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IFI44L 作为正向调控因子增强宿主抗结核反应。

IFI44L as a Forward Regulator Enhancing Host Antituberculosis Responses.

机构信息

State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.

College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

出版信息

J Immunol Res. 2021 Oct 20;2021:5599408. doi: 10.1155/2021/5599408. eCollection 2021.

Abstract

Interferon-induced protein 44-like (IFI44L) gene is a type I interferon-stimulated gene (ISG) that plays a critical role in antiviral activity and constitutes a promising diagnostic marker. However, its precise role and function in tuberculosis have not been unveiled. This study showed that IFI44L acts as an antimicrobial target and positive modulator in human macrophages. Knockdown of IFI44L led to increased intracellular survival. Moreover, IFI44L was significantly upregulated, and it restricted the intracellular survival of H37Rv strains at 72 h after rifampicin treatment. Individuals with cutaneous tuberculosis (CTB) were found to have significantly higher IFI44L expression after 6 months of rifampicin therapy than after only 1 month. These results demonstrated that IFI44L induced positive regulation and clearance of from human macrophages. This antimicrobial activity of IFI44L makes it a possible target for therapeutic applications against .

摘要

干扰素诱导蛋白 44 样(IFI44L)基因是一种 I 型干扰素刺激基因(ISG),在抗病毒活性中发挥关键作用,并构成有前途的诊断标志物。然而,其在结核病中的确切作用和功能尚未揭示。本研究表明,IFI44L 作为一种抗菌靶点和人巨噬细胞中的正调节剂。IFI44L 的敲低导致细胞内存活增加。此外,IFI44L 显著上调,并限制了利福平处理后 72 小时 H37Rv 株的细胞内存活。在利福平治疗 6 个月后,皮肤结核(CTB)患者的 IFI44L 表达明显高于治疗 1 个月后。这些结果表明,IFI44L 诱导了人巨噬细胞中 的正调节和清除。IFI44L 的这种抗菌活性使其成为针对 的治疗应用的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/163b/8550841/993b3767081a/JIR2021-5599408.001.jpg

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