首页> 外文期刊>Journal of Translational Medicine >Correlation of pharmacodynamic activity, pharmacokinetics, and anti-product antibody responses to anti-IL-21R antibody therapeutics following IV administration to cynomolgus monkeys
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Correlation of pharmacodynamic activity, pharmacokinetics, and anti-product antibody responses to anti-IL-21R antibody therapeutics following IV administration to cynomolgus monkeys

机译:药物动力学活性,药代动力学和抗体抗体对抗IL-21R抗体治疗剂的相关性对硫代莫酮猴进行抗IL-21R抗体治疗剂

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Background Anti-IL-21R antibodies are potential therapeutics for the treatment of autoimmune diseases. This study evaluated correlations between the pharmacodynamic (PD) activity, pharmacokinetics, and anti-product antibody responses of human anti-IL-21R antibodies Ab-01 and Ab-02 following IV administration to cynomolgus monkeys. Methods The PD assay was based on the ability of recombinant human IL-21 (rhuIL-21) to induce expression of the IL-2RA gene in cynomolgus monkey whole blood samples ex vivo. Monkeys screened for responsiveness to rhuIL-21 stimulation using the PD assay, were given a single 10 mg/kg IV dosage of Ab-01, Ab-02, or a control antibody (3/group), and blood samples were evaluated for PD activity (inhibition of IL-2RA expression) for up to 148 days. Anti-IL-21R antibody concentrations and anti-product antibody responses were measured in serum using immunoassays and flow cytometry. Results Following IV administration of Ab-01 and Ab-02 to cynomolgus monkeys, PD activity was observed as early as 5 minutes (first time point sampled). This PD activity had good correlation with the serum concentrations and anti-product antibody responses throughout the study. The mean terminal half-life (t1/2) was ~10.6 and 2.3 days for Ab-01 and Ab-02, respectively. PD activity was lost at ~5-13 weeks for Ab-01 and at ~2 weeks for Ab-02, when serum concentrations were relatively low. The estimated minimum concentrations needed to maintain PD activity were ~4-6 nM for Ab-01 and ~2.5 nM for Ab-02, and were consistent with the respective KD values for binding to human IL-21R. For Ab-01, there was noticeable inter-animal variability in t1/2 values (~6-14 days) and the resulting PD profiles, which correlated with the onset of anti-product antibody formation. While all three Ab-01-dosed animals were positive for anti-Ab-01 antibodies, only one monkey (with the shortest t1/2 and the earliest loss of PD activity) had evidence of neutralizing anti-Ab-01 antibodies. All three Ab-02-dosed monkeys developed neutralizing anti-Ab-02 antibodies. Conclusions For anti-IL-21R antibodies Ab-01 and Ab-02, there was good correlation between PD activity and PK profiles following IV administration to cynomolgus monkeys. Compared with Ab-01, Ab-02 was eliminated markedly faster from the circulation, which correlated with a shorter duration of PD activity.
机译:背景技术抗IL-21R抗体是治疗自身免疫疾病的潜在治疗方法。该研究评估了IV局给予CynOmolgus猴子后,将人抗IL-21R抗体AB-01和AB-02之后的药效学(Pd)活性,药代动力学和抗产物抗体反应之间的相关性。方法PD测定基于重组人IL-21(rhuil-21)的能力诱导诱导Cynomolgus猴子全血样品中的IL-2RA基因的表达。用Pd测定筛选使用PD测定对rhuil-21刺激刺激的猴子,给出了AB-01,AB-02或对照抗体(3 /组)的单个10mg / kg IV剂量,并评估血液样品PD活动(抑制IL-2RA表达),最长可达148天。使用免疫测定和流式细胞术,在血清中测量抗IL-21R抗体浓度和抗产物抗体应答。结果施用AB-01和AB-02至Cynomolgus猴,早于5分钟观察PD活性(第一次采样)。该PD活性与在整个研究中与血清浓度和抗产品抗体反应良好的相关性。 AB-01和AB-02分别为AB-01和AB-02的平均末端半衰期(T 1/2 )是〜10.6和2.3天。当血清浓度相对较低时,AB-01和AB-02的〜2周损失PD活性在〜5-13周。保持Pd活性所需的估计最小浓度为AB-02的AB-01和〜2.5nm的4-6nm,并且与相应的K d 值一致,用于与人IL结合 - 21r。对于AB-01,在T 1/2 值(〜6-14天)和所得的PD型材中,有明显的动物间变异性,与抗产物抗体形成的开始相关。虽然所有三种AB-01剂量的动物对抗AB-01抗体呈阳性,但只有一只猴子(具有最短的T 1/2 并且最早的PD活性损失)具有中和抗的证据-Ab-01抗体。所有三种AB-02剂猴子都开发了中和抗AB-02抗体。抗IL-21R抗体AB-01和AB-02的结论​​,在IV给予Cynomolgus猴后,Pd活性和PK型材之间存在良好的相关性。与AB-01相比,从循环中显着消除AB-02,其与较短的PD活性持续时间相关。

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