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在自然感染恶性疟原虫期间诱导产生的人类抗体对变异型利芬抗原的识别。

Recognition of variant Rifin antigens by human antibodies induced during natural Plasmodium falciparum infections.

作者信息

Abdel-Latif Mohamed S, Khattab Ayman, Lindenthal Christoph, Kremsner Peter G, Klinkert Mo-Quen

机构信息

Department of Parasitology, Institute for Tropical Medicine, University of Tübingen, Germany.

出版信息

Infect Immun. 2002 Dec;70(12):7013-21. doi: 10.1128/IAI.70.12.7013-7021.2002.

Abstract

Antibodies from individuals living in areas where malaria is endemic are known to react with parasite-derived erythrocyte surface proteins. The major immunogenic and clonally variant surface antigen described to date is Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP-1), which is encoded by members of the multicopy var gene family. We report here that rifin proteins (RIF proteins), belonging to the largest known family of variable infected erythrocyte surface-expressed proteins, are also naturally immunogenic. Recombinant RIF proteins were used to analyze the antibody responses of individuals living in an area of intense malaria transmission. Elevated anti-rifin antibody levels were detected in the majority of the adult population tested, whereas the prevalence of such antibodies was much lower in malaria-exposed children. Despite the high degree of diversity between rif sequences and the high gene copy number, it appears that P. falciparum infections can induce antibodies that cross-react with several variant rifin molecules in many parasite isolates in a given community, and the immune response is most likely to be stable over time in a hyperendemic area. The protein was localized by fluorescence microscopy on the membrane of ring and young trophozoite-infected erythrocytes with antibodies from human immune sera with specificities for recombinant RIF protein.

摘要

已知生活在疟疾流行地区的个体产生的抗体可与寄生虫衍生的红细胞表面蛋白发生反应。迄今为止描述的主要免疫原性和克隆变异表面抗原是恶性疟原虫红细胞膜蛋白1(PfEMP-1),它由多拷贝var基因家族的成员编码。我们在此报告,属于已知最大的可变感染红细胞表面表达蛋白家族的利芬蛋白(RIF蛋白)同样具有天然免疫原性。利用重组RIF蛋白分析了生活在疟疾传播活跃地区的个体的抗体反应。在大多数接受检测的成年人群中检测到抗利芬抗体水平升高,而在接触过疟疾的儿童中,此类抗体的流行率要低得多。尽管利芬序列之间存在高度多样性且基因拷贝数很高,但恶性疟原虫感染似乎能够诱导抗体与特定社区中许多寄生虫分离株中的几种变异利芬分子发生交叉反应,并且在高度流行地区,免疫反应很可能随时间推移保持稳定。利用来自对重组RIF蛋白具有特异性的人免疫血清的抗体,通过荧光显微镜将该蛋白定位在环状体和年轻滋养体感染的红细胞膜上。

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