Possible contribution of chemokine receptor CCR2 and CCR5 polymorphisms in the pathogenesis of chronic spontaneous autoreactive urticaria

被引:9
作者
Brzoza, Z. [1 ]
Grzeszczak, W. [2 ]
Rogala, B. [1 ]
Trautsolt, W. [2 ]
Moczulski, D. [3 ]
机构
[1] Med Univ Silesia, Allergol & Clin Immunol, Chair & Clin Dept Internal Dis, PL-40007 Katowice, Poland
[2] Med Univ Silesia, Diabetol & Nephrol, Chair & Clin Dept Internal Dis, PL-40007 Katowice, Poland
[3] Med Univ Lodz, Chair & Clin Dept Internal Dis & Nephrodiabetol, Lodz, Poland
关键词
CCR2; CCR5; Chronic urticaria; Polymorphism; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS; TYROSINE-PHOSPHATASE; GENE POLYMORPHISMS; DIABETES-MELLITUS; ASSOCIATION; ASTHMA; LYMPHOCYTES; EXPRESSION; DELETION;
D O I
10.1016/j.aller.2013.02.003
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Autoimmune mechanisms play a role in the pathophysiology of chronic urticaria. As the genetic background of autoimmunity is well proven, the role of genetics in chronic urticaria is hypothesised. Methods: 153 unrelated chronic spontaneous urticaria patients with a positive result of autologous serum skin test were included into the study, as were 115 healthy volunteers as control group. In all subjects we analysed CCR2 G190A and CCR5 d32 polymorphisms. Results: We noticed higher prevalence of CCR2 A allele as well as lower frequency of CCR5 d32 in chronic urticaria group in comparison to control group, with borderline statistical significance. Additionally, we assumed haplotype Gd statistically significant negative chronic urticaria association with tendency to higher frequency of Aw haplotype in this group. Conclusions: The results of our study imply the role of autoimmune components in chronic urticaria pathogenesis and present chronic urticaria as possibly genetically related disorder. (C) 2012 SEICAP. Published by Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:302 / 306
页数:5
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