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基于核酸的COVID-19治疗方法:适体和小干扰RNA的潜在疗效

Nucleic Acid-Based Treatments Against COVID-19: Potential Efficacy of Aptamers and siRNAs.

作者信息

Khanali Javad, Azangou-Khyavy Mohammadreza, Asaadi Yasaman, Jamalkhah Monire, Kiani Jafar

机构信息

School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

出版信息

Front Microbiol. 2021 Nov 8;12:758948. doi: 10.3389/fmicb.2021.758948. eCollection 2021.

Abstract

Despite significant efforts, there are currently no approved treatments for COVID-19. However, biotechnological approaches appear to be promising in the treatment of the disease. Accordingly, nucleic acid-based treatments including aptamers and siRNAs are candidates that might be effective in COVID-19 treatment. Aptamers can hamper entry and replication stages of the SARS-CoV-2 infection, while siRNAs can cleave the viral genomic and subgenomic RNAs to inhibit the viral life cycle and reduce viral loads. As a conjugated molecule, aptamer-siRNA chimeras have proven to be dual-functioning antiviral therapy, acting both as virus-neutralizing and replication-interfering agents as well as being a siRNA targeted delivery approach. Previous successful applications of these compounds against various stages of the pathogenesis of diseases and viral infections, besides their advantages over other alternatives, might provide sufficient rationale for the application of these nucleic acid-based drugs against the SARS-CoV-2. However, none of them are devoid of limitations. Here, the literature was reviewed to assess the plausibility of using aptamers, siRNAs, and aptamer-siRNA chimeras against the SARS-CoV-2 based on their previously established effectiveness, and discussing challenges lie in applying these molecules.

摘要

尽管付出了巨大努力,但目前尚无获批的新冠病毒治疗方法。然而,生物技术方法在该疾病的治疗中似乎很有前景。因此,包括适体和小干扰RNA(siRNA)在内的基于核酸的治疗方法是可能对新冠病毒治疗有效的候选方案。适体可以阻碍严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的进入和复制阶段,而siRNA可以切割病毒基因组和亚基因组RNA以抑制病毒生命周期并降低病毒载量。作为一种共轭分子,适体-siRNA嵌合体已被证明是一种双功能抗病毒疗法,既可以作为病毒中和剂和复制干扰剂,也是一种siRNA靶向递送方法。这些化合物先前在针对疾病和病毒感染发病机制的各个阶段成功应用,以及它们相对于其他替代方案的优势,可能为应用这些基于核酸的药物对抗SARS-CoV-2提供充分的理论依据。然而,它们都并非没有局限性。在此,对文献进行了综述,以根据适体、siRNA和适体-siRNA嵌合体先前已确立的有效性评估其用于对抗SARS-CoV-2的合理性,并讨论应用这些分子所面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1627/8630580/9b3658452533/fmicb-12-758948-g001.jpg

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