Arinola O G, Louis J S, Tacchini-Cottier F, Aseffa A, Salimonu L S
Department of Chemical Pathology and Immunology, College of Medicine, University of Ibadan, Oyo State, Nigeria.
Afr J Med Med Sci. 2005 Mar;34(1):65-70.
To determine if gestational factors affect the severity of L. major infection, this study assessed the levels of IL-4 mRNA and IFN-gamma mRNA in popliteal lymph node cells of pregnant C57BL/6 mice mated at 5 hours, 16 hours and 15 days post L. major infection using PCR. Infected pregnant C57BL/6 mice developed larger cutaneous footpad lesions compared with non-pregnant infected C57BL/6 mice. The resolution of footpad lesions commenced after 8th week in C57BL/6 mice mated at 16 hrs post L. major infection but 12 weeks in C57BL/6 mice mated at 5 hrs and 15 days post L. major infection. C57BL/6 mice that were infected 20 days post partum resolved L. major infection effectively. But, the lesions in infected pregnant C57BL/6 mice and infected non-pregnant C57BL/6 mice were not as large as in susceptible BALB/c mice. The mean litter weights were similar in pregnant infected C57BL/6 mice mated at different stages of L. major infection but were slightly lower than weights of litters from pregnant uninfected C57BL/6 mice. In 5 days infected pregnant C57BL/6 mice, the levels of IFN-gamma were raised compared with the levels of IL-4 but those mated at 15 days post L. major infection had highest level of IFN-gamma mRNA. In 10 days pregnant infected C57BL/6 mice, levels of IL-4 were raised compared with IFN-gamma but mice mated at 16 hrs post L. major infection had highest level of IL-4. In 15 days pregnant infected mice, the levels of IL-4 were higher than IFN-gamma irrespective of the stage of L. major infection when the mice were mated. Mice infected with L. major 20 days post-partum produced more IFN-gamma than IL-4 from 16 hrs post L. major infection onwards. It may be concluded that increased IL-4 in pregnant infected C57BL/6 mice impairs the resistance of C57BL/6 mice to L. major infection especially in mice that were pregnant before effective immunity (5 hours post L. major infection) is mounted against L. major infection.
为了确定妊娠因素是否会影响硕大利什曼原虫感染的严重程度,本研究使用聚合酶链反应(PCR)评估了在硕大利什曼原虫感染后5小时、16小时和15天交配的怀孕C57BL/6小鼠腘窝淋巴结细胞中白细胞介素-4(IL-4)信使核糖核酸(mRNA)和干扰素-γ(IFN-γ)mRNA的水平。与未怀孕的感染C57BL/6小鼠相比,感染的怀孕C57BL/6小鼠出现了更大的皮肤足垫病变。在硕大利什曼原虫感染后16小时交配的C57BL/6小鼠中,足垫病变在第8周开始消退,但在硕大利什曼原虫感染后5小时和15天交配的C57BL/6小鼠中,足垫病变在第12周开始消退。产后20天感染的C57BL/6小鼠有效清除了硕大利什曼原虫感染。但是,感染的怀孕C57BL/6小鼠和感染的未怀孕C57BL/6小鼠中的病变不如易感的BALB/c小鼠中的病变大。在硕大利什曼原虫感染不同阶段交配的怀孕感染C57BL/6小鼠的平均窝仔重量相似,但略低于未感染的怀孕C57BL/6小鼠的窝仔重量。在感染5天的怀孕C57BL/6小鼠中,IFN-γ水平相对于IL-4水平升高,但在硕大利什曼原虫感染后15天交配的小鼠中,IFN-γ mRNA水平最高。在怀孕感染10天的C57BL/6小鼠中,IL-4水平相对于IFN-γ水平升高,但在硕大利什曼原虫感染后16小时交配的小鼠中,IL-4水平最高。在怀孕感染15天的小鼠中,无论小鼠交配时硕大利什曼原虫感染处于何种阶段,IL-4水平均高于IFN-γ水平。产后20天感染硕大利什曼原虫的小鼠从硕大利什曼原虫感染后16小时起产生的IFN-γ比IL-4更多。可以得出结论,怀孕感染的C57BL/6小鼠中IL-4的增加会损害C57BL/6小鼠对硕大利什曼原虫感染的抵抗力,尤其是在针对硕大利什曼原虫感染建立有效免疫(硕大利什曼原虫感染后5小时)之前就已怀孕的小鼠中。