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UB-612 疫苗加强针后,针对严重急性呼吸综合征冠状病毒 2 奥密克戎 BA.1 和 BA.2 的高中和抗体水平。

High Neutralizing Antibody Levels Against Severe Acute Respiratory Syndrome Coronavirus 2 Omicron BA.1 and BA.2 After UB-612 Vaccine Booster.

机构信息

Vaxxinity Inc, Dallas, Texas, USA.

United Biomedical Inc Asia, Hsinchu, Taiwan.

出版信息

J Infect Dis. 2022 Oct 17;226(8):1401-1406. doi: 10.1093/infdis/jiac241.

DOI:10.1093/infdis/jiac241
PMID:35723969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9278180/
Abstract

The highly transmissible severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has caused high rates of breakthrough infections in those previously vaccinated with ancestral strain coronavirus disease 2019 (COVID-19) vaccines. Here, we demonstrate that a booster dose of UB-612 vaccine candidate delivered 7-9 months after primary vaccination increased neutralizing antibody levels by 131-, 61-, and 49-fold against ancestral SARS-CoV-2 and the Omicron BA.1 and BA.2 variants, respectively. Based on the receptor-binding domain protein binding antibody responses, the UB-612 third-dose booster may lead to an estimated approximately 95% efficacy against symptomatic COVID-19 caused by the ancestral strain. Our results support UB-612 as a potential potent booster against current and emerging SARS-CoV-2 variants.

摘要

高度传染性的严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)奥密克戎变体导致先前接种过原始株冠状病毒病 2019(COVID-19)疫苗的人突破性感染率很高。在这里,我们证明,在初次接种疫苗后 7-9 个月接种 UB-612 候选疫苗加强针,分别使针对原始 SARS-CoV-2 以及奥密克戎 BA.1 和 BA.2 变体的中和抗体水平提高了 131 倍、61 倍和 49 倍。基于受体结合域蛋白结合抗体反应,UB-612 第三剂加强针可能使针对由原始株引起的有症状 COVID-19 的估计有效率达到约 95%。我们的结果支持 UB-612 作为针对当前和新兴 SARS-CoV-2 变体的潜在有效加强针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/9574663/60a0959e3efd/jiac241f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/9574663/8f038eb3dffc/jiac241f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/9574663/60a0959e3efd/jiac241f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/9574663/8f038eb3dffc/jiac241f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/9574663/60a0959e3efd/jiac241f2.jpg

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1
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Nature. 2022 Jul;607(7917):128-134. doi: 10.1038/s41586-022-04778-y. Epub 2022 Apr 21.
2
Vaccine protection against the SARS-CoV-2 Omicron variant in macaques.疫苗对猕猴体内 SARS-CoV-2 奥密克戎变异株的保护作用。
Cell. 2022 Apr 28;185(9):1549-1555.e11. doi: 10.1016/j.cell.2022.03.024. Epub 2022 Mar 17.
3
A multitope SARS-CoV-2 vaccine provides long-lasting B cell and T cell immunity against Delta and Omicron variants.
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Vaccines (Basel). 2023 Dec 29;12(1):40. doi: 10.3390/vaccines12010040.
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Beta-spike-containing boosters induce robust and functional antibody responses to SARS-CoV-2 in macaques primed with distinct vaccines.含 Beta 棘突蛋白的加强针在以不同疫苗为基础免疫的猕猴中诱导针对 SARS-CoV-2 的强大且有功能的抗体反应。
Cell Rep. 2023 Nov 28;42(11):113292. doi: 10.1016/j.celrep.2023.113292. Epub 2023 Oct 28.
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Front Immunol. 2023 Jun 19;14:1160065. doi: 10.3389/fimmu.2023.1160065. eCollection 2023.
6
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7
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8
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9
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Viruses. 2023 Feb 24;15(3):624. doi: 10.3390/v15030624.
10
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Microbiol Spectr. 2023 Mar 13;11(2):e0419422. doi: 10.1128/spectrum.04194-22.
一种多表位 SARS-CoV-2 疫苗可提供针对 Delta 和奥密克戎变异株的持久 B 细胞和 T 细胞免疫。
J Clin Invest. 2022 May 16;132(10). doi: 10.1172/JCI157707.
4
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N Engl J Med. 2022 Apr 21;386(16):1532-1546. doi: 10.1056/NEJMoa2119451. Epub 2022 Mar 2.
5
Neutralizing Antibody Responses to SARS-CoV-2 in Recovered COVID-19 Patients Are Variable and Correlate With Disease Severity and Receptor-Binding Domain Recognition.恢复期 COVID-19 患者对 SARS-CoV-2 的中和抗体反应具有变异性,与疾病严重程度和受体结合域识别相关。
Front Immunol. 2022 Jan 31;13:830710. doi: 10.3389/fimmu.2022.830710. eCollection 2022.
6
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N Engl J Med. 2022 Mar 17;386(11):1088-1091. doi: 10.1056/NEJMc2119912. Epub 2022 Jan 26.
7
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Nat Med. 2022 Mar;28(3):481-485. doi: 10.1038/s41591-022-01705-6. Epub 2022 Jan 20.
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Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa.南非 SARS-CoV-2 奥密克戎变异株的快速流行扩张。
Nature. 2022 Mar;603(7902):679-686. doi: 10.1038/s41586-022-04411-y. Epub 2022 Jan 7.
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Science. 2022 Feb 11;375(6581):678-680. doi: 10.1126/science.abn7591. Epub 2022 Jan 18.
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Vaccine. 2022 Jan 21;40(2):306-315. doi: 10.1016/j.vaccine.2021.12.006. Epub 2021 Dec 15.