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Association of the +874 T/A interferon gamma polymorphism with infections in sickle cell disease
Author(s) -
Joannes M. O.,
Loko G.,
Deloumeaux J.,
Chout R.,
MariannePepin T.
Publication year - 2010
Publication title -
international journal of immunogenetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.41
H-Index - 47
eISSN - 1744-313X
pISSN - 1744-3121
DOI - 10.1111/j.1744-313x.2010.00912.x
Subject(s) - genotype , immunology , allele , interferon gamma , disease , medicine , interferon , cytokine , biology , genetics , gene
Summary Infectious complications are a leading cause of morbidity and mortality in patients with sickle cell disease. Several mechanisms are supposed to contribute to this susceptibility. The exact reasons for the susceptibility of sickle cell patients to infection are not clear and are still a matter of debate. Interferon gamma (IFNγ) is a key cytokine involved mainly in the defence against intracellular pathogens. We investigated a possible association of an IFNγ +874 T/A polymorphism and infectious complications in sickle cell patients. Seventy‐two sickle cell patients were typed for +874 T/A IFNγ polymorphism. Genotype frequencies were different between cases and controls. Indeed, the T allele frequency was significantly higher in patients with infections than in patients without infections ( P = 0.014). Our results suggest that the +874 T/A IFNγ polymorphism is associated with infectious complications in sickle cell patients. T allele could be involved in infections in sickle cell patients.