Evidence map›Paper›PMID 35260724›Full record

ArticleScientific reports2022

ACE2 protein expression in lung tissues of severe COVID-19 infection.

Atish Gheware, Animesh Ray, Deeksha Rana, Prashant Bajpai, Aruna Nambirajan, S Arulselvi, Purva Mathur, Anjan Trikha, Sudheer Arava, Prasenjit Das and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
8.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. COVID-19, the disease that changed the world.Medicine and pharmacy reports · 2026
    Review
  4. Expression of angiotensin-converting enzyme 2, transmembrane serine protease 2, and sirtuin 1 proteins in lungs of different age groups.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 2 institutions in 1 country.

Atish GhewareDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Animesh RayDepartment of Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India.
Deeksha RanaDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Prashant BajpaiEmory Vaccine Center, International Center for Genetic Engineering and Biotechnology, New Delhi, 110067, India.
Aruna NambirajanDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
S ArulselviDepartment of Laboratory Medicine, JPNATC, All India Institute of Medical Sciences, New Delhi, 110029, India.
Purva MathurDepartment of Laboratory Medicine, JPNATC, All India Institute of Medical Sciences, New Delhi, 110029, India.
Anjan TrikhaDepartment of Anaesthesiology, Critical Care and Pain Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India.
Sudheer AravaDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Prasenjit DasDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Asit Ranjan MridhaDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Geetika SinghDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Manish SonejaDepartment of Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India.
Neeraj NischalDepartment of Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India.
Sanjeev LalwaniDivision of Forensic Pathology and Molecular Laboratory, All India Institute of Medical Sciences, New Delhi, 110029, India.
Naveet WigDepartment of Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India.
Chitra SarkarDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Deepali JainDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India. deepalijain76@gmail.com.
All India Institute of Medical Sciences · INInternational Centre for Genetic Engineering and Biotechnology · IN

Funding

This work is supported by intramural funding from the research section of the All India Institute of Medical Sciences (AIIMS), New Delhi, India. A-COVID 40
6 · The paper itself

Abstract

Angiotensin-converting enzyme 2 (ACE2) is a key host protein by which severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) enters and multiplies within cells. The level of ACE2 expression in the lung is hypothesised to correlate with an increased risk of severe infection and complications in COrona VIrus Disease 2019 (COVID-19). To test this hypothesis, we compared the protein expression status of ACE2 by immunohistochemistry (IHC) in post-mortem lung samples of patients who died of severe COVID-19 and lung samples obtained from non-COVID-19 patients for other indications. IHC for CD61 and CD163 was performed for the assessment of platelet-rich microthrombi and macrophages, respectively. IHC for SARS-CoV-2 viral antigen was also performed. In a total of 55, 44 COVID-19 post-mortem lung samples were tested for ACE2, 36 for CD163, and 26 for CD61, compared to 15 non-covid 19 control lung sections. Quantification of immunostaining, random sampling, and correlation analysis were used to substantiate the morphologic findings. Our results show that ACE2 protein expression was significantly higher in COVID-19 post-mortem lung tissues than in controls, regardless of sample size. Histomorphology in COVID-19 lungs showed diffuse alveolar damage (DAD), acute bronchopneumonia, and acute lung injury with SARS-CoV-2 viral protein detected in a subset of cases. ACE2 expression levels were positively correlated with increased expression levels of CD61 and CD163. In conclusion, our results show significantly higher ACE2 protein expression in severe COVID-19 disease, correlating with increased macrophage infiltration and microthrombi, suggesting a pathobiological role in disease severity.

Indexed as

Acute Lung InjuryAdolescentAdultAgedAged, 80 and overAngiotensin-Converting Enzyme 2Antigens, CDAntigens, Differentiation, MyelomonocyticAutopsyCase-Control StudiesCD163 AntigenCOVID-19FemaleHumansImmunohistochemistryIntegrin beta3ACE2 protein, humanAngiotensin-Converting Enzyme 2Antigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenIntegrin beta3Receptors, Cell Surface

Identifiers

PMID35260724
PMCPMC8902283
OpenAlexW4221022908

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.