针对 SARS-CoV-2 穗状糖蛋白的单克隆抗体的特征:与Delta和Omicron BA.1 个变体。

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Journal of virological methods Pub Date : 2024-08-30 DOI:10.1016/j.jviromet.2024.115027
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引用次数: 0

摘要

由于 SARS-CoV-2 感染具有跨物种传播性,因此有必要开发用于检测不同动物物种感染情况的特异性试剂。SARS-CoV-2 的尖峰糖蛋白参与病毒的进入,是一种高免疫原性蛋白。为了开发针对这种蛋白的检测方法,我们生成了八种针对 SARS CoV-2 S1 蛋白的单克隆抗体(mAbs)和七种针对 S1/S2 蛋白(外显子)的单克隆抗体(mAbs)。根据在酶联免疫吸附试验(ELISA)中观察到的中和能力和反应谱,与单独针对 S1 结构域产生的抗体相比,针对 S1/S2 抗原产生的 mAbs 具有更广泛的表位特异性。全长外结构域诱导的抗体可以中和大流行期间遇到的两种最重要的病毒变体,即 Delta 和 Omicron。这些试剂的问世将大大促进用于检测各种宿主物种中 COVID-19 感染的精确诊断方法的开发,并推动基于 mAb 的疗法的进步。
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Characterization of monoclonal antibodies targeting SARS-CoV-2 spike glycoprotein: Reactivity against Delta and Omicron BA.1 variants

The cross-species transmissibility of SARS-CoV-2 infection has necessitated development of specific reagents for detecting infection in various animal species. The spike glycoprotein of SARS-CoV-2, which is involved in viral entry, is a highly immunogenic protein. To develop assays targeting this protein, we generated eight monoclonal antibodies (mAbs) against the S1 and seven against the S1/S2 protein (ectodomain) of SARS CoV-2. Based on neutralization capability and reactivity profile observed in ELISA, the mAbs generated against the S1/S2 antigen exhibited a broader spectrum of epitope specificity than those produced against the S1 domain alone. The full-length ectodomain induced antibodies that could neutralize the two most important variants of the virus encountered during the pandemic, namely Delta and Omicron. The availability of these reagents could greatly enhance the development of precise diagnostics for detecting COVID-19 infections in various host species and contribute to the advancement of mAb-based therapeutics.

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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
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