Bockman J M, Prusiner S B, Tateishi J, Kingsbury D T
Ann Neurol. 1987 Jun;21(6):589-95. doi: 10.1002/ana.410210611.
Creutzfeldt-Jakob disease (CJD) is a rare dementia that is generally found in older people and is caused by unusual infectious pathogens or prions. Using rabbit antisera raised against hamster scrapie prion proteins (HaPrPSc), we identified by immunoblotting human CJD prion proteins (HuPrPCJD) in the brains of 14 patients dying of CJD. Extracts from 6 of the patients were transmitted to mice after prolonged incubation. The rabbit antisera raised against HaPrPSc also reacted with the mouse CJD prion proteins (MoPrPCJD) found in the brains of these experimentally infected mice. When mice were immunized with HuPrPCJD, they produced antibodies that reacted with HuPrPCJD but not with MoPrPCJD. Mice immunized with MoPrPCJD produced antibodies to neither murine nor human prion proteins. Our results provide evidence for host species-specific epitopes on prion proteins. The existence of such epitopes is consistent with the apparent lack of an immune response during prion infections and the finding that prion protein molecules are encoded by host genes.
克雅氏病(CJD)是一种罕见的痴呆症,通常在老年人中发现,由异常的传染性病原体或朊病毒引起。使用针对仓鼠瘙痒病朊病毒蛋白(HaPrPSc)产生的兔抗血清,我们通过免疫印迹法在14例死于CJD的患者大脑中鉴定出人类CJD朊病毒蛋白(HuPrPCJD)。其中6例患者的提取物在长时间孵育后接种给小鼠。针对HaPrPSc产生的兔抗血清也与这些实验感染小鼠大脑中发现的小鼠CJD朊病毒蛋白(MoPrPCJD)发生反应。当用HuPrPCJD免疫小鼠时,它们产生的抗体与HuPrPCJD发生反应,但不与MoPrPCJD发生反应。用MoPrPCJD免疫的小鼠既不产生针对鼠源也不产生针对人源朊病毒蛋白的抗体。我们的结果为朊病毒蛋白上宿主物种特异性表位提供了证据。这些表位的存在与朊病毒感染期间明显缺乏免疫反应以及朊病毒蛋白分子由宿主基因编码的发现是一致的。