HUMANIZED ANTI-LEWIS-Y ANTIBODIES - IN-VITRO PROPERTIES AND PHARMACOKINETICS IN RHESUS-MONKEYS

ABL 364 is a murine monoclonal IgG3 antibody directed against the Lewi s Y carbohydrate antigen (Le(y)) expressed on the surface of many epit helial cell tumors, The antibody mediates cytotoxicity via activation of human complement or human effector cells, and has been evaluated in several clinical trials including two Phase I/II trials in relapsed s mall cell lung cancer and metastatic breast cancer, To improve the eff ector functions of the antibody, increase its half-life in circulation , and avoid the human antimouse antibody response, two chimeric and se veral humanized antibodies were constructed for evaluation, The chimer ic IgG1 is more potent than the murine IgG3 in tumor cell lysis via ac tivation of human peripheral mononuclear cells (10-fold), but somewhat less effective in complement-dependent lysis (2-3-fold). The chimeric IgG3 is slightly less potent than the IgG1. A humanized IgG1 was cons tructed by combining the complementarity-determining regions of the AB L 364 antibody with human framework and constant regions, Several addi tional variants were subsequently constructed to improve the binding a ffinity and increase expression of the antibody, Two of the variants, designated I and K, differ by a single amino acid at position 75 of th e heavy chain, Both variants have affinity within 2-fold of the chimer ic IgG1 antibody and retain the cytolytic activities toward tumor cell lines, However, it was possible to express variant K at a significant ly higher level (5-10-fold) than variant I, Pharmacokinetics of the hu manized ABL 364 antibody variant K was compared with that of the paren t murine antibody in rhesus monkeys, It was shown that the terminal ha lf-life of the humanized antibody in rhesus monkeys is 14-20 days, wit h a mean of 16.3 days, while that of the parent murine antibody is onl y 1.9 days.