重组ACE2-Ig融合蛋白中和SARS-CoV-2

Q4 Immunology and Microbiology Journal of Bacteriology and Virology Pub Date : 2022-03-31 DOI:10.4167/jbv.2022.52.1.039
Jin-Woo Song, Young‐Sang Koh
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引用次数: 0

摘要

新型冠状病毒(SARS-CoV-2)是新冠肺炎大流行的病原体,需要有效的抗病毒药物。血管紧张素转换酶2(ACE2)已被证明是严重急性呼吸系统综合征冠状病毒和严重急性呼吸综合征冠状病毒2型的细胞受体。为了对ACE2进行治疗验证,产生了由与IgG1-Fc结构域融合的ACE2细胞外结构域组成的重组蛋白(ACE2-Ig)。ACE2-Ig表现出适当的药理学特性,并与严重急性呼吸系统综合征冠状病毒和严重急性呼吸综合征冠状病毒2受体结合结构域具有高亲和力。此外,它还能用严重急性呼吸系统综合征冠状病毒和严重急性呼吸综合征冠状病毒2型刺突蛋白中和病毒。总的来说,这些数据表明ACE2-Ig具有显著的抗严重急性呼吸系统综合征冠状病毒2型特性,值得进一步研究其在治疗严重急性呼吸综合征冠状病毒2中的潜在应用。©2022细菌与病毒学杂志。
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Recombinant ACE2-Ig Fusion Protein Neutralizes SARS-CoV-2
A novel coronavirus (SARS-CoV-2) is the causative agent for the COVID-19 pandemic, and needs for effective antiviral drugs have been demanded. Angiotensin-converting enzyme 2 (ACE2) has been shown to be a cellular receptor for SARS-CoV and SARS-CoV-2. For the therapeutic validation of ACE2, a recombinant protein consisting of the ACE2 extracellular domain fused to the IgG1 Fc domain (ACE2-Ig) was generated. ACE2-Ig exhibits proper pharmacological properties and binds with a high affinity to SARS-CoV and SARS-CoV-2 receptor-binding domain. Further, it neutralizes virus with SARS-CoV and SARS-CoV-2 spike proteins. Taken overall, these data suggest that ACE2-Ig has substantial anti-SARS-CoV-2 properties and warrant further study concerning its potential applications for the treatment of SARS-CoV-2. © 2022 Journal of Bacteriology and Virology.
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来源期刊
Journal of Bacteriology and Virology
Journal of Bacteriology and Virology Immunology and Microbiology-Immunology
CiteScore
0.80
自引率
0.00%
发文量
16
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