Cellular and humoral immune responses to vaccines of hepatitis B type
and rabies were inhibited by specific inhibitors of cathepsin B, speci
fic synthetic substrates of cathepsin B and anti-cathepsin B antibody.
Therefore the lysosomal cathepsin B of antigen presenting cells plays
an essential role in processing of these antigens for presentation to
MHC class II. One of the active sites of cathepsin B, VN217-222 Share
s highly homologous sequences with a part of the desetope, a binding d
omain of antigenic peptides, VN57-62 of MHC class II, beta-chain. This
evidence suggests that the peptides processed by the substrate specif
icity of cathepsin B exhibit a common affinity to bind with the deseto
pe of MHC class II, beta-chain.