• 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

了解 SARS-CoV-2 感染及其免疫学的复杂性:迈向基于免疫的治疗方法。

Understanding the complexities of SARS-CoV2 infection and its immunology: A road to immune-based therapeutics.

机构信息

Children's Health Queensland Clinical Unit, School of Clinical Medicine, Faculty of Medicine, Mater Research, University of Queensland, ST Lucia, Brisbane, Queensland 4078, Australia; School of Biomedical Sciences, Faculty of Medicine, University of Queensland, ST Lucia, Brisbane, Queensland 4078, Australia.

出版信息

Int Immunopharmacol. 2020 Nov;88:106980. doi: 10.1016/j.intimp.2020.106980. Epub 2020 Sep 8.

DOI:10.1016/j.intimp.2020.106980
PMID:33182073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7843151/
Abstract

Emerging infectious diseases always pose a threat to humans along with plant and animal life. SARS-CoV2 is the recently emerged viral infection that originated from Wuhan city of the Republic of China in December 2019. Now, it has become a pandemic. Currently, SARS-CoV2 has infected more than 27.74 million people worldwide, and taken 901,928 human lives. It was named first 'WH 1 Human CoV' and later changed to 2019 novel CoV (2019-nCoV). Scientists have established it as a zoonotic viral disease emerged from Chinese horseshoe bats, which do not develop a severe infection. For example, Rhinolophus Chinese horseshoe bats harboring severe acute respiratory syndrome-related coronavirus (SARSr-CoV) or SARSr-Rh-BatCoV appear healthy and clear the virus within 2-4 months period. The article introduces first the concept of EIDs and some past EIDs, which have affected human life. Next section discusses mysteries regarding SARS-CoV2 origin, its evolution, and human transfer. Third section describes COVID-19 clinical symptoms and factors affecting susceptibility or resistance. The fourth section introduces the SARS-CoV2 entry in the host cell, its replication, and the establishment of productive infection. Section five describes the host's immune response associated with asymptomatic, symptomatic, mild to moderate, and severe COVID-19. The subsequent seventh and eighth sections mention the immune status in COVID-19 convalescent patients and re-emergence of COVID-19 in them. Thereafter, the eighth section describes viral strategies to hijack the host antiviral immune response and generate the "cytokine storm". The ninth section describes about transgenic humane ACE2 (hACE2) receptor expressing mice to study immunity, drugs, and vaccines. The article ends with the development of different immunomodulatory and immunotherapeutics strategies, including vaccines waiting for their approval in humans as prophylaxis or treatment measures.

摘要

新发传染病总是对人类、动植物生命构成威胁。SARS-CoV2 是一种新出现的病毒感染,于 2019 年 12 月起源于中华民国武汉市。如今,它已成为一种大流行疾病。目前,SARS-CoV2 已在全球范围内感染了超过 2774 万人,并夺走了 901928 人的生命。它最初被命名为“WH 1 人冠状病毒”,后来更改为 2019 年新型冠状病毒(2019-nCoV)。科学家们已经确定它是一种源自中国马蹄蝠的人畜共患病毒性疾病,而这些蝙蝠本身不易受到严重感染。例如,携带严重急性呼吸系统综合征相关冠状病毒(SARSr-CoV)或 SARSr-Rh-BatCoV 的中华菊头蝠似乎健康无恙,并能在 2-4 个月内清除病毒。本文首先介绍了新发传染病的概念以及一些曾对人类生命造成影响的过去的新发传染病。接下来的一节讨论了 SARS-CoV2 的起源、进化和人际传播的奥秘。第三节描述了 COVID-19 的临床症状以及影响易感性或抵抗力的因素。第四节介绍了 SARS-CoV2 进入宿主细胞、复制和建立有性感染的过程。第五节描述了宿主与无症状、有症状、轻度至中度和重度 COVID-19 相关的免疫反应。随后的第七和第八节提到了 COVID-19 康复患者的免疫状态以及他们再次感染 COVID-19 的情况。此后,第八节描述了病毒劫持宿主抗病毒免疫反应并引发“细胞因子风暴”的策略。第九节介绍了表达转基因人类 ACE2(hACE2)受体的转基因小鼠,用于研究免疫、药物和疫苗。本文最后介绍了不同的免疫调节和免疫治疗策略的发展,包括等待在人类中获得批准作为预防或治疗措施的疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/dc0b57e601d4/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/3ffed1a44758/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/8fc9c3b57289/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/d40a0e74492a/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/77778cbc42d1/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/ccd3e63d3d5b/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/bdcd53ced1e8/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/71b77ea16ea7/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/dc0b57e601d4/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/3ffed1a44758/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/8fc9c3b57289/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/d40a0e74492a/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/77778cbc42d1/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/ccd3e63d3d5b/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/bdcd53ced1e8/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/71b77ea16ea7/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/7843151/dc0b57e601d4/gr7_lrg.jpg

相似文献

1
Understanding the complexities of SARS-CoV2 infection and its immunology: A road to immune-based therapeutics.了解 SARS-CoV-2 感染及其免疫学的复杂性:迈向基于免疫的治疗方法。
Int Immunopharmacol. 2020 Nov;88:106980. doi: 10.1016/j.intimp.2020.106980. Epub 2020 Sep 8.
2
Hypothesis for potential pathogenesis of SARS-CoV-2 infection-a review of immune changes in patients with viral pneumonia.关于 SARS-CoV-2 感染潜在发病机制的假说——病毒性肺炎患者免疫变化的综述。
Emerg Microbes Infect. 2020 Dec;9(1):727-732. doi: 10.1080/22221751.2020.1746199.
3
Prevention and treatment of COVID-19 disease by controlled modulation of innate immunity.通过对固有免疫的控制调节来预防和治疗 COVID-19 疾病。
Eur J Immunol. 2020 Jul;50(7):932-938. doi: 10.1002/eji.202048693. Epub 2020 Jun 15.
4
An update on SARS-CoV-2/COVID-19 with particular reference to its clinical pathology, pathogenesis, immunopathology and mitigation strategies.SARS-CoV-2/COVID-19 的最新进展,特别参考其临床病理学、发病机制、免疫病理学和缓解策略。
Travel Med Infect Dis. 2020 Sep-Oct;37:101755. doi: 10.1016/j.tmaid.2020.101755. Epub 2020 May 30.
5
Immune response to SARS-CoV-2 and mechanisms of immunopathological changes in COVID-19.针对 SARS-CoV-2 的免疫反应和 COVID-19 中免疫病理变化的机制。
Allergy. 2020 Jul;75(7):1564-1581. doi: 10.1111/all.14364.
6
SARS-CoV-2 jumping the species barrier: Zoonotic lessons from SARS, MERS and recent advances to combat this pandemic virus.SARS-CoV-2 跨越物种屏障:SARS、MERS 带来的人畜共患病教训及应对此次大流行病毒的最新进展。
Travel Med Infect Dis. 2020 Sep-Oct;37:101830. doi: 10.1016/j.tmaid.2020.101830. Epub 2020 Aug 2.
7
Angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 and the pathophysiology of coronavirus disease 2019 (COVID-19).血管紧张素转化酶 2(ACE2)、严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)与 2019 冠状病毒病(COVID-19)的病理生理学。
J Pathol. 2020 Jul;251(3):228-248. doi: 10.1002/path.5471. Epub 2020 Jun 10.
8
COVID-19: The Immune Responses and Clinical Therapy Candidates.新型冠状病毒肺炎:免疫应答与临床治疗候选药物。
Int J Mol Sci. 2020 Aug 3;21(15):5559. doi: 10.3390/ijms21155559.
9
Immune responses and pathogenesis of SARS-CoV-2 during an outbreak in Iran: Comparison with SARS and MERS.伊朗暴发期间 SARS-CoV-2 的免疫反应和发病机制:与 SARS 和 MERS 的比较。
Rev Med Virol. 2020 May;30(3):e2107. doi: 10.1002/rmv.2107. Epub 2020 Apr 8.
10
The pathogenicity of SARS-CoV-2 in hACE2 transgenic mice.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在人血管紧张素转换酶2(hACE2)转基因小鼠中的致病性。
Nature. 2020 Jul;583(7818):830-833. doi: 10.1038/s41586-020-2312-y. Epub 2020 May 7.

引用本文的文献

1
Eosinophils and COVID-19: Insights into immune complexity and vaccine safety.嗜酸性粒细胞与新冠病毒病:对免疫复杂性和疫苗安全性的见解
Clin Transl Allergy. 2025 Mar;15(3):e70050. doi: 10.1002/clt2.70050.
2
The Recognition Pathway of the SARS-CoV-2 Spike Receptor-Binding Domain to Human Angiotensin-Converting Enzyme 2.严重急性呼吸综合征冠状病毒2刺突蛋白受体结合域与人血管紧张素转换酶2的识别途径
Molecules. 2024 Apr 19;29(8):1875. doi: 10.3390/molecules29081875.
3
The Role of Perceived Risk in the Relationship Between Disgust Sensitivity and COVID-19 Vaccine Hesitancy.

本文引用的文献

1
ACE2-IgG1 fusions with improved and activity against SARS-CoV-2.对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)具有改善活性的血管紧张素转换酶2(ACE2)-免疫球蛋白G1(IgG1)融合蛋白
iScience. 2022 Jan 21;25(1):103670. doi: 10.1016/j.isci.2021.103670. Epub 2021 Dec 20.
2
Network Analysis and Transcriptome Profiling Identify Autophagic and Mitochondrial Dysfunctions in SARS-CoV-2 Infection.网络分析和转录组分析揭示新冠病毒感染中的自噬和线粒体功能障碍
Front Genet. 2021 Mar 16;12:599261. doi: 10.3389/fgene.2021.599261. eCollection 2021.
3
Male sex identified by global COVID-19 meta-analysis as a risk factor for death and ITU admission.
感知风险在厌恶敏感性与新冠疫苗犹豫关系中的作用
Cognit Ther Res. 2023 May 24:1-12. doi: 10.1007/s10608-023-10391-8.
4
Cellular and Molecular Mechanisms of Pathogenic and Protective Immune Responses to SARS-CoV-2 and Implications of COVID-19 Vaccines.针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的致病性和保护性免疫反应的细胞和分子机制以及2019冠状病毒病(COVID-19)疫苗的影响
Vaccines (Basel). 2023 Mar 8;11(3):615. doi: 10.3390/vaccines11030615.
5
Review on the Biogenesis of Platelets in Lungs and Its Alterations in SARS-CoV-2 Infection Patients.肺部血小板的发生机制及其在 SARS-CoV-2 感染患者中的变化综述。
J Renin Angiotensin Aldosterone Syst. 2023 Feb 27;2023:7550197. doi: 10.1155/2023/7550197. eCollection 2023.
6
BCG and SARS-CoV-2-What Have We Learned?卡介苗与严重急性呼吸综合征冠状病毒2——我们学到了什么?
Vaccines (Basel). 2022 Sep 30;10(10):1641. doi: 10.3390/vaccines10101641.
7
Have General Surgery Practices Decreased During the COVID-19 Pandemic?普通外科手术量在新冠疫情期间有所减少吗?
Cureus. 2022 Jul 26;14(7):e27270. doi: 10.7759/cureus.27270. eCollection 2022 Jul.
8
Monoclonal antibodies: a remedial approach to prevent SARS-CoV-2 infection.单克隆抗体:一种预防新型冠状病毒2019感染的补救方法。
3 Biotech. 2022 Sep;12(9):227. doi: 10.1007/s13205-022-03281-5. Epub 2022 Aug 17.
9
In silico analysis of SARS-CoV-2 spike protein N501Y and N501T mutation effects on human ACE2 binding.基于 SARS-CoV-2 刺突蛋白 N501Y 和 N501T 突变对人 ACE2 结合影响的计算机分析。
J Mol Graph Model. 2022 Nov;116:108260. doi: 10.1016/j.jmgm.2022.108260. Epub 2022 Jul 1.
10
SARS-CoV-2: Molecular Structure, Pathogenesis, Potential Therapeutic Targets, and Immune Response of the Infected Subject.严重急性呼吸综合征冠状病毒2:分子结构、发病机制、潜在治疗靶点及感染个体的免疫反应
Interdiscip Perspect Infect Dis. 2022 Jun 2;2022:7856659. doi: 10.1155/2022/7856659. eCollection 2022.
全球 COVID-19 荟萃分析显示,男性性别是死亡和 ICU 入院的风险因素。
Nat Commun. 2020 Dec 9;11(1):6317. doi: 10.1038/s41467-020-19741-6.
4
Robust T Cell Immunity in Convalescent Individuals with Asymptomatic or Mild COVID-19.无症状或轻症 COVID-19 康复者体内具有强大的 T 细胞免疫。
Cell. 2020 Oct 1;183(1):158-168.e14. doi: 10.1016/j.cell.2020.08.017. Epub 2020 Aug 14.
5
Human B Cell Clonal Expansion and Convergent Antibody Responses to SARS-CoV-2.人类 B 细胞克隆扩增和对 SARS-CoV-2 的趋同抗体反应。
Cell Host Microbe. 2020 Oct 7;28(4):516-525.e5. doi: 10.1016/j.chom.2020.09.002. Epub 2020 Sep 3.
6
Non-neuronal expression of SARS-CoV-2 entry genes in the olfactory system suggests mechanisms underlying COVID-19-associated anosmia.SARS-CoV-2 进入基因在嗅觉系统中的非神经元表达提示了 COVID-19 相关嗅觉丧失的潜在机制。
Sci Adv. 2020 Jul 31;6(31). doi: 10.1126/sciadv.abc5801. Epub 2020 Jul 24.
7
Neutralization of SARS-CoV-2 by Destruction of the Prefusion Spike.通过破坏融合前刺突来中和严重急性呼吸综合征冠状病毒2
Cell Host Microbe. 2020 Sep 9;28(3):497. doi: 10.1016/j.chom.2020.07.002.
8
Growth Factor Receptor Signaling Inhibition Prevents SARS-CoV-2 Replication.生长因子受体信号抑制可预防 SARS-CoV-2 复制。
Mol Cell. 2020 Oct 1;80(1):164-174.e4. doi: 10.1016/j.molcel.2020.08.006. Epub 2020 Aug 11.
9
Humoral Immune Response to SARS-CoV-2 in Iceland.冰岛人针对 SARS-CoV-2 的体液免疫反应。
N Engl J Med. 2020 Oct 29;383(18):1724-1734. doi: 10.1056/NEJMoa2026116. Epub 2020 Sep 1.
10
A mouse-adapted model of SARS-CoV-2 to test COVID-19 countermeasures.一种适应 SARS-CoV-2 的小鼠模型,用于测试 COVID-19 对策。
Nature. 2020 Oct;586(7830):560-566. doi: 10.1038/s41586-020-2708-8. Epub 2020 Aug 27.