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PDL1 基因 rs4143815 多态性与伊朗东北部无症状献血者 HTLV-1 感染和前病毒载量的关联。

Association of the rs4143815 polymorphism of PDL1 gene with HTLV-1 infection and proviral load in asymptomatic blood donors in northeast Iran.

机构信息

Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.

出版信息

Microbiol Immunol. 2022 Jun;66(6):324-329. doi: 10.1111/1348-0421.12976. Epub 2022 Apr 12.

DOI:10.1111/1348-0421.12976
PMID:35289428
Abstract

It is obvious that genetic differences, including mutations and polymorphisms, can play an important role in viral infections. In this case-control study, which included 81 human T-cell leukemia virus type 1 (HTLV-1) asymptomatic carriers (AC) and 162 healthy controls (HC), the rs4143815 polymorphism of PDL1 gene was investigated. This polymorphism is the site of miR-570 binding and it can influence immune system responses. The rs4143815 polymorphism was evaluated by allele-specific polymerase chain reaction (AS-PCR) and the proviral load levels by quantitative real-time PCR (q PCR). The results demonstrated that the C allele (P = 0.027) and the CC genotype (P = 0.031) of rs4143815 polymorphism was significantly higher in the AC group than in the HC group, also the proviral load in the AC group with the C allele (P = 0.020) was significantly higher. Thus, the rs4143815 polymorphism can play a vital role in HTLV-1 infection.

摘要

很明显,遗传差异,包括突变和多态性,可能在病毒感染中发挥重要作用。在这项包括 81 例人类 T 细胞白血病病毒 1 型(HTLV-1)无症状携带者(AC)和 162 例健康对照(HC)的病例对照研究中,研究了 PDL1 基因的 rs4143815 多态性。该多态性是 miR-570 结合的位点,可影响免疫系统反应。通过等位基因特异性聚合酶链反应(AS-PCR)评估 rs4143815 多态性,通过定量实时 PCR(qPCR)评估前病毒载量水平。结果表明,rs4143815 多态性的 C 等位基因(P=0.027)和 CC 基因型(P=0.031)在 AC 组中显著高于 HC 组,AC 组中具有 C 等位基因的前病毒载量(P=0.020)也显著升高。因此,rs4143815 多态性在 HTLV-1 感染中可能起重要作用。

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引用本文的文献

1
Analysis of Programmed Cell Death-1 (PD-1) Gene Variations (re11568821 and rs41386349) in HTLV-1 Infection Using One Primer Pair and Proviral Load.利用一条引物和前病毒载量分析 HTLV-1 感染中的程序性细胞死亡受体-1(PD-1)基因变异(re11568821 和 rs41386349)
J Mol Evol. 2023 Aug;91(4):562-566. doi: 10.1007/s00239-023-10104-5. Epub 2023 Apr 5.