• 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

长期随访和 SARS-CoV-2 恢复期患者疫苗接种过程中刺突蛋白和核衣壳特异性免疫的动态变化。

Dynamics of spike-and nucleocapsid specific immunity during long-term follow-up and vaccination of SARS-CoV-2 convalescents.

机构信息

Institute of Virology, Helmholtz-Zentrum München/Technical University of Munich, School of Medicine, Munich, Germany.

Institute of Molecular Immunology and Experimental Oncology, Technical University of Munich, School of Medicine, Munich, Germany.

出版信息

Nat Commun. 2022 Jan 10;13(1):153. doi: 10.1038/s41467-021-27649-y.

DOI:10.1038/s41467-021-27649-y
PMID:35013191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8748966/
Abstract

Anti-viral immunity continuously declines over time after SARS-CoV-2 infection. Here, we characterize the dynamics of anti-viral immunity during long-term follow-up and after BNT162b2 mRNA-vaccination in convalescents after asymptomatic or mild SARS-CoV-2 infection. Virus-specific and virus-neutralizing antibody titers rapidly declined in convalescents over 9 months after infection, whereas virus-specific cytokine-producing polyfunctional T cells persisted, among which IL-2-producing T cells correlated with virus-neutralizing antibody titers. Among convalescents, 5% of individuals failed to mount long-lasting immunity after infection and showed a delayed response to vaccination compared to 1% of naïve vaccinees, but successfully responded to prime/boost vaccination. During the follow-up period, 8% of convalescents showed a selective increase in virus-neutralizing antibody titers without accompanying increased frequencies of circulating SARS-CoV-2-specific T cells. The same convalescents, however, responded to vaccination with simultaneous increase in antibody and T cell immunity revealing the strength of mRNA-vaccination to increase virus-specific immunity in convalescents.

摘要

SARS-CoV-2 感染后,抗病毒免疫力会随时间持续下降。在这里,我们描述了无症状或轻症 SARS-CoV-2 感染后恢复期个体在长期随访期间及 BNT162b2 mRNA 疫苗接种后的抗病毒免疫动态。感染后 9 个月内,恢复期个体的病毒特异性和中和抗体滴度迅速下降,而病毒特异性细胞因子产生的多功能 T 细胞持续存在,其中产生 IL-2 的 T 细胞与中和抗体滴度相关。在恢复期个体中,有 5%的个体在感染后未能产生持久免疫力,且与未感染的疫苗接种者相比,对疫苗的反应延迟,但成功地对加强针疫苗产生了应答。在随访期间,有 8%的恢复期个体表现出病毒中和抗体滴度的选择性增加,而循环 SARS-CoV-2 特异性 T 细胞的频率没有相应增加。然而,这些相同的恢复期个体对疫苗接种的反应是抗体和 T 细胞免疫同时增加,这揭示了 mRNA 疫苗在增强恢复期个体病毒特异性免疫方面的强大效力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/c68890e7a1d0/41467_2021_27649_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/136bc3bef674/41467_2021_27649_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/139cf940bb4a/41467_2021_27649_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/d7c8ac9d463e/41467_2021_27649_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/44a09bf18d73/41467_2021_27649_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/f7a98a778295/41467_2021_27649_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/4454a454afae/41467_2021_27649_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/c68890e7a1d0/41467_2021_27649_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/136bc3bef674/41467_2021_27649_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/139cf940bb4a/41467_2021_27649_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/d7c8ac9d463e/41467_2021_27649_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/44a09bf18d73/41467_2021_27649_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/f7a98a778295/41467_2021_27649_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/4454a454afae/41467_2021_27649_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401e/8748966/c68890e7a1d0/41467_2021_27649_Fig7_HTML.jpg

相似文献

1
Dynamics of spike-and nucleocapsid specific immunity during long-term follow-up and vaccination of SARS-CoV-2 convalescents.长期随访和 SARS-CoV-2 恢复期患者疫苗接种过程中刺突蛋白和核衣壳特异性免疫的动态变化。
Nat Commun. 2022 Jan 10;13(1):153. doi: 10.1038/s41467-021-27649-y.
2
B Cell Response Induced by SARS-CoV-2 Infection Is Boosted by the BNT162b2 Vaccine in Primary Antibody Deficiencies.SARS-CoV-2 感染诱导的 B 细胞反应可被 BNT162b2 疫苗增强原发性抗体缺陷。
Cells. 2021 Oct 27;10(11):2915. doi: 10.3390/cells10112915.
3
A single mRNA vaccine dose in COVID-19 patients boosts neutralizing antibodies against SARS-CoV-2 and variants of concern.在 COVID-19 患者中接种一剂 mRNA 疫苗可提高针对 SARS-CoV-2 及关注变异株的中和抗体。
Cell Rep Med. 2021 Dec 14;3(1):100486. doi: 10.1016/j.xcrm.2021.100486. eCollection 2022 Jan 18.
4
Anti-SARS-CoV-2 Immunoglobulin Isotypes, and Neutralization Activity Against Viral Variants, According to BNT162b2-Vaccination and Infection History.根据 BNT162b2 疫苗接种和感染史,抗 SARS-CoV-2 免疫球蛋白同种型和对病毒变异体的中和活性。
Front Immunol. 2021 Dec 17;12:793191. doi: 10.3389/fimmu.2021.793191. eCollection 2021.
5
B and T cell response to SARS-CoV-2 vaccination in health care professionals with and without previous COVID-19.医护人员中有无既往 COVID-19 史者对 SARS-CoV-2 疫苗接种的 B 和 T 细胞应答。
EBioMedicine. 2021 Aug;70:103539. doi: 10.1016/j.ebiom.2021.103539. Epub 2021 Aug 12.
6
Cutting Edge: Serum but Not Mucosal Antibody Responses Are Associated with Pre-Existing SARS-CoV-2 Spike Cross-Reactive CD4 T Cells following BNT162b2 Vaccination in the Elderly.前沿:血清而非黏膜抗体反应与 BNT162b2 疫苗接种后老年人中预先存在的 SARS-CoV-2 刺突交叉反应性 CD4 T 细胞有关。
J Immunol. 2022 Mar 1;208(5):1001-1005. doi: 10.4049/jimmunol.2100990. Epub 2022 Feb 4.
7
Longitudinal analysis of antibody dynamics in COVID-19 convalescents reveals neutralizing responses up to 16 months after infection.对 COVID-19 康复者的抗体动态进行纵向分析显示,感染后长达 16 个月仍存在中和反应。
Nat Microbiol. 2022 Mar;7(3):423-433. doi: 10.1038/s41564-021-01051-2. Epub 2022 Feb 7.
8
Three exposures to the spike protein of SARS-CoV-2 by either infection or vaccination elicit superior neutralizing immunity to all variants of concern.通过感染或接种疫苗,三次接触 SARS-CoV-2 的刺突蛋白会引发对所有令人关注的变异体更好的中和免疫。
Nat Med. 2022 Mar;28(3):496-503. doi: 10.1038/s41591-022-01715-4. Epub 2022 Jan 28.
9
Sequential Analysis of Binding and Neutralizing Antibody in COVID-19 Convalescent Patients at 14 Months After SARS-CoV-2 Infection.新冠病毒感染 14 个月后 COVID-19 恢复期患者结合抗体和中和抗体的动态分析。
Front Immunol. 2021 Nov 26;12:793953. doi: 10.3389/fimmu.2021.793953. eCollection 2021.
10
Cellular and humoral functional responses after BNT162b2 mRNA vaccination differ longitudinally between naive and subjects recovered from COVID-19.BNT162b2 mRNA 疫苗接种后细胞和体液功能反应在 COVID-19 初治和恢复期患者中具有纵向差异。
Cell Rep. 2022 Jan 11;38(2):110235. doi: 10.1016/j.celrep.2021.110235. Epub 2021 Dec 21.

引用本文的文献

1
The Role of SARS-CoV-2 Nucleocapsid Protein in Host Inflammation.严重急性呼吸综合征冠状病毒2核衣壳蛋白在宿主炎症中的作用
Viruses. 2025 Jul 27;17(8):1046. doi: 10.3390/v17081046.
2
Predicting SARS-CoV-2-specific CD4 and CD8 T-cell responses elicited by inactivated vaccines in healthy adults using machine learning models.使用机器学习模型预测灭活疫苗在健康成年人中引发的SARS-CoV-2特异性CD4和CD8 T细胞反应。
Clin Exp Med. 2025 Jul 8;25(1):236. doi: 10.1007/s10238-025-01772-2.
3
Protective Potential and Functional Role of Antibodies Against SARS-CoV-2 Nucleocapsid Protein.

本文引用的文献

1
SARS-CoV-2 vaccine breakthrough infections with the alpha variant are asymptomatic or mildly symptomatic among health care workers.在医护人员中,感染新冠病毒阿尔法变异株的突破性病例通常无症状或症状轻微。
Nat Commun. 2021 Oct 15;12(1):6032. doi: 10.1038/s41467-021-26154-6.
2
Broadly directed SARS-CoV-2-specific CD4+ T cell response includes frequently detected peptide specificities within the membrane and nucleoprotein in patients with acute and resolved COVID-19.广泛靶向 SARS-CoV-2 的特异性 CD4+ T 细胞反应包括急性和已解决的 COVID-19 患者中经常检测到的膜和核蛋白内的肽特异性。
PLoS Pathog. 2021 Sep 16;17(9):e1009842. doi: 10.1371/journal.ppat.1009842. eCollection 2021 Sep.
3
抗SARS-CoV-2核衣壳蛋白抗体的保护潜力及功能作用
Antibodies (Basel). 2025 May 28;14(2):45. doi: 10.3390/antib14020045.
4
Incidence of dynamic seroconversion in subjects received the first dose of the SARS-COV-2 vaccine (AstraZeneca, Moderna and Pfizer) in Kinshasa, Democratic Republic of Congo: prospective cohort study.刚果民主共和国金沙萨接受第一剂新冠病毒疫苗(阿斯利康、莫德纳和辉瑞)的受试者中动态血清转化的发生率:前瞻性队列研究。
BMC Infect Dis. 2025 Mar 11;25(1):342. doi: 10.1186/s12879-025-10754-4.
5
Vaccination with Plasmids Encoding the Fusion Proteins D-S1, D-S1N and O-SN from SARS-CoV-2 Induces an Effective Humoral and Cellular Immune Response in Mice.用编码来自严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的融合蛋白D-S1、D-S1N和O-SN的质粒进行疫苗接种可在小鼠中诱导有效的体液免疫和细胞免疫反应。
Vaccines (Basel). 2025 Jan 28;13(2):134. doi: 10.3390/vaccines13020134.
6
Co-immunization with spike and nucleocapsid based DNA vaccines for long-term protective immunity against SARS-CoV-2 Omicron.基于刺突蛋白和核衣壳的DNA疫苗联合免疫以获得针对SARS-CoV-2奥密克戎毒株的长期保护性免疫。
NPJ Vaccines. 2024 Dec 19;9(1):252. doi: 10.1038/s41541-024-01043-3.
7
Characterisation of the antibody-mediated selective pressure driving intra-host evolution of SARS-CoV-2 in prolonged infection.描述抗体介导的选择压力如何驱动 SARS-CoV-2 在持续性感染期间在宿主内进化。
PLoS Pathog. 2024 Oct 15;20(10):e1012624. doi: 10.1371/journal.ppat.1012624. eCollection 2024 Oct.
8
Escalating SARS-CoV-2 specific humoral immune response in rheumatoid arthritis patients and healthy controls.类风湿关节炎患者和健康对照者 SARS-CoV-2 特异性体液免疫应答逐渐增强。
Front Immunol. 2024 Jun 7;15:1397052. doi: 10.3389/fimmu.2024.1397052. eCollection 2024.
9
Evaluation of novel Epstein-Barr virus-derived antigen formulations for monitoring virus-specific T cells in pediatric patients with infectious mononucleosis.评价新型 Epstein-Barr 病毒衍生抗原制剂在监测传染性单核细胞增多症患儿病毒特异性 T 细胞中的作用。
Virol J. 2024 Jun 14;21(1):139. doi: 10.1186/s12985-024-02411-0.
10
SARS-CoV-2 seroprevalence among healthcare workers in a highly vaccinated Japanese medical center from 2020-2023.2020-2023 年日本一家高度接种疫苗的医疗中心医护人员中 SARS-CoV-2 的血清流行率。
Hum Vaccin Immunother. 2024 Dec 31;20(1):2337984. doi: 10.1080/21645515.2024.2337984. Epub 2024 Apr 15.
Resurgence of Ebola virus in 2021 in Guinea suggests a new paradigm for outbreaks.
2021 年在几内亚再次出现埃博拉病毒,表明疫情暴发出现了新的模式。
Nature. 2021 Sep;597(7877):539-543. doi: 10.1038/s41586-021-03901-9. Epub 2021 Sep 15.
4
Pre-activated antiviral innate immunity in the upper airways controls early SARS-CoV-2 infection in children.上呼吸道预先激活的抗病毒先天免疫可控制儿童早期 SARS-CoV-2 感染。
Nat Biotechnol. 2022 Mar;40(3):319-324. doi: 10.1038/s41587-021-01037-9. Epub 2021 Aug 18.
5
Differential effects of the second SARS-CoV-2 mRNA vaccine dose on T cell immunity in naive and COVID-19 recovered individuals.第二剂 SARS-CoV-2 mRNA 疫苗对初免人群和 COVID-19 康复者 T 细胞免疫的差异影响。
Cell Rep. 2021 Aug 24;36(8):109570. doi: 10.1016/j.celrep.2021.109570. Epub 2021 Aug 4.
6
SARS-CoV-2 Variants in Patients with Immunosuppression.免疫抑制患者中的新型冠状病毒2型变体
N Engl J Med. 2021 Aug 5;385(6):562-566. doi: 10.1056/NEJMsb2104756.
7
Rapid and stable mobilization of CD8 T cells by SARS-CoV-2 mRNA vaccine.SARS-CoV-2 mRNA 疫苗可快速稳定地动员 CD8 T 细胞。
Nature. 2021 Sep;597(7875):268-273. doi: 10.1038/s41586-021-03841-4. Epub 2021 Jul 28.
8
Dynamic innate immune response determines susceptibility to SARS-CoV-2 infection and early replication kinetics.动态先天免疫反应决定了对 SARS-CoV-2 感染的易感性和早期复制动力学。
J Exp Med. 2021 Aug 2;218(8). doi: 10.1084/jem.20210583. Epub 2021 Jun 15.
9
Naturally enhanced neutralizing breadth against SARS-CoV-2 one year after infection.感染 SARS-CoV-2 一年后自然增强的对其的中和广度。
Nature. 2021 Jul;595(7867):426-431. doi: 10.1038/s41586-021-03696-9. Epub 2021 Jun 14.
10
Tissues, not blood, are where immune cells function.免疫细胞发挥功能的场所是组织,而非血液。
Nature. 2021 May;593(7860):506-509. doi: 10.1038/d41586-021-01396-y.