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感染伯氏疟原虫(NK65)并用药物治疗的小鼠体内抗疟间接荧光抗体的产生与消退

Development and decline of antiplasmodial indirect fluorescent antibodies in mice infected with Plasmodium berghei (NK65) and treated with drugs.

作者信息

Waki S, Suzuki M

出版信息

Bull World Health Organ. 1974;50(6):521-6.

Abstract

Malaria parasites in mice present a simplified rodent model for the immunological study of malaria. Experiments have been performed to determine the pattern and persistence of malaria antibody as detected by the indirect fluorescent antibody (IFA) test utilizing specific antimouse IgM and IgG conjugates. The antibody levels in mice inoculated with Plasmodium berghei and treated with antimalarial drugs were traced after complete elimination of the parasites from the host. Within 1-2 weeks after inoculation, both specific IgM and IgG reached peak levels, which thereafter declined rapidly. The results suggest that a high IFA titre may be taken as an indication of recent parasitaemia when the parasites are absent from the host. The protective role of the specific immunoglobulin was not found in the cured animals at the time when the animals showed a high IFA titer. It seems that the detected IFA may not reflect protective immunity against reinfection with malaria parasites.

摘要

小鼠体内的疟原虫为疟疾免疫学研究提供了一个简化的啮齿动物模型。已开展实验以确定通过间接荧光抗体(IFA)试验利用特异性抗小鼠IgM和IgG缀合物检测到的疟疾抗体的模式和持续性。在用抗疟药物治疗感染伯氏疟原虫的小鼠后,在寄生虫从宿主体内完全清除后追踪抗体水平。接种后1-2周内,特异性IgM和IgG均达到峰值水平,此后迅速下降。结果表明,当宿主体内没有寄生虫时,高IFA滴度可被视为近期寄生虫血症的指标。在动物显示高IFA滴度时,在治愈的动物中未发现特异性免疫球蛋白的保护作用。似乎检测到的IFA可能无法反映针对疟原虫再感染的保护性免疫。

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Fluorescent antibody staining of human malaria parasites.人类疟原虫的荧光抗体染色。
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Acquired immunity to Plasmodium vinckei in mice.小鼠对文氏疟原虫的获得性免疫
Parasitology. 1966 Nov;56(4):719-32. doi: 10.1017/s0031182000071742.

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