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CD209(DC-SIGN)-336A>G 启动子多态性与香港华人的严重急性呼吸综合征。

CD209 (DC-SIGN) -336A>G promoter polymorphism and severe acute respiratory syndrome in Hong Kong Chinese.

机构信息

Department of Pathology, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong SAR, China.

出版信息

Hum Immunol. 2010 Jul;71(7):702-7. doi: 10.1016/j.humimm.2010.03.006. Epub 2010 May 4.

Abstract

CD209 (DC-SIGN) is an important C-type lectin which acts a receptor of many pathogens. The single nucleotide polymorphism (SNP) -336A>G in the CD209 promoter has been demonstrated to regulate promoter activity and to be associated with several important infectious diseases, such as human immunodeficiency virus-1 (HIV-1), Mycobacterium tuberculosis, and Dengue fever. CD209 facilitates severe acute respiratory syndrome (SARS)-coronavirus spike protein-bearing pseudotype driven infection of permissive cells in vitro. In keeping with previously published findings, our in vitro studies confirmed that this SNP modulates gene promoter activity. Genetic association analysis of this SNP with clinico-pathologic outcomes in 824 serologic confirmed SARS patients showed that the -336AG/GG genotype SARS patients was associated with lower standardized lactate-dehydrogenase (LDH) levels compared with the -336AA patients (p = 0.014, odds ratio = 0.40). High LDH levels are known to be an independent predictor for poor clinical outcome, probably related to tissue destruction from immune hyperactivity. Hence, SARS patients with the CD209 -336 AA genotype carry a 60% chance of having a poorer prognosis. This association is in keeping with the role of CD209 in modulating immune response to viral infection. The relevance of these findings for other infectious diseases and inflammatory conditions would be worth investigating.

摘要

CD209(DC-SIGN)是一种重要的 C 型凝集素,作为许多病原体的受体。已经证明 CD209 启动子中的单核苷酸多态性(SNP)-336A>G 调节启动子活性,并与几种重要的传染病有关,如人类免疫缺陷病毒-1(HIV-1)、结核分枝杆菌和登革热。CD209 促进体外允许细胞中严重急性呼吸综合征(SARS)-冠状病毒刺突蛋白携带假型的感染。与先前发表的研究结果一致,我们的体外研究证实了该 SNP 调节基因启动子活性。对 824 例血清学确诊 SARS 患者中该 SNP 与临床病理结果的遗传关联分析表明,与 -336AA 患者相比,-336AG/GG 基因型 SARS 患者的标准化乳酸脱氢酶(LDH)水平较低(p=0.014,优势比=0.40)。已知高 LDH 水平是临床预后不良的独立预测因子,可能与免疫活性引起的组织破坏有关。因此,携带 CD209-336AA 基因型的 SARS 患者有 60%的可能性预后较差。这种关联与 CD209 在调节病毒感染免疫反应中的作用一致。这些发现对于其他传染病和炎症性疾病的相关性值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/7115401/931d11a42132/gr1.jpg

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