A quadri-fluorescence SARS-CoV-2 pseudovirus system for efficient antigenic characterization of multiple circulating variants.

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS
Cell Reports Methods Pub Date : 2024-09-16 Epub Date: 2024-09-06 DOI:10.1016/j.crmeth.2024.100856
Jijing Chen, Zehong Huang, Jin Xiao, Shuangling Du, Qingfang Bu, Huilin Guo, Jianghui Ye, Shiqi Chen, Jiahua Gao, Zonglin Li, Miaolin Lan, Shaojuan Wang, Tianying Zhang, Jiming Zhang, Yangtao Wu, Yali Zhang, Ningshao Xia, Quan Yuan, Tong Cheng
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引用次数: 0

Abstract

The ongoing co-circulation of multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strains necessitates advanced methods such as high-throughput multiplex pseudovirus systems for evaluating immune responses to different variants, crucial for developing updated vaccines and neutralizing antibodies (nAbs). We have developed a quadri-fluorescence (qFluo) pseudovirus platform by four fluorescent reporters with different spectra, allowing simultaneous measurement of the nAbs against four variants in a single test. qFluo shows high concordance with the classical single-reporter assay when testing monoclonal antibodies and human plasma. Utilizing qFluo, we assessed the immunogenicities of the spike of BA.5, BQ.1.1, XBB.1.5, and CH.1.1 in hamsters. An analysis of cross-neutralization against 51 variants demonstrated superior protective immunity from XBB.1.5, especially against prevalent strains such as "FLip" and JN.1, compared to BA.5. Our finding partially fills the knowledge gap concerning the immunogenic efficacy of the XBB.1.5 vaccine against current dominant variants, being instrumental in vaccine-strain decisions and insight into the evolutionary path of SARS-CoV-2.

用于对多种循环变种进行高效抗原表征的四荧光 SARS-CoV-2 伪病毒系统。
多种严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)病毒株的持续共同流行需要先进的方法,如高通量多重伪病毒系统,以评估对不同变种的免疫反应,这对开发最新疫苗和中和抗体(nAbs)至关重要。我们开发的四重荧光(qFluo)伪病毒平台由四种不同光谱的荧光报告物组成,可在一次测试中同时测量针对四种变体的 nAbs。利用 qFluo,我们评估了 BA.5、BQ.1.1、XBB.1.5 和 CH.1.1 的尖峰在仓鼠体内的免疫原性。对 51 个变种的交叉中和分析表明,与 BA.5 相比,XBB.1.5 的保护性免疫力更强,尤其是针对 "FLip "和 JN.1 等流行毒株。我们的发现部分填补了有关 XBB.1.5 疫苗对当前优势变异株免疫原性功效的知识空白,有助于疫苗株决策和深入了解 SARS-CoV-2 的进化路径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
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