Koraka Penelopie, Benton Sabrina, van Amerongen Geert, Stittelaar Koert J, Osterhaus Albert D M E
Department of Virology, Erasmus MC, Dr. Molewaterplein 50, 3015 GE Rotterdam, The Netherlands.
Microbes Infect. 2007 Jul;9(8):940-6. doi: 10.1016/j.micinf.2007.03.012. Epub 2007 Apr 5.
Since studying the pathogenesis of dengue virus associated disease in humans has several limitations, an appropriate animal model is needed. Therefore, we investigated kinetics of viremia as well as humoral and cellular immune responses, after primary, secondary and tertiary heterologous dengue virus infections in cynomolgus macaques: these parameters were largely similar to those observed in natural human infection upon primary infection. Both antibody and T-cell responses measured were largely cross-reactive. Upon secondary infection with a heterologous virus serotype, T-cell responses specific for the primary infecting serotype were more pronounced, especially when the immune system was primed with dengue 1 virus. Measurement of transcription levels of pro- and anti-inflammatory cytokines in white blood cells upon primary and secondary infection generally showed a balanced response. In addition, a region of the NS2A protein of dengue viruses was identified that induces T-cell responses in macaques.
由于研究登革热病毒相关疾病在人类中的发病机制存在若干局限性,因此需要合适的动物模型。为此,我们研究了食蟹猴在初次、二次和三次异源登革热病毒感染后的病毒血症动力学以及体液和细胞免疫反应:这些参数与初次感染时人类自然感染中观察到的参数基本相似。所检测的抗体和T细胞反应大多具有交叉反应性。在用异源病毒血清型进行二次感染时,针对初次感染血清型的T细胞反应更为明显,尤其是当免疫系统用登革热1型病毒启动时。初次和二次感染时白细胞中促炎和抗炎细胞因子转录水平的测量总体上显示出平衡的反应。此外,还鉴定出登革热病毒NS2A蛋白的一个区域,该区域可在食蟹猴中诱导T细胞反应。