RC98:犬科猴体内的程序性细胞死亡配体 1 单克隆抗体

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ling Wang, Qiaoning Li, Chenglian Deng, Zhihao Liu, Fang Wang, Shenjun Li, Lihou Dong, Jing Jiang
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引用次数: 0

摘要

简介RC98是针对程序性细胞死亡配体1(PD-L1)的单克隆抗体。相关报道证实,肿瘤细胞表达的 PD-L1 对抗肿瘤 CD8+ T 细胞反应的影响特征明显,但免疫细胞表达的 PD-L1 的影响尚未明确。研究目的本研究旨在设计一项 RC98 在正常犬科猴体内的药代动力学/药理学(PK/PD)研究,以研究其对免疫系统的影响。研究方法给猴子静脉注射 RC98 和药物,剂量为 15 毫克/千克,每周一次,连续注射 4 周,以评估 PK 和 PD 之间的关系。药效学活性通过CD3+ T细胞中的PD-L1受体占据率(RO)、T细胞依赖性抗体反应(TDAR)和可溶性PD-L1的浓度来测量。结果药代动力学结果显示,最后一次给药的暴露量低于第一次给药,这可能是由于产生了免疫原性。全身暴露量与 CD3+ T 细胞中的 RO 存在很强的相关性,但最后一次给药后 RO 水平下降,这间接反映了 T 细胞的活化。RC98 组的锁孔帽状血蓝蛋白(KLH)诱导的 TDAR 高于车辆组。使用 RC98 后,可溶性 PD-L1 的浓度呈反馈性升高,且多次给药后可溶性 PD-L1 的浓度维持在比给药前更高的水平。结论这些数据表明,免疫系统明显被激活。此外,非临床数据可为其在临床试验中的疗效评估提供依据:这些数据表明,免疫系统明显被激活。非临床数据可为其在临床试验中的疗效评估提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical Pharmacokinetics and Pharmacology Study of RC98: A Programmed Cell Death Ligand 1 Monoclonal Antibody in Cynomolgus Monkeys
Introduction:: RC98 is the monoclonal antibody against Programmed Cell Death Ligand 1 (PD-L1). Relevant reports have confirmed that the influence of PD-L1 expressed by tumor cells on antitumor CD8+ T cell responses is well characterized, but the impact of PD-L1 expressed by immune cells has not been well defined. Objective:: This study aimed to design a Pharmacokinetics/Pharmacology (PK/PD) study of RC98 in normal cynomolgus monkeys to research the effect on the immune system. Methods:: RC98 and vehicle were administered to cynomolgus monkeys at 15 mg/kg via intravenous infusion once a week for 4 weeks to evaluate the relationship between PK and PD. The pharmacodynamic activity was measured by the PD-L1 receptor occupancy (RO) in CD3+ T cells, A T-cell-dependent antibody response (TDAR), and the concentration of soluble PD-L1. Results:: The pharmacokinetic result showed that the exposure from the last administration was lower than that of the first administration, probably due to immunogenicity production. There was a strong correlation between systemic exposure and RO in CD3+ T cells but decreased RO levels after the last dose, which indirectly reflected the activation of T cells. The keyhole limpet hemocyanin (KLH)-induced TDAR in the RC98 group was higher than in the vehicle group. The concentration of soluble PD-L1 had increased feedback with RC98, and the concentration of soluble PD-L1 was maintained at a higher level after multiple doses than before dosing. Conclusion:: These data indicate that the immune system was clearly activated. In addition, the non-clinical data could provide a basis for its efficacy evaluation in clinical trials. conclusion: These data indicate that the immune system was clearly activated. The non-clinical data could provide a basis for its efficacy evaluation in clinical trials.
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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