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- Title
Proinflammatory cytokine gene single nucleotide polymorphisms in common variable immunodeficiency.
- Authors
Rezaei, Nima; Amirzargar, A. A.; Shakiba, Y.; Mahmoudi, M.; Moradi, B.; Aghamohammadi, A.
- Abstract
Common variable immunodeficiency (CVID) is a heterogeneous group of primary immunodeficiency diseases. Cytokine production could be affected in CVID patients, whereas its alteration could be due to genetic polymorphisms within coding and promoter regions of the cytokine genes. This study was performed to analyse the proinflammatory cytokine single nucleotide polymorphisms in CVID. The allele and genotype frequencies of a number polymorphic genes coding tumour necrosis factor (TNF)-α, interleukin (IL)-1α, IL-1β, IL-1R, IL-1RA and IL-6 were investigated and compared between two groups of CVID patients and controls. The IL-6 GA genotype at position nt565 was significantly over-represented in the patient group ( P < 0·001), while the IL-6 GG genotype at position −174 ( P = 0·006) and the GG genotype at position nt565 ( P < 0·001) were significantly lower than controls. The TNF-α AG genotype at position −308 in the patient group was increased significantly in comparison with controls ( P = 0·027), but the GG genotype at the same position was significantly decreased ( P = 0·011). IL-6 CA and GA haplotypes were the most frequent haplotypes in the patients ( P < 0·005), whereas TNF-α GA ( P = 0·002) and IL-6 GG ( P < 0·001) haplotypes were decreased significantly in the patients in comparison with controls. Cytokine single nucleotide polymorphisms could have a role in pathophysiology of CVID. High production of TNF-α is expected in some CVID patients based on the frequency of genotypes/haplotypes of these cytokine gene polymorphisms.
- Subjects
IMMUNODEFICIENCY; TUMOR necrosis factors; CYTOKINES; GENETIC polymorphism research; INTERLEUKIN-6; THERAPEUTICS
- Publication
Clinical & Experimental Immunology, 2009, Vol 155, Issue 1, p21
- ISSN
0009-9104
- Publication type
Article
- DOI
10.1111/j.1365-2249.2008.03790.x