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接种异源疫苗的个体中出现的新冠病毒奥密克戎突破性变异株增强了对BA.2原始谱系的中和抗体抑制性能。

Breakthrough SARS-CoV-2 Omicron Variant in Individuals Primed with Heterologous Vaccines Enhances Inhibition Performance of Neutralizing Antibody to BA.2 Parental Lineage.

作者信息

Szekely Jidapa, Swangphon Piyawut, Nanakorn Natthaphon, Chaimuti Panuttha, Nualnoi Teerapat, Wongwitwichot Paweena, Somapa Namchoke, Somapa Denpong, Pengsakul Theerakamol

机构信息

Faculty of Medical Technology, Prince of Songkla University, Hat Yai 90110, Thailand.

Immunology and Virology Unit, Department of Medical Technology and Clinical Pathology, Hat Yai Hospital, Hat Yai 90110, Thailand.

出版信息

Vaccines (Basel). 2023 Jul 11;11(7):1230. doi: 10.3390/vaccines11071230.

Abstract

This study aims to analyze the neutralization ability against Omicron parental variants in five clusters of individuals with different Coronavirus disease (COVID-19) immunity backgrounds, including individuals receiving a homologous or heterologous vaccine without prior infection, recovered patients with homologous or heterologous vaccination, and recovery patients without vaccination. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) surrogate virus neutralization assay was performed on serum samples. Spearman correlation analysis showed that the percent inhibition against Omicron B.1.1.529 and BA.2 was significantly related to the period of serum collection ( = 0.730 and 0.787, < 0.001, respectively). Very strong correlation between percent inhibition of neutralizing antibody against Omicron B.1.1.529 and BA.2 variants ( = 0.973, < 0.001) was also observed. The neutralizing activity of the sera from recovery patients receiving homologous and heterologous vaccine against the wild-type, B.1.1.529, and BA.2 Omicron variants was significantly higher ( < 0.001) than that of recovery patients without vaccination. This study robustly showed that the breakthrough SARS-CoV-2 Omicron variant in individuals who received homologous and heterologous vaccines had a high level of neutralizing activity against B.1.1.529 and BA.2 parental lineage of XBB subvariants. Therefore, the next-generation COVID-19 vaccine against emerging variants is needed to improve resilience against ongoing variants, particularly for persons who have never been infected.

摘要

本研究旨在分析五组具有不同新冠病毒病(COVID-19)免疫背景的个体对奥密克戎原始毒株的中和能力,这些个体包括未感染过但接受同源或异源疫苗接种的个体、接种过同源或异源疫苗的康复患者以及未接种疫苗的康复患者。对血清样本进行了严重急性呼吸综合征冠状病毒2(SARS-CoV-2)替代病毒中和试验。Spearman相关性分析表明,针对奥密克戎B.1.1.529和BA.2的抑制百分比与血清采集时间显著相关(分别为r = 0.730和0.787,P < 0.001)。还观察到针对奥密克戎B.1.1.529和BA.2变异株的中和抗体抑制百分比之间存在非常强的相关性(r = 0.973,P < 0.001)。接受同源和异源疫苗的康复患者血清对野生型、B.1.1.529和BA.2奥密克戎变异株的中和活性显著高于未接种疫苗的康复患者(P < 0.001)。本研究有力地表明,接种同源和异源疫苗的个体中出现的突破性SARS-CoV-2奥密克戎变异株对XBB亚变异株的B.1.1.529和BA.2原始谱系具有高水平的中和活性。因此,需要研发针对新出现变异株的下一代COVID-19疫苗,以提高对现有变异株的抵抗力,特别是对于从未感染过的人群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc8/10383937/69d8a3b3ea89/vaccines-11-01230-g001.jpg

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