啮齿动物模型系统中恶性疟原虫和间日疟原虫环孢子子疫苗的Muramyl肽佐剂。

Biotechnology therapeutics Pub Date : 1992-01-01
I C Bathurst, H L Gibson, J Kansopon, B K Hahm, M R Hollingdale, P J Barr
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引用次数: 0

摘要

恶性疟原虫和间日疟原虫的环孢子子蛋白在酿酒酵母中高水平表达。重组蛋白在长度和天然氨基酸重复基序的数量上都有所不同。这些蛋白被纯化并用于小鼠、豚鼠和兔子的免疫。通过ELISA检测、固定孢子体的间接免疫荧光检测以及活孢子体对培养肝细胞的侵袭,研究人员使用了新型的muramyl肽佐剂,增强了免疫应答。这些结果表明,通过改变重组蛋白的设计和使用新的佐剂系统,可以改善重组环孢子子疫苗的体液应答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Muramyl peptide adjuvants for Plasmodium falciparum and Plasmodium vivax circumsporozoite vaccines in rodent model systems.

Circumsporozoite proteins from the malaria parasites Plasmodium falciparum and Plasmodium vivax were expressed at high levels in the yeast Saccharomyces cerevisiae. Recombinant proteins varied both in length and in number of the natural amino acid repeat motifs. The proteins were purified and used to immunize mice, guinea pigs, and rabbits. Novel muramyl peptide adjuvants were used that increased the immune response as measured by ELISA assays, indirect immunofluorescence of fixed sporozoites, and the invasion of cultured liver cells by live sporozoites. These results suggest that an improved humoral response to recombinant circumsporozoite vaccines might be achieved by varying the design of the recombinant protein and by the use of novel adjuvant systems.

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