SARS-CoV-2 spike protein expression as an identification in quality control testing for Adenovector based COVID-19 vaccine

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of immunological methods Pub Date : 2024-05-03 DOI:10.1016/j.jim.2024.113680
Harit Kasana , Ajay Kumar Ade , Jaipal Meena, Archana Sayal, Faraz Sheikh, Anupkumar R. Anvikar, Harish Chander
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Abstract

Aim

Quality control testing of the vaccine for lot release is of paramount importance in public health. A recent pandemic caused by the SARS-CoV-2 virus brought together all spheres of vaccine to combat the virus. The scientific advancement in the development of vaccines facilitated the scientists to develop the vaccine against SARS-CoV-2 in a record time. Thus, these vaccines should be stringently monitored for their safety and efficacy as per the latest WHO and national regulatory guidelines, and quality control evaluation of the product should be done at national control laboratories before releasing the product into the market as it assures the quality and safety of the vaccine.

Methods

The SARS-CoV-2 exploited the ACE2 (Angiotensin Converting Enzyme 2) receptor, a surface protein on mammalian cells to gain entry into the host cells. The viral surface protein that interacted with the ACE2 receptor is the Spike protein of SARS-CoV-2. Thus, in the development of the vaccine and assessing its quality, the Spike protein of SARS-CoV-2 became an attractive immunodominant antigen. In National Institute of Biologicals, an apex body in the testing of biologicals in India, received the Adenovector (Adenovirus + vector) based COVID-19 vaccine, a finished product for quality evaluation. Due to the lack of a pharmacopeial monograph, the testing of the vaccine was done as per the manufacturer's specifications and methods. The routine assays of identification employed by the manufacturer do not reflect the expression of Spike protein which is required for the immune system to get activated. In this report, we showed the determination of Spike protein expression by immunoblotting and immunofluorescence for identification parameters in the quality testing of the COVID-19 vaccine. We determined the translation of the SARS-CoV-2 Spike gene cloned into an Adenovector.

Results

The results from these experiments indicated the expression of Spike protein upon infection of mammalian cells with viral particles suggested that the expression of immunodominant Spike protein of SARS-CoV-2 may be employed by quality control laboratories as a parameter for identification.

Conclusion

The study suggested that the determination of the expression of Spike protein is pertinent to identifying the Adenovector based vaccines against COVID-19.

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SARS-CoV-2 尖峰蛋白表达作为基于 Adenovector 的 COVID-19 疫苗质量控制测试的鉴定方法。
目的:对批量生产的疫苗进行质量控制测试对公共卫生至关重要。最近由 SARS-CoV-2 病毒引起的大流行汇集了所有疫苗领域的力量来对抗该病毒。疫苗开发方面的科学进步促进了科学家们在创纪录的时间内开发出 SARS-CoV-2 疫苗。因此,应根据世界卫生组织和各国最新的监管准则对这些疫苗的安全性和有效性进行严格监测,并在产品投放市场前在国家控制实验室对产品进行质量控制评估,以确保疫苗的质量和安全性:SARS-CoV-2利用哺乳动物细胞表面蛋白ACE2(血管紧张素转换酶2)受体进入宿主细胞。与 ACE2 受体相互作用的病毒表面蛋白是 SARS-CoV-2 的穗状蛋白。因此,在开发疫苗和评估疫苗质量的过程中,SARS-CoV-2 的尖峰蛋白成为一种有吸引力的免疫优势抗原。印度国家生物制品研究所是印度生物制品检测的最高机构,该研究所接收了基于 Adenovector(腺病毒+载体)的 COVID-19 疫苗成品进行质量评估。由于缺乏药典专著,疫苗的检测是按照制造商的规格和方法进行的。生产商采用的常规鉴定方法不能反映免疫系统激活所需的斯派克蛋白的表达。在本报告中,我们展示了在 COVID-19 疫苗的质量检测中,通过免疫印迹和免疫荧光来确定斯派克蛋白表达的鉴定参数。我们测定了克隆到腺病毒载体中的 SARS-CoV-2 Spike 基因的翻译结果:结果:这些实验结果表明,哺乳动物细胞感染病毒颗粒后会表达 Spike 蛋白,这表明 SARS-CoV-2 的免疫显性 Spike 蛋白的表达可被质量控制实验室用作鉴定参数:研究表明,测定尖峰蛋白的表达与鉴定基于腺病毒载体的 COVID-19 疫苗有关。
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
CiteScore
4.10
自引率
0.00%
发文量
120
审稿时长
3 months
期刊介绍: The Journal of Immunological Methods is devoted to covering techniques for: (1) Quantitating and detecting antibodies and/or antigens. (2) Purifying immunoglobulins, lymphokines and other molecules of the immune system. (3) Isolating antigens and other substances important in immunological processes. (4) Labelling antigens and antibodies. (5) Localizing antigens and/or antibodies in tissues and cells. (6) Detecting, and fractionating immunocompetent cells. (7) Assaying for cellular immunity. (8) Documenting cell-cell interactions. (9) Initiating immunity and unresponsiveness. (10) Transplanting tissues. (11) Studying items closely related to immunity such as complement, reticuloendothelial system and others. (12) Molecular techniques for studying immune cells and their receptors. (13) Imaging of the immune system. (14) Methods for production or their fragments in eukaryotic and prokaryotic cells. In addition the journal will publish articles on novel methods for analysing the organization, structure and expression of genes for immunologically important molecules such as immunoglobulins, T cell receptors and accessory molecules involved in antigen recognition, processing and presentation. Submitted full length manuscripts should describe new methods of broad applicability to immunology and not simply the application of an established method to a particular substance - although papers describing such applications may be considered for publication as a short Technical Note. Review articles will also be published by the Journal of Immunological Methods. In general these manuscripts are by solicitation however anyone interested in submitting a review can contact the Reviews Editor and provide an outline of the proposed review.
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