Suppr超能文献

应对宿主对新发病毒疾病的反应:从脓毒症、肺炎、流感和埃博拉疫情中汲取的经验教训。

Treating the host response to emerging virus diseases: lessons learned from sepsis, pneumonia, influenza and Ebola.

作者信息

Fedson David S

机构信息

Formerly, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA.

出版信息

Ann Transl Med. 2016 Nov;4(21):421. doi: 10.21037/atm.2016.11.03.

Abstract

There is an ongoing threat of epidemic or pandemic diseases that could be caused by influenza, Ebola or other emerging viruses. It will be difficult and costly to develop new drugs that target each of these viruses. Statins and angiotensin receptor blockers (ARBs) have been effective in treating patients with sepsis, pneumonia and influenza, and a statin/ARB combination appeared to dramatically reduce mortality during the recent Ebola outbreak. These drugs target (among other things) the endothelial dysfunction found in all of these diseases. Most scientists work on new drugs that target viruses, and few accept the idea of treating the host response with generic drugs. A great deal of research will be needed to show conclusively that these drugs work, and this will require the support of public agencies and foundations. Investigators in developing countries should take an active role in this research. If the next Public Health Emergency of International Concern is caused by an emerging virus, a "top down" approach to developing specific new drug treatments is unlikely to be effective. However, a "bottom up" approach to treatment that targets the host response to these viruses by using widely available and inexpensive generic drugs could reduce mortality in any country with a basic health care system. In doing so, it would make an immeasurable contribution to global equity and global security.

摘要

流感、埃博拉病毒或其他新兴病毒有可能引发大规模流行疾病,这一威胁始终存在。研发针对每种此类病毒的新药既困难又昂贵。他汀类药物和血管紧张素受体阻滞剂(ARB)在治疗败血症、肺炎和流感患者方面已显示出疗效,在近期埃博拉疫情期间,他汀类药物与ARB的联合使用似乎能显著降低死亡率。这些药物(除其他作用外)针对所有这些疾病中出现的内皮功能障碍。大多数科学家致力于研发针对病毒的新药,很少有人接受用通用药物治疗宿主反应的理念。要确凿证明这些药物有效,还需要大量研究,而这需要公共机构和基金会的支持。发展中国家的研究人员应积极参与此项研究。如果下一次国际关注的突发公共卫生事件是由某种新兴病毒引发,“自上而下”研发特定新药疗法的方法不太可能奏效。然而,通过使用广泛可得且价格低廉的通用药物来针对宿主对这些病毒的反应进行“自下而上”的治疗方法,在任何具备基本医疗体系的国家都能降低死亡率。这样做将为全球公平和全球安全做出不可估量的贡献。

相似文献

2
Clinician-initiated research on treating the host response to pandemic influenza.
Hum Vaccin Immunother. 2018 Mar 4;14(3):790-795. doi: 10.1080/21645515.2017.1378292. Epub 2017 Oct 31.
3
What treating Ebola means for pandemic influenza.
J Public Health Policy. 2018 Aug;39(3):268-282. doi: 10.1057/s41271-018-0138-8.
4
COVID-19, host response treatment, and the need for political leadership.
J Public Health Policy. 2021 Mar;42(1):6-14. doi: 10.1057/s41271-020-00266-7. Epub 2020 Dec 2.
5
Treating influenza with statins and other immunomodulatory agents.
Antiviral Res. 2013 Sep;99(3):417-35. doi: 10.1016/j.antiviral.2013.06.018. Epub 2013 Jul 4.
7
Influenza, evolution, and the next pandemic.
Evol Med Public Health. 2018 Oct 3;2018(1):260-269. doi: 10.1093/emph/eoy027. eCollection 2018.
9
Treating COVID-19: Targeting the Host Response, Not the Virus.
Life (Basel). 2023 Mar 6;13(3):712. doi: 10.3390/life13030712.

引用本文的文献

1
Molecular Insight into the Role of Vitamin D in Immune-Mediated Inflammatory Diseases.
Int J Mol Sci. 2025 May 16;26(10):4798. doi: 10.3390/ijms26104798.
4
Impact of prior antihypertensive treatment on COVID-19 outcomes, by active ingredient.
Inflammopharmacology. 2024 Jun;32(3):1805-1815. doi: 10.1007/s10787-024-01475-2. Epub 2024 Apr 15.
6
Physiological Basis for Using Vitamin D to Improve Health.
Biomedicines. 2023 May 26;11(6):1542. doi: 10.3390/biomedicines11061542.
8
Treating COVID-19: Targeting the Host Response, Not the Virus.
Life (Basel). 2023 Mar 6;13(3):712. doi: 10.3390/life13030712.
10
Role of endothelial dysfunction in the severity of COVID‑19 infection (Review).
Mol Med Rep. 2022 Nov;26(5). doi: 10.3892/mmr.2022.12867. Epub 2022 Oct 5.

本文引用的文献

1
Sepsis and septic shock.
Nat Rev Dis Primers. 2016 Jun 30;2:16045. doi: 10.1038/nrdp.2016.45.
2
Looking Across and Looking Beyond the Knowledge Frontier: Intellectual Distance, Novelty, and Resource Allocation in Science.
Manage Sci. 2016 Oct;62(10):2765-2783. doi: 10.1287/mnsc.2015.2285. Epub 2016 Jan 8.
3
Dysregulation of angiopoietin-1 plays a mechanistic role in the pathogenesis of cerebral malaria.
Sci Transl Med. 2016 Sep 28;8(358):358ra128. doi: 10.1126/scitranslmed.aaf6812.
4
Angiotensin receptors and β-catenin regulate brain endothelial integrity in malaria.
J Clin Invest. 2016 Oct 3;126(10):4016-4029. doi: 10.1172/JCI87306. Epub 2016 Sep 19.
6
Systems Biology-Based Investigation of Cellular Antiviral Drug Targets Identified by Gene-Trap Insertional Mutagenesis.
PLoS Comput Biol. 2016 Sep 15;12(9):e1005074. doi: 10.1371/journal.pcbi.1005074. eCollection 2016 Sep.
9
Clinical and Virological Characteristics of Ebola Virus Disease Patients Treated With Favipiravir (T-705)-Sierra Leone, 2014.
Clin Infect Dis. 2016 Nov 15;63(10):1288-1294. doi: 10.1093/cid/ciw571. Epub 2016 Aug 23.
10
Atorvastatin promotes the expansion of myeloid-derived suppressor cells and attenuates murine colitis.
Immunology. 2016 Dec;149(4):432-446. doi: 10.1111/imm.12662. Epub 2016 Sep 20.

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