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大麻素受体 2:在严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2,即 CoV-19)感染中是否为一个可能的靶点?

Cannabinoid Receptor Type 2: A Possible Target in SARS-CoV-2 (CoV-19) Infection?

机构信息

Department of Woman, Child and General and Specialist Surgery, University of Campania "Luigi Vanvitelli", L. De Crecchio 4, 80138 Naples, Italy.

Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", S. Maria di Costantinopoli 16, 80138 Naples, Italy.

出版信息

Int J Mol Sci. 2020 May 27;21(11):3809. doi: 10.3390/ijms21113809.

Abstract

In late December 2019, a novel coronavirus (SARS-CoV-2 or CoV-19) appeared in Wuhan, China, causing a global pandemic. SARS-CoV-2 causes mild to severe respiratory tract inflammation, often developing into lung fibrosis with thrombosis in pulmonary small vessels and causing even death. COronaVIrus Disease (COVID-19) patients manifest exacerbated inflammatory and immune responses, cytokine storm, prevalence of pro-inflammatory M1 macrophages and increased levels of resident and circulating immune cells. Men show higher susceptibility to SARS-CoV-2 infection than women, likely due to estrogens production. The protective role of estrogens, as well as an immune-suppressive activity that limits the excessive inflammation, can be mediated by cannabinoid receptor type 2 (CB2). The role of this receptor in modulating inflammation and immune response is well documented in fact in several settings. The stimulation of CB2 receptors is known to limit the release of pro-inflammatory cytokines, shift the macrophage phenotype towards the anti-inflammatory M2 type and enhance the immune-modulating properties of mesenchymal stromal cells. For these reasons, we hypothesize that CB2 receptor can be a therapeutic target in COVID-19 pandemic emergency.

摘要

2019 年 12 月底,一种新型冠状病毒(SARS-CoV-2 或 CoV-19)在中国武汉出现,引发了全球大流行。SARS-CoV-2 引起轻度至重度呼吸道炎症,常发展为肺小血管血栓形成的肺纤维化,并导致死亡。COronaVIrus Disease(COVID-19)患者表现出炎症和免疫反应加剧、细胞因子风暴、促炎 M1 巨噬细胞增多和常驻及循环免疫细胞水平升高。男性比女性更容易感染 SARS-CoV-2,这可能与雌激素的产生有关。雌激素的保护作用以及抑制过度炎症的免疫抑制活性,可由大麻素受体 2(CB2)介导。事实上,在多种情况下,该受体在调节炎症和免疫反应方面的作用已有充分的记载。已知 CB2 受体的刺激可限制促炎细胞因子的释放,将巨噬细胞表型向抗炎 M2 型转变,并增强间充质基质细胞的免疫调节特性。基于这些原因,我们假设 CB2 受体可能是 COVID-19 大流行紧急情况下的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4016/7312493/e1948e5c3441/ijms-21-03809-g001.jpg

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