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Allelic family-specific humoral responses to merozoite surface protein 2 (MSP2) in Gabonese residents with Plasmodium falciparum infections

机译:加蓬恶性疟原虫感染者对裂殖子表面蛋白2(MSP2)的等位基因家族特异性体液反应

摘要

Merozoite surface protein 2 (MSP2) expressed by Plasmodium falciparum asexual blood stages has been identified as a promising vaccine candidate. In order to explore allelic family-specific humoral responses which may be responsible for parasite neutralization during natural infections, isolates from individuals with either asymptomatic infections or uncomplicated malaria and residing in a Central African area where Plasmodium transmission is high and perennial, were analysed using MSP2 as polymorphic marker. The family-specific antibody responses were assessed by ELISA using MSP2 synthetic peptides. We observed an age-dependence of P. falciparum infection complexity. The decrease of infection complexity around 15 years of age was observed simultaneously with an increase in the mean number of MSP2 variants recognized. No significant difference in the P. falciparum genetic diversity and infection complexity was found in isolates from asymptomatic subjects and patients with uncomplicated malaria. The longitudinal follow-up showed a rapid development of immune responses to various regions of MSP2 variants within one week. Comparing humoral responses obtained with the other major antigen on the merozoite surface, MSP1, our findings suggest that different pathways of responsiveness are involved in antibody production to merozoite surface antigens.
机译:恶性疟原虫无性血液阶段表达的裂殖子表面蛋白2(MSP2)已被确认为有前途的疫苗候选物。为了探索可能导致自然感染过程中寄生虫中和的等位基因家族特异性体液反应,使用MSP2分析了无症状感染或疟疾简单且居住在中非疟原虫传播频繁且多年生的个体的分离株。作为多态标记。使用MSP2合成肽通过ELISA评估家族特异性抗体反应。我们观察到了恶性疟原虫感染的年龄依赖性。同时观察到大约15岁时感染复杂性的降低,以及公认的MSP2变体平均数量的增加。在无症状受试者和无并发症疟疾患者的分离物中,恶性疟原虫的遗传多样性和感染复杂性没有显着差异。纵向随访显示在一周内对MSP2变体各个区域的免疫反应迅速发展。比较与裂殖子表面上的其他主要抗原(MSP1)获得的体液反应,我们的发现表明,对裂殖子表面抗原的抗体生产涉及不同的反应途径。

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