Hou Wei, Xia Bing, Yuan Anlong, Li Jin, Yang Zhanqiu, Mao Lin
Department of Internal Medicine and Research Center of Digestive Diseases, Wuhan University Zhongnan Hospital, Wuhan, China.
Inflamm Bowel Dis. 2005 Jul;11(7):653-6. doi: 10.1097/01.mib.0000165112.25934.36.
Ulcerative colitis (UC) is characterized by chronic inflammation of the colon and rectum as a result of an exaggerated T-cell response. Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) is a T cell-restricted surface molecule induced with TCR or CD28 activation. There is evidence for genetic involvement of CTLA-4 in several autoimmune diseases, with the focus on the possible role of genetic variation of the CTLA-4 locus. The aim of this study was to investigate CTLA-4 gene polymorphisms in patients with UC in a Chinese population with Han nationality.
The C-318T polymorphism in the promoter region and A+49G polymorphism in exon 1 of the CTLA-4 gene were studied by a polymerase chain reaction-sequence-specific primer method. We studied 82 unrelated patients with UC and 204 healthy controls in a Chinese population with Han nationality.
The frequency of the haplotype 2,3 (-318C+49G/-318T+49A) was 26% in patients with UC and 41% in healthy controls (Fisher exact test P = 0.0147, odds ratio = 0.4918, 95% confidence interval: 0.2784 - 0.8688), but this significance disappeared when Bonferoni correction was applied. No other significant differences in the distribution of allele and genotype frequencies were observed between C-318T and A+49G gene polymorphisms and UC in the Chinese Han population.
The C-318T and A+49G polymorphisms of the CTLA-4 gene were not associated with UC in Chinese Han patients.
溃疡性结肠炎(UC)的特征是结肠和直肠的慢性炎症,这是由于T细胞反应过度所致。细胞毒性T淋巴细胞相关抗原4(CTLA-4)是一种T细胞限制性表面分子,在TCR或CD28激活时被诱导产生。有证据表明CTLA-4基因参与了几种自身免疫性疾病,重点关注CTLA-4基因座的遗传变异可能发挥的作用。本研究的目的是调查中国汉族人群中UC患者的CTLA-4基因多态性。
采用聚合酶链反应-序列特异性引物法研究CTLA-4基因启动子区的C-318T多态性和外显子1的A+49G多态性。我们在中国汉族人群中研究了82例无亲缘关系的UC患者和204例健康对照。
单倍型2,3(-318C+49G/-318T+49A)在UC患者中的频率为26%,在健康对照中的频率为41%(Fisher精确检验P = 0.0147,优势比 = 0.4918,95%置信区间:0.2784 - 0.8688),但应用Bonferroni校正后该显著性消失。在中国汉族人群中,C-318T和A+49G基因多态性与UC之间在等位基因和基因型频率分布上未观察到其他显著差异。
CTLA-4基因的C-318T和A+49G多态性与中国汉族UC患者无关。