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间日疟原虫无症状带虫者血清中交叉反应性抗 PfCLAG9 抗体。

Cross-reactive anti-PfCLAG9 antibodies in the sera of asymptomatic parasite carriers of Plasmodium vivax.

机构信息

Centro de Pesquisa em Medicina Tropical, Porto Velho, RO, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2013 Feb;108(1):98-105. doi: 10.1590/s0074-02762013000100016.

Abstract

The PfCLAG9 has been extensively studied because their immunogenicity. Thereby, the gene product is important for therapeutics interventions and a potential vaccine candidate. Antibodies against synthetic peptides corresponding to selected sequences of the Plasmodium falciparum antigen PfCLAG9 were found in sera of falciparum malaria patients from Rondônia, in the Brazilian Amazon. Much higher antibody titres were found in semi-immune and immune asymptomatic parasite carriers than in subjects suffering clinical infections, corroborating original findings in Papua Guinea. However, sera of Plasmodium vivax patients from the same Amazon area, in particular from asymptomatic vivax parasite carriers, reacted strongly with the same peptides. Bioinformatic analyses revealed regions of similarity between P. falciparum Pfclag9 and the P. vivax ortholog Pvclag7. Indirect fluorescent microscopy analysis showed that antibodies against PfCLAG9 peptides elicited in BALB/c mice react with human red blood cells (RBCs) infected with both P. falciparum and P. vivax parasites. The patterns of reactivity on the surface of the parasitised RBCs are very similar. The present observations support previous findings that PfCLAG9 may be a target of protective immune responses and raises the possibility that the cross reactive antibodies to PvCLAG7 in mixed infections play a role in regulate the fate of Plasmodium mixed infections.

摘要

PfCLAG9 因其免疫原性而被广泛研究。因此,该基因产物对于治疗干预和潜在疫苗候选物很重要。在来自巴西亚马逊地区朗多尼亚的恶性疟患者的血清中发现了针对恶性疟原虫抗原 PfCLAG9 选定序列的合成肽的抗体。在半免疫和免疫无症状寄生虫携带者中发现的抗体滴度要比在患有临床感染的患者中高得多,这与巴布亚新几内亚的原始发现相符。然而,来自同一亚马逊地区的间日疟患者(特别是无症状间日疟寄生虫携带者)的血清也与相同的肽强烈反应。生物信息学分析显示,恶性疟原虫 Pfclag9 与间日疟原虫 Pfclag9 之间存在相似性。间接荧光显微镜分析表明,在 BALB/c 小鼠中诱导的针对 PfCLAG9 肽的抗体与感染了恶性疟原虫和间日疟原虫的人红细胞(RBC)反应。寄生虫 RBC 表面的反应模式非常相似。目前的观察结果支持先前的发现,即 PfCLAG9 可能是保护性免疫反应的靶标,并提出了在混合感染中对 PvCLAG7 具有交叉反应性的抗体可能在调节疟疾混合感染的命运中发挥作用的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bbe/3974312/ede9dcc79ece/0074-0276-mioc-108-01-0098-gf01.jpg

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