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接种 INO-4800 后对 501Y.V1 和 501Y.V2 SARS-CoV-2 变异株的活病毒中和作用

Live Virus Neutralisation of the 501Y.V1 and 501Y.V2 SARS-CoV-2 Variants following INO-4800 Vaccination of Ferrets.

机构信息

Commonwealth Scientific and Industrial Research Organisation, Australian Centre for Disease Preparedness, Geelong, VIC, Australia.

Commonwealth Scientific and Industrial Research Organisation, Data61, Docklands, VIC, Australia.

出版信息

Front Immunol. 2021 Jun 25;12:694857. doi: 10.3389/fimmu.2021.694857. eCollection 2021.

Abstract

The ongoing COVID-19 pandemic has resulted in significant global morbidity and mortality on a scale similar to the influenza pandemic of 1918. Over the course of the last few months, a number of SARS-CoV-2 variants have been identified against which vaccine-induced immune responses may be less effective. These "variants-of-concern" have garnered significant attention in the media, with discussion around their impact on the future of the pandemic and the ability of leading COVID-19 vaccines to protect against them effectively. To address concerns about emerging SARS-CoV-2 variants affecting vaccine-induced immunity, we investigated the neutralisation of representative 'G614', '501Y.V1' and '501Y.V2' virus isolates using sera from ferrets that had received prime-boost doses of the DNA vaccine, INO-4800. Neutralisation titres against G614 and 501Y.V1 were comparable, but titres against the 501Y.V2 variant were approximately 4-fold lower, similar to results reported with other nucleic acid vaccines and supported by biomolecular modelling. The results confirm that the vaccine-induced neutralising antibodies generated by INO-4800 remain effective against current variants-of-concern, albeit with lower neutralisation titres against 501Y.V2 similar to other leading nucleic acid-based vaccines.

摘要

持续的 COVID-19 大流行导致了类似 1918 年流感大流行的全球发病率和死亡率。在过去的几个月里,已经确定了一些针对疫苗诱导的免疫反应可能不太有效的 SARS-CoV-2 变体。这些“值得关注的变体”在媒体上引起了广泛关注,讨论了它们对大流行未来的影响,以及领先的 COVID-19 疫苗有效预防它们的能力。为了解决对新型 SARS-CoV-2 变体影响疫苗诱导免疫的担忧,我们使用接受了 DNA 疫苗 INO-4800 初免-加强剂量的雪貂血清,研究了代表性的“G614”、“501Y.V1”和“501Y.V2”病毒分离株的中和作用。针对 G614 和 501Y.V1 的中和效价相当,但针对 501Y.V2 变体的效价约低 4 倍,与其他核酸疫苗的报告结果相似,并得到生物分子建模的支持。研究结果证实,INO-4800 诱导的疫苗产生的中和抗体仍然对当前的关注变体有效,尽管针对 501Y.V2 的中和效价较低,与其他领先的基于核酸的疫苗相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8623/8269317/ce7f5abb9431/fimmu-12-694857-g001.jpg

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