模型 | 成本 | 与人体数据的相关性 |
---|---|---|
体外 | 低 | 低 |
普通小鼠 | 中等 | 低 |
人源化 FcRn 小鼠 | 中等 | 极高 |
非人灵长类动物 | 高 | 极高 |
特色 FcRn 小鼠模型
B6.Cg-Fcgrttm1Dcr Tg(FCGRT)32Dcr/DcrJ (014565)小鼠具有靶向突变导致的基因缺失,且存在一个在内源性启动子 (hTg32) 驱动下表达的人 FcRn 的转基因。这些小鼠对人源化 IgG 抗体具有最高、最类似人类的保护作用,是在需要最大半衰期数据时使用的最佳模型。
B6.Cg-Fcgrttm1Dcr Tg(CAG-FCGRT)276Dcr/DcrJ (004919)小鼠具有靶向突变导致的基因缺失和表达人 FcRn 的转基因。人 FcRn 转基因 (hTg276) 的半合子小鼠最适合检测体内抗体持久性的细微差异。
B6.Cg-Fcgrttm1Dcr Prkdcscid Tg(FCGRT)32Dcr/DcrJ (018441)小鼠表达 hTg32 转基因,同时免疫缺陷。这些小鼠对人源化 IgG 具有最高、最类似人类的保护作用,可用于评价具有潜在免疫原性或涉及异种移植物的基于 Fc 结构域的治疗药物。
B6.Cg-Alb<em12Mvw> Fcgrt<tm1Dcr> Tg(FCGRT)32Dcr/MvwJ (025201)白蛋白敲除 hTg32 小鼠是一种有效的类人模型,可用于表征白蛋白融合药物或基于白蛋白的疗法的药代动力学。
模型 | 内源性启动子 | 最长的半衰期 | 评价 PK 值的细微差异 | 免疫缺陷 | 白蛋白 PK |
---|---|---|---|---|---|
FcRn Tg32 (014565) |
是 | 是 | 否 | 否 | 否 |
FcRn Tg276 (004919) |
否 | 否 | 是 | 否 | 否 |
Tg32 Scid (018441) |
是 | 是 | 否 | 是 | 否 |
Tg276 Scid* (021146) |
否 | 否 | 是 | 是 | 否 |
Tg276 Rag1* (016919) |
否 | 否 | 是 | 是 | 否 |
Tg32 Alb KO (025201) |
是 | 是 | 否 | 否 | 是 |
*需冷冻复苏
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- 一项使用了 6 只 B6.Cg-Fcgrttm1Dcr Tg(FCGRT)32Dcr/DcrJ (014565) 小鼠的标准研究。
- 实验药物及空白对照均通过 IV(静脉注射)给药。
- 实验药物经 IV 给药后 1、2、6、10、14、18、22 和 26 天采集血样。
- 通过 ELISA 定量分析实验药物的浓度,并使用 PK Solutions 软件计算药代动力学数据。
- 一项使用了 6 只 B6.Cg-Fcgrttm1Dcr Tg(FCGRT)32Dcr/DcrJ (014565) 小鼠的标准研究。
- 通过 IV 给予小鼠人 IgG,24 小时后采集血样。
- 采血后 1 小时,通过 IV 给予实验药物和空白对照。
- 32、48、56、72、96、120 和 144 小时后采集血样。
- 通过 ELISA 定量分析人 IgG 或白蛋白的浓度,并使用 PK Solutions 软件计算药效学数据。