
14 patients with hepatocellular carcinoma and one with a hepatoblastoma were given AFP antibodies and changes in serum AFP levels and clinical courses were observed. Anti-human AFP horse IgG was purified by immunoadsorbent column chromatography. 1 mg of the purified antibody was able to bind 100-150 micrograms of AFP. 200-800 mg were given to each patient, according to their AFP levels. Also, conventional anti-cancer agents were administered consecutively. In all cases, the serum AFP levels measured by RIA decreased rapidly to undetectable levels within 24-48 h after the infusion. Then, in seven of 15 cases, the relatively low level was maintained for periods of 10-96 weeks. In the remaining eight cases, the serum AFP level increased again after 1-2 weeks and rose further with clinical deterioration. Since the antibody administered was undetectable in the serum within 2 weeks after its infusion, it is suggested that the AFP antibody had an inhibitory effect on the production or the release of AFP in some patients.
Adult, Male, Carcinoma, Hepatocellular, Liver Neoplasms, Immunization, Passive, Radioimmunoassay, Middle Aged, Antibodies, Child, Preschool, Immunoglobulin G, Humans, Female, alpha-Fetoproteins, Aged, Follow-Up Studies
Adult, Male, Carcinoma, Hepatocellular, Liver Neoplasms, Immunization, Passive, Radioimmunoassay, Middle Aged, Antibodies, Child, Preschool, Immunoglobulin G, Humans, Female, alpha-Fetoproteins, Aged, Follow-Up Studies
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