Vascular Immunology Unit, Department of Pathology, Faculty of Medicine and Health, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Human Health, Nuclear Science, Technology, and Landmark Infrastructure, Australian Nuclear Science and Technology Organisation, Sydney, NSW, Australia.
Front Immunol. 2019 Apr 17;10:830. doi: 10.3389/fimmu.2019.00830. eCollection 2019.
Complications from malaria parasite infections still cost the lives of close to half a million people every year. The most severe is cerebral malaria (CM). Employing murine models of CM, autopsy results, experiments, neuroimaging and microscopic techniques, decades of research activity have investigated the development of CM immunopathology in the hope of identifying steps that could be therapeutically targeted. Yet important questions remain. This review summarizes recent findings, primarily mechanistic insights on the essential cellular and molecular players involved gained within the murine experimental cerebral malaria model. It also highlights recent developments in (a) cell-cell communication events mediated through extracellular vesicles (EVs), (b) mounting evidence for innate immune memory, leading to "trained" increased or tolerised responses, and (c) modulation of immune cell function through metabolism, that could shed light on why some patients develop this life-threatening condition whilst many do not.
疟疾寄生虫感染的并发症每年仍导致近 50 万人死亡。最严重的是脑型疟疾(CM)。利用 CM 的鼠模型、尸检结果、实验、神经影像学和显微镜技术,数十年的研究活动已经研究了 CM 免疫病理学的发展,以期确定可以进行治疗靶向的步骤。然而,仍有一些重要的问题有待解决。本综述总结了最近的发现,主要是在鼠实验性脑疟疾模型中获得的与所涉及的基本细胞和分子参与者相关的机制见解。它还强调了(a)通过细胞外囊泡(EVs)介导的细胞间通讯事件,(b)先天免疫记忆的证据不断增加,导致“训练”增强或耐受反应,以及(c)通过代谢调节免疫细胞功能,这可能有助于解释为什么有些患者会出现这种危及生命的情况,而许多患者则不会。