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亚急性海绵状脑病的发病机制。

Pathogenesis of subacute spongiform encephalopathies.

作者信息

Asher D M, Gibbs C J, Gajdusek D C

出版信息

Ann Clin Lab Sci. 1976 Jan-Feb;6(1):84-103.

PMID:129025
Abstract

The subacute spongiform encephalopathies include scrapie of sheep, transmissible mink encephalopathy, and kuru and Creutzfeldt-Jakob disease of man. These diseases are caused by filterable infectious agents with unique physical properties. The usual sources of infection in nature are not completely known. Epidemiological evidence suggests that the agents may enter the body through breaks in the skin and mucous membranes. Experimental studies of scrapie after subcutaneous inoculation demonstrated early replication of the agent in lymphoid tissues and later appearance in other organs; as the amount of agent in the central nervous system (CNS) increased, it decreased in or disappeared from lymphoid tissues. In preliminary studies of kuru and Creutzfeldt-Jakob disease, the infectious agents were regularly recovered from the brains of clinically-ill patients and experimental animals but only occasionally from organs outside the CNS. It remains to be seen if early events in the pathogenesis of the two human diseases, before the appearance of clinical signs, are similar to those in scrapie.

摘要

亚急性海绵状脑病包括绵羊瘙痒病、传染性水貂脑病以及人类的库鲁病和克雅氏病。这些疾病由具有独特物理特性的可滤过性传染因子引起。自然界中常见的感染源尚不完全清楚。流行病学证据表明,这些因子可能通过皮肤和黏膜破损处进入人体。对皮下接种瘙痒病后的实验研究表明,该因子早期在淋巴组织中复制,随后出现在其他器官;随着中枢神经系统(CNS)中因子数量的增加,其在淋巴组织中的数量减少或消失。在对库鲁病和克雅氏病的初步研究中,传染性因子经常从临床患病患者和实验动物的大脑中检出,但仅偶尔从CNS以外的器官中检出。这两种人类疾病在出现临床症状之前的发病早期事件是否与瘙痒病相似,仍有待观察。

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