Jiangsu Institute of Clinical Immunology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Medical Biotechnology Institute, Soochow University, Suzhou 215006, China ; Wuxi Red Cross Blood Center, Wuxi 214021, China.
Int J Genomics. 2014;2014:247637. doi: 10.1155/2014/247637. Epub 2014 Apr 3.
Objective. Programmed cell death 1 (PD-1) induces negative signals to T cells during interaction with its ligands and is therefore a candidate gene in the development of autoimmune diseases such as rheumatoid arthritis (RA). Herein, we investigate the association of PDCD-1 polymorphisms with the risk of RA among Chinese patients and healthy controls. Methods. Using the PCR-direct sequencing analysis, 4 PDCD-1 SNPs (rs36084323, rs11568821, rs2227982, and rs2227981) were genotyped in 320 RA patients and 309 matched healthy controls. Expression of PD-1 was determined in peripheral blood lymphocytes by flow cytometry and quantitative real-time reverse transcriptase polymerase chain reaction. Results. We observed that the GG genotype of rs36084323 was associated with a increased risk for developing RA (OR 1.70, 95% 1.11-2.61, P = 0.049). Patients carrying G/G genotype displayed an increased mRNA level of PD-1 (P = 0.04) compared with A/A genotype and healthy controls. Meanwhile, patients homozygous for rs36084323 had induced basal PD-1 expression on activated CD4+ T cells. Conclusion. The PDCD-1 polymorphism rs36084323 was significantly associated with RA risk in Han Chinese population. This SNP, which effectively influenced the expression of PD-1, may be a biomarker of early diagnosis of RA and a suitable indicator of utilizing PD-1 inhibitor for treatment of RA.
程序性细胞死亡 1(PD-1)在与配体相互作用时向 T 细胞诱导负信号,因此是类风湿关节炎(RA)等自身免疫性疾病发展的候选基因。在此,我们研究了 PDCD-1 多态性与中国患者和健康对照者 RA 风险的关联。
使用 PCR-直接测序分析,在 320 名 RA 患者和 309 名匹配的健康对照者中对 4 个 PDCD-1 SNP(rs36084323、rs11568821、rs2227982 和 rs2227981)进行了基因分型。通过流式细胞术和实时定量逆转录聚合酶链反应测定外周血淋巴细胞中 PD-1 的表达。
我们观察到 rs36084323 的 GG 基因型与发生 RA 的风险增加相关(OR 1.70,95%CI 1.11-2.61,P = 0.049)。与 A/A 基因型和健康对照者相比,携带 G/G 基因型的患者 PD-1 的 mRNA 水平升高(P = 0.04)。同时,rs36084323 纯合子患者在激活的 CD4+T 细胞上诱导了基础 PD-1 表达。
PDCD-1 多态性 rs36084323 与汉族人群的 RA 风险显著相关。该 SNP 有效影响 PD-1 的表达,可能是 RA 早期诊断的生物标志物,也是利用 PD-1 抑制剂治疗 RA 的合适指标。