The sickle cell trait is associated with enhanced immunoglobulin G antibody responses to Plasmodium falciparum variant surface antigens.
Publication year
2005Source
The Journal of Infectious Diseases, 191, 10, (2005), pp. 1631-8ISSN
Publication type
Article / Letter to editor
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Organization
Medical Microbiology
Journal title
The Journal of Infectious Diseases
Volume
vol. 191
Issue
iss. 10
Page start
p. 1631
Page end
p. 8
Subject
N4i 1: Pathogenesis and modulation of inflammation; UMCN 4.1: Microbial pathogenesis and host defenseAbstract
The sickle cell trait (HbAS) protects against severe Plasmodium falciparum malaria in young African children. We investigated the extent of the association between HbAS and antibodies directed to parasite-derived variant surface antigens (VSAs) on the membrane of infected erythrocytes. We measured immunoglobulin G (IgG) responses with specificity for VSAs of 2 heterologous parasite isolates in 458 Gabonese children aged between 6 months and 11 years. Logistic regression analyses showed a highly significant independent association (P<.001) between carriage of HbAS and the presence of IgG anti-VSA responses; this association was related specifically to IgG1 and IgG4 subclasses in the anti-VSA profile. IgG2 and IgG3 anti-VSA responses were both independently associated with older age, consistent with the pattern observed in semi-immune adults. The results imply that enhanced levels of cross-reactive anti-VSA responses in children with HbAS may be intimately associated with the protection they have against malaria.
This item appears in the following Collection(s)
- Academic publications [246625]
- Faculty of Medical Sciences [93367]
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