Type I interferons, which are mostly a-interferons (either as single agents
or in combination with antiviral drugs), are currently the standard therap
y for chronic viral hepatitis B, B/D, and C. Side-effects are not uncommon
and include exacerbation of preexisting autoimmune disorders or the de novo
induction of autoimmunity. These adverse effects are attributed to the imm
unomodulatory properties of type I interferons, and should be distinguished
from autoimmunity associated with chronic viral hepatitis in which interfe
ron treatment may indeed be beneficial. The major autoimmune side-effects o
f interferon therapy for chronic viral hepatitis are thyroid or liver disea
se. Therefore, screening for thyroid antibodies and auto-antibodies indicat
ive of autoimmune hepatitis both before, during, and after interferon thera
py is strongly recommended. The presence of high concentrations of thyroid
auto-antibodies or antibodies associated with autoimmune hepatitis can be c
ontraindicative to interferon therapy. However, treatment is not contraindi
cated in viral hepatitis (in particular chronic hepatitis C) associated wit
h autoimmune phenomena - including low-titer thyroid antibodies or other no
n-organ specific autoantibodies. If interferon-induced autoimmunity occurs,
the necessity of therapy has to be balanced carefully against the risks of
autoimmune disease. Further research is needed to identify the factors whi
ch determine susceptibility to interferon-associated autoimmunity in indivi
dual patients. (C) 1999 Elsevier, Paris.