以恶性疟原虫环孢子子蛋白基因重组蛋白或DNA接种小鼠引起的体液免疫应答

Z. Fang, Y-W Liu, Y. Shi, X-B. Yu, W-Q Huang, X. Ji
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引用次数: 3

摘要

摘要本文比较了不同剂量、不同途径接种含恶性疟原虫FCC1/HN环孢子子蛋白(CSP)基因的质粒DNA与基于CSP基因的重组表达蛋白接种引起的小鼠体液应答。对于DNA疫苗,肌肉注射似乎最有效,其次是静脉注射,然后是皮下注射,每种情况下的反应都是剂量依赖性的。在标准ELISA和dot-ELISA中,用DNA免疫的小鼠血清中抗疟疾抗体的滴度明显低于用重组蛋白免疫的小鼠血清。尽管这两种“疫苗”都在BALB/c小鼠中引发了体液免疫反应,但基于质粒DNA的疫苗比重组蛋白诱导高滴度抗体反应所需的时间要长得多。
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The humoral immune responses elicited in mice by inoculations with a recombinant protein or DNA based on the circumsporozoite-protein gene of Plasmodium falciparum
Abstract The humoral responses elicited in mice by inoculation, in various doses and by several routes, with plasmid DNA containing the gene coding for the circumsporozoite protein (CSP) of Plasmodium falciparum FCC1/HN were compared with those evoked by inoculation with a recombinant expressed protein based on the CSP. With the DNA vaccine, intramuscular inoculations appeared the most effective, followed by intravenous and then subcutaneous injections, the responses in each case being dose-dependent. In both standard ELISA and dot-ELISA, sera from the mice immunized with the DNA were found to have much lower titres of antimalarial antibodies than the corresponding sera from mice immunized with the recombinant protein. Although both 'vaccines' elicited humoral immune responses in BALB/c mice, that based on plasmid DNA took much longer than the recombinant protein to induce high-titre antibody responses.
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