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韩国系统性红斑狼疮患者的肿瘤坏死因子β基因多态性

TNFB gene polymorphism in patients with systemic lupus erythematosus in Korean.

作者信息

Kim H Y, Lee S H, Yang H I, Park S H, Cho C S, Kim T G, Han H, Kim D J

机构信息

Department of Internal Medicine, Microbiology, Catholic University, Medical College, Seoul, Korea.

出版信息

Korean J Intern Med. 1995 Jul;10(2):130-6. doi: 10.3904/kjim.1995.10.2.130.

Abstract

OBJECTIVES

To elucidate the gene frequency of TNFB Ncol polymorphism and its association with HLA class II antigen in patients with systemic lupus erythematosus(SLE) in Korea.

METHODS

We investigated the gene frequency of the TNFB alleles using DNA obtained from peripheral mononuclar cells in 141 healthy controls and in 58 patients with SLE. The polymorphisms of TNFB gene (735 bp) were studied by Ncol PCR-RELP. A portion of TNFB gene(735 bp) was amplified by PCR and its products were digested with Ncol restriction enzyme. The digested samples of amplified DNA were analyzed by agarose gel electrophoresis. TNFB1 and TNFB2 alleles were identified according to polymorphic fragments on Ncol restriction site in the first intron of the TNFB gene. The generic types of HLA-DRBI were also determined by PCR with sequence specific primers(SSP) using genomic DNA from the same subjects.

RESULTS

The genotypic frequency of TNFB2 homozygote was significantly increased in patients with SLE compared with controls(RR = 2.36, P = 0.011). The frequency of HLA-DRBI15 was also significantly increased in patients (RR = 2.27, P = 0.029). However, the increased frequency of TNFB2 homozygote was apparently increased in nephritis group (RR = 2.79, P = 0.035), whereas the significance of TNFB2 homozygote was weakend in non-nephritis group.

CONCLUSIONS

Our results suggest that genetic predisposition of TNFB2 homozygote is another risk factor in Korean SLE, especially in DR2 negative patients. In addition, TNFB2 homozygote could have a tendency for the development of nephritis in patients with SLE.

摘要

目的

阐明韩国系统性红斑狼疮(SLE)患者中TNFB Ncol多态性的基因频率及其与HLA II类抗原的关联。

方法

我们使用从141名健康对照者和58名SLE患者外周血单个核细胞中提取的DNA,研究TNFB等位基因的基因频率。通过Ncol PCR-RELP研究TNFB基因(735 bp)的多态性。用PCR扩增TNFB基因的一部分(735 bp),其产物用Ncol限制性内切酶消化。通过琼脂糖凝胶电泳分析扩增DNA的消化样品。根据TNFB基因第一内含子Ncol限制性位点的多态性片段鉴定TNFB1和TNFB2等位基因。还使用来自同一受试者的基因组DNA,通过序列特异性引物(SSP)PCR测定HLA-DRBI的基因型。

结果

与对照组相比,SLE患者中TNFB2纯合子的基因型频率显著增加(RR = 2.36,P = 0.011)。患者中HLA-DRBI15的频率也显著增加(RR = 2.27,P = 0.029)。然而,TNFB2纯合子频率的增加在肾炎组中明显增加(RR = 2.79,P = 0.035),而在非肾炎组中TNFB2纯合子的显著性减弱。

结论

我们的结果表明,TNFB2纯合子的遗传易感性是韩国SLE患者的另一个危险因素,尤其是在DR2阴性患者中。此外,TNFB2纯合子可能使SLE患者有发生肾炎的倾向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ad/4532044/dbd8abbfeddf/kjim-10-2-130-8f1.jpg

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