Herrera S, Herrera M A, Certa U, Corredor A, Guerrero R
Depto. de Microbiologia, Universidad del Valle, Cali, Colombia.
Mem Inst Oswaldo Cruz. 1992;87 Suppl 3:423-8. doi: 10.1590/s0074-02761992000700071.
The protective efficacy of several recombinant and a synthetic Plasmodium falciparum protein was assessed in Aotus monkeys. The rp41 aldolase, the 190L fragment of the MSA-1 protein and fusion 190L-CS. T3 protein containing the CS.T3 helper "universal" epitope were emulsified in Freund's adjuvants and injected 3 times in groups of 4-5 monkeys each one. The synthetic polymer Spf (66)30 also emulsified in Freund's adjuvants was injected 6 times. Control groups for both experiments were immunized with saline solution in the same adjuvant following the same schedules. Serology for malaria specific antibodies showed seroconversion in monkeys immunized with the recombinant proteins but not in those immunized with the polymer nor in the controls. Challenge was performed with the 10(5) parasites from the P. falciparum FVO isolate. Neither rp41 nor Spf(66)30 induced protection, whereas 190L induced significant delay of parasitemia. The fusion of the CS.T3 epitope to 190L significantly increased its protective capacity.
在夜猴中评估了几种重组和一种合成的恶性疟原虫蛋白的保护效力。将rp41醛缩酶、MSA-1蛋白的190L片段以及含有CS.T3辅助“通用”表位的融合蛋白190L-CS.T3蛋白在弗氏佐剂中乳化,并以每组4 - 5只猴子的数量分3次注射。同样在弗氏佐剂中乳化的合成聚合物Spf(66)30分6次注射。两个实验的对照组均按照相同的时间表用含相同佐剂的盐溶液进行免疫。疟疾特异性抗体的血清学检测显示,用重组蛋白免疫的猴子出现了血清转化,而用聚合物免疫的猴子以及对照组猴子则未出现血清转化。用来自恶性疟原虫FVO分离株的10⁵个疟原虫进行攻击。rp41和Spf(66)30均未诱导出保护作用,而190L诱导了显著的寄生虫血症延迟。CS.T3表位与190L的融合显著提高了其保护能力。