp. 965-968
To study the prevalence and clinical features of hepatitis G virus (HG
V)/GB virus C (GBV-C) infection in bone marrow transplantation (BMT),
we examined frozen serum samples from 95 bone marrow allograft patient
s for HGV/GBV-C RNA by RT-PCR. Twenty-eight out of 95 (29.5 %) were po
sitive and 14 of the HGV(+) patients were already positive before tran
splantation. The mean numbers of blood donors to whom the HGV(-) and H
GV(+) populations were exposed before BMT were not significantly diffe
rent (Kruskal-Wallis test, P = 0.08, NS) but did reveal that the HGV() population had been transfused more often. Moreover, all but one of
the patients who were HGV(+) before graft, had had hematological disea
ses which needed heavy transfusion protocols suggesting, a role of blo
od products in HGV transmission. Fifty out of the 95 patients received
Gammagard intravenous immunoglobulin (IVIG) batches suspected of havi
ng transmitted HCV. However, no significant difference appeared betwee
n these recipients and those receiving other IVIG. Despite their immun
odeficiency, no clinical or biological evidence of liver disease poten
tially linked to HGV infection has as yet been observed. The clinical
outcome, in terms of acute GVHD, chronic GVHD or veno-occlusive diseas
e was similar in HGV(+) and HGV(-) recipients suggesting the absence o
f adverse effects of HGV infection on the early outcome of allogenic B
MT. Long-term evolution remains to be prospectively studied.