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首页> 外文期刊>Infection and immunity >Protective immunity induced in Aotus monkeys by a recombinant SERA protein of Plasmodium falciparum: further studies using SERA 1 and MF75.2 adjuvant.
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Protective immunity induced in Aotus monkeys by a recombinant SERA protein of Plasmodium falciparum: further studies using SERA 1 and MF75.2 adjuvant.

机译:恶性疟原虫的重组SERA蛋白在大猿猴中诱导的保护性免疫:使用SERA 1和MF75.2佐剂的进一步研究。

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We describe the third of three vaccination trials of Panamanian Aotus monkeys with a recombinant blood-stage antigen derived from the malaria parasite Plasmodium falciparum. Immunization was performed with an N-terminal region of the SERA antigen (serine repeat antigen protein), SERA 1, that contains a 262-amino-acid fragment including amino acids 24 to 285 of the 989-amino-acid SERA protein. Vaccinations were carried out with the recombinant protein mixed with either Freund's, MF75.2, or MF59.2 adjuvant. A control group that did not receive SERA 1 but only MF75.2 adjuvant was included. Monkeys vaccinated with the antigen MF59.2 mixture produced low anti-SERA 1 titers and were not protected. Monkeys vaccinated with antigen and Freund's adjuvant had, in general, a higher average anti-SERA 1 titer (107,278) than did monkeys immunized with SERA 1 and MF75.2 (40, 143), yet monkeys in both groups were well protected. Monkeys that received only MF75.2 developed neither detectable anti-SERA 1 nor anti-P. falciparum antibodies prior to or 10 days after parasite challenge, yet were apparently protected against infection. Monkeys vaccinated with either SERA 1 and Freund's, SERA 1 and MF75.2, or MF75.2 alone and that had been challenged but did not develop a countable parasitemia were treated with a curative dose of mefloquine 100 days after parasite challenge and then rechallenged 40 days later. None of the five rechallenged monkeys that had originally received SERA 1 and Freund's developed a countable parasitemia. Only one of five rechallenged monkeys that originally received SERA 1 and MF75.2 developed a high countable parasitemia, while two animals developed a barely countable parasitemia. Four of the rechallenged monkeys that had originally received only MF75.2 developed a moderate to high countable parasitemia. The results indicate that vaccination with SERA 1 and either Freund's or MF75.2 adjuvant provides protection and vaccination with MF75.2 alone can provide a temporary protection unrelated to the induction of anti-SERA 1 or antimalarial antibodies.
机译:我们描述了来自疟疾寄生虫恶性疟原虫的重组血液阶段抗原对巴拿马Aotus猴子进行的三项疫苗接种试验中的第三项。用SERA抗原(丝氨酸重复抗原蛋白)SERA 1的N-末端区域进行免疫,所述SERA 1含有262个氨基酸的片段,所述片段包含989个氨基酸的SERA蛋白的24-285位氨基酸。用与弗氏,MF75.2或MF59.2佐剂混合的重组蛋白进行疫苗接种。对照组不接受SERA 1,而仅接受MF75.2佐剂。接种了抗原MF59.2混合物的猴子产生的抗SERA 1滴度低,并且没有受到保护。一般而言,接种了抗原和弗氏佐剂的猴子比使用SERA 1和MF75.2免疫的猴子(40、143)具有更高的平均平均抗SERA 1滴度(107,278),但是两组的猴子都受到了很好的保护。仅接受MF75.2的猴子既没有检测到抗SERA 1也没有抗P。寄生虫攻击之前或之后10天的恶性疟原虫抗体,但显然已受到保护,不会感染。接种了SERA 1和Freund's,SERA 1和MF75.2或MF75.2且已被攻击但没有发展为可计数的寄生虫的猴子在寄生虫攻击后100天用治愈剂量的甲氟喹治疗,然后再次攻击40几天后。最初接受SERA 1和弗氏(Freund's)的五只再挑战的猴子均未出现可计数的寄生虫病。最初接受SERA 1和MF75.2的五只再挑战的猴子中只有一只发展为高度可计数的寄生虫病,而两只动物则发展为几乎不可计数的寄生虫病。最初仅接受MF75.2的四只再挑战猴发展为中度至高度可计数的寄生虫病。结果表明,用SERA 1和弗氏或MF75.2佐剂进行疫苗接种可提供保护,而仅用MF75.2疫苗接种可提供与诱导抗SERA 1或抗疟疾抗体无关的临时保护。

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