• 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

相似文献

1
Protective and pathogenic role of humoral responses in COVID-19.体液免疫反应在 COVID-19 中的保护作用和致病作用。
J Microbiol. 2022 Mar;60(3):268-275. doi: 10.1007/s12275-022-2037-8. Epub 2022 Mar 2.
2
Hybrid Immunity Shifts the Fc-Effector Quality of SARS-CoV-2 mRNA Vaccine-Induced Immunity.杂合免疫改变了 SARS-CoV-2 mRNA 疫苗诱导免疫的 Fc 效应子质量。
mBio. 2022 Oct 26;13(5):e0164722. doi: 10.1128/mbio.01647-22. Epub 2022 Aug 24.
3
Characterization of SARS-CoV-2-specific humoral immunity and its potential applications and therapeutic prospects.SARS-CoV-2 特异性体液免疫的特性及其潜在的应用和治疗前景。
Cell Mol Immunol. 2022 Feb;19(2):150-157. doi: 10.1038/s41423-021-00774-w. Epub 2021 Oct 13.
4
Previous Infection Combined with Vaccination Produces Neutralizing Antibodies with Potency against SARS-CoV-2 Variants.既往感染与疫苗接种产生针对 SARS-CoV-2 变异株的中和抗体效力。
mBio. 2021 Dec 21;12(6):e0265621. doi: 10.1128/mBio.02656-21. Epub 2021 Dec 7.
5
Longitudinal immune profiling reveals dominant epitopes mediating long-term humoral immunity in COVID-19-convalescent individuals.纵向免疫分析揭示了介导 COVID-19 恢复期个体长期体液免疫的优势表位。
J Allergy Clin Immunol. 2022 Apr;149(4):1225-1241. doi: 10.1016/j.jaci.2022.01.005. Epub 2022 Jan 21.
6
High-Throughput Neutralization and Serology Assays Reveal Correlated but Highly Variable Humoral Immune Responses in a Large Population of Individuals Infected with SARS-CoV-2 in the US between March and August 2020.高通量中和和血清学检测揭示了 2020 年 3 月至 8 月间美国大量感染 SARS-CoV-2 的个体中相关但高度可变的体液免疫反应。
mBio. 2023 Apr 25;14(2):e0352322. doi: 10.1128/mbio.03523-22. Epub 2023 Feb 14.
7
Comprehensive characterization of the antibody responses to SARS-CoV-2 Spike protein finds additional vaccine-induced epitopes beyond those for mild infection.全面描述了针对 SARS-CoV-2 刺突蛋白的抗体反应,发现了除轻度感染诱导的表位之外的其他疫苗诱导的表位。
Elife. 2022 Jan 24;11:e73490. doi: 10.7554/eLife.73490.
8
Heterogeneous SARS-CoV-2-Neutralizing Activities After Infection and Vaccination.感染和接种后对 SARS-CoV-2 的异源中和活性。
Front Immunol. 2022 May 30;13:888794. doi: 10.3389/fimmu.2022.888794. eCollection 2022.
9
Characterization of SARS-CoV-2-Specific Humoral and Cellular Immune Responses Induced by Inactivated COVID-19 Vaccines in a Real-World Setting.在真实环境中评估灭活 COVID-19 疫苗诱导的 SARS-CoV-2 特异性体液和细胞免疫应答的特征。
Front Immunol. 2021 Dec 22;12:802858. doi: 10.3389/fimmu.2021.802858. eCollection 2021.
10
Comparative kinetics of SARS-CoV-2 anti-spike protein RBD IgGs and neutralizing antibodies in convalescent and naïve recipients of the BNT162b2 mRNA vaccine versus COVID-19 patients.比较 BNT162b2 mRNA 疫苗接种者的恢复期和未接种者的 SARS-CoV-2 抗刺突蛋白 RBD IgG 和中和抗体与 COVID-19 患者的动力学。
BMC Med. 2021 Aug 23;19(1):208. doi: 10.1186/s12916-021-02090-6.

引用本文的文献

1
Rise in broadly cross-reactive adaptive immunity against human β-coronaviruses in MERS-recovered patients during the COVID-19 pandemic.在 COVID-19 大流行期间,MERS 康复患者中针对人类 β 冠状病毒的广泛交叉反应性适应性免疫增加。
Sci Adv. 2024 Mar;10(9):eadk6425. doi: 10.1126/sciadv.adk6425. Epub 2024 Feb 28.
2
Distinctive Combinations of RBD Mutations Contribute to Antibody Evasion in the Case of the SARS-CoV-2 Beta Variant.SARS-CoV-2 贝塔变异株中 RBD 突变的独特组合导致抗体逃逸。
J Microbiol Biotechnol. 2023 Dec 28;33(12):1587-1295. doi: 10.4014/jmb.2308.08020. Epub 2023 Nov 3.
3
Immune evasion of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2); molecular approaches.严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)的免疫逃逸;分子方法。
Mol Immunol. 2023 Apr;156:10-19. doi: 10.1016/j.molimm.2022.11.020. Epub 2022 Nov 24.
4
Two years of COVID-19 pandemic: where are we now?两年的 COVID-19 大流行:我们现在在哪里?
J Microbiol. 2022 Mar;60(3):235-237. doi: 10.1007/s12275-022-1679-x.

本文引用的文献

1
Omicron variant showed lower neutralizing sensitivity than other SARS-CoV-2 variants to immune sera elicited by vaccines after boost.奥密克戎变异株对疫苗加强后免疫血清的中和敏感性低于其他 SARS-CoV-2 变异株。
Emerg Microbes Infect. 2022 Dec;11(1):337-343. doi: 10.1080/22221751.2021.2022440.
2
The antibody response to SARS-CoV-2 Beta underscores the antigenic distance to other variants.针对 SARS-CoV-2 Beta 的抗体反应突显了与其他变体的抗原距离。
Cell Host Microbe. 2022 Jan 12;30(1):53-68.e12. doi: 10.1016/j.chom.2021.11.013. Epub 2021 Nov 27.
3
The state of complement in COVID-19.COVID-19 中的补体状态。
Nat Rev Immunol. 2022 Feb;22(2):77-84. doi: 10.1038/s41577-021-00665-1. Epub 2021 Dec 15.
4
Universal Coronavirus Vaccines - An Urgent Need.通用冠状病毒疫苗——迫切需求
N Engl J Med. 2022 Jan 27;386(4):297-299. doi: 10.1056/NEJMp2118468. Epub 2021 Dec 15.
5
Activation of Intracellular Complement in Lungs of Patients With Severe COVID-19 Disease Decreases T-Cell Activity in the Lungs.重症 COVID-19 患者肺部细胞内补体的激活会降低肺部 T 细胞活性。
Front Immunol. 2021 Nov 24;12:700705. doi: 10.3389/fimmu.2021.700705. eCollection 2021.
6
A monoclonal antibody that neutralizes SARS-CoV-2 variants, SARS-CoV, and other sarbecoviruses.一种能够中和 SARS-CoV-2 变体、SARS-CoV 和其他沙贝科病毒的单克隆抗体。
Emerg Microbes Infect. 2022 Dec;11(1):147-157. doi: 10.1080/22221751.2021.2011623.
7
SARS-CoV-2 Variants, RBD Mutations, Binding Affinity, and Antibody Escape.SARS-CoV-2 变体、RBD 突变、结合亲和力和抗体逃逸。
Int J Mol Sci. 2021 Nov 9;22(22):12114. doi: 10.3390/ijms222212114.
8
SARS-CoV-2 Antibodies Mediate Complement and Cellular Driven Inflammation.SARS-CoV-2 抗体介导补体和细胞驱动的炎症反应。
Front Immunol. 2021 Nov 2;12:767981. doi: 10.3389/fimmu.2021.767981. eCollection 2021.
9
Seronegative Erosive Arthritis Following SARS-CoV-2 Infection.新型冠状病毒感染后的血清阴性侵蚀性关节炎
Rheumatol Ther. 2022 Feb;9(1):295-301. doi: 10.1007/s40744-021-00395-9. Epub 2021 Nov 16.
10
The intersection of COVID-19 and autoimmunity.COVID-19 与自身免疫的交集。
J Clin Invest. 2021 Dec 15;131(24). doi: 10.1172/JCI154886.

体液免疫反应在 COVID-19 中的保护作用和致病作用。

Protective and pathogenic role of humoral responses in COVID-19.

机构信息

Department of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul, 03080, Republic of Korea.

Department of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, 03080, Republic of Korea.

出版信息

J Microbiol. 2022 Mar;60(3):268-275. doi: 10.1007/s12275-022-2037-8. Epub 2022 Mar 2.

DOI:10.1007/s12275-022-2037-8
PMID:35235178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8890013/
Abstract

Since the advent of SARS-CoV-2 in Dec. 2019, the global endeavor to identify the pathogenic mechanism of COVID-19 has been ongoing. Although humoral immunity including neutralizing activity play an important role in protection from the viral pathogen, dysregulated antibody responses may be associated with the pathogenic progression of COVID-19, especially in high-risk individuals. In addition, SARS-CoV-2 spike-specific antibodies acquired by prior infection or vaccination act as immune pressure, driving continuous population turnover by selecting for antibody-escaping mutations. Here, we review accumulating knowledge on the potential role of humoral immune responses in COVID-19, primarily focusing on their beneficial and pathogenic properties. Understanding the multifaceted regulatory mechanisms of humoral responses during SARS-CoV-2 infection can help us to develop more effective therapeutics, as well as protective measures against the ongoing pandemic.

摘要

自 2019 年 12 月 SARS-CoV-2 出现以来,全球一直在努力确定 COVID-19 的发病机制。虽然包括中和活性在内的体液免疫在防止病毒病原体方面发挥着重要作用,但失调的抗体反应可能与 COVID-19 的发病进展有关,尤其是在高危人群中。此外,先前感染或接种疫苗获得的 SARS-CoV-2 刺突特异性抗体充当免疫压力,通过选择逃逸抗体的突变来推动持续的人群更替。在这里,我们回顾了关于体液免疫反应在 COVID-19 中潜在作用的累积知识,主要关注其有益和致病特性。了解 SARS-CoV-2 感染期间体液反应的多方面调节机制有助于我们开发更有效的治疗方法以及针对持续大流行的保护措施。