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针对 PfEMP1、RIFIN、MSP3 和 GLURP 的抗体是在初次感染的志愿者中受控制的恶性疟原虫感染期间获得的。

Antibodies against PfEMP1, RIFIN, MSP3 and GLURP are acquired during controlled Plasmodium falciparum malaria infections in naïve volunteers.

机构信息

Department of International Health, Centre for Medical Parasitology, University of Copenhagen, Copenhagen, Denmark.

出版信息

PLoS One. 2011;6(12):e29025. doi: 10.1371/journal.pone.0029025. Epub 2011 Dec 12.

Abstract

Antibodies to polymorphic antigens expressed during the parasites erythrocytic stages are important mediators of protective immunity against P. falciparum malaria. Therefore, polymorphic blood stage antigens like MSP3, EBA-175 and GLURP and variant surface antigens PfEMP1 and RIFIN are considered vaccine candidates. However, to what extent these antibodies to blood stage antigens are acquired during naive individuals' first infections has not been studied in depth. Using plasma samples collected from controlled experimental P. falciparum infections we show that antibodies against variant surface antigens, PfEMP1 and RIFIN as well as MSP3 and GLURP, are acquired during a single short low density P. falciparum infection in non-immune individuals including strain transcendent PfEMP1 immune responses. These data indicate that the immunogenicity of the variant surface antigens is similar to the less diverse merozoite antigens. The acquisition of a broad and strain transcendent repertoire of PfEMP1 antibodies may reflect a parasite strategy of expressing most or all PfEMP1 variants at liver release optimizing the likelihood of survival and establishment of chronic infections in the new host.

摘要

针对疟原虫红细胞阶段表达的多态性抗原的抗体是针对恶性疟原虫疟疾的保护性免疫的重要介质。因此,多态性红内期抗原(如 MSP3、EBA-175 和 GLURP)和变异表面抗原 PfEMP1 和 RIFIN 被认为是疫苗候选物。然而,在无免疫力的个体的首次感染中,这些针对红内期抗原的抗体在多大程度上被获得尚未深入研究。我们使用从受控的恶性疟原虫感染中收集的血浆样本表明,针对变异表面抗原 PfEMP1 和 RIFIN 以及 MSP3 和 GLURP 的抗体,是在无免疫力个体的单次短暂低密度恶性疟原虫感染中获得的,包括对 PfEMP1 免疫的个体。这些数据表明,变异表面抗原的免疫原性与多样化程度较低的裂殖子抗原相似。广泛且跨越株系的 PfEMP1 抗体的获得可能反映了寄生虫在肝脏释放时表达大多数或所有 PfEMP1 变体的策略,从而优化了在新宿主中存活和建立慢性感染的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c5/3236238/b2f7894f2147/pone.0029025.g001.jpg

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