Proceedings of the National Academy of Sciences · 1987 · 203 citations · 25 references
PharmacyImmunologyOncologyAntibody EngineeringCancer ImmunologyMonoclonal AntibodiesAntibody-antigen RecognitionChimeric AntibodiesHybridoma TechnologyTherapeutic Monoclonal AntibodiesTumor AntigensTumor-associated AntigensAntibody Structure-function RelationshipsAntibody Therapeutic EfficacyAntibody-dependent Cell-mediated CytotoxicityAntibody-dependent Cellular CytotoxicityCdna CloningChimeric Antibody ProductionMonoclonal Antibodies In CancerMonoclonal Antibodies In Oncology
A chimeric mouse-human antibody has been created that recognizes an antigen found on the surface of cells from many carcinomas. Immunoglobulin constant (C) domains of the mouse monoclonal antibody L6, C gamma 2a and C kappa, were substituted by the human C gamma 1 and C kappa by recombining cDNA modules encoding variable or C domains. The cDNA constructs were transfected into lymphoid cells for antibody production. The chimeric antibody and mouse L6 antibody bound to carcinoma cells with equal affinity and mediated complement-dependent cytolysis. In the presence of human effector cells, the chimeric antibody gave antibody-dependent cellular cytotoxicity at 100 times lower concentration than that needed for the mouse L6 antibody. The chimeric antibody, but not the mouse L6 antibody, is effective against a melanoma line expressing small amounts of the L6 antigen. The findings point to the usefulness of the chimeric antibody approach for obtaining agents with strong antitumor activity for possible therapeutic use in man.
25
A simple and very efficient method for generating cDNA libraries
Ueli Gubler, Beth J. Hoffman · Gene · 1983 · 4.6K citations