A PRETRANSPLANT INFECTION WITH PRECORE MUTANTS OF HEPATITIS-B VIRUS DOES NOT INFLUENCE THE OUTCOME OF ORTHOTOPIC LIVER-TRANSPLANTATION IN PATIENTS ON HIGH-DOSE ANTI-HEPATITIS-B VIRUS SURFACE-ANTIGEN IMMUNOPROPHYLAXIS
U. Naumann et al., A PRETRANSPLANT INFECTION WITH PRECORE MUTANTS OF HEPATITIS-B VIRUS DOES NOT INFLUENCE THE OUTCOME OF ORTHOTOPIC LIVER-TRANSPLANTATION IN PATIENTS ON HIGH-DOSE ANTI-HEPATITIS-B VIRUS SURFACE-ANTIGEN IMMUNOPROPHYLAXIS, Hepatology, 26(2), 1997, pp. 478-484
Hepatitis B virus (HBV) infection of the liver graft is a major compli
cation after orthotropic liver transplantation (OLT) for HBV-related c
irrhosis. A high viral load before OLT is a known risk factor, whereas
the relevance of precore mutants of HBV is a subject of controversy.
The aim of this study was to correlate the pretransplantation viral lo
ad and a pretransplantation infection with precore mutant HBV (pmHBV)
or wildtype HBV (wtHBV) with allograft damage, graft failure, and surv
ival after OLT. Sixty-nine patients with HBV cirrhosis underwent OLT u
nder high dose immunoprophylaxis with anti-hepatitis B surface (HBs) t
ype immunoglobulins (HBIg), A pretransplantation infection with pmHBV
and wtHBV was detected by polymerase chain reaction (PCR) and direct s
equencing in 30 patients each (pmHBV and wtHBV group), Nine of 69 pati
ents were PCR-negative (noHBV group), Median pretransplantation levels
of HBV DNA assessed by hybridization assay were 42 pg/mL for pmHBV an
d 54 pg/mL for wtHBV patients. HDV recurred ill 17 of 30 (57%) of pmHB
V and in 14 of 30 (47%) of wtHBV patients and graft failure occurred i
n 6 of 30 (20%) of pmHBV and 7 of 30 (23%) of wtHBV patients. Neither
HBV recurrence nor graft failure occurred in patients in whom no HBV D
NA could be detected by PCR using primers flanking the HBV precore reg
ion (noHBV) patients. Allograft damage assessed by histology activity
index (HAI) scoring was median 6 for pmHBV and 7 for wtHBV patients, C
umulative survival after 5 years was 72% for pmHBV, 74% for wtHBV, and
100% for noHBV patients, In this study, we protide evidence that pret
ransplantation viral load, but not infection with pmHBV, determines th
e outcome after OLT in patients on high. dose HBIg prophylaxis.