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本文引用的文献

1
Cytokine Storm in Novel Coronavirus Disease (COVID-19): Expert Management Considerations.新型冠状病毒肺炎(COVID-19)中的细胞因子风暴:专家管理考量
Indian J Crit Care Med. 2020 Jun;24(6):429-434. doi: 10.5005/jp-journals-10071-23415.
2
Simultaneous Treatment of COVID-19 With Serine Protease Inhibitor Camostat and/or Cathepsin L Inhibitor?丝氨酸蛋白酶抑制剂卡莫司他和/或组织蛋白酶L抑制剂联合治疗新型冠状病毒肺炎?
J Clin Med Res. 2020 May;12(5):320-322. doi: 10.14740/jocmr4161. Epub 2020 May 8.
3
Association between age and clinical characteristics and outcomes of COVID-19.年龄与 COVID-19 的临床特征和结局的关系。
Eur Respir J. 2020 May 27;55(5). doi: 10.1183/13993003.01112-2020. Print 2020 May.
4
Potential benefits of precise corticosteroids therapy for severe 2019-nCoV pneumonia.精准皮质类固醇治疗对重症2019新型冠状病毒肺炎的潜在益处。
Signal Transduct Target Ther. 2020 Feb 21;5(1):18. doi: 10.1038/s41392-020-0127-9.
5
Surviving Sepsis Campaign: guidelines on the management of critically ill adults with Coronavirus Disease 2019 (COVID-19).拯救脓毒症运动:2019 冠状病毒病(COVID-19)危重症成人管理指南。
Intensive Care Med. 2020 May;46(5):854-887. doi: 10.1007/s00134-020-06022-5. Epub 2020 Mar 28.
6
COVID-19: consider cytokine storm syndromes and immunosuppression.2019冠状病毒病:考虑细胞因子风暴综合征和免疫抑制。
Lancet. 2020 Mar 28;395(10229):1033-1034. doi: 10.1016/S0140-6736(20)30628-0. Epub 2020 Mar 16.
7
SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor.严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)进入细胞依赖于 ACE2 和 TMPRSS2,可被一种临床验证的蛋白酶抑制剂所阻断。
Cell. 2020 Apr 16;181(2):271-280.e8. doi: 10.1016/j.cell.2020.02.052. Epub 2020 Mar 5.
8
On the use of corticosteroids for 2019-nCoV pneumonia.关于皮质类固醇在2019新型冠状病毒肺炎中的应用。
Lancet. 2020 Feb 29;395(10225):683-684. doi: 10.1016/S0140-6736(20)30361-5. Epub 2020 Feb 12.
9
Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention.中国2019年冠状病毒病(COVID-19)疫情的特征及重要经验教训:来自中国疾病预防控制中心72314例病例报告的总结
JAMA. 2020 Apr 7;323(13):1239-1242. doi: 10.1001/jama.2020.2648.
10
Clinical evidence does not support corticosteroid treatment for 2019-nCoV lung injury.临床证据不支持使用皮质类固醇治疗2019新型冠状病毒肺炎肺损伤。
Lancet. 2020 Feb 15;395(10223):473-475. doi: 10.1016/S0140-6736(20)30317-2. Epub 2020 Feb 7.

重症新型冠状病毒肺炎:病毒感染诱发的脓毒症?及其免疫调节治疗。

The severe COVID-19: A sepsis induced by viral infection? And its immunomodulatory therapy.

作者信息

Lin Hong-Yuan

机构信息

Forth Medical Center, General Hospital of PLA, Beijing, China.

出版信息

Chin J Traumatol. 2020 Aug;23(4):190-195. doi: 10.1016/j.cjtee.2020.06.002. Epub 2020 Jun 15.

DOI:10.1016/j.cjtee.2020.06.002
PMID:32690231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7451584/
Abstract

COVID-19 is known for its magical infectivity, fast transmission and high death toll based on the large number of infected people. From the perspective of the clinical manifestation, autopsy examination and pathophysiology, the essence of COVID-19 should be viewed as a sepsis induced by viral infection, and has the essential characteristics as sepsis induced by other pathogens. Therefore, in addition to etiological and supportive treatment, immunomodulatory therapy is also appropriate to severe COVID-19. Although there is still a lack of consensus on immunotherapy for sepsis so far, relatively rich experiences have been accumulated in the past decades, which will help us in the treatment of severe COVID-19. This article will elaborate immunotherapy of sepsis, though it may not be consistent.

摘要

新冠病毒肺炎(COVID-19)以其惊人的传染性、快速传播以及基于大量感染人群的高死亡率而闻名。从临床表现、尸检检查及病理生理学角度来看,COVID-19的本质应被视为一种由病毒感染诱发的脓毒症,具备其他病原体诱发脓毒症的基本特征。因此,对于重症COVID-19,除病原学及支持治疗外,免疫调节治疗同样适用。尽管目前对于脓毒症的免疫治疗仍缺乏共识,但在过去几十年里已积累了较为丰富的经验,这将有助于我们治疗重症COVID-19。本文将阐述脓毒症的免疫治疗,尽管可能并不全面。