Grau Georges E, Mackenzie Charles D, Carr Richard A, Redard Mireille, Pizzolato Giampaolo, Allasia Claude, Cataldo Claude, Taylor Terrie E, Molyneux Malcolm E
Experimental Parasitology Unit, IFR48, Université de la Méditerranée, Marseille, France.
J Infect Dis. 2003 Feb 1;187(3):461-6. doi: 10.1086/367960. Epub 2003 Jan 24.
The pathogenesis of fatal cerebral malaria (CM) is not well understood, in part because data from patients in whom a clinical diagnosis was established prior to death are rare. In a murine CM model, platelets accumulate in brain microvasculature, and antiplatelet therapy can improve outcome. We determined whether platelets are also found in cerebral vessels in human CM, and we performed immunohistopathology for platelet-specific glycoprotein, GPIIb-IIIa, on tissue from multiple brain sites in Malawian children whose fatal illness was severe malarial anemia, CM, or nonmalarial encephalopathy. Platelets were observed in 3 locations within microvessels: between malaria pigment and leukocytes, associated with malaria pigment, or alone. The mean surface area of platelet staining and the proportion of vessels showing platelet accumulation were significantly higher in patients with CM than in those without it. Platelet accumulation occurs in the microvasculature of patients with CM and may play a role in the pathogenesis of the disease.
致命性脑型疟疾(CM)的发病机制尚未完全明确,部分原因是在死亡前已确立临床诊断的患者数据很少。在小鼠CM模型中,血小板会在脑微血管中积聚,抗血小板治疗可改善预后。我们确定了在人类CM患者的脑血管中是否也能发现血小板,并对马拉维儿童多个脑区的组织进行了血小板特异性糖蛋白GPIIb-IIIa的免疫组织病理学检查,这些儿童的致命疾病为严重疟疾贫血、CM或非疟疾性脑病。在微血管的3个位置观察到了血小板:在疟色素与白细胞之间、与疟色素相关或单独存在。CM患者血小板染色的平均表面积以及显示血小板积聚的血管比例显著高于非CM患者。血小板积聚发生在CM患者的微血管中,可能在该疾病的发病机制中起作用。