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首页> 外文期刊>Infection and immunity >Antibodies Reactive with the N-Terminal Domain ofPlasmodium falciparum Serine Repeat Antigen Inhibit Cell Proliferation by Agglutinating Merozoites and Schizonts
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Antibodies Reactive with the N-Terminal Domain ofPlasmodium falciparum Serine Repeat Antigen Inhibit Cell Proliferation by Agglutinating Merozoites and Schizonts

机译:与恶性疟原虫丝氨酸重复抗原的N-末端结构域反应的抗体可通过凝集裂殖子和裂殖体抑制细胞增殖。

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摘要

The serine repeat antigen (SERA) is a vaccine candidate antigen ofPlasmodium falciparum. Immunization of mice withEscherichia coli-produced recombinant protein of the SERA N-terminal domain (SE47′) induced an antiserum that was inhibitory to parasite growth in vitro. Affinity-purified mouse antibodies specific to the recombinant protein inhibited parasite growth between the schizont and ring stages but not between the ring and schizont stages. When Percoll-purified schizonts were cultured with the affinity-purified SE47′-specific antibodies, schizonts and merozoites were agglutinated. Indirect-immunofluorescence assays with unfixed parasite cells showed that SE47′-specific immunoglobulin G (IgG) bound to SERA molecules on rupturing schizonts and merozoites but the IgG did not react with the schizont-infected erythrocytes (RBC). Furthermore, double-fluorescence staining against SE47′-specific IgG and anti-human RBC membrane IgG showed that the RBC membrane disappeared from SE47′-specific-IgG-bound schizonts after cultivation. These observations suggest that the SE47′-specific antibodies inhibit parasite growth by cross-linking SERA molecules that are associated with merozoites in rupturing schizonts with partly broken RBC and parasitophorous vacuole membranes, blocking merozoite release.
机译:丝氨酸重复抗原(SERA)是恶性疟原虫的疫苗候选抗原。用大肠埃希菌生产的SERA N末端域重组蛋白(SE47')免疫小鼠后,产生的抗血清可抑制体外寄生虫的生长。对重组蛋白具有特异性的亲和纯化的小鼠抗体可抑制裂殖体和环阶段之间的寄生虫生长,但不能抑制裂殖体和环之间的寄生虫生长。当用亲和纯化的SE47'特异性抗体培养Percoll纯化的裂殖体时,将裂殖体和裂殖子凝集。未固定寄生虫细胞的间接免疫荧光分析表明,SE47'特异性免疫球蛋白G(IgG)在裂殖子裂殖子和裂殖子破裂时与SERA分子结合,但IgG不与裂殖体感染的红细胞(RBC)反应。此外,对SE47'特异性IgG和抗人RBC膜IgG的双荧光染色显示,培养后,RBC膜从SE47'特异性IgG结合的裂殖体中消失。这些观察结果表明,SE47'特异性抗体通过交联与裂殖子相关的SERA分子在部分裂开的RBC和寄生虫液泡膜的裂殖裂裂中阻断了裂殖子的释放,从而抑制了寄生虫的生长。

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