Association of the+874 T/A interferon gamma polymorphism with infections in sickle cell disease

被引:4
作者
Joannes, M. O.
Loko, G.
Deloumeaux, J. [2 ]
Chout, R. [3 ]
Marianne-Pepin, T. [1 ]
机构
[1] Univ Antilles Guyane, UFR Sci Exactes & Nat, Dept Biol, Campus Fouillole,BP592, F-97157 Pointe A Pitre, Guadeloupe, France
[2] Ctr Hosp Univ Pointe A Pitre, Dept Med Informat, Pointe A Pitre, Guadeloupe, France
[3] Ctr Hosp Univ Pointe A Pitre, Lab Hematol Immunol, F-97159 Pointe A Pitre, Guadeloupe, France
关键词
CHILDREN; SEPTICEMIA; GENE; MENINGITIS; DEFICIENCY;
D O I
10.1111/j.1744-313X.2010.00912.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
P>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 (IFN gamma) is a key cytokine involved mainly in the defence against intracellular pathogens. We investigated a possible association of an IFN gamma +874 T/A polymorphism and infectious complications in sickle cell patients. Seventy-two sickle cell patients were typed for +874 T/A IFN gamma 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 IFN gamma polymorphism is associated with infectious complications in sickle cell patients. T allele could be involved in infections in sickle cell patients.
引用
收藏
页码:219 / 223
页数:5
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