Suppr超能文献

干扰素途径狼疮风险等位基因调节急性 COVID-19 死亡风险。

Interferon pathway lupus risk alleles modulate risk of death from acute COVID-19.

机构信息

Colton Center for Autoimmunity, NYU Grossman School of Medicine, New York, New York.

Center for Human Genetics and Genomics, NYU Grossman School of Medicine, New York, New York.

出版信息

Transl Res. 2022 Jun;244:47-55. doi: 10.1016/j.trsl.2022.01.007. Epub 2022 Jan 31.

Abstract

Type I interferon (IFN) is critical in our defense against viral infections. Increased type I IFN pathway activation is a genetic risk factor for systemic lupus erythematosus (SLE), and a number of common risk alleles contribute to the high IFN trait. We hypothesized that these common gain-of-function IFN pathway alleles may be associated with protection from mortality in acute COVID-19. We studied patients admitted with acute COVID-19 (756 European-American and 398 African-American ancestry). Ancestral backgrounds were analyzed separately, and mortality after acute COVID-19 was the primary outcome. In European-American ancestry, we found that a haplotype of interferon regulatory factor 5 (IRF5) and alleles of protein kinase cGMP-dependent 1 (PRKG1) were associated with mortality from COVID-19. Interestingly, these were much stronger risk factors in younger patients (OR = 29.2 for PRKG1 in ages 45-54). Variants in the IRF7 and IRF8 genes were associated with mortality from COVID-19 in African-American subjects, and these genetic effects were more pronounced in older subjects. Combining genetic information with blood biomarker data such as C-reactive protein, troponin, and D-dimer resulted in significantly improved predictive capacity, and in both ancestral backgrounds the risk genotypes were most relevant in those with positive biomarkers (OR for death between 14 and 111 in high risk genetic/biomarker groups). This study confirms the critical role of the IFN pathway in defense against COVID-19 and viral infections, and supports the idea that some common SLE risk alleles exert protective effects in antiviral immunity.

摘要

I 型干扰素(IFN)在我们对抗病毒感染的防御中至关重要。I 型 IFN 途径的激活增加是系统性红斑狼疮(SLE)的遗传风险因素,许多常见的风险等位基因导致 IFN 表型高。我们假设这些常见的 IFN 途径获得性功能等位基因可能与急性 COVID-19 患者的死亡率降低相关。我们研究了因急性 COVID-19 住院的患者(756 名欧洲裔美国人和 398 名非裔美国人)。分别分析了祖先背景,急性 COVID-19 后的死亡率是主要结局。在欧洲裔美国人中,我们发现干扰素调节因子 5(IRF5)的单倍型和蛋白激酶 cGMP 依赖性 1(PRKG1)的等位基因与 COVID-19 相关的死亡率相关。有趣的是,这些在年轻患者中是更强的风险因素(PRKG1 在年龄为 45-54 岁时的 OR = 29.2)。IRF7 和 IRF8 基因的变体与非裔美国人 COVID-19 死亡率相关,这些遗传效应在老年患者中更为明显。将遗传信息与 C 反应蛋白、肌钙蛋白和 D-二聚体等血液生物标志物数据相结合,可显著提高预测能力,并且在两个祖先背景中,风险基因型在标志物阳性的患者中最为相关(在高风险遗传/生物标志物组中,死亡的 OR 在 14 到 111 之间)。这项研究证实了 IFN 途径在对抗 COVID-19 和病毒感染中的关键作用,并支持一些常见的 SLE 风险等位基因在抗病毒免疫中发挥保护作用的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f4d/8802623/a9254114b5a8/gr1_lrg.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验