Mouse/human chimeric anti-HIV-1 gp120 antibody to the principal neutralizing determinant: Tolerability and pharmacokinetics in cynomolgus monkeys,Macaca fascicularis
Autor: | Wayne Gordon, Tse Wen Chang, Michael S. C. Fung, Walter Bee, Luigi Botta, Fred Gudat, Dietmar G. Braun, Ruey-Shyan Liou, Nancy T. Chang, Ulrich Zühlke, Sam McKinney, Daniel Gygax |
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Rok vydání: | 1992 |
Předmět: |
Male
medicine.medical_specialty HIV Antigens medicine.drug_class Ratón Recombinant Fusion Proteins Enzyme-Linked Immunosorbent Assay HIV Antibodies HIV Envelope Protein gp120 Pharmacology Monoclonal antibody Epitopes Mice Pharmacokinetics Neutralization Tests Internal medicine Immunopathology medicine Animals Humans Hematology biology Immunogenicity Antibodies Monoclonal Macaca fascicularis Tolerability Immunology biology.protein Female Antibody |
Zdroj: | Biotherapy. 5:291-299 |
ISSN: | 1573-8280 0921-299X |
DOI: | 10.1007/bf02179047 |
Popis: | In preparing for testing a pharmaceutical grade preparation of chimeric (mouse/human) antibody CGP 47,439 in HIV-1 infected individuals, it was administered to Macaca fascicularis (cynomolgus) monkeys to study tolerability, immunogenicity and pharmacokinetics. Four groups of monkeys, three males and three females per group, received respectively four infusions of 0, 1.43, 4.3, and 14.3 mg of CGP 47,439/kg body weight at one-week intervals. The chimeric antibody induced no fever, was tolerated well throughout the 50-day observation period, elicited no tissue damage and no anti-antibody response. The pharmacokinetic profile was similar at all dose levels with a mean T1/2 alpha of 14.2 h (range 11.8-19.3 h) and a mean T1/2 beta of 172.6 h (range 137.2-220.5h). Following four successive antibody infusions serum concentrations of CGP 47,439 increased without reaching a steady state, and its measured concentrations were comparable to the simulated values. Collectively the study has provided safety and pharmacokinetic data that would allow human studies with this antibody in AIDS patients. |
Databáze: | OpenAIRE |
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