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MEK 抑制剂作为新型宿主靶向抗病毒药物,针对过度炎症性呼吸道病毒病具有双重作用模式。

MEK inhibitors as novel host-targeted antivirals with a dual-benefit mode of action against hyperinflammatory respiratory viral diseases.

机构信息

Institute of Virology (IVM), Westfaelian Wilhelms University Muenster (WWU) and University Clinics (UKM), Muenster, Germany.

Institute of Medical Virology, Justus Liebig University, Giessen, Germany; German Center for Infection Research (DZIF), partner site Giessen, Germany.

出版信息

Curr Opin Virol. 2023 Apr;59:101304. doi: 10.1016/j.coviro.2023.101304. Epub 2023 Feb 24.

Abstract

Acute hyperinflammatory virus infections, such as influenza or coronavirus disease-19, are still a major health burden worldwide. In these diseases, a massive overproduction of pro-inflammatory cytokines and chemokines (cytokine storm syndrome) determine the severity of the disease, especially in late stages. Direct-acting antivirals against these pathogens have to be administered very early after infection to be effective and may induce viral resistance. Here, we summarize data on a host-targeted strategy using inhibitors of the cellular Raf/MEK/ERK kinase cascade that not only block replication of different RNA viruses but also suppress the hyperinflammatory cytokine response upon infection. In the first phase-II clinical trial of that approach, the MEK inhibitor Zapnometinib shows evidence of clinical benefit.

摘要

急性高炎症病毒感染,如流感或新型冠状病毒病-19,仍然是全球范围内的主要健康负担。在这些疾病中,大量促炎细胞因子和趋化因子的过度产生(细胞因子风暴综合征)决定了疾病的严重程度,尤其是在晚期。针对这些病原体的直接作用抗病毒药物必须在感染后非常早期使用才有效,并且可能会诱导病毒产生耐药性。在这里,我们总结了使用细胞 Raf/MEK/ERK 激酶级联抑制剂的宿主靶向策略的数据,该策略不仅可以阻断不同 RNA 病毒的复制,还可以抑制感染时的过度炎症细胞因子反应。在该方法的首次 II 期临床试验中,MEK 抑制剂 Zapnometinib 显示出临床获益的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d0b/10091867/2f664e597e05/gr1_lrg.jpg

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