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Acquisition of naturally acquired antibody response to Plasmodium falciparum erythrocyte membrane protein 1-DBLα and differential regulation of IgG subclasses in severe and uncomplicated malaria

机译:在严重和不复杂的疟疾中获得对恶性疟原虫红细胞膜蛋白1-DBLα的自然获得性抗体应答和IgG亚类的差异调节

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摘要

Objectives: To explore whether individuals infected with Plasmodium falciparum(P. falciparum) develop antibodies directed against Pf EMP1-DBLa, and to assess their IgG subclass distribution in severe and uncomplicated malaria.Methods: The anti-PfDBLα IgG and their IgG subclass distributions in plasma of severe(SM) and uncomplicated malaria(UCM) were assessed by enzyme-linked immunoabsorbent assay. The antibody profiles to P. falciparum blood stage antigens were evaluated. CD36 binding ability was determined by static receptor-binding assays.Rosette formation was performed by staining with acridine orange.Results: Significantly higher number of UCM(86.48%) than SM(57.78%) plasma contained total acquisition of specific IgG to P. falciparum antigens(P = 0.000). Similar manners were seen in response to P. falciparum DBLa with significant difference(UCM,59.46% vs SM, 40.00%; P = 0.014). Anti-PfDBLα-IgG1 and-IgG3 were the predominant subclasses. Similar percentage of UCM(31.82%) and SM(33.33%) plasma contained only IgG1, while 13.64% of UCM and 27.78% of SM plasma contained only IgG3. AntiPfDBLα-IgG1 coexpressed with more than one subclass was noted(UCM, 27.27%; SM,16.67%). Obviously, IgG1 coexpressed with IgG3(9.09%) was observed in only UCM plasma. IgG1 was coexpressed with IgG2 in UCM(9.09%) and SM(11.11%) plasma,while IgG1 was coexpressed with IgG4 only in UCM plasma(4.55%). IgG subclasses to P. falciparum antigens were distributed in a similar manner. Only the levels of IgG1, but not IgG3 were significantly higher in UCM than in SM.Conclusions: These data suggest that individuals infected with P. falciparum can develop the anti-Pf EMP1 antibodies with the major contribution of specific IgG subclasses. The balance and the levels of anti-PfDBLα IgG subclasses play a crucial role in antibody mediated protection against severe malaria.
机译:目的:探讨恶性疟原虫(P. falciparum)感染者是否产生针对Pf EMP1-DBLa的抗体,并评估其在严重且不复杂的疟疾中的IgG亚类分布。方法:抗PfDBLαIgG及其IgG亚类分布酶联免疫吸附法测定重症(SM)和单纯性疟疾(UCM)血浆。评估了恶性疟原虫血阶段抗原的抗体谱。通过静态受体结合测定法确定CD36结合能力,通过a啶橙染色来形成子弹头。结果:UCM(86.48%)的数量显着高于SM(57.78%)血浆所含的针对恶性疟原虫的特异性IgG。抗原(P = 0.000)。对恶性疟原虫DBLa的反应相似,差异有统计学意义(UCM,59.46%vs SM,40.00%; P = 0.014)。抗-PfDBLα-IgG1和-IgG3是主要的亚类。 UCM(31.82%)和SM(33.33%)血浆的相似百分比仅包含IgG1,而UCM的13.64%和SM血浆的27.78%仅包含IgG3。注意到与一种以上亚类共表达的抗PfDBLα-IgG1(UCM,27.27%; SM,16.67%)。显然,仅在UCM血浆中观察到IgG1与IgG3共表达(9.09%)。 IgG1与IgG2在UCM血浆中共表达(9.09%)和SM(11.11%),而IgG1仅在UCM血浆中与IgG4共表达(4.55%)。恶性疟原虫抗原的IgG亚类以相似的方式分布。结论:这些数据表明,感染恶性疟原虫的个体可以发展出抗-Pf EMP1抗体,而这些抗体主要是特定IgG亚类的。抗PfDBLαIgG亚类的平衡和水平在抗体介导的针对严重疟疾的保护中起着至关重要的作用。

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  • 来源
    《亚太热带生物医学杂志:英文版》 |2017年第012期|P.1055-1061|共7页
  • 作者单位

    Faculty of Medical Technology, Huachiew Chalermprakiet University;

    Department of Biochemistry, Faculty of Science, Kasetsart University;

    Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University;

    Center for Emerging and Neglected Infectious Diseases, Mahidol University;

    Faculty of Medical Technology, Huachiew Chalermprakiet University;

    Department of Biochemistry, Faculty of Science, Kasetsart University;

    Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University;

    Center for Emerging and Neglected Infectious Diseases, Mahidol University;

    Faculty of Medical Technology, Huachiew Chalermprakiet University;

    Department of Biochemistry, Faculty of Science, Kasetsart University;

    Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University;

    Center for Emerging and Neglected Infectious Diseases, Mahidol University;

    Faculty of Medical Technology, Huachiew Chalermprakiet University;

    Department of Biochemistry, Faculty of Science, Kasetsart University;

    Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University;

    Center for Emerging and Neglected Infectious Diseases, Mahidol University;

    Faculty of Medical Technology, Huachiew Chalermprakiet University;

    Department of Biochemistry, Faculty of Science, Kasetsart University;

    Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University;

    Center for Emerging and Neglected Infectious Diseases, Mahidol University;

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  • 原文格式 PDF
  • 正文语种 CHI
  • 中图分类 医学原虫学;
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