H. Schupper et al., PERIPHERAL-BLOOD MONONUCLEAR CELL RESPONSES TO RECOMBINANT HEPATITIS-C VIRUS-ANTIGENS IN PATIENTS WITH CHRONIC HEPATITIS-C, Hepatology, 18(5), 1993, pp. 1055-1060
Peripheral blood mononuclear cell proliferative responses in vitro to
recombinant yeast or Escherichia coli hepatitis C virus fusion protein
s were evaluated in 20 patients with chronic hepatitis C who were reac
tive for antibody to hepatitis C virus (on enzyme immunoassay, version
2.0, and a four-antigen recombinant immunoblot assay). Twenty age-mat
ched, healthy individuals negative for antibody to hepatitis C virus w
ere used as a control group. Peripheral-blood mononuclear cells from a
ll chronic hepatitis C patients with antibodies to hepatitis C virus a
ntigens c22 and c100-3 proliferated in vitro in response to the corres
ponding recombinant hepatitis C virus fusion protein. Peripheral-blood
mononuclear cells from 75% of patients infected with hepatitis C viru
s proliferated in response to cytidine monophosphate-keto-3-deoxyoctul
osonic acid-core recombinant antigen but there was no proliferative re
sponse to cytidine monophosphate-keto-3-deoxyoctulosonic acid-EF (deri
ved from the NS5 region). All hepatitis C virus-infected patients had
33c antibody, but peripheral-blood mononuclear cells from only 9 of 14
(64%) proliferated in vitro in response to 33c. Ninety-five percent o
f all hepatitis C virus-infected patients had peripheral-blood mononuc
lear cells that proliferated in response to at least one recombinant h
epatitis C virus fusion protein. The numbers and percentages of CD3 T
cells, CD19 B cells and natural killer cells from patients with chroni
c hepatitis C virus infection did not differ from those in the healthy
control group. However, the number of non-major histocompatibility co
mplex-restricted cytotoxic T cells (CD3-positive, CD56-positive, CD16-
positive) was increased in patients with chronic hepatitis C virus inf
ection (p < 0.05).