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进入抑制剂:阻断病毒感染的有效手段。

Entry Inhibitors: Efficient Means to Block Viral Infection.

机构信息

School of Chemistry, Sambalpur University, Jyoti Vihar, Burla, Odisha, 768 019, India.

Centre of Excellence in Natural Products and Therapeutics, Sambalpur University, Jyoti Vihar, Burla, Odisha, 768 019, India.

出版信息

J Membr Biol. 2020 Oct;253(5):425-444. doi: 10.1007/s00232-020-00136-z. Epub 2020 Aug 30.

Abstract

The emerging and re-emerging viral infections are constant threats to human health and wellbeing. Several strategies have been explored to develop vaccines against these viral diseases. The main effort in the journey of development of vaccines is to neutralize the fusion protein using antibodies. However, significant efforts have been made in discovering peptides and small molecules that inhibit the fusion between virus and host cell, thereby inhibiting the entry of viruses. This class of inhibitors is called entry inhibitors, and they are extremely efficient in reducing viral infection as the entry of the virus is considered as the first step of infection. Nevertheless, these inhibitors are highly selective for a particular virus as antibody-based vaccines. The recent COVID-19 pandemic lets us ponder to shift our attention towards broad-spectrum antiviral agents from the so-called 'one bug-one drug' approach. This review discusses peptide and small molecule-based entry inhibitors against class I, II, and III viruses and sheds light on broad-spectrum antiviral agents.

摘要

新兴和再现的病毒感染是对人类健康和福祉的持续威胁。已经探索了几种策略来开发针对这些病毒性疾病的疫苗。疫苗开发过程中的主要努力是使用抗体中和融合蛋白。然而,人们在发现抑制病毒与宿主细胞融合从而抑制病毒进入的肽和小分子方面做出了巨大努力。这类抑制剂称为进入抑制剂,由于病毒进入被认为是感染的第一步,因此它们在降低病毒感染方面非常有效。然而,与基于抗体的疫苗不同,这些抑制剂对特定病毒具有高度选择性。最近的 COVID-19 大流行让我们考虑将注意力从所谓的“一种病菌一种药物”方法转移到广谱抗病毒药物上。这篇综述讨论了针对 I 型、II 型和 III 型病毒的基于肽和小分子的进入抑制剂,并探讨了广谱抗病毒药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53d7/7456447/b6ea8ab63e52/232_2020_136_Fig1_HTML.jpg

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