Several new technologies to generate and modify established hybridomas
that produce monoclonal antibodies have recently been presented and f
urther development should make them more suitable for diagnostic and t
herapeutic techniques. Different proteolytic procedures have been used
for the fragmentation of intact antibodies to Fab(2)' and Fab fragmen
ts and recombinant DNA techniques have made it possible to obtain chim
eric, humanized, Fv fragments and single-chain Fvs. A review of the ne
w approaches is presented and the future implications are discussed.