Liver allografts from HBcAb(+), IgM(-), HEsAg(-) donors can transmit H
BV to uninfected recipients. We currently no longer accept these liver
s for transplantation while continuing to accept the kidneys. The purp
ose of this study is to determine the risk of donor-transmitted HBV in
fections from HBcAb(+), HBIgM(-), HBsAg(-) organ donors and determine
if the risk of donor-transmitted HBV infections and their severity is
dependent on the organ being transplanted. This study consists of a re
trospective review of the posttransplant course of recipients of HBcAb
(+), HBIgM(-), HBsAg(-) donors accepted at UCSF from 6/85 to 12/93. Tr
ansmitted HBV infection was defined as one in which the recipient chan
ged from HBsAg(-) prior to transplantation to HBsAg(+) posttransplant,
with no other source. There were 25 of 1190 donors who were HBcAb(f),
HBIgM(-), HBsAg(-); 1/42 kidney, 3/6 liver, and 0/7 heart HBsAg(-) tr
ansplant recipients of organs from these donors became HBsAg(f) after
transplantation. This difference in infection rate (liver vs, kidney a
nd heart) is statistically significant. The clinical course of the liv
er recipients was also more severe. Ah of the patients who became infe
cted were HBsAb(-) and HBcAb(-) prior to transplant. We conclude that
(1) HBV can be transmitted from HBcAb(+), HBIgM(-), HBsAg(-) organ don
ors, (2) the rate of transmission is highest and severity of infection
is worst in the liver recipients; and (3) we will continue to transpl
ant kidneys from these donors, preferably into immunized recipients.