Vugmeyster Yulia, Beyer Joseph, Howell Kathy, Combs Dan, Fielder Paul, Yang Jihong, Qureshi Ferhan, Sandlund Bryan, Kawaguchi Ly, Dummer Wolfgang, Lowman Henry, McKeever Kathleen
Genentech, Inc., South San Francisco, California 94080, USA.
J Immunother. 2005 May-Jun;28(3):212-9. doi: 10.1097/01.cji.0000155050.03916.04.
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.
PRO70769是一种针对正常和恶性B细胞上存在的CD20分子的人源化IgG1单克隆抗体。PRO70769正在接受评估,用于治疗B细胞介导的疾病,目前正处于类风湿性关节炎的1期试验阶段。作为临床前毒理学评估的一部分,在食蟹猴中评估了PRO70769的B细胞清除情况和安全性。在第1天和第15天给动物静脉注射10、50或100mg/kg的PRO70769,并在第二次给药后2周和3个月的恢复期后处死动物。在一项平行研究中,动物不进行尸检,而是按照相同方案接受第二个周期的PRO70769治疗。PRO70769将血液中的B细胞抑制到检测不到的水平,并显著减少淋巴组织中的B细胞。与淋巴结B细胞相比,脾脏B细胞的耗竭程度更大。与一个治疗周期后的耗竭情况相比,第二个治疗周期导致淋巴组织中的耗竭程度更大;然而,即使在最高剂量下,淋巴组织中的残留B细胞仍然可以检测到。外周血中B细胞的恢复率在一个和两个治疗周期之间似乎相似。耗竭后,淋巴结B细胞亚群的分布发生了变化。恢复后,B细胞亚群恢复到正常水平。表达CD20的细胞耗竭和淋巴滤泡萎缩是仅有的与治疗相关的效应。