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首页> 外文期刊>Immunology and Cell Biology >Human antibodies to the polymorphic block 2 domain of the Plasmodium falciparum merozoite surface protein 1 (MSP-1) exhibit a highly skewed, peptide-specific light chain distribution.
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Human antibodies to the polymorphic block 2 domain of the Plasmodium falciparum merozoite surface protein 1 (MSP-1) exhibit a highly skewed, peptide-specific light chain distribution.

机译:恶性疟原虫裂殖子表面蛋白1(MSP-1)的多态性block 2域的人类抗体表现出高度偏斜的,肽特异性的轻链分布。

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摘要

Summary Antibodies to polymorphic block 2 of the Plasmodium falciparum merozoite surface protein 1 (MSP-1) present a paradoxical association with acquired protection against clinical malaria, while showing restricted and fixed specificity, reminiscent of antigenic sin. We report here that these antibodies present a highly imbalanced, peptide-specific light chain distribution. This was not observed with several other parasite-derived peptides or antigens. These data point to a skewed immune response to MSP-1 block 2 that is constrained both in specificity and chain usage. This is the first report of a biased response to polymorphic epitopes of a surface antigen in malaria parasites.
机译:小结恶性疟原虫裂殖子表面蛋白1(MSP-1)多态性块2的抗体与获得的针对临床疟疾的保护呈反常联系,同时表现出限制性和固定的特异性,让人联想到抗原性罪恶。我们在这里报告这些抗体呈现高度不平衡的,肽特异性轻链分布。在其他几种寄生虫衍生的肽或抗原中未观察到这一点。这些数据表明对MSP-1嵌段2的偏向免疫反应受到了特异性和链使用的限制。这是疟疾寄生虫对表面抗原多态性表位的偏向反应的首次报道。

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