R. Repp et al., CLINICAL AND IMMUNOLOGICAL ASPECTS OF HEPATITIS-B VIRUS-INFECTION IN CHILDREN RECEIVING MULTIDRUG CANCER-CHEMOTHERAPY, Archives of virology, 1993, pp. 103-111
For two reasons hepatitis B virus infection is an important problem in
patients with cancer. First, multidrug cancer chemotherapy may reacti
vate or worsen a previously benign chronic HBV infection. Second, pati
ents undergoing cancer chemotherapy are at an increased risk of acquir
ing and spreading HBV which may result in an endemic infection. HBV re
activation may precipitate into a severe acute disease including fulmi
nant hepatitis. In contrast, the acquisition of HBV during cancer chem
otherapy commonly takes a mild clinical course but frequently leads to
persistently high viremia. This state of immunotolerance to viral ant
igens allows viral replication without any sign of liver cell destruct
ion. Withdrawal of chemotherapy does not cause significant changes if
infection occurred during cytotoxic chemotherapy. Infection with HBV d
uring cancer chemotherapy, therefore, may be considered as a model of
an induced antigen-specific immunotolerance. In agreement with this hy
pothesis, vaccination against HBV during cancer chemotherapy does not
prevent spread of HBV in oncology wards as it does not produce signifi
cant anti-HBs titers. Furthermore, vaccination even suppresses the imm
une response to later booster doses after chemotherapy has been withdr
awn.