Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Trends Parasitol. 2010 Jan;26(1):11-5. doi: 10.1016/j.pt.2009.10.007. Epub 2009 Nov 22.
P.berghei ANKA infection in CBA or CB57BL/6 mice is used widely as a murine 'model' of human cerebral malaria (HCM), despite markedly different histopathological features. The pathology of the murine model is characterised by marked inflammation with little or no intracerebral sequestration of parasitised erythrocytes, whereas HCM is associated with intense intracerebral sequestration, often with little inflammatory response. There are now more than ten times as many studies each year of the murine model than on HCM. Of 48 adjunctive interventions evaluated in the murine model, 44 (92%) were successful, compared with only 1 (6%) of 17 evaluated in HCM during the same period. The value of the mouse model in identifying pathological processes or therapeutic interventions in human cerebral malaria is questionable.
尽管在组织病理学特征上存在明显差异,但是 CBA 或 CB57BL/6 小鼠中的 P.berghei ANKA 感染仍被广泛用作人类脑型疟疾(HCM)的“模型”。该小鼠模型的病理学特征是明显的炎症,很少或没有寄生红细胞的颅内扣押,而 HCM 与强烈的颅内扣押有关,通常炎症反应很少。目前,每年对该小鼠模型的研究数量是 HCM 的十倍以上。在该小鼠模型中评估的 48 种辅助干预措施中,有 44 种(92%)成功,而在同期评估的 17 种 HCM 中只有 1 种(6%)成功。该小鼠模型在确定人类脑型疟疾中的病理过程或治疗干预措施方面的价值是值得怀疑的。