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吸烟者 COVID-19 肺炎肺组织中血管紧张素转换酶 2 受体基因表达降低。

Lower Gene Expression of Angiotensin Converting Enzyme 2 Receptor in Lung Tissues of Smokers with COVID-19 Pneumonia.

机构信息

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova Medical School, 35128 Padova, Italy.

Department of Medicine, University of Padova Medical School, 35128 Padova, Italy.

出版信息

Biomolecules. 2021 May 26;11(6):796. doi: 10.3390/biom11060796.

DOI:10.3390/biom11060796
PMID:34073591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8226817/
Abstract

Angiotensin-converting enzyme 2 (ACE-2) is the main cell entry receptor for severe acute respiratory syndrome-Coronavirus-2 (SARS-CoV-2), thus playing a critical role in causing Coronavirus disease 2019 (COVID-19). The role of smoking habit in the susceptibility to infection is still controversial. In this study we correlated lung ACE-2 gene expression with several clinical/pathological data to explore susceptibility to infection. This is a retrospective observational study on 29 consecutive COVID-19 autopsies. SARS-CoV-2 genome and ACE-2 mRNA expression were evaluated by real-time polymerase chain reaction in lung tissue samples and correlated with several data with focus on smoking habit. Smoking was less frequent in high than low ACE-2 expressors ( = 0.014). A Bayesian regression also including age, gender, hypertension, and virus quantity confirmed that smoking was the most probable risk factor associated with low ACE-2 expression in the model. A direct relation was found between viral quantity and ACE-2 expression ( = 0.028). Finally, high ACE-2 expressors more frequently showed a prevalent pattern of vascular injury than low expressors ( = 0.049). In conclusion, ACE-2 levels were decreased in the lung tissue of smokers with severe COVID-19 pneumonia. These results point out complex biological interactions between SARS-CoV-2 and ACE-2 particularly concerning the aspect of smoking habit and need larger prospective case series and translational studies.

摘要

血管紧张素转换酶 2(ACE-2)是严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的主要细胞进入受体,因此在引起 2019 年冠状病毒病(COVID-19)方面发挥着关键作用。吸烟习惯在易感染方面的作用仍存在争议。在这项研究中,我们将肺 ACE-2 基因表达与几项临床/病理数据相关联,以探讨易感性。这是一项对 29 例连续 COVID-19 尸检的回顾性观察性研究。通过实时聚合酶链反应评估肺组织样本中的 SARS-CoV-2 基因组和 ACE-2 mRNA 表达,并将其与吸烟习惯等几个数据相关联。在高 ACE-2 表达者中,吸烟者比低 ACE-2 表达者少(=0.014)。包括年龄、性别、高血压和病毒量在内的贝叶斯回归也证实,吸烟是该模型中与低 ACE-2 表达最相关的可能危险因素。病毒量与 ACE-2 表达呈直接相关(=0.028)。最后,高 ACE-2 表达者比低表达者更频繁地表现出血管损伤的普遍模式(=0.049)。总之,在患有严重 COVID-19 肺炎的吸烟者的肺组织中,ACE-2 水平降低。这些结果指出了 SARS-CoV-2 和 ACE-2 之间复杂的生物学相互作用,特别是在吸烟习惯方面,需要更大的前瞻性病例系列和转化研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/70e2e23f9962/biomolecules-11-00796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/99f54ce3280d/biomolecules-11-00796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/97a0d14d906c/biomolecules-11-00796-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/70e2e23f9962/biomolecules-11-00796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/99f54ce3280d/biomolecules-11-00796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/97a0d14d906c/biomolecules-11-00796-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/69e74df4d451/biomolecules-11-00796-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/767a7d65e696/biomolecules-11-00796-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c1/8226817/70e2e23f9962/biomolecules-11-00796-g005.jpg

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J Pathol. 2021 Jun;254(2):173-184. doi: 10.1002/path.5653. Epub 2021 Mar 30.
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Association of smoking history with severe and critical outcomes in COVID-19 patients: A systemic review and meta-analysis.
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