# Investigation of Biomarkers in Allergic Patients with Long COVID

**Authors:** Fabio Romano Selvi, David Longhino, Gabriele Lucca, Ilaria Baglivo, Maria Antonietta Zavarella, Chiara Laface, Laura Bruno, Sara Gamberale, Ludovica Fabbroni, Angela Rizzi, Arianna Aruanno, Rosa Buonagura, Marina Curci, Alessandro Buonomo, Marinella Viola, Gianluca Ianiro, Francesco Landi, Matteo Tosato, Antonio Gasbarrini, Cristiano Caruso

PMC · DOI: 10.3390/jpm16010031 · Journal of Personalized Medicine · 2026-01-05

## TL;DR

This study explores how allergic inflammation and immune markers are linked to long-lasting symptoms in people with allergies and long COVID.

## Contribution

The study identifies elevated ECP and FLCs as potential biomarkers associated with persistent long-COVID symptoms in allergic patients.

## Key findings

- Elevated kappa FLC levels were significantly associated with high ECP and increased IgE in allergic long-COVID patients.
- Higher ECP and FLC levels correlated with persistent respiratory and systemic symptoms like fatigue and dyspnea.
- The findings suggest a model of sustained inflammation and delayed epithelial recovery in allergic long-COVID patients.

## Abstract

Background: Long COVID remains a challenging and heterogeneous condition, with mechanisms that are still incompletely understood. Emerging evidence suggests that patients with allergic disease may experience more persistent post-COVID symptoms, possibly due to immune dysregulation and epithelial barrier fragility. Methods: We carried out an observational, single-center study at the Allergy and Clinical Immunology Unit of Policlinico Universitario A. Gemelli IRCCS (Rome, Italy). Seventeen adults with confirmed allergic disease and long COVID were evaluated between July and December 2024. Biomarkers reflecting allergic inflammation and barrier integrity, blood eosinophil count, total immunoglobulin E (IgE), eosinophil cationic protein (ECP), and serum free light chains (FLCs), were measured and analyzed for interrelationships and symptom correlations. Results: Participants (10 men, 7 women; mean age 43.7 years) showed variable biomarker profiles, consistent with the heterogeneity of allergic inflammation. Mean eosinophil count was 179 ± 72 cells/µL, total IgE 165.4 ± 140.6 kU/L, ECP 64.2 ± 48.5 ng/mL, and the kappa/lambda FLC ratio 1.20 ± 0.69. Notably, elevated kappa FLC levels (>19.4 mg/L) were significantly associated with high ECP (>20 ng/mL) (χ2 = 10.6, p = 0.001) and increased IgE (>200 kU/L) (χ2 = 6.0, p = 0.015). Individuals with higher ECP and FLCs more often reported respiratory and systemic symptoms, especially fatigue, dyspnea, and cognitive fog, that persisted beyond six months. Conclusions: These findings suggest that biomarkers of allergic inflammation and barrier dysfunction, particularly ECP and FLCs, may contribute to the persistence of long-COVID symptoms in allergic patients. The observed links between humoral activation, eosinophilic activity, and prolonged symptom burden support a model of sustained inflammation and delayed epithelial recovery. Larger, longitudinal studies including non-allergic controls are warranted to confirm these associations and to explore whether restoring barrier integrity could shorten recovery trajectories in this vulnerable population.

## Linked entities

- **Proteins:** IGHE (immunoglobulin heavy constant epsilon), RNASE3 (ribonuclease A family member 3)
- **Diseases:** allergic disease (MONDO:0005271)

## Full-text entities

- **Genes:** RNASE3 (ribonuclease A family member 3) [NCBI Gene 6037] {aka ECP, RAF1, RNS3}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** dyspnea (MESH:D004417), fatigue (MESH:D005221), cognitive fog (MESH:D003072), Long COVID (MESH:D000094024), allergic inflammation (MESH:D007249), allergic disease (MESH:D004342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12842890/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12842890/full.md

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Source: https://tomesphere.com/paper/PMC12842890