Efficient Clearance of Poly(Ethylene Glycol)Modified Immunoenzyme with Anti-Peg Monoclonal-Antibody for Prodrug Cancer-Therapy

The F(ab')(2) fragment of the anti-TAG-72 antibody, B72.3, was covalently linked to Escherichia coli-derived P- glucuronidase that was modified with methoxypoly(ethylene glycol). The conjugate (B72.3-beta G-PEG) localized to a peak concentration in LS174T xenografts within 48 h after injection, but enzyme activity persisted in plasma such that prodrug administration had to be delayed for at least 4 days to avoid systemic prodrug activation and associated toxicity. Conjugate levels in tumors decreased to 36% of peak levels at this time. Intravenous administration of AGP3 , an IgM mAb against methoxypoly(ethylene glycol), accelerated clearance of conjugate from serum and increased the tumor/blood ratio of B 72.3-beta G-PEG from 3.9 to 29.6 without significantly decreasing the accumulation of conjugate in tumors. Treatment of nude mice bearing established human colon adenocarcinoma xenografts with B72.3 -beta G-PEG followed 48 h later with AGP3 and a glucuronide prodrug of p- hydroxyaniline mustard significantly (p less than or equal to 0.0005) delayed tumor growth with minimal toxicity compared to therapy with a control conjugate or conventional chemotherapy