Suppr超能文献

TIM-3 基因变异通过干扰 CD4+T 细胞中的干扰素 γ 影响骨关节炎易感性。

TIM-3 Genetic Variations Affect Susceptibility to Osteoarthritis by Interfering with Interferon Gamma in CD4+ T Cells.

机构信息

Department of Orthopedics, Qianfoshan Hospital, Shandong University, 16766 Jing Shi Road, Jinan, Shandong, 250014, China,

出版信息

Inflammation. 2015 Oct;38(5):1857-63. doi: 10.1007/s10753-015-0164-7.

Abstract

Osteoarthritis (OA) is the most common type of arthritis, in which T cell responses and cytokines may play critical roles in the development of the disease. TIM-3 may affect immune responses and is correlated with decreased expression of interferon gamma (INF-γ) in CD4+ T cells. In the current study, we investigated the association between polymorphisms in the TIM-3 gene and susceptibility to OA. Two polymorphisms in TIM-3, -574G/T and +4259T/G polymorphisms, were identified in OA cases and healthy donors by polymerase chain reaction-restriction fragment length polymorphism method. Data revealed that the prevalence of TIM-3 +4259T/G genotype was significantly elevated in OA patients than in the healthy donors after adjustment (Odds ratio [OR] = 2.67, 95% confidence interval [CI] 1.32-5.11, P < 0.001). Similarly, the TIM-3 +4259G allele presented a positive association with the risk of OA after adjustment (OR = 2.58, 95% CI 1.29-4.82, P = 0.003). The TIM-3 -574G/T polymorphism did not show any correlation with the disease. We further examined whether the two TIM-3 polymorphisms could affect INF-γ expression in CD4+ T cells. Data revealed that subjects carrying polymorphic +4259TG genotype had significantly higher mRNA and protein levels of INF-γ in CD4+ T cells compared to wild-type GG genotype (P < 0.001 and P < 0.01). These results indicated that TIM-3 polymorphism is associated with increased susceptibility to OA possibly by upregulating INF-γ expression in CD4+ T cells.

摘要

骨关节炎(OA)是最常见的关节炎类型,其中 T 细胞反应和细胞因子可能在疾病的发展中起关键作用。TIM-3 可能影响免疫反应,并与 CD4+T 细胞中干扰素γ(INF-γ)表达降低相关。在本研究中,我们研究了 TIM-3 基因多态性与 OA 易感性的关系。通过聚合酶链反应-限制性片段长度多态性方法,在 OA 病例和健康供体中鉴定了 TIM-3 的两个多态性-574G/T 和 +4259T/G 多态性。数据显示,TIM-3 +4259T/G 基因型在 OA 患者中的患病率明显高于健康供体(调整后的优势比[OR] = 2.67,95%置信区间[CI] 1.32-5.11,P < 0.001)。同样,调整后,TIM-3 +4259G 等位基因与 OA 发病风险呈正相关(OR = 2.58,95%CI 1.29-4.82,P = 0.003)。TIM-3 -574G/T 多态性与疾病无任何关联。我们进一步检查了这两个 TIM-3 多态性是否能影响 CD4+T 细胞中 INF-γ 的表达。数据显示,携带多态性 +4259TG 基因型的受试者 CD4+T 细胞中 INF-γ 的 mRNA 和蛋白水平明显高于野生型 GG 基因型(P < 0.001 和 P < 0.01)。这些结果表明,TIM-3 多态性与 OA 的易感性增加有关,可能是通过上调 CD4+T 细胞中 INF-γ 的表达。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验