Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Infect Immun. 2012 Sep;80(9):2997-3007. doi: 10.1128/IAI.06185-11. Epub 2012 Jun 11.
Lack of an adequate animal model of Plasmodium falciparum severe malarial anemia (SMA) has hampered the understanding of this highly lethal condition. We developed a model of SMA by infecting C57BL/6 mice with P. chabaudi followed after recovery by P. berghei infection. P. chabaudi/P. berghei-infected mice had an initial 9- to 10-day phase of relatively low parasitemia and severe anemia, followed by a second phase of hyperparasitemia, more profound anemia, reticulocytosis, and death 14 to 21 days after infection. P. chabaudi/P. berghei-infected animals had more intense splenic hematopoiesis, higher interleukin-10 (IL-10)/tumor necrosis factor alpha and IL-12/gamma interferon (IFN-γ) ratios, and higher antibody levels against P. berghei and P. chabaudi antigens than P. berghei-infected or P. chabaudi-recovered animals. Early treatment with chloroquine or artesunate did not prevent the anemia, suggesting that the bulk of red cell destruction was not due to the parasite. Red cells from P. chabaudi/P. berghei-infected animals had increased surface IgG and C3 by flow cytometry. However, C3(-/-) mice still developed anemia. Tracking of red cells labeled ex vivo and in vivo and analysis of frozen tissue sections by immunofluorescence microscopy showed that red cells from P. chabaudi/P. berghei-infected animals were removed at an accelerated rate in the liver by erythrophagocytosis. This model is practical and reproducible, and its similarities with P. falciparum SMA in humans makes it an appealing system with which to study the pathogenesis of this condition and explore potential immunomodulatory interventions.
疟原虫恶性疟疾贫血(SMA)缺乏足够的动物模型,阻碍了对这一高致命性疾病的理解。我们通过感染伯氏疟原虫(P. berghei)后再感染约氏疟原虫(P. chabaudi)来建立 SMA 模型。感染约氏疟原虫和伯氏疟原虫的小鼠最初经历 9-10 天的相对低寄生虫血症和严重贫血期,然后进入第二阶段的高寄生虫血症、更严重的贫血、网织红细胞增多和感染后 14-21 天死亡。感染约氏疟原虫和伯氏疟原虫的动物脾脏造血作用更强烈,白细胞介素-10(IL-10)/肿瘤坏死因子-α和 IL-12/γ干扰素(IFN-γ)比值更高,针对伯氏疟原虫和约氏疟原虫抗原的抗体水平也更高。早期用氯喹或青蒿琥酯治疗并不能预防贫血,表明大部分红细胞破坏不是由寄生虫引起的。感染约氏疟原虫和伯氏疟原虫的红细胞通过流式细胞术显示表面 IgG 和 C3 增加。然而,C3(-/-) 小鼠仍发生贫血。用体外和体内标记的红细胞进行追踪,并通过免疫荧光显微镜分析冷冻组织切片显示,感染约氏疟原虫和伯氏疟原虫的动物肝脏中红细胞通过红细胞吞噬作用以更快的速度被清除。该模型实用且可重复,其与人类恶性疟疾贫血的相似性使其成为研究该疾病发病机制和探索潜在免疫调节干预措施的有吸引力的系统。