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首页> 外文期刊>Malaria Journal >Parasite densities modulate susceptibility of mice to cerebral malaria during co-infection with Schistosoma japonicum and Plasmodium berghei
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Parasite densities modulate susceptibility of mice to cerebral malaria during co-infection with Schistosoma japonicum and Plasmodium berghei

机译:寄生虫密度调节小鼠与日本血吸虫和柏氏疟原虫共感染期间对脑疟疾的敏感性

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Background Malaria and schistosomiasis are endemic and co-exist in the same geographic areas, even co-infecting the same host. Previous studies have reported that concomitant infection with Schistosoma japonicum could offer protection against experimental cerebral malaria (ECM) in mice. This study was performed to evaluate whether alterations in parasite density could alter this protective effect. Methods Mice were inoculated with 100 or 200?S. japonicum cercariae followed by infection with high or low density of Plasmodium berghei ANKA strain eight weeks after the first infection. Then, parasitaemia, survival rate and blood–brain-barrier (BBB) damage were assessed. Interferon-gamma (IFN-γ), interleukin (IL)-4, IL-5, IL-13, IL-10, and TGF-β levels were determined in splenocyte supernatants using enzyme-linked immunosorbent assay (ELISA). Cell surface/intracellular staining and flow cytometry were used to analyse the level of CD4+/CD8+ T cells, CD4+CD25+Foxp3+ Tregs, IL-10-secreting Tregs, and IL-10+Foxp3-CD4+ T cells in the spleen, and CD4+/CD8+ T cells infiltrating the brain. Results Co-infection with low density P. berghei and increased S. japonicum cercariae significantly increased the levels of IL-4, IL-5, IL-13, TGF-β and Tregs, but significantly decreased the levels of IFN-γ and the percentage of CD4+ T cells and CD8+ T cells in the spleen and CD8+ T cell infiltration in the brain. Increased worm loads also significantly decreased mortality and BBB impairment during ECM. When challenged with higher numbers of P. berghei and increased cercariae, the observed cytokine changes were not statistically significant. The corresponding ECM mortality and BBB impairment also remained unchanged. Conclusions This study demonstrates that protection for ECM depends on the numbers of the parasites, S. japonicum and P. berghei, during co-infection. Alterations in the regulatory response appear to play a key role in this adaptation.
机译:背景疟疾和血吸虫病是地方性流行病,在同一地理区域内并存,甚至共同感染同一宿主。先前的研究已经报道,日本血吸虫的伴随感染可以对小鼠实验性脑疟疾(ECM)提供保护。进行这项研究是为了评估寄生虫密度的改变是否可以改变这种保护作用。方法给小鼠接种100或200?S。首次感染后八周,日本尾继之以高密度或低密度的伯氏疟原虫ANKA株感染。然后,评估了寄生虫血症,存活率和血脑屏障(BBB)损害。使用酶联免疫吸附测定(ELISA)测定脾细胞上清液中的干扰素-γ(IFN-γ),白介素(IL)-4,IL-5,IL-13,IL-10和TGF-β水平。细胞表面/细胞内染色和流式细胞仪用于分析脾脏中CD4 + / CD8 + T细胞,CD4 + CD25 + Foxp3 + Treg,IL-10-分泌Treg和IL-10 + Foxp3-CD4 + T细胞的水平,以及CD4 + / CD8 + T细胞渗入大脑。结果低密度伯氏疟原虫和日本尾and的共同感染显着增加了IL-4,IL-5,IL-13,TGF-β和Tregs的水平,但显着降低了IFN-γ和Tregs的水平。脾脏中CD4 + T细胞和CD8 + T细胞的百分比,以及脑中CD8 + T细胞的浸润。蠕虫负荷增加还显着降低了ECM期间的死亡率和BBB损害。当受到更高数量的伯氏疟原虫和尾增加的挑战时,观察到的细胞因子变化在统计学上并不显着。相应的ECM死亡率和BBB损害也保持不变。结论该研究表明,在共感染期间对ECM的保护取决于寄生虫S. japonicum和P. berghei的数量。监管反应的改变似乎在这种适应中起关键作用。

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