首页|用于中和抗体评价和进入抑制剂筛选的多变异株SARS-CoV-2假病毒体系构建与评估

用于中和抗体评价和进入抑制剂筛选的多变异株SARS-CoV-2假病毒体系构建与评估

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目的:构建一种高滴度SARS-CoV-2假病毒(PsV)体系,用于中和抗体体外评价与病毒进入抑制剂的筛选.方法:共转染慢病毒载体质粒psPAX2、pCDH-Luc与SARS-CoV-2 Spike(S)蛋白表达质粒,收获的假病毒上清感染ACE2-293T细胞.通过测定p24蛋白含量反映PsV滴度,Western blot检测S蛋白在PsV中的表达.利用原始株、D614G、Gamma、Delta、Omicron PsV亚型对1株S蛋白单克隆抗体的中和能力进行评价.采用两种已报道的病毒进入抑制剂氯喹、角叉菜胶检测对Omicron PsV进入的影响.结果:慢病毒载体成功掺入了S蛋白,Western blot结果显示665Y位突变的S蛋白表现出与野生型全长S蛋白(180 kD)不同的切割形式(90 kD).三质粒体系包装出的PsV滴度更高,S蛋白表达质粒、转移质粒与包装质粒比例在1∶3∶3时为原始株PsV包装的最佳条件.该条件下包装出的5种PsV滴度均在20 ng/ml以上.PsV可有效感染ACE2-293T细胞,双报告基因GFP与萤火虫荧光素酶表达明显,化学发光数值高达106.基于原始株S蛋白的单克隆抗体可有效中和原始株PsV,对原始株PsV的中和作用是对变异株PsV的10~30倍.病毒进入抑制剂氯喹与ι-角叉菜胶可显著抑制Omicron PsV进入宿主细胞.结论:成功构建了高滴度的SARS-CoV-2 PsV进入体系,该体系以荧光素酶报告基因为指示,包含原始株和D614G、PsV Gamma、Delta、Omicron 4种变异株PsV,可有效评价中和抗体与病毒进入抑制剂活性,区分二者对不同变异株的敏感性差异对抗SARS-CoV-2药物研发有重要意义.
Construction and evaluation of a multi-variant pseudovirus system of SARS-CoV-2 for antibody evaluation and virus entry inhibitors screening
Objective:A SARS-CoV-2 pseudovirus(PsV)system was established for neutralizing antibody evaluation and virus entry inhibitor screening.Methods:Lentiviral vector plasmids psPAX2,pCDH-Luc and SARS-CoV-2 Spike(S)protein expres-sion plasmids were co-transfected,and harvested pseudoviral supernatant was used to infect ACE2-293T cells.Protein content of p24 was determined to reflect titer of PsV,and expression of S protein in PsV was detected by Western blot.Neutralization capacity of an S protein monoclonal antibody was evaluated using original strain,D614G,Gamma,Delta,Omicron PsV.Two reported virus entry inhibitors,chloroquine and carrageenin,were used to detect effect on entry of Omicron PsV.Results:Lentiviral vector successfully incorporated S protein.Western blot results showed that S protein mutated at 665Y showed a different cleavage form(90 kD)than wild-type full-length S protein(180 kD).Titer of PsV packaged by three plasmids system was higher.Ratio of S protein expression plasmid,transfer plasmid and packaging plasmid at 1∶3∶3 was optimum condition for viral packaging.Titer of PsV packaged under this condi-tion was over 20 ng/ml.PsV could effectively infect ACE2-293T cells,and double reporter gene GFP and firefly luciferase were expressed obviously,whose chemiluminescence values reached 106.Monoclonal antibodies of S protein effectively neutralized four types of PsVs,but neutralization of original strain was 10~30 times greater than that of variant PsV.Virus entry inhibitors,chloroquine and ι-carrageenan significantly inhibited entry of Omicron PsV.Conclusion:SARS-CoV-2 PsV infection system we conducted can simu-late entry of SARS-CoV-2 successfully.Effective pharmacodynamic evaluation of neutralizing antibodies and virus entry inhibitors can be performed efficiently by the system,which can provide a technical platform for evaluation of neutralizing antibody of SARS-CoV-2 and screening of virus entry inhibitors,and would benefit R&D of anti-SARS-CoV-2 drugs.

SARS-CoV-2PseudovirusS proteinNeutralizing antibodyVirus entry inhibitor

李静璇、刘峰、王莹、程军平、肖智勇、周文霞

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军事科学院军事医学研究院毒物药物研究所,抗毒药物与毒理学国家重点实验室,北京 100850

SARS-CoV-2 假病毒 S蛋白 中和抗体 病毒进入抑制剂

天津市科技计划项目

22ZYJDSS00080

2024

中国免疫学杂志
中国免疫学会,吉林省医学期刊社

中国免疫学杂志

CSTPCD北大核心
影响因子:0.926
ISSN:1000-484X
年,卷(期):2024.40(4)
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