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对 COVID-19 进行免疫消毒:开发辅助性 T 细胞 I 和 II 激活疫苗是当务之急。

Sterilizing Immunity against COVID-19: Developing Helper T cells I and II activating vaccines is imperative.

机构信息

Department of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.

Department of Clinical Microbiology, School of Medicine and Health Sciences, University for Development Studies, Tamale, Ghana.

出版信息

Biomed Pharmacother. 2021 Dec;144:112282. doi: 10.1016/j.biopha.2021.112282. Epub 2021 Oct 2.

DOI:10.1016/j.biopha.2021.112282
PMID:34624675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8486642/
Abstract

Six months after the publication of the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) sequence, a record number of vaccine candidates were listed, and quite a number of them have since been approved for emergency use against the novel coronavirus disease 2019 (COVID-19). This unprecedented pharmaceutical feat did not only show commitment, creativity and collaboration of the scientific community, but also provided a swift solution that prevented global healthcare system breakdown. Notwithstanding, the available data show that most of the approved COVID-19 vaccines protect only a proportion of recipients against severe disease but do not prevent clinical manifestation of COVID-19. There is therefore the need to probe further to establish whether these vaccines can induce sterilizing immunity, otherwise, COVID-19 vaccination would have to become a regular phenomenon. The emergence of SARS-CoV-2 variants could further affect the capability of the available COVID-19 vaccines to prevent infection and protect recipients from a severe form of the disease. These notwithstanding, data about which vaccine(s), if any, can confer sterilizing immunity are unavailable. Here, we discuss the immune responses to viral infection with emphasis on COVID-19, and the specific adaptive immune response to SARS-CoV-2 and how it can be harnessed to develop COVID-19 vaccines capable of conferring sterilizing immunity. We further propose factors that could be considered in the development of COVID-19 vaccines capable of stimulating sterilizing immunity. Also, an old, but effective vaccine development technology that can be applied in the development of COVID-19 vaccines with sterilizing immunity potential is reviewed.

摘要

六个月后严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)序列公布,创纪录数量的疫苗候选者被列出,此后相当数量的疫苗已被批准用于针对新型冠状病毒病 2019(COVID-19)的紧急使用。这一前所未有的制药壮举不仅展示了科学界的承诺、创造力和合作精神,还提供了一个迅速的解决方案,防止了全球医疗保健系统的崩溃。尽管如此,现有数据表明,大多数批准的 COVID-19 疫苗仅能保护一部分接种者免受严重疾病的侵害,但不能预防 COVID-19 的临床症状。因此,有必要进一步探究这些疫苗是否能诱导出杀菌性免疫,否则,COVID-19 疫苗接种将不得不成为一种常规现象。SARS-CoV-2 变体的出现可能会进一步影响现有 COVID-19 疫苗预防感染和保护接种者免受严重疾病的能力。尽管如此,关于哪种(哪些)疫苗如果有的话可以赋予杀菌性免疫的数据尚不可用。在这里,我们讨论了针对病毒感染的免疫反应,重点是 COVID-19,以及针对 SARS-CoV-2 的特定适应性免疫反应,以及如何利用它来开发能够赋予杀菌性免疫的 COVID-19 疫苗。我们进一步提出了在开发能够刺激杀菌性免疫的 COVID-19 疫苗时可以考虑的因素。此外,还回顾了一种古老但有效的疫苗开发技术,该技术可应用于开发具有杀菌性免疫潜力的 COVID-19 疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/b87e039b8e6c/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/4494858a3919/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/37a91390d769/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/c02c4f1b9442/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/b56b079e9cd4/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/834db61b278b/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/b87e039b8e6c/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/4494858a3919/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/37a91390d769/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/c02c4f1b9442/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/b56b079e9cd4/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/834db61b278b/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da3/8486642/b87e039b8e6c/gr5_lrg.jpg

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本文引用的文献

1
Methodological Analysis: Randomized Controlled Trials for Pfizer and Moderna COVID-19 Vaccines.方法学分析:辉瑞和莫德纳 COVID-19 疫苗的随机对照试验。
J Pediatr Health Care. 2021 Jul-Aug;35(4):443-448. doi: 10.1016/j.pedhc.2021.04.001. Epub 2021 May 31.
2
Neutralization of Beta and Delta variant with sera of COVID-19 recovered cases and vaccinees of inactivated COVID-19 vaccine BBV152/Covaxin.用 COVID-19 恢复期患者和灭活 COVID-19 疫苗 BBV152/Covaxin 接种者的血清中和 Beta 和 Delta 变异株。
J Travel Med. 2021 Oct 11;28(7). doi: 10.1093/jtm/taab104.
3
Cross-reactive serum and memory B-cell responses to spike protein in SARS-CoV-2 and endemic coronavirus infection.
SARS-CoV-2 检测面临的挑战:侧向流动免疫分析的发展——作为病毒诊断的有价值工具。
Biosensors (Basel). 2022 Sep 5;12(9):728. doi: 10.3390/bios12090728.
4
Zika virus-like particle vaccine fusion loop mutation increases production yield but fails to protect AG129 mice against Zika virus challenge.寨卡病毒样颗粒疫苗融合环突变提高了产量,但不能保护 AG129 小鼠免受寨卡病毒挑战。
PLoS Negl Trop Dis. 2022 Jul 6;16(7):e0010588. doi: 10.1371/journal.pntd.0010588. eCollection 2022 Jul.
5
Antimicrobial Resistance in the COVID-19 Landscape: Is There an Opportunity for Anti-Infective Antibodies and Antimicrobial Peptides?新型冠状病毒肺炎疫情下的抗菌药物耐药性:抗感染抗体和抗菌肽是否有机会?
Front Immunol. 2022 Jun 2;13:921483. doi: 10.3389/fimmu.2022.921483. eCollection 2022.
6
Asymptomatic COVID-19 CT image denoising method based on wavelet transform combined with improved PSO.基于小波变换结合改进粒子群优化算法的无症状新冠肺炎CT图像去噪方法
Biomed Signal Process Control. 2022 Jul;76:103707. doi: 10.1016/j.bspc.2022.103707. Epub 2022 Apr 18.
7
Antibodies: A Double Leg Takedown Against COVID-19.抗体:对抗新冠病毒的双重攻势
J Infect Dis. 2022 May 16;225(10):1685-1687. doi: 10.1093/infdis/jiac061.
8
COVID-19 Vaccination: The Mainspring of Challenges and the Seed of Remonstrance.新冠疫苗接种:挑战的根源与谏言的种子
Vaccines (Basel). 2021 Dec 13;9(12):1474. doi: 10.3390/vaccines9121474.
血清中和抗体及记忆 B 细胞对 SARS-CoV-2 刺突蛋白和地方性冠状病毒感染的交叉反应性。
Nat Commun. 2021 May 19;12(1):2938. doi: 10.1038/s41467-021-23074-3.
4
Effectiveness of the Pfizer-BioNTech and Oxford-AstraZeneca vaccines on covid-19 related symptoms, hospital admissions, and mortality in older adults in England: test negative case-control study.辉瑞-生物科技疫苗和牛津-阿斯利康疫苗对英格兰老年人新冠病毒相关症状、住院及死亡率的有效性:检测阴性病例对照研究
BMJ. 2021 May 13;373:n1088. doi: 10.1136/bmj.n1088.
5
Role of Circulating T Follicular Helper Cells and Stem-Like Memory CD4 T Cells in the Pathogenesis of HIV-2 Infection and Disease Progression.循环滤泡辅助性 T 细胞和干细胞样记忆 CD4 T 细胞在 HIV-2 感染和疾病进展中的作用。
Front Immunol. 2021 Apr 16;12:666388. doi: 10.3389/fimmu.2021.666388. eCollection 2021.
6
Ebola virus disease: current vaccine solutions.埃博拉病毒病:现有疫苗解决方案。
Curr Opin Immunol. 2021 Aug;71:27-33. doi: 10.1016/j.coi.2021.03.008. Epub 2021 Apr 17.
7
COVID-19 vaccines: modes of immune activation and future challenges.COVID-19 疫苗:免疫激活模式和未来挑战。
Nat Rev Immunol. 2021 Apr;21(4):195-197. doi: 10.1038/s41577-021-00526-x.
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Cell. 2021 Apr 1;184(7):1858-1864.e10. doi: 10.1016/j.cell.2021.02.010. Epub 2021 Feb 9.
9
Multiscale Modeling of Germinal Center Recapitulates the Temporal Transition From Memory B Cells to Plasma Cells Differentiation as Regulated by Antigen Affinity-Based Tfh Cell Help.基于抗原亲和力的滤泡辅助性 T 细胞帮助的生发中心多尺度建模再现了从记忆 B 细胞到浆细胞分化的时间转变。
Front Immunol. 2021 Feb 5;11:620716. doi: 10.3389/fimmu.2020.620716. eCollection 2020.
10
Epitope mimicry analysis of SARS-COV-2 surface proteins and human lung proteins.SARS-COV-2 表面蛋白和人肺蛋白的表位模拟分析。
J Mol Graph Model. 2021 Jun;105:107836. doi: 10.1016/j.jmgm.2021.107836. Epub 2021 Feb 4.