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首页> 外文期刊>The journal of immunology >3D7-Derived Plasmodium falciparum Erythrocyte Membrane Protein 1 Is a Frequent Target of Naturally Acquired Antibodies Recognizing Protein Domains in a Particular Pattern Independent of Malaria Transmission Intensity
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3D7-Derived Plasmodium falciparum Erythrocyte Membrane Protein 1 Is a Frequent Target of Naturally Acquired Antibodies Recognizing Protein Domains in a Particular Pattern Independent of Malaria Transmission Intensity

机译:3D7来源的恶性疟原虫红细胞膜蛋白1是自然获得的抗体的常见目标,这些抗体以特定的模式识别蛋白结构域,而与疟疾的传播强度无关。

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摘要

Protection against Plasmodium falciparum malaria is largely mediated by IgG against surface Ags such as the erythrocyte membrane protein 1 family (PfEMP1) responsible for antigenic variation and sequestration of infected erythrocytes. PfEMP1 molecules can be divided into groups A, B/A, B, C, and B/C. We have previously suggested that expression of groups A and B/A PfEMP1 is associated with severe disease and that Abs to these molecules are acquired earlier in life than Abs to PfEMP1 belonging to groups B, B/C, and C PfEMP1. In this study, we compared the acquisition of IgG to 20 rPfEMP1 domains derived from 3D7 in individuals living under markedly different malaria transmission intensity and were unable to find differences in the Ab acquisition rate to PfEMP1 of different groupings (A, B, or C) or domain type (α, β, γ, δ, ε, or x). Abs were acquired early in life in individuals living in the high transmission village and by the age of 2–4 years most individuals had Abs against most constructs. This level of reactivity was found at the age of 10–20 years in the medium transmission village and was never reached by individuals living under low transmission. Nevertheless, the sequence by which individuals acquired Abs to particular constructs was largely the same in the three villages. This indicates that the pattern of PfEMP1 expression by parasites transmitted at the different sites was similar, suggesting that PfEMP1 expression is nonrandom and shaped by host-parasite relationship factors operating at all transmission intensities.
机译:抵御恶性疟原虫疟疾的保护作用很大程度上是由IgG介导的,针对表面抗原(例如负责抗原变异和隔离感染红细胞的红细胞膜蛋白1家族(PfEMP1))的IgG介导的。 PfEMP1分子可分为A,B / A,B,C和B / C组。我们先前曾提出,A和B / A组PfEMP1的表达与严重疾病有关,并且这些分子的Abs的生命要早于属于B,B / C和C PfEMP1组的PfEMP1的Abs。在这项研究中,我们比较了在疟疾传播强度明显不同且无法找到不同组别(A,B或C)与PfEMP1的抗体获取率差异的个体中,IgG的获取与3D7衍生的20 rPfEMP1域的比较或域类型(α,β,γ,δ,ε或x)。 Abs是生活在高传播村庄中的人在生命早期获得的,到2-4岁时,大多数人对大多数建筑物都具有Abs。在中等传播村庄发现这种反应水平的年龄为10-20岁,生活在低传播村庄的人们从未达到过这种反应水平。然而,在这三个村庄中,个人获取特定构造抗体的顺序基本相同。这表明在不同位点传播的寄生虫的PfEMP1表达模式是相似的,这表明PfEMP1表达是非随机的,并且受在所有传播强度下运行的宿主-寄生虫相关因素的影响。

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