• 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

观点:降低 SARS-CoV2 感染性及其相关免疫病理学。

Perspective: Reducing SARS-CoV2 Infectivity and Its Associated Immunopathology.

机构信息

Department of Biological Sciences, Indian Institute of Science Education and Research Mohali, Mohali, India.

Biomedical and Diagnostic Sciences, College of Veterinary Medicine, The University of Tennessee, Knoxville, TN, United States.

出版信息

Front Immunol. 2020 Oct 22;11:581076. doi: 10.3389/fimmu.2020.581076. eCollection 2020.

DOI:10.3389/fimmu.2020.581076
PMID:33193385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7642257/
Abstract

COVID-19 has become difficult to contain in our interconnected world. In this article, we discuss some approaches that could reduce the consequences of COVID-19. We elaborate upon the utility of camelid single-domain antibodies (sdAbs), also referred to as nanobodies, which are naturally poised to neutralize viruses without enhancing its infectivity. Smaller sized sdAbs can be easily selected using microbes or the subcellular organelle display methods and can neutralize SARS-CoV2 infectivity. We also discuss issues related to their production using scalable platforms. The favorable outcome of the infection is evident in patients when the inflammatory response is adequately curtailed. Therefore, we discuss approaches to mitigate hyperinflammatory reactions initiated by SARS-CoV2 but orchestrated by immune mediators.

摘要

在这个相互关联的世界中,COVID-19 已经难以控制。在本文中,我们讨论了一些可能降低 COVID-19 后果的方法。我们详细介绍了骆驼单域抗体(sdAb)的用途,也称为纳米抗体,它们具有天然中和病毒而不增强其感染力的能力。较小的 sdAb 可以使用微生物或亚细胞细胞器展示方法轻松选择,并可以中和 SARS-CoV2 的感染力。我们还讨论了使用可扩展平台生产它们的相关问题。当炎症反应得到充分抑制时,感染的有利结果在患者中是明显的。因此,我们讨论了减轻由 SARS-CoV2 引发但由免疫介质协调的过度炎症反应的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/7642257/78da82f2d798/fimmu-11-581076-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/7642257/e889cee62b46/fimmu-11-581076-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/7642257/78da82f2d798/fimmu-11-581076-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/7642257/e889cee62b46/fimmu-11-581076-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/7642257/78da82f2d798/fimmu-11-581076-g002.jpg

相似文献

1
Perspective: Reducing SARS-CoV2 Infectivity and Its Associated Immunopathology.观点:降低 SARS-CoV2 感染性及其相关免疫病理学。
Front Immunol. 2020 Oct 22;11:581076. doi: 10.3389/fimmu.2020.581076. eCollection 2020.
2
The role of single-domain antibodies (or nanobodies) in SARS-CoV-2 neutralization.单域抗体(或纳米抗体)在 SARS-CoV-2 中和中的作用。
Mol Biol Rep. 2022 Jan;49(1):647-656. doi: 10.1007/s11033-021-06819-7. Epub 2021 Oct 14.
3
Zinc and vitamin C intake increases spike and neutralising antibody production following SARS-CoV-2 infection.感染新冠病毒后,摄入锌和维生素C可增加刺突抗体和中和抗体的产生。
Clin Transl Med. 2022 Feb;12(2):e731. doi: 10.1002/ctm2.731.
4
Nanobodies as powerful pulmonary targeted biotherapeutics against SARS-CoV-2, pharmaceutical point of view.纳米抗体作为针对 SARS-CoV-2 的强大肺部靶向生物疗法,从药物角度来看。
Biochim Biophys Acta Gen Subj. 2021 Nov;1865(11):129974. doi: 10.1016/j.bbagen.2021.129974. Epub 2021 Jul 31.
5
Nasal delivery of single-domain antibody improves symptoms of SARS-CoV-2 infection in an animal model.鼻腔给药的单域抗体可改善动物模型中 SARS-CoV-2 感染的症状。
PLoS Pathog. 2021 Oct 14;17(10):e1009542. doi: 10.1371/journal.ppat.1009542. eCollection 2021 Oct.
6
Drugs, Metabolites, and Lung Accumulating Small Lysosomotropic Molecules: Multiple Targeting Impedes SARS-CoV-2 Infection and Progress to COVID-19.药物、代谢物和肺内蓄积的小溶酶体靶向小分子:多靶点抑制阻碍 SARS-CoV-2 感染和 COVID-19 进展。
Int J Mol Sci. 2021 Feb 11;22(4):1797. doi: 10.3390/ijms22041797.
7
Escape from neutralizing antibodies by SARS-CoV-2 spike protein variants.通过 SARS-CoV-2 刺突蛋白变体逃避中和抗体。
Elife. 2020 Oct 28;9:e61312. doi: 10.7554/eLife.61312.
8
Neutralization of SARS-CoV-2 by highly potent, hyperthermostable, and mutation-tolerant nanobodies.高效、超耐热且耐突变的纳米抗体对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的中和作用
EMBO J. 2021 Oct 1;40(19):e107985. doi: 10.15252/embj.2021107985. Epub 2021 Aug 9.
9
COVID-19 Updates: Monoclonal Antibodies for COVID-19.新冠疫情最新消息:用于治疗新冠的单克隆抗体
Med Lett Drugs Ther. 2022 Jan 24;64(1642):16.
10
Characterization and antiviral susceptibility of SARS-CoV-2 Omicron BA.2.奥密克戎 BA.2 型 SARS-CoV-2 的特征和抗病毒敏感性
Nature. 2022 Jul;607(7917):119-127. doi: 10.1038/s41586-022-04856-1. Epub 2022 May 16.

引用本文的文献

1
In vitro and in vivo neutralization of Dengue virus by a single domain antibody.单域抗体对登革病毒的体外和体内中和作用
Immunohorizons. 2025 Mar 26;9(5). doi: 10.1093/immhor/vlaf012.
2
Can the triumph of mRNA vaccines against COVID-19 be extended to other viral infections of humans and domesticated animals?mRNA 疫苗对抗 COVID-19 的胜利能否扩展到人类和驯养动物的其他病毒感染?
Microbes Infect. 2023 Jan-Feb;25(1-2):105078. doi: 10.1016/j.micinf.2022.105078. Epub 2022 Nov 23.
3
Robust anti-SARS-CoV2 single domain antibodies cross neutralize multiple viruses.

本文引用的文献

1
SARS-CoV-2 in Environmental Samples of Quarantined Households.新冠病毒在隔离家庭环境样本中的情况。
Viruses. 2022 May 17;14(5):1075. doi: 10.3390/v14051075.
2
Preexisting and de novo humoral immunity to SARS-CoV-2 in humans.人类对 SARS-CoV-2 的预先存在和新产生的体液免疫。
Science. 2020 Dec 11;370(6522):1339-1343. doi: 10.1126/science.abe1107. Epub 2020 Nov 6.
3
Divergent SARS-CoV-2-specific T- and B-cell responses in severe but not mild COVID-19 patients.在重症 COVID-19 患者中而非轻症 COVID-19 患者中存在不同的 SARS-CoV-2 特异性 T 细胞和 B 细胞反应。
强大的抗SARS-CoV-2单域抗体可交叉中和多种病毒。
iScience. 2022 Jul 15;25(7):104549. doi: 10.1016/j.isci.2022.104549. Epub 2022 Jun 9.
4
A Novel Potent Carrier for Unconventional Protein Export in .一种用于……中非常规蛋白质输出的新型强效载体 。 (你提供的原文“A Novel Potent Carrier for Unconventional Protein Export in.”似乎不完整,缺少具体的物种或环境等信息)
Front Cell Dev Biol. 2022 Jan 10;9:816335. doi: 10.3389/fcell.2021.816335. eCollection 2021.
Eur J Immunol. 2020 Dec;50(12):1998-2012. doi: 10.1002/eji.202048908. Epub 2020 Nov 16.
4
Immunosuppressive Drugs and COVID-19: A Review.免疫抑制药物与新型冠状病毒肺炎:综述
Front Pharmacol. 2020 Aug 28;11:1333. doi: 10.3389/fphar.2020.01333. eCollection 2020.
5
Antibody-dependent enhancement and SARS-CoV-2 vaccines and therapies.抗体依赖性增强作用与 SARS-CoV-2 疫苗和疗法。
Nat Microbiol. 2020 Oct;5(10):1185-1191. doi: 10.1038/s41564-020-00789-5. Epub 2020 Sep 9.
6
SARS-CoV-2 infections in children and young people.儿童和青少年感染 SARS-CoV-2。
Clin Immunol. 2020 Nov;220:108588. doi: 10.1016/j.clim.2020.108588. Epub 2020 Sep 6.
7
Age-Related Differences in Immunological Responses to SARS-CoV-2.年龄相关的对 SARS-CoV-2 的免疫反应差异。
J Allergy Clin Immunol Pract. 2020 Nov-Dec;8(10):3251-3258. doi: 10.1016/j.jaip.2020.08.026. Epub 2020 Aug 27.
8
Potential small-molecule drugs as available weapons to fight novel coronavirus (2019-nCoV): A review.潜在的小分子药物可作为对抗新型冠状病毒(2019-nCoV)的现有武器:综述。
Cell Biochem Funct. 2021 Jan;39(1):4-9. doi: 10.1002/cbf.3576. Epub 2020 Aug 17.
9
The type I interferon response in COVID-19: implications for treatment.COVID-19 中的 I 型干扰素反应:治疗意义。
Nat Rev Immunol. 2020 Oct;20(10):585-586. doi: 10.1038/s41577-020-00429-3.
10
Selective and cross-reactive SARS-CoV-2 T cell epitopes in unexposed humans.未暴露于 SARS-CoV-2 人群中的选择性和交叉反应性 T 细胞表位。
Science. 2020 Oct 2;370(6512):89-94. doi: 10.1126/science.abd3871. Epub 2020 Aug 4.