Inhibitory Antibodies Specific for the 19-Kilodalton Fragment of Merozoite Surface Protein 1 Do Not Correlate with Delayed Appearance of Infection with Plasmodium falciparum in Semi-Immune Individuals in Vietnam

被引:17
|
作者
Murhandarwati, E. Elsa Herdiana [1 ]
Wang, Lina [1 ]
Black, Casilda G. [1 ]
Nhan, Doan Hanh [2 ]
Richie, Thomas L. [3 ]
Coppel, Ross L. [1 ]
机构
[1] Monash Univ, Dept Microbiol, Clayton, Vic 3800, Australia
[2] Inst Malariol Parasitol & Entomol, Hanoi, Vietnam
[3] USN, US Mil Malaria Vaccine Program, Med Res Ctr, Walter Reed Army Inst Res, Silver Spring, MD 20910 USA
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
C-TERMINAL FRAGMENT; 19-KDA FRAGMENT; PARASITE GROWTH; MALARIA; MECHANISMS; RESPONSES; CHILDREN; IMMUNOGENICITY; ACQUISITION; PROTECTION;
D O I
10.1128/IAI.00360-09
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inhibitory antibodies specific for the 19-kDa fragment of merozoite surface protein 1 (MSP1(19)) are a significant component of inhibitory responses in individuals immune to malaria. Nevertheless, conflicting results have been obtained in determining whether this antibody specificity correlates with protection in residents of areas where malaria is endemic. In this study, we examined sera collected from a population of semi-immune individuals living in an area of Vietnam with meso-endemicity during a 6-month period. We used two Plasmodium falciparum parasite lines that express either endogenous MSP1(19) or the homologous region from Plasmodium yoelii to measure the MSP1(19)-specific inhibitory activity. We showed that (i) the level of MSP1(19)-specific inhibitory antibodies was not associated with a delay in P. falciparum infection, (ii) MSP1(19)-specific inhibitory antibodies declined significantly during the convalescent period after infection, and (iii) there was no significant correlation between the MSP1(19)-specific inhibitory antibodies and the total antibodies measured by enzyme-linked immunosorbent assay. These results have implications for understanding naturally acquired immunity to malaria and for the development and evaluation of MSP1(19)-based vaccines.
引用
收藏
页码:4510 / 4517
页数:8
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