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恶性疟原虫裂殖子表面蛋白-2(MSP-2)四种等位基因变体的差异性抗体识别

Differential antibody recognition of four allelic variants of the merozoite surface protein-2 (MSP-2) of Plasmodium falciparum.

作者信息

Tonhosolo R, Wunderlich G, Ferreira M U

机构信息

Department of Parasitology, Institute for Biomedical Sciences, University of São Paulo, SP, Brazil.

出版信息

J Eukaryot Microbiol. 2001 Sep-Oct;48(5):556-64. doi: 10.1111/j.1550-7408.2001.tb00191.x.

Abstract

The merozoite surface protein-2 (MSP-2) is a major vaccine candidate for the asexual blood stage of Plasmodium falciparum. MSP-2 is essentially dimorphic, and allelic families are named after the representative isolates FC27 and IC1. The polymorphic central region contains immunodominant repeats, which vary in number, length, and sequence within and between allelic families. We have examined the antibody recognition of repeat regions from both MSP-2 allelic families expressed as recombinant fusion peptides. The results are summarized as follows. (1) Immunization of mice with the fusion peptides elicited IgG antibodies that cross-reacted with the native MSP-2 molecule in an allelic family-specific manner. (2) These mouse antibodies recognized the recombinant proteins in both a variant-specific and a family-specific manner, as shown in inhibition immunoassays. Antibodies raised against the peptide FC27 seemed to be essentially variant-specific, since the soluble form of the S20 antigen (a member of FC27 family) had relatively little inhibitory effect on them. (3) The overall pattern of human IgG antibody responses to MSP-2 in Karitiana Indians, a population continuously exposed to hypoendemic malaria in the Brazilian Amazon Region, differs from that described in hyperendemic areas in Africa and Papua New Guinea in two important features: there was no clear age-dependent increase in the prevalence and mean concentration of specific IgG antibodies, and there was no skewing towards the IgG3 subclass in antibody responses. (4) The relatively poor correlation between concentrations of IgG antibodies that are specific for members of the same allelic family suggests that recognition of MSP-2 peptides by naturally acquired antibodies was largely variant-specific in this population. The potential role of naturally acquired variant-specific antibodies in immune evasion, by selecting mutant parasites carrying insertions or deletions of repeat sequences, is briefly discussed.

摘要

裂殖子表面蛋白2(MSP-2)是恶性疟原虫无性血液阶段的主要候选疫苗。MSP-2本质上是二态的,等位基因家族以代表性分离株FC27和IC1命名。多态性中心区域包含免疫显性重复序列,其数量、长度和序列在等位基因家族内部和之间有所不同。我们已经检测了以重组融合肽形式表达的两个MSP-2等位基因家族重复区域的抗体识别情况。结果总结如下:(1)用融合肽免疫小鼠可诱导产生IgG抗体,这些抗体以等位基因家族特异性方式与天然MSP-2分子发生交叉反应。(2)如抑制免疫测定所示,这些小鼠抗体以变异体特异性和家族特异性方式识别重组蛋白。针对肽FC27产生的抗体似乎基本上是变异体特异性的,因为S20抗原(FC27家族成员)的可溶性形式对它们的抑制作用相对较小。(3)在巴西亚马逊地区持续暴露于低流行疟疾的卡里蒂亚纳印第安人中,人类对MSP-2的IgG抗体反应总体模式在两个重要特征上与非洲和巴布亚新几内亚高流行地区所描述的不同:特异性IgG抗体的患病率和平均浓度没有明显的年龄依赖性增加,并且抗体反应中没有偏向IgG3亚类。(4)针对同一等位基因家族成员的IgG抗体浓度之间相对较差的相关性表明,在该人群中,天然获得的抗体对MSP-2肽的识别在很大程度上是变异体特异性的。本文简要讨论了天然获得的变异体特异性抗体通过选择携带重复序列插入或缺失的突变寄生虫在免疫逃避中的潜在作用。

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