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伯氏疟原虫感染后期网织红细胞的优先侵袭导致循环中网织红细胞水平降低。

Preferential invasion of reticulocytes during late-stage Plasmodium berghei infection accounts for reduced circulating reticulocyte levels.

作者信息

Cromer Deborah, Evans Krystal J, Schofield Louis, Davenport Miles P

机构信息

Department of Haematology, Prince of Wales Hospital, University of New South Wales, Kensington, NSW 2052, Australia.

出版信息

Int J Parasitol. 2006 Nov;36(13):1389-97. doi: 10.1016/j.ijpara.2006.07.009. Epub 2006 Sep 1.

Abstract

Insufficient circulating reticulocytes have been observed during severe malarial anaemia in both human and murine infection, and are often attributed to reduced production of red cell precursors. However, a number of Plasmodium species display a preference for invading reticulocytes rather than erythrocytes. Thus, the reduction in circulating reticulocyte numbers may arise as a result both of increased parasitization and lysis of reticulocytes, as well as decreased production. We have analysed both circulating reticulocyte numbers and the percentage of infected reticulocytes during murine Plasmodium berghei infection. We found a large reduction in circulating numbers when compared with an equivalent chemically induced anaemia. However, mathematical analysis of parasite and red cell numbers revealed the preference of P. berghei for reticulocytes to be approximately 150-fold over that for erythrocytes, leading to increased destruction of reticulocytes. Although erythropoietic suppression is evident during the first week of P. berghei infection, this preferential infection and destruction of reticulocytes is sufficient to mediate ongoing reduced levels of circulating reticulocytes during the latter stages of infection, following compensatory erythropoiesis in response to haemolytic anaemia.

摘要

在人类和鼠类感染严重疟疾性贫血期间,均观察到循环网织红细胞不足,这通常归因于红细胞前体生成减少。然而,许多疟原虫物种表现出优先侵入网织红细胞而非红细胞的倾向。因此,循环网织红细胞数量的减少可能是由于网织红细胞的寄生和裂解增加以及生成减少所致。我们分析了鼠类感染伯氏疟原虫期间循环网织红细胞数量和感染网织红细胞的百分比。与同等化学诱导的贫血相比,我们发现循环数量大幅减少。然而,对寄生虫和红细胞数量的数学分析表明,伯氏疟原虫对网织红细胞的偏好比对红细胞的偏好约高150倍,导致网织红细胞破坏增加。尽管在伯氏疟原虫感染的第一周红细胞生成抑制明显,但这种对网织红细胞优先感染和破坏足以在感染后期介导循环网织红细胞水平持续降低,这是在溶血性贫血后进行代偿性红细胞生成之后出现的情况。

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