Institute of Medical Microbiology and Hospital Hygiene, Otto-von-Guericke University of Magdeburg, Magdeburg, Germany; Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany.
Trends Parasitol. 2019 Jul;35(7):516-528. doi: 10.1016/j.pt.2019.04.010. Epub 2019 May 27.
Cerebral malaria is a life-threatening complication of malaria caused by the parasite Plasmodium falciparum. The growing problem of drug resistance and the dearth of new antiparasitic drugs are a serious threat to the antimalaria treatment regimes. Studies on humans and the murine model have implicated the disruption of the blood-brain barrier (BBB) in the lethal course of the disease. Therefore, efforts to alleviate the BBB dysfunction could serve as an adjunct therapy. Here, we review the mechanisms associated with the disruption of the BBB. In addition, we discuss the current, still limited, knowledge on the contribution of different cell types, microparticles, and the kynurenine pathway in the regulation of BBB dysfunction, and how these molecules could be used as potential new therapeutic targets.
脑型疟疾是由疟原虫引起的危及生命的疟疾并发症。抗药性日益严重和新的抗寄生虫药物短缺,对疟疾治疗方案构成严重威胁。人类和鼠类模型的研究表明,血脑屏障(BBB)的破坏与疾病的致命过程有关。因此,减轻 BBB 功能障碍的努力可以作为辅助治疗。在这里,我们回顾了与 BBB 破坏相关的机制。此外,我们还讨论了目前仍然有限的关于不同细胞类型、微粒体和犬尿氨酸途径在调节 BBB 功能障碍中的作用的知识,以及这些分子如何可以用作潜在的新治疗靶点。