Human antibodies to hepatitis C virus core, NS4A and NS3 were cloned i
n a prokaryotic vector and expressed as soluble Fab fragments and as p
hage-displayed Fabs. The recombinant Fabs were shown to be a suitable
tool for immunohistochemistry, since they recognize the cognate antige
n expressed in mammalian cells. The nucleotide sequence of the cDNA fo
r the variable domains of these antibodies was determined and the V-ge
ne usage was derived. On the basis of the deduced amino acid sequence,
a structural model of the V domains of the Fabs was constructed.