Depletion of B Cells by a Humanized Anti-CD20 Antibody PRO70769 in Macaca Fascicularis

Yulia Vugmeyster(Foundation for Human Potential), Joseph C. Beyer(Foundation for Human Potential), Kathy Howell(Foundation for Human Potential), Dan Combs(Foundation for Human Potential), Paul J. Fielder(Foundation for Human Potential), Jihong Yang(Foundation for Human Potential), Ferhan Qureshi(Foundation for Human Potential), Bryan Sandlund(Foundation for Human Potential), Ly Kawaguchi(Foundation for Human Potential), Wolfgang Dummer(Foundation for Human Potential), Henry B. Lowman(Foundation for Human Potential), Kathleen McKeever(Foundation for Human Potential)
Journal of Immunotherapy
April 18, 2005
Cited by 79

Abstract

PRO70769 is a humanized IgG1 monoclonal antibody against the CD20 molecule that is present on normal and malignant B cells. PRO70769 is being evaluated for treatment of B-cell-mediated diseases and is in a phase 1 trial for rheumatoid arthritis. As part of the preclinical toxicology evaluation, B-cell depletion profiles and safety of PRO70769 were assessed in cynomolgus monkeys. Animals were administered drug (IV) on days 1 and 15 with 10, 50, or 100 mg/kg PRO70769 and killed 2 weeks after the second dose and after a 3-month recovery period. In a parallel study, animals were not necropsied but instead were retreated with a second cycle of PRO70769 administered under an identical regimen. PRO70769 suppressed B cells in the blood to undetectable levels and significantly reduced B cells in lymphoid tissues. Splenic B cells were depleted to a greater extent compared with lymph node B cells. A second cycle of treatment resulted in a greater extent of depletion in lymphoid tissues compared with the depletion observed after one cycle of treatment; however, residual B cells in lymphoid tissues were still detectable, even at the highest dose. The rate of B-cell recovery in peripheral blood appeared similar between one and two cycles of treatment. Upon depletion there was a change in the profile of lymph node B-cell subsets. After recovery, B-cell subsets were reconstituted to normal levels. Depletion of CD20-expressing cells and lymphoid follicular atrophy were the only treatment-related effects.


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