Association of the TNF-α, IL-2, and IL-2RB gene variants with susceptibility to psoriasis in a Turkish cohort

被引:6
作者
Gulel, Aslihan [1 ]
Inaloz, Huseyin Serhat [1 ]
Nursal, Ayse Feyda [2 ]
Sever, Tugce [1 ]
Pehlivan, Sacide [3 ]
机构
[1] Gaziantep Univ, Dept Dermatol, Fac Med, Gaziantep, Turkey
[2] Hitit Univ, Dept Med Genet, Fac Med, Corum, Turkey
[3] Istanbul Univ, Dept Med Biol, Istanbul Fac Med, Istanbul, Turkey
关键词
psoriasis; tumour necrosis factor alpha; variant; interleukin; 2; IL-2 receptor beta; JUVENILE-ONSET PSORIASIS; PROMOTER POLYMORPHISM; JAPANESE PATIENTS; SPANISH PATIENTS; HAN POPULATION; SERUM-LEVELS; T-CELLS; ARTHRITIS; REGION; VULGARIS;
D O I
10.5114/ceji.2018.74873
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim of the study: The aim of this study was to investigate the role TNF-alpha, IL-2, and IL-2RB variants in psoriasis (Ps) and to evaluate the association between these variants and clinical features. Material and methods: A total of 74 psoriatic patients and 74 healthy individuals were genotyped for these variants by PCR and/or RFLP. Results: The AA genotype of TNF-alpha (-308) was significantly more common in the patients (p = 0.013). TIVF-alpha (-238) AA genotype was significantly increased in the patients (p = 0.028), while the GG genotype was decreased in the patient group, compared to the controls (p = 0.016). IL-2 (-330) variant GG and TT genotype was more common in the patients (p = 0.037, p = 0.009, respectively), while IL-2 (-330) GT genotype was increased in the control subjects (p = 0.001). IL-2 (-330) GG genotype frequency was significantly decreased (p = 0.021) and the TT genotype frequency was significantly increased among patients with psoriatic arthritis in comparison with Ps patients (p = 0.014). IL-2RB TC genotype frequency was significantly decreased and TT genotype frequency was significantly increased in the patients with positive family history of Ps compared to those who had a negative family history (p = 0.017, p = 0.014, respectively). Also, IL-2RB CC genotype was significantly increased among the patients with late-onset Ps in comparison with the early onset Ps group (p = 0.009). The frequency of IL-2 (-330) TT genotype was significantly higher in mild Ps patients than moderate-severe patients (p = 0.043). Conclusions: Our data suggest a potential role of these genes as candidate genes for susceptibility to Ps in a Turkish cohort.
引用
收藏
页码:50 / 57
页数:8
相关论文
共 39 条
[1]   Serum levels of proinflammatory cytokines in psoriasis patients from Saudi Arabia [J].
Abanmi, A ;
Al Harthi, F ;
Khan, HA ;
Tariq, M .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2005, 44 (01) :82-83
[2]   TNF-α promoter polymorphisms in multiple sclerosis: no association with-308 and-238 alleles, but the-857 alleles in associated with the disease in Turkish patients [J].
Akcali, A. ;
Pehlivan, S. ;
Pehlivan, M. ;
Sever, T. ;
Akgul, P. ;
Neyal, M. .
INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2010, 37 (02) :91-95
[3]  
Arias AI, 1997, EXP CLIN IMMUNOGENET, V14, P118
[4]   Cytokines in psoriasis [J].
Baliwag, Jaymie ;
Barnes, Drew H. ;
Johnston, Andrew .
CYTOKINE, 2015, 73 (02) :342-350
[5]  
Baran W, 2006, ACTA DERMATOVEN ALP, V15, P113
[6]   Association between psoriasis and polymorphisms in the TNF, IL12B, and IL23R genes in Spanish patients [J].
Cabaleiro, Teresa ;
Roman, Manuel ;
Gallo, Elena ;
Ochoa, Dolores ;
Tudelilla, Fatima ;
Talegon, Maria ;
Prieto-Perez, Rocio ;
Garcia-Diez, Amaro ;
Dauden, Esteban ;
Abad-Santos, Francisco .
EUROPEAN JOURNAL OF DERMATOLOGY, 2013, 23 (05) :640-645
[7]   Genetic and epigenetic basis of psoriasis pathogenesis [J].
Chandra, Aditi ;
Ray, Aditi ;
Senapati, Swapan ;
Chatterjee, Raghunath .
MOLECULAR IMMUNOLOGY, 2015, 64 (02) :313-323
[8]   Cytokine gene polymorphisms in Chinese patients with psoriasis [J].
Chang, Y. T. ;
Chou, C. T. ;
Yu, C. W. ;
Lin, M. W. ;
Shiao, Y. M. ;
Chen, C. C. ;
Huang, C. H. ;
Lee, D. D. ;
Liu, H. N. ;
Wang, W. J. ;
Tsai, S. F. .
BRITISH JOURNAL OF DERMATOLOGY, 2007, 156 (05) :899-905
[9]   Psoriasis as a disease associated with the immune system disorders [J].
Chomiczewska-Skora, Dorota ;
Trznadel-Grodzka, Ewa ;
Rotsztejn, Helena .
CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY, 2013, 38 (01) :129-133
[10]  
DALFONSO S, 1994, IMMUNOGENETICS, V39, P150