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基于寡核苷酸的抑制登革病毒复制方法。

Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication.

机构信息

Dengue & Chikungunya Group, ICMR-National Institute of Virology, 20-A, Dr. Ambedkar Road, Pune 411001, India.

出版信息

Molecules. 2021 Feb 11;26(4):956. doi: 10.3390/molecules26040956.

Abstract

Dengue fever is one of the most common viral infections affecting humans. It is an expanding public health problem, particularly in tropical and subtropical regions. No effective vaccine or antiviral therapies against Dengue virus (DENV) infection are available. Therefore, there is a strong need to develop safe and effective therapeutic strategies that can reduce the burden and duration of hospitalizations due to this life-threatening disease. Oligonucleotide-based strategies are considered as an attractive means of inhibiting viral replication since oligonucleotides can be designed to interact with any viral RNA, provided its sequence is known. The resultant targeted destruction of viral RNA interferes with viral replication without inducing any adverse effects on cellular processes. In this review, we elaborate the ribozymes, RNA interference, CRISPR, aptamer and morpholino strategies for the inhibition of DENV replication and discuss the challenges involved in utilizing such approaches.

摘要

登革热是影响人类的最常见病毒感染之一。它是一个日益严重的公共卫生问题,特别是在热带和亚热带地区。目前尚无针对登革病毒(DENV)感染的有效疫苗或抗病毒疗法。因此,迫切需要开发安全有效的治疗策略,以减轻这种危及生命的疾病导致的住院负担和时间。基于寡核苷酸的策略被认为是抑制病毒复制的一种有吸引力的手段,因为只要知道其序列,寡核苷酸就可以被设计成与任何病毒 RNA 相互作用。这种靶向破坏病毒 RNA 会干扰病毒复制,而不会对细胞过程产生任何不利影响。在这篇综述中,我们详细阐述了核酶、RNA 干扰、CRISPR、适体和吗啉代寡核苷酸策略在抑制 DENV 复制方面的应用,并讨论了利用这些方法所涉及的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b4/7918374/54f61cda71a6/molecules-26-00956-g001.jpg

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