首页> 外文期刊>Nuclear Medicine and Biology >Fusion of hIgG1-Fc to In-111-anti-amyloid single domain antibody fragment VHH-pa2H prolongs blood residential time in APP/PS1 mice but does not increase brain uptake
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Fusion of hIgG1-Fc to In-111-anti-amyloid single domain antibody fragment VHH-pa2H prolongs blood residential time in APP/PS1 mice but does not increase brain uptake

机译:hIgG1-Fc与In-111-抗淀粉样蛋白单结构域抗体片段VHH-pa2H的融合可延长APP / PS1小鼠的血液停留时间,但不会增加脑摄取

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Introduction: Llama single domain antibody fragments (VHH), which can pass endothelial barriers, are being investigated for targeting amyloid plaque load in Alzheimer's disease (AD). Contrary to conventional human or murine antibodies consisting of IgG or F(ab')2 antibody fragments, VHH are able to effectively pass the blood brain barrier (BBB) in vitro. However, in earlier in vivo studies, anti-amyloid VHH showed poor BBB passage due to their short serum half-lives. It would be of interest to develop a VHH based protein with elongated serum half-life to enhance BBB passage, allowing the VHH to more easily reach the cerebral amyloid deposits.
机译:简介:正在研究可通过内皮屏障的骆马单结构域抗体片段(VHH),以靶向阿尔茨海默病(AD)中的淀粉样斑块负载。与由IgG或F(ab')2抗体片段组成的常规人或鼠抗体相反,VHH能够在体外有效通过血脑屏障(BBB)。但是,在较早的体内研究中,抗淀粉样蛋白VHH由于其血清半衰期短而显示出较差的BBB传递。开发具有延长的血清半衰期以增强BBB通过,使VHH更容易到达脑淀粉样蛋白沉积物的基于VHH的蛋白质将是令人感兴趣的。

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