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

**Authors:** Yufeng Song, Frances Mehl, Lyndsey M. Muehling, Glenda Canderan, Kyle Enfield, Jie Sun, Michael T. Yin, Sarah J. Ratcliffe, Jeffrey M. Wilson, Alexandra Kadl, Judith A. Woodfolk, Steven L. Zeichner

PMC · DOI: 10.1128/mbio.01735-25 · 2025-07-22

## TL;DR

Some people recovering from COVID-19 produce antibodies that mimic ACE2 enzyme activity, which may contribute to long-term symptoms like blood pressure issues.

## Contribution

Identified ACE2-like enzymatic activity in convalescent patients, linking it to persistent symptoms in long COVID.

## Key findings

- ACE2-like abzymes are present in convalescent patients with persistent pulmonary symptoms.
- ACE2-like activity correlates with blood pressure changes during exercise tests.
- These abzymes may play a role in the pathogenesis of long COVID.

## 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.

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.

## Linked entities

- **Proteins:** ACE2 (angiotensin converting enzyme 2)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}
- **Diseases:** inflammation (MESH:D007249), neuropsychiatric complaints (MESH:C000631768), infection (MESH:D007239), coagulopathies (MESH:D001778), LC (MESH:D000094024), brain fog (MESH:D005222), gastrointestinal problems (MESH:D012817), COVID-19 (MESH:D000086382)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12345163/full.md

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Source: https://tomesphere.com/paper/PMC12345163