PD-1基因多态性与多发性硬化易感性之间的关系。

IF 2.7 Q3 IMMUNOLOGY
Nasrin Hassani, Arash Salmaninejad, Saeed Aslani, Eskandar Kamali-Sarvestani, Mahmood Vessal
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引用次数: 2

摘要

程序性细胞死亡1 (PD-1)是一种免疫检查点,据报道与几种自身免疫性疾病有关。我们旨在研究人类PD-1基因(PDCD1)多态性与多发性硬化症(MS)之间的关系。本研究对229例多发性硬化症患者和246名健康对照者进行了病例对照研究。采用PCR-RFLP技术对rs36084323 (PD-1.1 G/A)、rs11568821 (PD-1.3 G/A)和rs2227981 (PD-1.5 C/T)多态性进行基因分型。PD-1.1基因型和等位基因频率(-536 G/A)在患者和健康对照组之间差异无统计学意义。对于PD-1.3, AA + AG基因型在对照组中相对较高。在PD-1.5 (+7785 C/T)中,MS患者T等位基因携带者(TT + CT)的频率相对较高,差异无统计学意义(p = .07)。PD-1基因多态性可能与MS有关;然而,准确的结论需要更多样本的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The association between PD-1 gene polymorphisms and susceptibility to multiple sclerosis.

Programmed cell death 1 (PD-1) is an immune checkpoint and has been reported to be associated with several autoimmune diseases. We aimed to investigate the association between human PD-1 gene (PDCD1) polymorphisms and multiple sclerosis (MS). This case-control study was conducted on 229 MS patients and 246 healthy controls. Genotyping of rs36084323 (PD-1.1 G/A), rs11568821 (PD-1.3 G/A) and rs2227981 (PD-1.5 C/T) polymorphisms was performed by PCR-RFLP technique. The frequency difference of PD-1.1 genotypes and alleles (-536 G/A) between patients and healthy controls was not significant. Regarding PD-1.3, the AA + AG genotype was found to be relatively higher in the control group. Concerning PD-1.5 (+7785 C/T), the frequency of T allele carriers (TT + CT) was relatively higher in MS patients, which was marginally insignificant (p = .07). PD-1 gene polymorphisms may be associated with MS; however, accurate conclusions require further studies with a larger number of samples.

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来源期刊
Immunological Medicine
Immunological Medicine Medicine-Immunology and Allergy
CiteScore
7.10
自引率
2.30%
发文量
19
审稿时长
19 weeks
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