Validity of Modelling Cerebral Malaria in Mice: Argument and Counter Argument

A. Taylor-Robinson
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引用次数: 14

Abstract

The clinical manifestations of Plasmodium falciparum infection of humans that are collectively recognised as cerebral malaria produce profound changes in mental status and induce coma. The histopathological hallmark of this encephalopathy is the sequestration of cerebral capillaries and venules with both infected and uninfected erythrocytes. The underlying cause of cerebral malaria is the subject of vigorous debate. A major reason for this is that human brain tissue is only available post mortem. In order to dissect the pathology of this acute disease, therefore, a number of models using murine malarias have been developed. While these have undoubtedly proved useful in helping to identify immunological mechanisms involved, recognition of the differences between the pathological processes during cerebral malaria in mice and man has led to some researchers questioning the validity of extrapolating findings from mouse models to the human condition with a view to informing therapeutic interventions. In turn, this has provoked lively debate within the malaria research community. This commentary sets out our current understanding of cerebral disease in humans and evaluates what meaningful contribution the study of mouse models has made to this knowledge.
小鼠脑疟疾模型的有效性:论证与反论证
人类感染恶性疟原虫的临床表现被统称为脑型疟疾,其精神状态发生深刻变化并诱发昏迷。这种脑病的组织病理学特征是感染和未感染红细胞的脑毛细血管和小静脉的隔离。脑型疟疾的根本原因是激烈辩论的主题。造成这种情况的一个主要原因是人类的脑组织只有在死后才能得到。因此,为了解剖这种急性疾病的病理,已经开发了许多使用小鼠疟疾的模型。虽然这些无疑证明有助于确定所涉及的免疫机制,但认识到小鼠和人类脑疟疾期间病理过程之间的差异,导致一些研究人员质疑将小鼠模型的发现外推到人类状况的有效性,从而为治疗干预提供信息。反过来,这在疟疾研究界引发了激烈的争论。这篇评论阐述了我们目前对人类大脑疾病的理解,并评估了小鼠模型研究对这一知识的有意义的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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