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Comprehensive innate immune profiling of chikungunya virus infection in pediatric cases.小儿基孔肯雅热病毒感染的全面固有免疫分析。
Mol Syst Biol. 2018 Aug 27;14(8):e7862. doi: 10.15252/msb.20177862.
2
Defective cholesterol metabolism in haematopoietic stem cells promotes monocyte-driven atherosclerosis in rheumatoid arthritis.造血干细胞胆固醇代谢缺陷促进类风湿关节炎中单核细胞驱动的动脉粥样硬化。
Eur Heart J. 2018 Jun 14;39(23):2158-2167. doi: 10.1093/eurheartj/ehy119.
3
Cholesterol Efflux Pathways Suppress Inflammasome Activation, NETosis, and Atherogenesis.胆固醇外排途径抑制炎症小体激活、NETosis 和动脉粥样硬化形成。
Circulation. 2018 Aug 28;138(9):898-912. doi: 10.1161/CIRCULATIONAHA.117.032636.
4
Chikungunya virus: a rheumatologist's perspective.基孔肯雅热病毒:风湿病学家的视角。
Clin Exp Rheumatol. 2018 May-Jun;36(3):494-501. Epub 2018 Mar 2.
5
Specific inhibition of NLRP3 in chikungunya disease reveals a role for inflammasomes in alphavirus-induced inflammation.特异性抑制寨卡病毒病中的 NLRP3 炎症小体揭示了炎症小体在甲病毒诱导的炎症中的作用。
Nat Microbiol. 2017 Oct;2(10):1435-1445. doi: 10.1038/s41564-017-0015-4. Epub 2017 Aug 28.
6
The challenges and promise of targeting the Liver X Receptors for treatment of inflammatory disease.针对肝 X 受体治疗炎症性疾病的挑战与前景。
Pharmacol Ther. 2018 Jan;181:1-12. doi: 10.1016/j.pharmthera.2017.07.010. Epub 2017 Jul 16.
7
Chikungunya virus: an update on the biology and pathogenesis of this emerging pathogen.基孔肯雅热病毒:对这种新兴病原体的生物学和发病机制的最新研究。
Lancet Infect Dis. 2017 Apr;17(4):e107-e117. doi: 10.1016/S1473-3099(16)30385-1. Epub 2017 Feb 1.
8
An LXR-Cholesterol Axis Creates a Metabolic Co-Dependency for Brain Cancers.肝X受体-胆固醇轴为脑癌创造了一种代谢共同依赖性。
Cancer Cell. 2016 Nov 14;30(5):683-693. doi: 10.1016/j.ccell.2016.09.008. Epub 2016 Oct 13.
9
Cholesterol homeostasis: How do cells sense sterol excess?胆固醇稳态:细胞如何感知胆固醇过量?
Chem Phys Lipids. 2016 Sep;199:170-178. doi: 10.1016/j.chemphyslip.2016.02.011. Epub 2016 Mar 15.
10
Liver X receptors in lipid metabolism: opportunities for drug discovery.肝脏 X 受体在脂代谢中的作用:药物研发的机遇。
Nat Rev Drug Discov. 2014 Jun;13(6):433-44. doi: 10.1038/nrd4280. Epub 2014 May 16.

肝 X 受体激动剂抑制原代人成纤维细胞中的基孔肯雅病毒复制。

Inhibition of Chikungunya Virus Replication in Primary Human Fibroblasts by Liver X Receptor Agonist.

机构信息

Section of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA

Section of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

Antimicrob Agents Chemother. 2019 Aug 23;63(9). doi: 10.1128/AAC.01220-19. Print 2019 Sep.

DOI:10.1128/AAC.01220-19
PMID:31307983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6709483/
Abstract

The mosquito-borne chikungunya virus (CHIKV) causes acute pain and joint inflammation, and in recent years the virus has caused large epidemics in previously CHIKV-free geographic areas. To advance the understanding of host factors that antagonize CHIKV, we show that synthetic agonist of liver X receptor (LXR-623) inhibits CHIKV replication by upregulating the cholesterol exporter ABCA1 and that endogenous and pharmacological activation of interferon signaling pathway partners with LXR-623 to generate a superior antiviral state.

摘要

虫媒传播的基孔肯雅病毒(CHIKV)可引起急性疼痛和关节炎症,近年来,该病毒已在以前无 CHIKV 的地理区域引发了大规模疫情。为了深入了解拮抗 CHIKV 的宿主因素,我们发现合成肝 X 受体(LXR-623)激动剂可通过上调胆固醇外排蛋白 ABCA1 抑制 CHIKV 复制,内源性和药理学激活干扰素信号通路与 LXR-623 协同作用可产生更优的抗病毒状态。