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恶性疟原虫的抗原多样性与抗体介导的寄生虫中和作用。

Antigenic diversity of Plasmodium falciparum and antibody-mediated parasite neutralization.

作者信息

Bolad A, Berzins K

机构信息

Stockholm University, Department of Immunology, SE-106 91 Stockholm, Sweden.

出版信息

Scand J Immunol. 2000 Sep;52(3):233-9. doi: 10.1046/j.1365-3083.2000.00787.x.

Abstract

The malaria parasite Plasmodium falciparum, causing the most severe form of the disease in humans, is characterized by a broad antigenic diversity between different strains and isolates of the parasite. The antigenic diversity reflects on the one hand polymorphisms in allelic gene products and, on the other hand, antigenic variation as a result of expression of alternative genes in multigene families. Using selected polymorphic regions in two merozoite surface antigens, a method for genotyping P. falciparum parasites has been developed. This has resulted in new information on the clonal multiplicity and dynamics of parasite populations. Observations from in vivo and in vitro studies have identified many potential parasite-neutralizing immune responses and several of the target antigens are being explored as vaccine candidates. Studies of antibody-mediated neutralization of parasites in P. falciparum in vitro cultures, with or without leukocytes as effector cells, have been instrumental in identifying potential target antigens for protective immunity and for elucidation of the effects of immune pressure on the dynamics of parasite populations and their antigenic plasticity.

摘要

疟原虫恶性疟原虫可导致人类最严重的疟疾形式,其特点是不同菌株和分离株之间存在广泛的抗原多样性。抗原多样性一方面反映在等位基因产物的多态性上,另一方面反映在多基因家族中替代基因表达导致的抗原变异上。利用两种裂殖子表面抗原中的选定多态性区域,已开发出一种对恶性疟原虫进行基因分型的方法。这带来了关于寄生虫群体克隆多样性和动态的新信息。体内和体外研究的观察结果已确定了许多潜在的寄生虫中和免疫反应,并且正在探索几种靶抗原作为候选疫苗。在有或没有白细胞作为效应细胞的情况下,对恶性疟原虫体外培养物中抗体介导的寄生虫中和作用的研究,有助于确定保护性免疫的潜在靶抗原,并阐明免疫压力对寄生虫群体动态及其抗原可塑性的影响。

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