Cavanagh David R, Dodoo Daniel, Hviid Lars, Kurtzhals Jørgen A L, Theander Thor G, Akanmori Bartholomew D, Polley Spencer, Conway David J, Koram Kojo, McBride Jana S
Institute of Cell, Animal and Population Biology, School of Biological Sciences, University of Edinburgh, King's Buildings, West Mains Rd., EH9 3JT, Scotland, UK.
Infect Immun. 2004 Nov;72(11):6492-502. doi: 10.1128/IAI.72.11.6492-6502.2004.
This longitudinal prospective study shows that antibodies to the N-terminal block 2 region of the Plasmodium falciparum merozoite surface protein 1 (MSP-1) are associated with protection against clinical malaria in an area of stable but seasonal malaria transmission of Ghana. Antibodies to the block 2 region of MSP-1 were measured in a cohort of 280 children before the beginning of the major malaria transmission season. The cohort was then actively monitored for malaria, clinically and parasitologically, over a period of 17 months. Evidence is presented for an association between antibody responses to block 2 and a significantly reduced risk of subsequent clinical malaria. Furthermore, statistical survival analysis provides new information on the duration of the effect over time. The results support a conclusion that the block 2 region of MSP-1 is a target of protective immunity against P. falciparum and, thus, a promising new candidate for the development of a malaria vaccine.
这项纵向前瞻性研究表明,在加纳疟疾传播稳定但有季节性的地区,针对恶性疟原虫裂殖子表面蛋白1(MSP-1)N端2区的抗体与预防临床疟疾有关。在280名儿童组成的队列中,于主要疟疾传播季节开始前检测了针对MSP-1 2区的抗体。随后对该队列进行了为期17个月的疟疾临床和寄生虫学主动监测。有证据表明,针对2区的抗体反应与随后临床疟疾风险显著降低之间存在关联。此外,统计生存分析提供了关于该效应随时间持续时间的新信息。这些结果支持这样一个结论,即MSP-1的2区是针对恶性疟原虫的保护性免疫靶点,因此是开发疟疾疫苗的一个有前景的新候选对象。