• 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

他汀类药物:针对传染病的宿主定向治疗的可行候选药物。

Statins: a viable candidate for host-directed therapy against infectious diseases.

机构信息

International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town-Component, Cape Town, South Africa.

Institute of Infectious Diseases and Molecular Medicine (IDM), Department of Pathology, Division of Immunology and South African Medical Research Council (SAMRC), Immunology of Infectious Diseases, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

出版信息

Nat Rev Immunol. 2019 Feb;19(2):104-117. doi: 10.1038/s41577-018-0094-3.

DOI:10.1038/s41577-018-0094-3
PMID:30487528
Abstract

Statins were first identified over 40 years ago as lipid-lowering drugs and have been remarkably effective in treating cardiovascular diseases. As research advanced, the protective effects of statins were additionally attributed to their anti-inflammatory, antioxidative, anti-thrombotic and immunomodulatory functions rather than lipid-lowering abilities alone. By promoting host defence mechanisms and inhibiting pathological inflammation, statins increase survival in human infectious diseases. At the cellular level, statins inhibit the intermediates of the host mevalonate pathway, thus compromising the immune evasion strategies of pathogens and their survival. Here, we discuss the potential use of statins as an inexpensive and practical alternative or adjunctive host-directed therapy for infectious diseases caused by intracellular pathogens, such as viruses, protozoa, fungi and bacteria.

摘要

他汀类药物最初在 40 多年前被发现具有降低血脂的作用,并且在治疗心血管疾病方面非常有效。随着研究的进展,他汀类药物的保护作用还归因于其抗炎、抗氧化、抗血栓形成和免疫调节功能,而不仅仅是降低血脂的能力。通过促进宿主防御机制和抑制病理性炎症,他汀类药物可提高人类感染性疾病的生存率。在细胞水平上,他汀类药物抑制宿主甲羟戊酸途径的中间产物,从而破坏病原体的免疫逃避策略及其生存能力。在这里,我们讨论了将他汀类药物作为一种廉价且实用的替代或辅助宿主导向疗法,用于治疗由细胞内病原体(如病毒、原生动物、真菌和细菌)引起的感染性疾病的可能性。

相似文献

1
Statins: a viable candidate for host-directed therapy against infectious diseases.他汀类药物:针对传染病的宿主定向治疗的可行候选药物。
Nat Rev Immunol. 2019 Feb;19(2):104-117. doi: 10.1038/s41577-018-0094-3.
2
Potential role of statins in inflammation and atherosclerosis.他汀类药物在炎症和动脉粥样硬化中的潜在作用。
J Atheroscler Thromb. 2003;10(3):140-4. doi: 10.5551/jat.10.140.
3
Pleiotropic use of Statins as non-lipid-lowering drugs.他汀类药物作为非降脂药物的多效性用途。
Int J Biol Sci. 2020 Aug 13;16(14):2704-2711. doi: 10.7150/ijbs.42965. eCollection 2020.
4
Statins reduce vascular inflammation in atherogenesis: A review of underlying molecular mechanisms.他汀类药物可减少动脉粥样硬化形成中的血管炎症:潜在分子机制的综述。
Int J Biochem Cell Biol. 2020 May;122:105735. doi: 10.1016/j.biocel.2020.105735. Epub 2020 Feb 29.
5
Antiinflammatory and immunomodulatory properties of statins.他汀类药物的抗炎和免疫调节特性。
Immunol Res. 2002;25(3):271-85. doi: 10.1385/IR:25:3:271.
6
Statins and inflammation: an update.他汀类药物与炎症:最新进展。
Curr Opin Cardiol. 2010 Jul;25(4):399-405. doi: 10.1097/HCO.0b013e3283398e53.
7
Novel prospects of statins as therapeutic agents in cancer.他汀类药物作为癌症治疗药物的新前景。
Pharmacol Res. 2014 Oct;88:84-98. doi: 10.1016/j.phrs.2014.06.013. Epub 2014 Jul 5.
8
To cardiovascular disease and beyond: new therapeutic perspectives of statins in autoimmune diseases and cancer.从心血管疾病到其他疾病:他汀类药物在自身免疫性疾病和癌症中的新治疗前景。
Curr Drug Targets. 2012 Jun;13(6):829-41. doi: 10.2174/138945012800564112.
9
Lipid homeostasis and mevalonate pathway in COVID-19: Basic concepts and potential therapeutic targets.新型冠状病毒肺炎中的脂质稳态和甲羟戊酸途径:基本概念和潜在治疗靶点。
Prog Lipid Res. 2021 Apr;82:101099. doi: 10.1016/j.plipres.2021.101099. Epub 2021 Apr 26.
10
Statins: pros and cons.他汀类药物:利弊。
Med Clin (Barc). 2018 May 23;150(10):398-402. doi: 10.1016/j.medcli.2017.11.030. Epub 2017 Dec 29.

引用本文的文献

1
Impact of Long-Term Statin Therapy on Incidence and Severity of Community-Acquired Pneumonia: A Real-World Data Analysis.长期他汀类药物治疗对社区获得性肺炎发病率和严重程度的影响:一项真实世界数据分析
Biomedicines. 2025 Jun 11;13(6):1438. doi: 10.3390/biomedicines13061438.
2
The Association Between Statin Therapy and the Subsequent Clinical Course of Patients With Melioidosis.他汀类药物治疗与类鼻疽病患者后续临床病程之间的关联。
J Trop Med. 2025 May 25;2025:8838580. doi: 10.1155/jotm/8838580. eCollection 2025.
3
Impact of statins as immune-modulatory agents on inflammatory markers in adults with chronic diseases: A systematic review and meta-analysis.
他汀类药物作为免疫调节剂对慢性病成年人炎症标志物的影响:一项系统评价和荟萃分析。
PLoS One. 2025 May 29;20(5):e0323749. doi: 10.1371/journal.pone.0323749. eCollection 2025.
4
Human γδ T Cell Function Is Impaired Upon Mevalonate Pathway Inhibition.甲羟戊酸途径受抑制后,人类γδ T细胞功能受损。
Immunology. 2025 Jul;175(3):300-322. doi: 10.1111/imm.13931. Epub 2025 Apr 22.
5
Association between statin use and 30-day mortality among patients with sepsis-associated encephalopathy: a retrospective cohort study.他汀类药物使用与脓毒症相关性脑病患者30天死亡率之间的关联:一项回顾性队列研究。
Front Neurol. 2024 Dec 27;15:1371314. doi: 10.3389/fneur.2024.1371314. eCollection 2024.
6
Impact of statin use on COVID-19 outcomes in hospitalized patients in Saudi Arabia: a retrospective cohort study.他汀类药物使用对沙特阿拉伯住院患者新冠病毒病结局的影响:一项回顾性队列研究
J Med Life. 2024 Nov;17(11):994-999. doi: 10.25122/jml-2024-0371.
7
Repurposed Drugs and Plant-Derived Natural Products as Potential Host-Directed Therapeutic Candidates for Tuberculosis.重新利用的药物和植物源天然产物作为结核病潜在的宿主导向治疗候选物
Biomolecules. 2024 Nov 24;14(12):1497. doi: 10.3390/biom14121497.
8
Itaconate facilitates viral infection via alkylating GDI2 and retaining Rab GTPase on the membrane.衣康酸盐通过烷基化GDI2并使Rab GTP酶保留在膜上促进病毒感染。
Signal Transduct Target Ther. 2024 Dec 27;9(1):371. doi: 10.1038/s41392-024-02077-8.
9
PET-CT outcomes from a randomised controlled trial of rosuvastatin as an adjunct to standard tuberculosis treatment.瑞舒伐他汀作为标准结核病治疗辅助药物的随机对照试验中的PET-CT结果。
Nat Commun. 2024 Dec 2;15(1):10475. doi: 10.1038/s41467-024-54419-3.
10
SARS-CoV-2 entry and fusion are independent of ACE2 localization to lipid rafts.严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)的进入和融合与血管紧张素转换酶2(ACE2)定位于脂筏无关。
J Virol. 2025 Jan 31;99(1):e0182324. doi: 10.1128/jvi.01823-24. Epub 2024 Nov 21.