Human antibodies to the polymorphic block 2 domain of the Plasmodium falciparum merozoite surface protein 1 (MSP-1) exhibit a highly skewed, peptide-specific light chain distribution

被引:3
|
作者
Jouin, H
Garraud, O
Longacre, S
Baleux, F
Mercereau-Puijalon, O
Milon, G
机构
[1] Inst Pasteur, Parasite Mol Immunol Unit, CNRS, URA 2581, F-75724 Paris, France
[2] Inst Pasteur, INSERM, U547, F-59019 Lille, France
[3] Univ St Etienne, Fac Med, EA 3064, GIMAP, St Etienne, France
[4] Inst Pasteur, Organ Chem Unit, Paris, France
[5] Inst Pasteur, Immunophysiol & Intracellular Parasitism Unit, Paris, France
来源
IMMUNOLOGY AND CELL BIOLOGY | 2005年 / 83卷 / 04期
关键词
antibodies; antigenic peptide/epitope; human; immunoglobulin light chain; protozoan parasite;
D O I
10.1111/j.1440-1711.2005.01343.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Antibodies to polymorphic block 2 of the Plasmodium falciparum merozoite surface protein 1 (MSP-1) present a paradoxical association with acquired protection against clinical malaria, while showing restricted and fixed specificity, reminiscent of antigenic sin. We report here that these antibodies present a highly imbalanced, peptide-specific light chain distribution. This was not observed with several other parasite-derived peptides or antigens. These data point to a skewed immune response to MSP-1 block 2 that is constrained both in specificity and chain usage. This is the first report of a biased response to polymorphic epitopes of a surface antigen in malaria parasites.
引用
收藏
页码:392 / 395
页数:4
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