• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

靶向脂筏——COVID-19 的潜在治疗方法。

Targeting Lipid Rafts-A Potential Therapy for COVID-19.

机构信息

Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.

Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.

出版信息

Front Immunol. 2020 Sep 29;11:574508. doi: 10.3389/fimmu.2020.574508. eCollection 2020.

DOI:10.3389/fimmu.2020.574508
PMID:33133090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7550455/
Abstract

COVID-19 is a global pandemic currently in an acute phase of rapid expansion. While public health measures remain the most effective protection strategy at this stage, when the peak passes, it will leave in its wake important health problems. Historically, very few viruses have ever been eradicated. Instead, the virus may persist in communities causing recurrent local outbreaks of the acute infection as well as several chronic diseases that may arise from the presence of a "suppressed" virus or as a consequence of the initial exposure. An ideal solution would be an anti-viral medication that (i) targets multiple stages of the viral lifecycle, (ii) is insensitive to frequent changes of viral phenotype due to mutagenesis, (iii) has broad spectrum, (iv) is safe and (v) also targets co-morbidities of the infection. In this Perspective we discuss a therapeutic approach that owns these attributes, namely "lipid raft therapy." Lipid raft therapy is an approach aimed at reducing the abundance and structural modifications of host lipid rafts or at targeted delivery of therapeutics to the rafts. Lipid rafts are the sites of the initial binding, activation, internalization and cell-to-cell transmission of SARS-CoV-2. They also are key regulators of immune and inflammatory responses, dysregulation of which is characteristic to COVID-19 infection. Lipid raft therapy was successful in targeting many viral infections and inflammatory disorders, and can potentially be highly effective for treatment of COVID-19.

摘要

COVID-19 是一种全球性的大流行病,目前正处于快速扩张的急性阶段。虽然公共卫生措施仍然是现阶段最有效的保护策略,但当高峰期过去后,它将留下重要的健康问题。从历史上看,很少有病毒被彻底消灭。相反,病毒可能会在社区中持续存在,导致急性感染的反复局部爆发,以及可能由“受抑制”病毒的存在或初始暴露引起的几种慢性疾病。一个理想的解决方案是一种抗病毒药物,它 (i) 针对病毒生命周期的多个阶段,(ii) 对由于突变导致的病毒表型频繁变化不敏感,(iii) 具有广谱性,(iv) 安全,(v) 还针对感染的合并症。在本观点中,我们讨论了一种具有这些特性的治疗方法,即“脂筏治疗”。脂筏治疗是一种旨在减少宿主脂筏的丰度和结构修饰或靶向递送至脂筏的治疗方法。脂筏是 SARS-CoV-2 最初结合、激活、内化和细胞间传播的部位。它们也是免疫和炎症反应的关键调节剂,COVID-19 感染的特征就是其失调。脂筏治疗在靶向多种病毒感染和炎症性疾病方面取得了成功,并且可能对 COVID-19 的治疗非常有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d97/7550455/cc2199d9f884/fimmu-11-574508-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d97/7550455/cc2199d9f884/fimmu-11-574508-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d97/7550455/cc2199d9f884/fimmu-11-574508-g0001.jpg

相似文献

1
Targeting Lipid Rafts-A Potential Therapy for COVID-19.靶向脂筏——COVID-19 的潜在治疗方法。
Front Immunol. 2020 Sep 29;11:574508. doi: 10.3389/fimmu.2020.574508. eCollection 2020.
2
The lysosome: A potential juncture between SARS-CoV-2 infectivity and Niemann-Pick disease type C, with therapeutic implications.溶酶体:SARS-CoV-2 感染性与尼曼-匹克病 C 型之间的潜在连接点,具有治疗意义。
FASEB J. 2020 Jun;34(6):7253-7264. doi: 10.1096/fj.202000654R. Epub 2020 May 5.
3
Inflammation resolution: a dual-pronged approach to averting cytokine storms in COVID-19?炎症消退:避免 COVID-19 中细胞因子风暴的双管齐下策略?
Cancer Metastasis Rev. 2020 Jun;39(2):337-340. doi: 10.1007/s10555-020-09889-4.
4
Emergence, Transmission, and Potential Therapeutic Targets for the COVID-19 Pandemic Associated with the SARS-CoV-2.与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)相关的2019冠状病毒病大流行的出现、传播及潜在治疗靶点
Cell Physiol Biochem. 2020 Aug 25;54(4):767-790. doi: 10.33594/000000254.
5
Discovering small-molecule therapeutics against SARS-CoV-2.寻找针对 SARS-CoV-2 的小分子治疗药物。
Drug Discov Today. 2020 Aug;25(8):1535-1544. doi: 10.1016/j.drudis.2020.06.017. Epub 2020 Jun 20.
6
Glycyrrhizin: An alternative drug for the treatment of COVID-19 infection and the associated respiratory syndrome?甘草酸:治疗 COVID-19 感染及相关呼吸综合征的替代药物?
Pharmacol Ther. 2020 Oct;214:107618. doi: 10.1016/j.pharmthera.2020.107618. Epub 2020 Jun 24.
7
[Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): Should we target the virus, the cell or the disease?].[严重急性呼吸综合征冠状病毒2(SARS-CoV-2):我们应该针对病毒、细胞还是疾病?]
Virologie (Montrouge). 2020 Jun 1;24(3):135-141. doi: 10.1684/vir.2020.0843.
8
COVID-19: Underpinning Research for Detection, Therapeutics, and Vaccines Development.新冠病毒:检测、治疗与疫苗研发的基础研究
Pharm Nanotechnol. 2020;8(4):323-353. doi: 10.2174/2211738508999200817163335.
9
The association between obesity and poor outcome after COVID-19 indicates a potential therapeutic role for montelukast.肥胖与 COVID-19 后不良结局之间的关联表明孟鲁司特可能具有潜在的治疗作用。
Med Hypotheses. 2020 Oct;143:109883. doi: 10.1016/j.mehy.2020.109883. Epub 2020 May 27.
10
SARS, MERS and SARS-CoV-2 (COVID-19) treatment: a patent review.严重急性呼吸综合征(SARS)、中东呼吸综合征(MERS)和严重急性呼吸综合征冠状病毒 2(COVID-19)治疗:专利述评。
Expert Opin Ther Pat. 2020 Aug;30(8):567-579. doi: 10.1080/13543776.2020.1772231. Epub 2020 Jun 7.

引用本文的文献

1
Fatty Acids and Inflammatory Protein Biomarkers From Coronavirus Disease 2019 Patients.2019冠状病毒病患者的脂肪酸和炎症蛋白生物标志物
Immun Inflamm Dis. 2025 Jul;13(7):e70218. doi: 10.1002/iid3.70218.
2
Lipid Rafts in Signalling, Diseases, and Infections: What Can Be Learned from Fluorescence Techniques?信号传导、疾病与感染中的脂筏:从荧光技术中能学到什么?
Membranes (Basel). 2025 Jan 1;15(1):6. doi: 10.3390/membranes15010006.
3
Membrane lipid nanodomains modulate HCN pacemaker channels in nociceptor DRG neurons.膜脂纳米域调节伤害感受器 DRG 神经元中的 HCN 起搏通道。

本文引用的文献

1
Coronavirus Interplay With Lipid Rafts and Autophagy Unveils Promising Therapeutic Targets.冠状病毒与脂筏和自噬的相互作用揭示了有前景的治疗靶点。
Front Microbiol. 2020 Aug 11;11:1821. doi: 10.3389/fmicb.2020.01821. eCollection 2020.
2
Does immunosuppressive treatment entail an additional risk for children with rheumatic diseases? A survey-based study in the era of COVID-19.免疫抑制治疗是否会给患有风湿病的儿童带来额外的风险?COVID-19 时代的一项基于调查的研究。
Rheumatol Int. 2020 Oct;40(10):1613-1623. doi: 10.1007/s00296-020-04663-9. Epub 2020 Aug 2.
3
COVID-19: Coagulopathy, Risk of Thrombosis, and the Rationale for Anticoagulation.
Nat Commun. 2024 Nov 15;15(1):9898. doi: 10.1038/s41467-024-54053-z.
4
SARS-CoV-2-associated lymphopenia: possible mechanisms and the role of CD147.SARS-CoV-2 相关的淋巴细胞减少症:可能的机制和 CD147 的作用。
Cell Commun Signal. 2024 Jul 4;22(1):349. doi: 10.1186/s12964-024-01718-3.
5
Association of Altered Plasma Lipidome with Disease Severity in COVID-19 Patients.新冠肺炎患者血浆脂质组改变与疾病严重程度的相关性研究。
Biomolecules. 2024 Mar 1;14(3):296. doi: 10.3390/biom14030296.
6
Research Advances on the Role of Lipids in the Life Cycle of Human Coronaviruses.脂质在人类冠状病毒生命周期中作用的研究进展
Microorganisms. 2023 Dec 28;12(1):63. doi: 10.3390/microorganisms12010063.
7
Direct regulation of the voltage sensor of HCN channels by membrane lipid compartmentalization.通过膜脂质区室化直接调节 HCN 通道的电压传感器。
Nat Commun. 2023 Oct 18;14(1):6595. doi: 10.1038/s41467-023-42363-7.
8
ARF6 is a host factor for SARS-CoV-2 infection .ARF6 是 SARS-CoV-2 感染的宿主因子。
J Gen Virol. 2023 Jun;104(6). doi: 10.1099/jgv.0.001868.
9
Metabolic alterations upon SARS-CoV-2 infection and potential therapeutic targets against coronavirus infection.新冠病毒感染后的代谢改变和针对冠状病毒感染的潜在治疗靶点。
Signal Transduct Target Ther. 2023 Jun 7;8(1):237. doi: 10.1038/s41392-023-01510-8.
10
Dual-targeting cyclic peptides of receptor-binding domain (RBD) and main protease (Mpro) as potential drug leads for the treatment of SARS-CoV-2 infection.作为治疗新型冠状病毒感染潜在药物先导物的受体结合域(RBD)和主要蛋白酶(Mpro)双靶向环肽
Front Pharmacol. 2022 Oct 19;13:1041331. doi: 10.3389/fphar.2022.1041331. eCollection 2022.
COVID-19:凝血功能障碍、血栓形成风险和抗凝治疗的理由。
Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620938149. doi: 10.1177/1076029620938149.
4
Main Clinical Features of COVID-19 and Potential Prognostic and Therapeutic Value of the Microbiota in SARS-CoV-2 Infections.新型冠状病毒肺炎的主要临床特征以及微生物群在严重急性呼吸综合征冠状病毒2感染中的潜在预后和治疗价值。
Front Microbiol. 2020 Jun 5;11:1302. doi: 10.3389/fmicb.2020.01302. eCollection 2020.
5
Determinants of COVID-19 disease severity in patients with cancer.癌症患者 COVID-19 疾病严重程度的决定因素。
Nat Med. 2020 Aug;26(8):1218-1223. doi: 10.1038/s41591-020-0979-0. Epub 2020 Jun 24.
6
Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections.无症状 SARS-CoV-2 感染的临床和免疫学评估。
Nat Med. 2020 Aug;26(8):1200-1204. doi: 10.1038/s41591-020-0965-6. Epub 2020 Jun 18.
7
Lipid-Raft-Mediated Direct Cytosolic Delivery of Polymer-Coated Soft Nanoparticles.脂质筏介导的聚合物包被软纳米颗粒的细胞质直接递送。
J Phys Chem B. 2020 Jun 25;124(25):5323-5333. doi: 10.1021/acs.jpcb.0c03444. Epub 2020 Jun 16.
8
SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues.SARS-CoV-2 受体 ACE2 是人类气道上皮细胞中的一种干扰素刺激基因,可在组织中的特定细胞亚群中检测到。
Cell. 2020 May 28;181(5):1016-1035.e19. doi: 10.1016/j.cell.2020.04.035. Epub 2020 Apr 27.
9
An outbreak of severe Kawasaki-like disease at the Italian epicentre of the SARS-CoV-2 epidemic: an observational cohort study.SARS-CoV-2 疫情意大年夜利中间爆发严重川崎病样病:一项不雅察性队列研究。
Lancet. 2020 Jun 6;395(10239):1771-1778. doi: 10.1016/S0140-6736(20)31103-X. Epub 2020 May 13.
10
The Challenges of Vaccine Development against a New Virus during a Pandemic.应对大流行期间新型病毒疫苗研发的挑战。
Cell Host Microbe. 2020 May 13;27(5):699-703. doi: 10.1016/j.chom.2020.04.021.