Is human malarial coma caused, or merely deepened, by sequestration?

被引:32
作者
Clark, Ian A. [1 ]
Alleva, Lisa M. [1 ]
机构
[1] Australian Natl Univ, Sch Biochem & Mol Biol, Canberra, ACT 0200, Australia
关键词
TUMOR-NECROSIS-FACTOR; NITRIC-OXIDE SYNTHASE; PLASMODIUM-VIVAX; TNF-ALPHA; CEREBROSPINAL-FLUID; CEREBRAL MALARIA; FALCIPARUM-MALARIA; SERUM-LEVELS; CHILDREN; DYSERYTHROPOIESIS;
D O I
10.1016/j.pt.2009.04.003
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程]; 100103 [病原生物学];
摘要
Much research into falciparum malaria coma assumes the primary event to be vascular obstruction by parasitized red blood cells. Recent evidence that vivax malaria, caused by a parasite traditionally thought not to block blood flow, seems to alter brain function to the same degree as falciparum malaria has seriously questioned this. These data are a timely call to reassess whether vascular obstruction should still be considered the primary cause of the coma of falciparum disease. They add to a growing literature that suggests that enhancement of brain-origin cytokines, such as tumour necrosis factor, by non-brain systemic inflammation and an appreciation of the degree to which neuronal homeostasis depends on them provide a more fruitful research direction.
引用
收藏
页码:314 / 318
页数:5
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