首页> 美国卫生研究院文献>Infection and Immunity >Immune responses to band 3 neoantigens on Plasmodium falciparum-infected erythrocytes in subjects living in an area of intense malaria transmission are associated with low parasite density and high hematocrit value.
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Immune responses to band 3 neoantigens on Plasmodium falciparum-infected erythrocytes in subjects living in an area of intense malaria transmission are associated with low parasite density and high hematocrit value.

机译:生活在严重疟疾传播地区的受试者对恶性疟原虫感染的红细胞对带3新抗原的免疫反应与低寄生虫密度和高血细胞比容值相关。

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摘要

During the intracellular development of the human malarial parasite, Plasmodium falciparum, cryptic regions of the erythrocyte band 3 protein are exposed. Antibodies against these band 3-related neoantigens block cytoadherence, and peptides based on amino acid sequences of putative exofacial loops of band 3 protein block the in vitro and in vivo adherence of P. falciparum-infected erythrocytes. At present, it is not known whether reactivity to these antigens is related to exposure to the malaria parasite or is correlated with protective immunity. The reactivities of plasma to peptides containing amino acid sequences of putative exofacial loops 3 and 7 of human band 3 protein were determined for children and adults living in an area of perennial malaria transmission (Liberia) and for donors who had never been exposed to malaria (Denmark). Plasma samples from children and adults living in an area of intense malaria transmission showed a much higher reactivity with the band 3 peptides than did those from nonimmune individuals. High reactivity to the loop 3 peptide (amino acids 546 to 555) was correlated with lower mean parasite density in children in the 5- to 9-year-old age group. The presence of antibodies against loop 3 and 7 peptides was not associated with a low packed erythrocyte volume (hematocrit); in fact, higher-than-average reactivities to both peptides were positively correlated with high hematocrit values, indicating that antibodies which specifically recognize the band 3-related neoantigens are not involved in hemolysis (autoimmunity).
机译:在人类疟疾寄生虫恶性疟原虫的细胞内发育过程中,暴露了红细胞带3蛋白的隐秘区域。针对这些与Band 3相关的新抗原的抗体会阻止细胞粘附,而基于带3蛋白推定的面部外环氨基酸序列的肽会阻断恶性疟原虫感染的红细胞的体外和体内粘附。目前,与这些抗原的反应性是否与暴露于疟疾寄生虫有关或与保护性免疫有关尚不清楚。确定了生活在常年疟疾传播地区(利比里亚)的儿童和成年人以及从未接触过疟疾的捐献者的血浆对含有人类乐队3蛋白推定面外环3和7氨基酸序列的肽的反应性(丹麦)。生活在高度疟疾传播地区的儿童和成年人的血浆样品显示的与乐队3肽的反应性比非免疫个体的高得多。在5至9岁年龄段的儿童中,对loop 3肽(氨基酸546至555)的高反应性与较低的平均寄生虫密度相关。抗环3和7肽的抗体的存在与低包装的红细胞体积(血细胞比容)无关;实际上,对两种肽的高于平均的反应性与高血细胞比容值呈正相关,表明特异性识别与带3相关的新抗原的抗体不参与溶血(自身免疫)。

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