Yang C, Xiao L, Tongren J E, Sullivan J, Lal A A, Collins W E
Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30341-3724, USA.
Am J Trop Med Hyg. 1999 Aug;61(2):226-9. doi: 10.4269/ajtmh.1999.61.226.
Plasmodium coatneyi infection in rhesus monkeys has been used as a model for studying human malaria. Cytokine production in this model, however, has so far not been examined. In this study, four rhesus monkeys were infected with P. coatneyi, with another four animals serving as uninfected controls. Blood samples were taken for the determination of daily parasitemia, and cytokine and prostaglandin E2 (PGE2) levels at days 0, 3, 5, 7, and 10. All inoculated animals became infected, with synchronized appearance of ring-stage parasites. Infected monkeys had increased plasma levels of proinflammatory cytokines (interleukin-1beta, interferon-gamma, and tumor necrosis factor-alpha) during the late stage of the infection. They also had increased production of ciliary neurotrophic factor. In conjunction with the production of proinflammatory cytokines, infected monkeys also had gradual increases in the production of PGE2. A continued definition of the P. coatneyi/rhesus monkey animal model should be useful for the elucidation of the immunopathogenesis of human malaria.
恒河猴感染柯氏疟原虫已被用作研究人类疟疾的模型。然而,该模型中的细胞因子产生情况迄今尚未得到研究。在本研究中,四只恒河猴感染了柯氏疟原虫,另外四只动物作为未感染对照。在第0、3、5、7和10天采集血样,用于测定每日的疟原虫血症以及细胞因子和前列腺素E2(PGE2)水平。所有接种的动物均被感染,环状体寄生虫同步出现。感染的猴子在感染后期血浆中促炎细胞因子(白细胞介素-1β、干扰素-γ和肿瘤坏死因子-α)水平升高。它们的睫状神经营养因子产生也增加。与促炎细胞因子的产生同时,感染的猴子PGE2的产生也逐渐增加。对柯氏疟原虫/恒河猴动物模型的持续定义对于阐明人类疟疾的免疫发病机制应该是有用的。