# Dysregulated monocyte compartment in PACS patients

**Authors:** Romy Kronstein-Wiedemann, Madeleine Teichert, Elisa Michel, Janina Berg, George Robinson, Kristin Tausche, Martin Kolditz, Johannes Bergleiter, Jessica Thiel, Dirk Koschel, Stephan R. Künzel, Kristina Hölig, Torsten Tonn, Manuela Rossol

PMC · DOI: 10.3389/fimmu.2025.1613034 · 2025-06-06

## TL;DR

Some patients with long-term symptoms after mild COVID-19 have altered monocyte populations in their blood, which may be linked to immune system dysfunction.

## Contribution

The study identifies specific monocyte subset changes in PACS patients, suggesting immune dysregulation even after recovery from mild disease.

## Key findings

- PACS patients showed increased intermediate and CD56+ monocytes compared to healthy donors.
- Non-classical monocyte levels were higher in PACS patients with cognitive dysfunction.
- Monocyte subset frequencies did not differ between PACS patients with fatigue, cough, or dyspnea and those without.

## Abstract

1-5% of all patients with COVID-19, a disease caused by infection with Severe Acute Respiratory Syndrome Virus 2 (SARS-Cov-2), even those with mild COVID-19 symptoms, continue to have symptoms after initial recovery. Symptoms associated with the post-acute sequelae of COVID-19 (PACS) include, among others, fatigue, shortness of breath, cough, and cognitive dysfunction. Since the dysregulated immune response appears to be caused by the sustained activation of certain immune cells, including monocytes, and the release of specific cytokines, the aim of our study was to investigate the effect of PACS disease on monocyte subpopulations.

Twenty-two healthy and thirty-two patients with PACS were included into this study. We performed blood gas analysis and measured hematological parameters from peripheral blood of PACS patients and compared them with healthy donors. Surface markers to identify monocyte subpopulations were analyzed by flow cytometry.

PACS patients had higher numbers of intermediate and CD56+ monocytes, whereas the numbers of total monocytes, classical and non-classical monocytes were normal compared to healthy donors. Comparison of patients with and without fatigue, cough, and dyspnea showed no difference in monocyte subset frequencies. However, patients with cognitive dysfunction had increased numbers of non-classical monocytes compared to patients without this symptom.

This suggests a disturbed homeostasis of the monocyte subsets in the peripheral blood of patients with PACS.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** NCAM1 (neural cell adhesion molecule 1) [NCBI Gene 4684] {aka CD56, MSK39, NCAM}
- **Diseases:** COVID-19 (MESH:D000086382), infection (MESH:D007239), dyspnea (MESH:D004417), cognitive dysfunction (MESH:D003072), fatigue (MESH:D005221), post-acute sequelae of COVID-19 (MESH:D000094024), PACS disease (MESH:D004194), cough (MESH:D003371)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12179141/full.md

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Source: https://tomesphere.com/paper/PMC12179141