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恶性疟原虫抗原之间的多种交叉反应会损害针对疟疾的保护性免疫的发展。

Multiple cross-reactivities amongst antigens of Plasmodium falciparum impair the development of protective immunity against malaria.

作者信息

Anders R F

出版信息

Parasite Immunol. 1986 Nov;8(6):529-39. doi: 10.1111/j.1365-3024.1986.tb00867.x.

Abstract

The majority of protein antigens of the malaria parasite Plasmodium falciparum contain short sequences that are extensively repeated in tandem arrays. Some antigens contain a single block of repeats whereas in other antigens there may be two or more blocks of related repeats. The repetitive sequences in an individual antigen may be highly conserved but more usually there is some degeneracy which occasionally is extensive. The repetitive sequences encode immunodominant epitopes to which much of the antibody response in malaria is directed. Recently, we have found that there are extensive cross-reactions amongst the epitopes encoded by related repetitive sequences. These cross-reactions may involve different blocks of repeats in the one antigen or repetitive sequences in different antigens. It is proposed that these cross-reactions interfere with the normal maturation of a high affinity antibody response in malaria by causing an abnormally high proportion of somatically-mutated B cells to be preserved during clonal expansion.

摘要

恶性疟原虫的大多数蛋白质抗原含有短序列,这些短序列以串联阵列的形式广泛重复。一些抗原包含单个重复块,而在其他抗原中可能有两个或更多相关重复块。单个抗原中的重复序列可能高度保守,但更常见的是存在一些简并性,偶尔这种简并性还很广泛。这些重复序列编码免疫显性表位,疟疾中的大部分抗体反应都针对这些表位。最近,我们发现相关重复序列编码的表位之间存在广泛的交叉反应。这些交叉反应可能涉及同一抗原中不同的重复块或不同抗原中的重复序列。有人提出,这些交叉反应通过导致在克隆扩增过程中异常高比例的体细胞突变B细胞被保留,从而干扰疟疾中高亲和力抗体反应的正常成熟。

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