4.7 Article

ACE2 Expression Is Increased in the Lungs of Patients With Comorbidities Associated With Severe COVID-19

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 222, 期 4, 页码 556-563

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiaa332

关键词

angiotensin converting enzyme 2; COVID-19; SARS-CoV-2; KDM5B

资金

  1. Brazilian National Council for Scientific and Technological Development [313662/2017-7]
  2. Sao Paulo Research Foundation [2017/50137-3, 2012/19278-6, 2018/14933-2, 2018/21934-5, 2013/08216-2]
  3. National Science Foundation (NSF) [DGE-1256082]
  4. NSF Graduate Research Opportunities Worldwide Fellowship
  5. National Institutes of Health STD and AIDS Research Training Fellowship Program [2T32AI007140-41]
  6. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [12/19278-6, 18/21934-5] Funding Source: FAPESP

向作者/读者索取更多资源

Patients who died from COVID-19 often had comorbidities, such as hypertension, diabetes, and chronic obstructive lung disease. Although angiotensin-converting enzyme 2 (ACE2) is crucial for SARS-CoV-2 to bind and enter host cells, no study has systematically assessed the ACE2 expression in the lungs of patients with these diseases. Here, we analyzed over 700 lung transcriptome samples from patients with comorbidities associated with severe COVID-19 and found that ACE2 was highly expressed in these patients compared to control individuals. This finding suggests that patients with such comorbidities may have higher chances of developing severe COVID-19. Correlation and network analyses revealed many potential regulators of ACE2 in the human lung, including genes related to histone modifications, such as HAT1, HDAC2, and KDM5B. Our systems biology approach offers a possible explanation for increased COVID-19 severity in patients with certain comorbidities.

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