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新型冠状病毒mRNA疫苗加强接种后血清中和抗体效价及广度的变化

Changes in serum-neutralizing antibody potency and breadth post-SARS-CoV-2 mRNA vaccine boost.

作者信息

Nair Manoj S, Ribeiro Ruy M, Wang Maple, Bowen Anthony D, Liu Lihong, Guo Yicheng, Chang Jennifer Y, Wang Pengfei, Sheng Zizhang, Sobieszczyk Magdalena E, Perelson Alan S, Huang Yaoxing, Ho David D

机构信息

Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA.

Theoretical Biology and Biophysics, Theoretical Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.

出版信息

iScience. 2023 Apr 21;26(4):106345. doi: 10.1016/j.isci.2023.106345. Epub 2023 Mar 6.

DOI:10.1016/j.isci.2023.106345
PMID:36925721
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9987605/
Abstract

A better understanding of the durability and breadth of serum-neutralizing antibody responses against multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants elicited by COVID-19 vaccines is crucial in addressing the current pandemic. In this study, we quantified the decay of serum neutralization antibodies (nAbs) after second and third doses of the original COVID-19 mRNA vaccine. Using an authentic virus-neutralization assay, we found that decay half-lives of WA1- and Delta-nAbs were both ∼60 days after second and third vaccine dose. Unexpectedly, the durability of serum antibodies that neutralize three different Omicron subvariants (BA.1.1, BA.5, BA.2.12.1) was substantially better, with half-lives of ≥6 months. A booster dose of the original COVID-19 vaccine was also found to broaden antibody responses against SARS-CoV and four other sarbecoviruses, in addition to multiple SARS-CoV-2 strains. These findings suggest that repeated vaccinations with the COVID-19 vaccine may confer a degree of protection against future spillover of sarbecoviruses from animal reservoirs.

摘要

更好地了解新冠病毒疾病(COVID-19)疫苗引发的针对多种严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体的血清中和抗体反应的持久性和广度,对于应对当前的大流行至关重要。在本研究中,我们对第二剂和第三剂原始COVID-19 mRNA疫苗后血清中和抗体(nAbs)的衰减进行了量化。使用真实病毒中和试验,我们发现第二剂和第三剂疫苗后,WA1和Delta nAbs的衰减半衰期均约为60天。出乎意料的是,中和三种不同奥密克戎亚变体(BA.1.1、BA.5、BA.2.12.1)的血清抗体的持久性要好得多,半衰期≥6个月。还发现,一剂原始COVID-19疫苗加强针除了能增强针对多种SARS-CoV-2毒株的抗体反应外,还能拓宽针对严重急性呼吸综合征冠状病毒(SARS-CoV)和其他四种沙贝病毒的抗体反应。这些发现表明,重复接种COVID-19疫苗可能会对未来沙贝病毒从动物宿主溢出提供一定程度的保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/2e4ff99ba88b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/588d294e713a/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/1cad2e6fc165/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/2e4ff99ba88b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/588d294e713a/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/1cad2e6fc165/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088d/10031112/2e4ff99ba88b/gr2.jpg

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本文引用的文献

1
Mapping SARS-CoV-2 antigenic relationships and serological responses.绘制 SARS-CoV-2 抗原关系和血清学反应图。
Science. 2023 Oct 6;382(6666):eadj0070. doi: 10.1126/science.adj0070.
2
Antigen presentation dynamics shape the antibody response to variants like SARS-CoV-2 Omicron after multiple vaccinations with the original strain.抗原呈递动力学塑造了对原始毒株多次接种后像 SARS-CoV-2 奥密克戎这样的变体的抗体反应。
Cell Rep. 2023 Apr 25;42(4):112256. doi: 10.1016/j.celrep.2023.112256. Epub 2023 Mar 6.
3
Alarming antibody evasion properties of rising SARS-CoV-2 BQ and XBB subvariants.
Three immunizations with Novavax's protein vaccines increase antibody breadth and provide durable protection from SARS-CoV-2.
接种三剂诺瓦瓦克斯公司的蛋白疫苗可增加抗体广度,并为抵御新冠病毒提供持久保护。
NPJ Vaccines. 2024 Jan 20;9(1):17. doi: 10.1038/s41541-024-00806-2.
令人担忧的 SARS-CoV-2 BQ 和 XBB 亚型不断出现的抗体逃逸特性。
Cell. 2023 Jan 19;186(2):279-286.e8. doi: 10.1016/j.cell.2022.12.018. Epub 2022 Dec 14.
4
Antibody evasion by SARS-CoV-2 Omicron subvariants BA.2.12.1, BA.4 and BA.5.SARS-CoV-2 奥密克戎亚变种 BA.2.12.1、BA.4 和 BA.5 的抗体逃逸
Nature. 2022 Aug;608(7923):603-608. doi: 10.1038/s41586-022-05053-w. Epub 2022 Jul 5.
5
BNT162b2 Vaccine Effectiveness against Omicron in Children 5 to 11 Years of Age.BNT162b2 疫苗对 5 至 11 岁儿童中奥密克戎的有效性。
N Engl J Med. 2022 Jul 21;387(3):227-236. doi: 10.1056/NEJMoa2205011. Epub 2022 Jun 29.
6
Antigenic cartography of SARS-CoV-2 reveals that Omicron BA.1 and BA.2 are antigenically distinct.SARS-CoV-2 抗原图谱显示,奥密克戎 BA.1 和 BA.2 具有不同的抗原性。
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7
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Nature. 2022 Jul;607(7918):351-355. doi: 10.1038/s41586-022-04865-0. Epub 2022 May 18.
8
Immune recall improves antibody durability and breadth to SARS-CoV-2 variants.免疫回忆可提高针对 SARS-CoV-2 变异株的抗体持久性和广谱性。
Sci Immunol. 2022 Dec 23;7(78):eabp8328. doi: 10.1126/sciimmunol.abp8328. Epub 2022 Dec 16.
9
Increased memory B cell potency and breadth after a SARS-CoV-2 mRNA boost.接种 SARS-CoV-2 mRNA 加强针后,记忆 B 细胞的效力和广度增加。
Nature. 2022 Jul;607(7917):128-134. doi: 10.1038/s41586-022-04778-y. Epub 2022 Apr 21.
10
An antibody class with a common CDRH3 motif broadly neutralizes sarbecoviruses.一种具有共同 CDRH3 基序的抗体类别广泛中和沙贝科病毒。
Sci Transl Med. 2022 May 25;14(646):eabn6859. doi: 10.1126/scitranslmed.abn6859.