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TLR4 作为 SARS-CoV-2 引起的呼吸和神经系统并发症的治疗靶点。

TLR4 as a therapeutic target for respiratory and neurological complications of SARS-CoV-2.

机构信息

Pharmacology Research Laboratory, University Institute of Pharmaceutical Sciences, UGC-Centre of Advanced Study, Punjab University, Chandigarh India.

Assistant Professor of Pharmaceutics, University Institute of Pharmaceutical Sciences UGC-Centre of Advanced Study, Panjab University, Chandigarh, India.

出版信息

Expert Opin Ther Targets. 2021 Jun;25(6):491-508. doi: 10.1080/14728222.2021.1918103. Epub 2021 Apr 28.

DOI:10.1080/14728222.2021.1918103
PMID:33857397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8095161/
Abstract

: The COVID-19 pandemic remains aglobal challenge. While there are mRNA agents on the horizon as apotential prevention, adefinitive drug therapy is an unmet medical need. The hyperinflammatory response, known as the 'cytokine storm', is chiefly responsible for complications and deaths. The binding of spike-glycoprotein of SARS-CoV-2 to TLR4 receptors has been documented in several studies and has been found to play arole in hyperinflammation; hence, there is an interest in TLR4 as apotential drug target.: This review discusses the neurological and respiratory complications of SARS-CoV-2 infection and progresses to examine the role of the 'cytokine storm' and the involvement of TLR4 receptors in these complications. The possibility of using TLR4 modulators to curb the complications are considered and finally, ashort perspective on future potential drug treatments is offered. Various databases were searched including Pub-Med, Google Scholar, and Medline. The search mainly included research articles, meta-analysis, retrospective studies, reports, and systematic reviews.: TLR4 modulators are being investigated in clinical trials for COVID-19. Challenges in terms of structural diversity of the agents, their natural origin, and efficacy demand extensive research.

摘要

: 新冠疫情仍然是一项全球性挑战。虽然有一些 mRNA 药物作为潜在的预防手段正在研发中,但针对这种疾病的确切治疗药物仍然是一个未满足的医疗需求。这种被称为“细胞因子风暴”的过度炎症反应主要是导致并发症和死亡的原因。有几项研究已经证明,SARS-CoV-2 的刺突糖蛋白与 TLR4 受体结合,并在过度炎症中发挥作用;因此,TLR4 作为一个潜在的药物靶点引起了人们的兴趣。

: 本综述讨论了 SARS-CoV-2 感染的神经和呼吸并发症,并进一步研究了“细胞因子风暴”的作用以及 TLR4 受体在这些并发症中的作用。考虑使用 TLR4 调节剂来抑制这些并发症的可能性,最后提供了对未来潜在药物治疗的简要展望。检索了各种数据库,包括 Pub-Med、Google Scholar 和 Medline。搜索主要包括研究文章、荟萃分析、回顾性研究、报告和系统评价。

: TLR4 调节剂正在临床试验中用于治疗 COVID-19。这些药物在结构多样性、天然来源和疗效方面存在挑战,需要进行广泛的研究。

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Nat Med. 2021 Apr;27(4):620-621. doi: 10.1038/s41591-021-01270-4. Epub 2021 Feb 8.
2
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Biochemistry (Mosc). 2020 Jul;85(7):833-837. doi: 10.1134/S0006297920070111.
3
SARS-CoV2-mediated suppression of NRF2-signaling reveals potent antiviral and anti-inflammatory activity of 4-octyl-itaconate and dimethyl fumarate.SARS-CoV2 介导的 NRF2 信号通路抑制揭示了 4-辛基衣康酸和富马酸二甲酯的强大抗病毒和抗炎活性。
Nat Commun. 2020 Oct 2;11(1):4938. doi: 10.1038/s41467-020-18764-3.
4
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J Korean Med Sci. 2020 Sep 28;35(38):e343. doi: 10.3346/jkms.2020.35.e343.
5
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6
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