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感染后对 SARS-CoV-2 变异株的交叉中和广度和持久性。

Cross-Neutralizing Breadth and Longevity Against SARS-CoV-2 Variants After Infections.

机构信息

Division of Clinical Virology, Center for Infectious Diseases, Kobe University Graduate School of Medicine, Kobe, Japan.

Division of Cardiovascular Medicine, Hyogo Prefectural Kakogawa Medical Center, Kakogawa, Japan.

出版信息

Front Immunol. 2022 Feb 24;13:773652. doi: 10.3389/fimmu.2022.773652. eCollection 2022.

DOI:10.3389/fimmu.2022.773652
PMID:35281007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8907139/
Abstract

BACKGROUND

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is the virus responsible for the Coronavirus Disease 2019 (COVID-19) pandemic. The emergence of variants of concern (VOCs) has become one of the most pressing issues in public health. To control VOCs, it is important to know which COVID-19 convalescent sera have cross-neutralizing activity against VOCs and how long the sera maintain this protective activity.

METHODS

Sera of patients infected with SARS-CoV-2 from March 2020 to January 2021 and admitted to Hyogo Prefectural Kakogawa Medical Center were selected. Blood was drawn from patients at 1-3, 3-6, and 6-8 months post onset. Then, a virus neutralization assay against SARS-CoV-2 variants (D614G mutation as conventional strain; B.1.1.7, P.1, and B.1.351 as VOCs) was performed using authentic viruses.

RESULTS

We assessed 97 sera from 42 patients. Sera from 28 patients showed neutralizing activity that was sustained for 3-8 months post onset. The neutralizing antibody titer against D614G significantly decreased in sera of 6-8 months post onset compared to those of 1-3 months post onset. However, the neutralizing antibody titers against the three VOCs were not significantly different among 1-3, 3-6, and 6-8 months post onset.

DISCUSSION

Our results indicate that neutralizing antibodies that recognize the common epitope for several variants may be maintained for a long time, while neutralizing antibodies having specific epitopes for a variant, produced in large quantities immediately after infection, may decrease quite rapidly.

摘要

背景

严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)是引发 2019 年冠状病毒病(COVID-19)大流行的病毒。关注变异株(VOC)的出现已成为公共卫生领域最紧迫的问题之一。为了控制 VOC,了解 COVID-19 恢复期血清对 VOC 具有交叉中和活性以及血清能维持这种保护活性的时间长短非常重要。

方法

选择 2020 年 3 月至 2021 年 1 月期间在兵库县加古川医疗中心因感染 SARS-CoV-2 而住院的患者的血清。在发病后 1-3、3-6 和 6-8 个月时从患者身上抽取血液。然后,使用真病毒对 SARS-CoV-2 变体(D614G 突变作为常规株;B.1.1.7、P.1 和 B.1.351 作为 VOC)进行病毒中和测定。

结果

我们评估了 42 名患者的 97 份血清。28 名患者的血清在发病后 3-8 个月保持中和活性。与发病后 1-3 个月相比,发病后 6-8 个月的血清对 D614G 的中和抗体滴度显著降低。然而,发病后 1-3、3-6 和 6-8 个月的血清对三种 VOC 的中和抗体滴度没有显著差异。

讨论

我们的结果表明,识别几个变体共有表位的中和抗体可能会长期维持,而针对变体特定表位的中和抗体在感染后立即大量产生,可能会迅速下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/2d2ea15ca8b8/fimmu-13-773652-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/d9ba0e858f32/fimmu-13-773652-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/60bed27522ea/fimmu-13-773652-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/2d2ea15ca8b8/fimmu-13-773652-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/d9ba0e858f32/fimmu-13-773652-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/60bed27522ea/fimmu-13-773652-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc93/8907139/2d2ea15ca8b8/fimmu-13-773652-g003.jpg

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本文引用的文献

1
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Lancet. 2022 Jan 15;399(10321):234-236. doi: 10.1016/S0140-6736(21)02844-0. Epub 2021 Dec 20.
2
Omicron and Delta variant of SARS-CoV-2: A comparative computational study of spike protein.SARS-CoV-2 的奥密克戎和德尔塔变体:刺突蛋白的比较计算研究。
J Med Virol. 2022 Apr;94(4):1641-1649. doi: 10.1002/jmv.27526. Epub 2021 Dec 27.
3
The significant immune escape of pseudotyped SARS-CoV-2 variant Omicron.
对原始新冠病毒感染的中和抗体反应广度与长期新冠症状的存在有关。
medRxiv. 2023 Mar 31:2023.03.30.23287923. doi: 10.1101/2023.03.30.23287923.
4
A DNA Vaccine Encoding the Full-Length Spike Protein of Beta Variant (B.1.351) Elicited Broader Cross-Reactive Immune Responses against Other SARS-CoV-2 Variants.一种编码β变异株(B.1.351)全长刺突蛋白的DNA疫苗引发了针对其他SARS-CoV-2变异株的更广泛的交叉反应性免疫应答。
Vaccines (Basel). 2023 Feb 22;11(3):513. doi: 10.3390/vaccines11030513.
5
COVID-19 and the Immune Response: A Multi-Phasic Approach to the Treatment of COVID-19.新型冠状病毒肺炎与免疫反应:新型冠状病毒肺炎治疗的多相策略。
Int J Mol Sci. 2022 Aug 3;23(15):8606. doi: 10.3390/ijms23158606.
6
Large-scale serosurveillance of COVID-19 in Japan: Acquisition of neutralizing antibodies for Delta but not for Omicron and requirement of booster vaccination to overcome the Omicron's outbreak.日本大规模的 COVID-19 血清学监测:获得针对 Delta 的中和抗体,但未获得针对奥密克戎的中和抗体,需要加强接种以克服奥密克戎的爆发。
PLoS One. 2022 Apr 5;17(4):e0266270. doi: 10.1371/journal.pone.0266270. eCollection 2022.
假型 SARS-CoV-2 变异株奥密克戎的显著免疫逃逸。
Emerg Microbes Infect. 2022 Dec;11(1):1-5. doi: 10.1080/22221751.2021.2017757.
4
Neutralizing antibody activity in convalescent sera from infection in humans with SARS-CoV-2 and variants of concern.感染 SARS-CoV-2 及关注变异株后康复患者血清中的中和抗体活性。
Nat Microbiol. 2021 Nov;6(11):1433-1442. doi: 10.1038/s41564-021-00974-0. Epub 2021 Oct 15.
5
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6
SARS-CoV-2 B.1.1.7 lineage rapidly spreads and replaces R.1 lineage in Japan: Serial and stationary observation in a community.SARS-CoV-2 B.1.1.7 谱系在日本迅速传播并取代 R.1 谱系:社区内的连续和定点观察。
Infect Genet Evol. 2021 Nov;95:105088. doi: 10.1016/j.meegid.2021.105088. Epub 2021 Sep 21.
7
Emerging SARS-CoV-2 variants of concern evade humoral immune responses from infection and vaccination.新出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变异株可逃避感染和疫苗接种所引发的体液免疫反应。
Sci Adv. 2021 Sep 3;7(36):eabj5365. doi: 10.1126/sciadv.abj5365.
8
Temporal maturation of neutralizing antibodies in COVID-19 convalescent individuals improves potency and breadth to circulating SARS-CoV-2 variants.COVID-19 恢复期个体中中和抗体的时间成熟提高了对流行的 SARS-CoV-2 变体的效力和广度。
Immunity. 2021 Aug 10;54(8):1841-1852.e4. doi: 10.1016/j.immuni.2021.06.015. Epub 2021 Jul 2.
9
SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19.严重急性呼吸综合征冠状病毒2型人类T细胞表位:针对2019冠状病毒病的适应性免疫反应
Cell Host Microbe. 2021 Jul 14;29(7):1076-1092. doi: 10.1016/j.chom.2021.05.010. Epub 2021 May 21.
10
Prevalence of neutralising antibodies against SARS-CoV-2 in acute infection and convalescence: A systematic review and meta-analysis.急性感染和恢复期针对 SARS-CoV-2 的中和抗体流行率:系统评价和荟萃分析。
PLoS Negl Trop Dis. 2021 Jul 8;15(7):e0009551. doi: 10.1371/journal.pntd.0009551. eCollection 2021 Jul.