# An engineered miniACE2 protein secreted by mesenchymal stromal cells effectively neutralizes multiple SARS-CoV- 2 variants in vitro

**Authors:** Sara Moreno-Jiménez, Gina Lopez-Cantillo, Jenny Andrea Arevalo-Romero, Ana María Perdomo-Arciniegas, Andrea Marisol Moreno-Gonzalez, Bellaneth Devia-Mejia, Bernardo Armando Camacho, Paulino Gómez-Puertas, Cesar A. Ramirez-Segura

PMC · DOI: 10.1186/s10020-025-01190-w · Molecular Medicine · 2025-04-23

## TL;DR

Researchers engineered a protein that can neutralize multiple SARS-CoV-2 variants when secreted by special cells, offering a potential treatment for vulnerable patients.

## Contribution

A novel therapeutic platform using mesenchymal stromal cells to secrete miniACE2 decoys for broad SARS-CoV-2 variant neutralization.

## Key findings

- BP2 protein secreted by MSCs effectively neutralizes SARS-CoV-2, including Omicron subvariants.
- The approach leverages MSCs for tissue repair and immunomodulation, enhancing therapeutic potential.
- This method offers a scalable strategy for treating severe COVID-19 across evolving viral variants.

## Abstract

SARS-CoV- 2 continues to evolve, producing novel Omicron subvariants through recombinant lineages that acquire new mutations, undermining existing antiviral strategies. The viral fitness and adaptive potential of SARS-CoV- 2 present significant challenges to emergency treatments, particularly monoclonal antibodies, which demonstrate reduced efficacy with the emergence of each new variant. Consequently, immunocompromised individuals, who are more susceptible to severe manifestations of COVID- 19 and face heightened risks of critical complications and mortality, remain vulnerable in the absence of effective emergency treatments. To develop translational approaches that can benefit this at-risk population and establish broader therapeutic strategies applicable across variants, we previously designed and engineered in silico miniACE2 decoys (designated BP2, BP9, and BP11). These decoys demonstrated promising efficacy in neutralizing Omicron subvariants. In this study, we leveraged the therapeutic potential of mesenchymal stromal cells (MSCs) for tissue repair and immunomodulation in lung injuries and used these cells as a platform for the secretion of BP2. Our innovative assays, which were conducted with the BP2 protein secreted into the culture supernatant of BP2-MSCs, demonstrated the potential for neutralizing SARS-CoV- 2, including Omicron subvariants. The development of these advanced therapeutic platforms holds significant promise for scalability to effectively mitigate the impact of severe COVID- 19, contributing to broader and more resilient treatment strategies against the evolving landscape of SARS-CoV- 2 variants.

The online version contains supplementary material available at 10.1186/s10020-025-01190-w.

## Linked entities

- **Proteins:** SYN1 (Rad21/Rec8-like family protein), Igkv9-119 (immunoglobulin kappa chain variable 9-119)
- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** BP2 [NCBI Gene 474257], BP9 [NCBI Gene 474199]
- **Diseases:** lung injuries (MESH:D055370), COVID- 19 (MESH:D000086382)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12016477