Evidence map›Paper›PMID 40693778›Full record

ArticlemBio2025

ACE-2-like enzymatic activity in COVID-19 convalescents with persistent pulmonary symptoms associated with immunoglobulin.

Yufeng Song, Frances Mehl, Lyndsey M Muehling, Glenda Canderan, Kyle Enfield, Jie Sun, Michael T Yin, Sarah J Ratcliffe, Jeffrey M Wilson, Alexandra Kadl and 2 more

Abstract read
In one paragraph

Article in mBio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Yufeng SongDepartment of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.ORCID 0009-0001-6788-1717
Frances MehlDepartment of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.ORCID 0009-0005-9929-3185
Lyndsey M MuehlingDepartment of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Glenda CanderanDepartment of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Kyle EnfieldDepartment of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Jie SunBeirne B. Carter Center for Immunology Research, University of Virginia, Charlottesville, Virginia, USA.
Michael T YinColumbia University Vagelos College of Physicians and Surgeons, New York, New York, USA.
Sarah J RatcliffeDivision of Biostatistics, Department of Public Health Sciences, University of Virginia, Charlottesville, Virginia, USA.
Jeffrey M WilsonDivision of Allergy and Clinical Immunology, Department of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Alexandra KadlDepartment of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Judith A WoodfolkDivision of Allergy and Clinical Immunology, Department of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Steven L ZeichnerDepartment of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0002-8922-9260

Funding

Globally Appropriate Genome Reduced Killed Whole Bacterial HIV VaccinesR01AI176515 · NIAID · UNIVERSITY OF VIRGINIA · PI Steven L. Zeichner · 2023 to 2026
$1.7M
Protective and Pathogenic T Cells Responding to SARS-CoV-2 in Health and DiseaseR21AI160334 · NIAID · UNIVERSITY OF VIRGINIA · PI WOODFOLK, JUDITH A · 2021 to 2022
$444k
Immune Programs and Related T Cell Mechanisms of Pulmonary Complications After COVID-19 IllnessR56AI178669 · NIAID · UNIVERSITY OF VIRGINIA · PI WOODFOLK, JUDITH A · 2023 to 2023
$410k
Alpha-1 Foundation AI178669Ivy FoundationManning Fund for COVID-19 Research at UVVANational Institute of Allergy and Infectious Diseases AI160334National Institute of Allergy and Infectious Diseases AI176515NIAID NIH HHS R01 AI176515NIAID NIH HHS R21 AI160334NIAID NIH HHS R56 AI178669The Pendleton Laboratory Fund for Pediatric Infectious Diseases
6 · The paper itself

Abstract

Many difficult-to-understand clinical features characterize COVID-19 and post-acute sequelae of COVID-19 (PASC or long COVID [LC]). These can include blood pressure instability, hyperinflammation, coagulopathies, and neuropsychiatric complaints. The pathogenesis of these features remains unclear. The SARS-CoV-2 Spike protein receptor-binding domain (RBD) binds angiotensin converting enzyme 2 (ACE2) on the surface of host cells to initiate infection. We hypothesized that some people convalescing from COVID-19 may produce anti-RBD antibodies that resemble ACE2 sufficiently to have ACE2-like catalytic activity, that is, they are ACE2-like proteolytic abzymes that may help mediate the pathogenesis of COVID-19 and LC. In previous work, we showed that some people with acute COVID-19 had immunoglobulin-associated ACE2-like proteolytic activity, suggesting that some people with COVID-19 indeed produced ACE2-like abzymes. However, it remained unknown whether ACE2-like abzymes were seen only in acute COVID-19 or whether ACE2-like abzymes could also be identified in people convalescing from COVID-19. Here, we show that some people convalescing from COVID-19 attending a clinic for people with persistent pulmonary symptoms also have ACE2-like abzymes and that the presence of ACE2-like catalytic activity correlates with alterations in blood pressure in an exercise test. IMPORTANCE: Patients who have had COVID-19 can sometimes have troublesome symptoms, termed post-acute sequelae of COVID-19 (PASC) or long COVID (LC), which can include problems with blood pressure regulation, gastrointestinal problems, inflammation, blood clotting, and symptoms like "brain fog." The proximate causes for these problems are not known, which makes these problems difficult to treat definitively. We previously found that some acute COVID-19 patients make antibodies against SARS-CoV-2, the virus that causes COVID-19, that act like an enzyme, angiotensin converting enzyme 2 (ACE2). ACE2 normally helps regulate blood pressure and serves as the receptor for SARS-CoV-2 in the body. We show that patients convalescing from COVID-19 also make antibodies that act like ACE2 and that the presence of those antibodies correlates with problems in blood pressure regulation. The findings provide a new opening to potentially understanding the causes of LC, and so provide direction for the development of new treatments.

Indexed as

Antibodies, CatalyticAntibodies, ViralCOVID-19Peptidyl-Dipeptidase AAdultAgedAngiotensin-Converting Enzyme 2ConvalescenceFemaleHumansMaleMiddle AgedPandemicsSARS-CoV-2Spike Glycoprotein, CoronavirusACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, CatalyticAntibodies, ViralPeptidyl-Dipeptidase ASpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2abzymeACE2COVID-19long COVIDPASCpathogenesisSARS-CoV-2

Identifiers

PMID40693778
PMCPMC12345163

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.