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Enhancing Blockade of Plasmodium falciparum Erythrocyte Invasion: Assessing Combinations of Antibodies against PfRH5 and Other Merozoite Antigens

机译:增强对恶性疟原虫红细胞侵袭的阻断:评估抗PfRH5和其他裂殖子抗原的抗体的组合。

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摘要

No vaccine has yet proven effective against the blood-stages of Plasmodium falciparum, which cause the symptoms and severe manifestations of malaria. We recently found that PfRH5, a P. falciparum-specific protein expressed in merozoites, is efficiently targeted by broadly-neutralizing, vaccine-induced antibodies. Here we show that antibodies against PfRH5 efficiently inhibit the in vitro growth of short-term-adapted parasite isolates from Cambodia, and that the EC50 values of antigen-specific antibodies against PfRH5 are lower than those against PfAMA1. Since antibody responses elicited by multiple antigens are speculated to improve the efficacy of blood-stage vaccines, we conducted detailed assessments of parasite growth inhibition by antibodies against PfRH5 in combination with antibodies against seven other merozoite antigens. We found that antibodies against PfRH5 act synergistically with antibodies against certain other merozoite antigens, most notably with antibodies against other erythrocyte-binding antigens such as PfRH4, to inhibit the growth of a homologous P. falciparum clone. A combination of antibodies against PfRH4 and basigin, the erythrocyte receptor for PfRH5, also potently inhibited parasite growth. This methodology provides the first quantitative evidence that polyclonal vaccine-induced antibodies can act synergistically against P. falciparum antigens and should help to guide the rational development of future multi-antigen vaccines.
机译:尚未证明任何疫苗可有效对抗恶性疟原虫的血液阶段,该阶段可导致疟疾的症状和严重表现。我们最近发现,PfRH5是一种在裂殖子中表达的恶性疟原虫特异性蛋白,可通过广泛中和疫苗诱导的抗体有效地靶向。在这里,我们显示了针对PfRH5的抗体有效抑制了柬埔寨短期适应性寄生虫分离株的体外生长,并且针对PfRH5的抗原特异性抗体的EC50值低于针对PfAMA1的抗原。由于推测由多种抗原引起的抗体反应可改善血液疫苗的功效,因此我们对PfRH5抗体与其他7种裂殖子抗原的抗体联合进行了寄生虫生长抑制的详细评估。我们发现针对PfRH5的抗体与针对某些其他裂殖子抗原的抗体(尤其是针对其他红细胞结合抗原,例如PfRH4)的抗体具有协同作用,以抑制同源恶性疟原虫克隆的生长。抗PfRH4和basinin(PfRH5的红细胞受体)的抗体的组合也有效抑制了寄生虫的生长。这种方法学提供了第一个定量证据,证明多克隆疫苗诱导的抗体可以协同作用对抗恶性疟原虫抗原,并应有助于指导未来多抗原疫苗的合理开发。

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