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恶性疟原虫EBA-140裂殖子配体杆状病毒表达结合区的免疫原性和抗原性研究

Studies on Immunogenicity and Antigenicity of Baculovirus-Expressed Binding Region of Plasmodium falciparum EBA-140 Merozoite Ligand.

作者信息

Zerka Agata, Rydzak Joanna, Lass Anna, Szostakowska Beata, Nahorski Wacław, Wroczyńska Agnieszka, Myjak Przemyslaw, Krotkiewski Hubert, Jaskiewicz Ewa

机构信息

Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.

Department of Tropical Parasitology, Institute of Maritime and Tropical Medicine in Gdynia, Medical University of Gdańsk, Gdańsk, Poland.

出版信息

Arch Immunol Ther Exp (Warsz). 2016 Apr;64(2):149-56. doi: 10.1007/s00005-015-0367-5. Epub 2015 Oct 6.

Abstract

The erythrocyte binding ligand 140 (EBA-140) is a member of the Plasmodium falciparum erythrocyte binding antigens (EBA) family, which are considered as prospective candidates for malaria vaccine development. EBA proteins were identified as important targets for naturally acquired inhibitory antibodies. Natural antibody response against EBA-140 ligand was found in individuals living in malaria-endemic areas. The EBA-140 ligand is a paralogue of the well-characterized P. falciparum EBA-175 protein. They both share homology of domain structure, including the binding region (Region II), which consists of two homologous F1 and F2 domains and is responsible for ligand-erythrocyte receptor interaction during merozoite invasion. It was shown that the erythrocyte receptor for EBA-140 ligand is glycophorin C-a minor human erythrocyte sialoglycoprotein. In studies on the immunogenicity of P. falciparum EBA ligands, the recombinant proteins are of great importance. In this report, we have demonstrated that the recombinant baculovirus-obtained EBA-140 Region II is immunogenic and antigenic. It can raise specific antibodies in rabbits, and it is recognized by natural antibodies present in sera of patients with malaria, and thus, it may be considered for inclusion in multicomponent blood-stage vaccines.

摘要

红细胞结合配体140(EBA - 140)是恶性疟原虫红细胞结合抗原(EBA)家族的成员,该家族被认为是疟疾疫苗开发的潜在候选对象。EBA蛋白被确定为天然获得性抑制抗体的重要靶点。在生活在疟疾流行地区的个体中发现了针对EBA - 140配体的天然抗体反应。EBA - 140配体是特征明确的恶性疟原虫EBA - 175蛋白的旁系同源物。它们在结构域结构上具有同源性,包括结合区域(区域II),该区域由两个同源的F1和F2结构域组成,负责裂殖子入侵期间配体与红细胞受体的相互作用。已表明EBA - 140配体的红细胞受体是血型糖蛋白C——一种次要的人类红细胞唾液糖蛋白。在对恶性疟原虫EBA配体免疫原性的研究中,重组蛋白非常重要。在本报告中,我们已经证明通过重组杆状病毒获得的EBA - 140区域II具有免疫原性和抗原性。它能在兔体内产生特异性抗体,并且能被疟疾患者血清中的天然抗体识别,因此,它可被考虑纳入多组分血液期疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/952e/4805696/614480a72a05/5_2015_367_Fig1_HTML.jpg

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