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Synthetic antigen based on the ligand domain of the Plasmodium vivax duffy binding protein

机译:基于间日疟原虫达菲结合蛋白的配体域的合成抗原

摘要

The disclosure provides compositions that are useful for eliciting a strain-transcending immune response in an animal or human directed against the blood-stage of the malarial parasite Plasmodium vivax. The compositions are based on the ligand domain of Plasmodium vivax Duffy binding protein (PvDBPII). Polar charged polymorphic residues within the dominant strain-specific B-cell epitope were mutated to uncharged residues (e.g. serine, alanine and threonine). This DEKnull variant of PvDBPII produced in bacteria can be purified and refolded in vitro to mimic conformation and erythrocyte binding function of native DBPII. Immunogenicity of DEKnull was confirmed by administration to mice. Compared to the naturally-occurring, strain variant DBPII, DEKnull elicits antibodies that are more broadly reactive with different strain variants of DBPII and enhances production of functional inhibitory antibodies to the shared protective epitopes of native DBPII.
机译:本公开提供了可用于在动物或人中引发针对疟疾寄生虫间日疟原虫的血液阶段的超越应变的免疫应答的组合物。该组合物基于间日疟原虫 Duffy结合蛋白(PvDBPII)的配体域。显性菌株特异性B细胞表位中的极性带电多态残基突变为不带电荷的残基(例如丝氨酸,丙氨酸和苏氨酸)。可以纯化细菌中产生的PvDBPII的DEKnull变体,并在体外重折叠以模拟天然DBPII的构象和红细胞结合功能。通过对小鼠给药证实了DEKnull的免疫原性。与天然存在的菌株变体DBPII相比,DEKnull引发与DBPII的不同菌株变体反应更广泛的抗体,并增强了针对天然DBPII共享保护性表位的功能性抑制抗体的产生。

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