# Evaluating the Role of the Renin-angiotensin System in COVID-19: Implications for ACE Inhibitor and ARB Use During SARS-CoV-2 Infection

**Authors:** Sarah R. Tritsch, Evelyn Mendoza-Torres, Mónica Gómez-Pulido, Jairo Castellar-López, Rebecca Lynch, Carlos Herrera Gomez, Hana Akselrod, Adrienne Poon, Sam Simmens, Christopher N. Mores, Gary Simon, Lauren C. Ray, Sarah Conway, Aileen Y. Chang

PMC · DOI: 10.33696/immunology.6.213 · Journal of cellular immunology · 2025-05-23

## TL;DR

This study examines the renin-angiotensin system in COVID-19 and finds no significant changes in key components or effects from ACE inhibitors and ARBs.

## Contribution

The study provides clinical and in vitro evidence that RAS components and ACE/ARB drugs are not significantly altered in COVID-19.

## Key findings

- No significant differences in RAS components were found between healthy and COVID-19 patient groups.
- ACE inhibitors and ARBs did not affect cell viability during SARS-CoV-2 infection in vitro.
- Findings support the safety of continuing ACE inhibitors and ARBs in COVID-19 patients.

## Abstract

This study aimed to investigate the role of the renin-angiotensin system (RAS) in COVID-19, particularly focusing on key components such as ACE, ACE2, and their related peptides, angiotensin-(1–7) and angiotensin-(1–9). Using serum samples from healthy controls and both non-severe and severe COVID-19 patients, ELISA assays revealed no significant differences in these RAS components between the groups. In addition, in vitro studies showed no impact of ACE inhibitors or Angiotensin Receptor Blockers (ARB) on cell viability during SARS-CoV-2 infection. These clinical findings suggest that RAS alterations may not be a major factor in COVID-19 severity and the in vitro data support current guidelines, indicating the safety of continuing ACE inhibitors and ARBs in COVID-19 patients without evidence of increased SARS-CoV-2 infectivity in the presence of these compounds. This study highlights the lack of significant changes in key RAS components during COVID-19 in a clinical cohort and provides critical in vitro evidence supporting the continued use of ACE inhibitors and ARBs in treating patients.

## Linked entities

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

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}
- **Diseases:** COVID-19 (MESH:D000086382)
- **Chemicals:** angiotensin-(1-9) (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12101613/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12101613/full.md

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Source: https://tomesphere.com/paper/PMC12101613