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我们真的需要基于奥密克戎 Spike 的更新版 COVID-19 疫苗吗?证据和研发管线。

Do We Really Need Omicron Spike-Based Updated COVID-19 Vaccines? Evidence and Pipeline.

机构信息

North-Western Tuscany Blood Bank, Pisa University Hospital, 56124 Pisa, Italy.

National Institute for Infectious Diseases "L. Spallanzani", 00161 Roma, Italy.

出版信息

Viruses. 2022 Nov 10;14(11):2488. doi: 10.3390/v14112488.

DOI:10.3390/v14112488
PMID:36366586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9692555/
Abstract

The wild-type SARS-CoV-2 Spike-based vaccines authorized so far have reduced COVID-19 severity, but periodic boosts are required to counteract the decline in immunity. An accelerated rate of immune escape to vaccine-elicited immunity has been associated with Spike protein antigenic shifts, as seen in the Omicron variant of concern and its sublineages, demanding the development of Omicron Spike-based vaccines. Herein, we review the evidence in animal models and topline results from ongoing clinical trials with such updated vaccines, discussing the pros and cons for their deployment.

摘要

迄今为止,获得授权的基于野生型 SARS-CoV-2 刺突蛋白的疫苗已经降低了 COVID-19 的严重程度,但需要定期加强针来对抗免疫的下降。正如在关注的奥密克戎变体及其亚谱系中所见,对疫苗诱导的免疫的免疫逃逸速度加快与刺突蛋白抗原转变有关,因此需要开发基于奥密克戎刺突蛋白的疫苗。在此,我们综述了这些更新的疫苗在动物模型中的证据和正在进行的临床试验的主要结果,讨论了它们部署的优缺点。

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Do We Really Need Omicron Spike-Based Updated COVID-19 Vaccines? Evidence and Pipeline.我们真的需要基于奥密克戎 Spike 的更新版 COVID-19 疫苗吗?证据和研发管线。
Viruses. 2022 Nov 10;14(11):2488. doi: 10.3390/v14112488.
2
Neutralizing antibodies to SARS-CoV-2 variants of concern including Delta and Omicron in subjects receiving mRNA-1273, BNT162b2, and Ad26.COV2.S vaccines.mRNA-1273、BNT162b2 和 Ad26.COV2.S 疫苗接种者对包括德尔塔和奥密克戎在内的关注变异株 SARS-CoV-2 的中和抗体。
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Clinical development of variant-adapted BNT162b2 COVID-19 vaccines: the early Omicron era.变异株适应型 BNT162b2 COVID-19 疫苗的临床开发:奥密克戎早期。
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Neutralization of Omicron sublineages and Deltacron SARS-CoV-2 by three doses of BNT162b2 vaccine or BA.1 infection.三剂 BNT162b2 疫苗或 BA.1 感染对奥密克戎亚谱系和德尔塔克戎 SARS-CoV-2 的中和作用。
Emerg Microbes Infect. 2022 Dec;11(1):1828-1832. doi: 10.1080/22221751.2022.2099305.
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A bivalent vaccine containing D614G and BA.1 spike trimer proteins or a BA.1 spike trimer protein booster shows broad neutralizing immunity.含有 D614G 和 BA.1 刺突三聚体蛋白的二价疫苗或 BA.1 刺突三聚体蛋白加强针可产生广泛的中和免疫。
J Med Virol. 2022 Sep;94(9):4287-4293. doi: 10.1002/jmv.27885. Epub 2022 Jun 2.
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Antibody evasion properties of SARS-CoV-2 Omicron sublineages.SARS-CoV-2 奥密克戎亚谱系的抗体逃逸特性。
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A mosaic-type trimeric RBD-based COVID-19 vaccine candidate induces potent neutralization against Omicron and other SARS-CoV-2 variants.一种基于三聚体 RBD 的马赛克型 COVID-19 疫苗候选物可诱导针对奥密克戎和其他 SARS-CoV-2 变体的强大中和作用。
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Antibody Avidity and Neutralizing Response against SARS-CoV-2 Omicron Variant after Infection or Vaccination.感染或接种疫苗后针对 SARS-CoV-2 奥密克戎变异株的抗体亲合力和中和反应。
J Immunol Res. 2022 Aug 31;2022:4813199. doi: 10.1155/2022/4813199. eCollection 2022.

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Cell Commun Signal. 2023 May 15;21(1):110. doi: 10.1186/s12964-023-01104-5.
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Convergent Evolution in SARS-CoV-2 Spike Creates a Variant Soup from Which New COVID-19 Waves Emerge.SARS-CoV-2 刺突蛋白的趋同进化导致了新的 COVID-19 浪潮的变体汤的出现。
Int J Mol Sci. 2023 Jan 23;24(3):2264. doi: 10.3390/ijms24032264.
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From Co-Administration to Co-Formulation: The Race for New Vaccines against COVID-19 and Other Respiratory Viruses.从联合给药到联合制剂:新型 COVID-19 及其他呼吸道病毒疫苗的研发竞赛
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本文引用的文献

1
Long-term humoral response following Delta and Omicron BA.1 co-infection.德尔塔毒株和奥密克戎毒株BA.1共同感染后的长期体液免疫反应。
NPJ Vaccines. 2023 Apr 20;8(1):57. doi: 10.1038/s41541-023-00652-8.
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Predicting the efficacy of variant-modified COVID-19 vaccine boosters.预测变异株改良 COVID-19 疫苗加强针的效力。
Nat Med. 2023 Mar;29(3):574-578. doi: 10.1038/s41591-023-02228-4. Epub 2023 Mar 2.
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Substantial Neutralization Escape by SARS-CoV-2 Omicron Variants BQ.1.1 and XBB.1.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎变种BQ.1.1和XBB.1的显著中和逃逸
N Engl J Med. 2023 Feb 16;388(7):662-664. doi: 10.1056/NEJMc2214314. Epub 2023 Jan 18.
4
Antibody Response to Omicron BA.4-BA.5 Bivalent Booster.对奥密克戎BA.4-BA.5二价加强针的抗体反应
N Engl J Med. 2023 Feb 9;388(6):567-569. doi: 10.1056/NEJMc2213907. Epub 2023 Jan 11.
5
Immunogenicity of BA.5 Bivalent mRNA Vaccine Boosters.BA.5二价mRNA疫苗加强针的免疫原性。
N Engl J Med. 2023 Feb 9;388(6):565-567. doi: 10.1056/NEJMc2213948. Epub 2023 Jan 11.
6
Neutralization against BA.2.75.2, BQ.1.1, and XBB from mRNA Bivalent Booster.来自mRNA二价加强针的针对BA.2.75.2、BQ.1.1和XBB的中和作用。
N Engl J Med. 2023 Jan 12;388(2):183-185. doi: 10.1056/NEJMc2214293. Epub 2022 Dec 21.
7
Low neutralization of SARS-CoV-2 Omicron BA.2.75.2, BQ.1.1 and XBB.1 by parental mRNA vaccine or a BA.5 bivalent booster.原始mRNA疫苗或BA.5二价加强针 对SARS-CoV-2奥密克戎BA.2.75.2、BQ.1.1和XBB.1的中和作用较低。
Nat Med. 2023 Feb;29(2):344-347. doi: 10.1038/s41591-022-02162-x. Epub 2022 Dec 6.
8
Extensive neutralization against SARS-CoV-2 variants elicited by Omicron-specific subunit vaccine as a heterologous booster.作为异源加强针的奥密克戎特异性亚单位疫苗引发的对新冠病毒变异株的广泛中和作用。
iScience. 2022 Nov 18;25(11):105465. doi: 10.1016/j.isci.2022.105465. Epub 2022 Oct 31.
9
Updated vaccine protects against SARS-CoV-2 variants including Omicron (B.1.1.529) and prevents transmission in hamsters.更新的疫苗可预防包括奥密克戎(B.1.1.529)在内的 SARS-CoV-2 变异株,并可预防仓鼠传播。
Nat Commun. 2022 Nov 4;13(1):6644. doi: 10.1038/s41467-022-34439-7.
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Bivalent mRNA vaccine booster induces robust antibody immunity against Omicron lineages BA.2, BA.2.12.1, BA.2.75 and BA.5.二价mRNA疫苗加强针可诱导针对奥密克戎谱系BA.2、BA.2.12.1、BA.2.75和BA.5的强大抗体免疫。
Cell Discov. 2022 Oct 11;8(1):108. doi: 10.1038/s41421-022-00473-4.