期刊
JOURNAL OF INFECTIOUS DISEASES
卷 225, 期 10, 页码 1786-1790出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiab548
关键词
IgG3 hinge region; cerebral malaria; polymorphism; IGHG3 gene; Plasmodium falciparum
资金
- Ministry of Foreign Affairs of Denmark (DFC) [14-P01-GHA]
- Multilateral Initiative on Malaria-Training in Tropical Diseases (MIM-TDR project) [A11034]
The study found an increased risk of cerebral malaria in Plasmodium falciparum-infected Ghanaian children with medium IgG3 hinge region length.
Cerebral malaria (CM) may cause death or long-term neurological damage in children, and several host genetic risk factors have been reported. Malaria-specific immunoglobulin (Ig) G3 antibodies are crucial to human immune response against malaria. The hinge region of IgG3 exhibits length polymorphism (with long [L], medium [M], and short [S] alleles), which may influence its functionality. We studied IgG3 hinge region length polymorphisms in 136 Ghanaian children with malaria. Using logistic regression models, we found that children with the recessive MM allotype encoding medium IgG3 hinge region length had an increased risk of CM (adjusted odds ratio, 6.67 [95% confidence interval,1.30-34.32]; P=.004) . This has implications for future epidemiological studies on CM. The hinge region of immunoglobulin (Ig) G3 exhibits length polymorphism (long, medium, and short alleles), which may influence its functionality. We found an increased risk of cerebral malaria in Plasmodium falciparum-infected Ghanaian children with medium IgG3 hinge region length.
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