Centre for Malaria and Tropical Diseases, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Rua da Junqueira, 100, Lisbon, 1349-008, Portugal.
Malar J. 2013 Mar 18;12:100. doi: 10.1186/1475-2875-12-100.
The malaria caused by Plasmodium falciparum remains a serious public health problem in the world, due largely to the absence of an effective vaccine. There is a lack of information on the structural properties and antigens capable of activating the immunological mechanisms for the induction of protective immunity. Therefore, the objective of this study is to evaluate the serological reactivity of sera from individuals with imported malaria and identify major immunogenic proteins.
The study was conducted in 227 individuals with imported malaria and 23 healthy individuals who had never been in areas endemic for malaria. The determination of anti-P. falciparum IgG antibodies was performed by an ELISA validated and optimized for this study. Sera showing higher reactivity to anti-P. falciparum by ELISA were analysed by immunoblotting and immunogenic proteins were identified by mass spectroscopy.
The results of anti-P. falciparum antibodies research by ELISA indicates 78 positive, 137 negative and 12 indeterminate sera. Analysis of immunoblotting demonstrated a consistent pattern with respect to immunoreactivity of antigens with molecular weights in the range of 40 to 60 kDa. Between 40 and 60 kDa six immunogenic proteins were identified: elongation factor-1 alpha (EF-1α), protein disulphide isomerase (PDI); phosphoglycerate kinase (PGK); 78 kDa glucose-regulated protein homologue (GRP-78); rhoptry-associated protein 2 (RAP-2) and rhoptry-associated protein 3 (RAP-3).
It was identified immunogenic proteins essential for parasite survival in the host, two of which (RAP-2 and RAP-3) are already described in the literature as proteins that play an important role in the invasion of erythrocytes by extracellular merozoites.
由于缺乏有效的疫苗,恶性疟原虫引起的疟疾仍然是世界上严重的公共卫生问题。目前缺乏关于能够激活免疫机制诱导保护性免疫的结构特性和抗原的信息。因此,本研究的目的是评估来自输入性疟疾个体的血清的血清学反应性,并鉴定主要免疫原性蛋白。
该研究在 227 名输入性疟疾患者和 23 名从未去过疟疾流行地区的健康个体中进行。通过 ELISA 测定抗疟原虫 IgG 抗体,该 ELISA 经过验证并为本研究进行了优化。通过 ELISA 显示对抗疟原虫具有更高反应性的血清进行免疫印迹分析,并通过质谱鉴定免疫原性蛋白。
ELISA 检测抗疟原虫抗体的结果表明,78 份血清为阳性,137 份血清为阴性,12 份血清为不确定。免疫印迹分析显示,抗原与分子量在 40 至 60 kDa 范围内的免疫反应性具有一致的模式。在 40 至 60 kDa 之间,鉴定出 6 种免疫原性蛋白:延伸因子-1α(EF-1α)、蛋白二硫键异构酶(PDI)、磷酸甘油酸激酶(PGK)、78 kDa 葡萄糖调节蛋白同源物(GRP-78)、泡颈相关蛋白 2(RAP-2)和泡颈相关蛋白 3(RAP-3)。
鉴定出了寄生虫在宿主中生存所必需的免疫原性蛋白,其中两种(RAP-2 和 RAP-3)已在文献中描述为在细胞外裂殖子入侵红细胞中起重要作用的蛋白。