The availability of monoclonal antibodies with well-defined specificit
ies to lymphoma-associated antigens promises to open new therapeutic o
pportunities in the treatment of patients with non-Hodgkin's lymphoma.
Monoclonal antibodies against lineage-specific surface markers such a
s CD19, CD20 or CD22 have been generated and employed in native or mod
ified forms in clinical phase I/II trials. Modified versions such as t
oxin-conjugated antibodies or antibodies with dual specificities (bisp
ecific antibodies) were introduced to enhance the cytotoxicity of mono
clonal antibodies since native antibodies were not able to induce long
-lasting remissions in patients with advanced disease although respons
es were seen and side-effects were usually mild. Future efforts should
concentrate on patients with minimal residual disease employing genet
ically engineered antibody fragments.