# Clara cell 16 kDa protein: an important marker for COVID-19 severity

**Authors:** Tineke Kardol-Hoefnagel, Bart Luijk, Leon Reteig, Saskia Haitjema, Helen L. Leavis, Henny G. Otten

PMC · DOI: 10.3389/fimmu.2025.1527377 · Frontiers in Immunology · 2025-04-01

## TL;DR

This study shows that higher levels of Clara cell 16 kDa protein (CC16) in the blood predict severe cases of COVID-19, helping identify patients who may need intensive care.

## Contribution

The study identifies CC16 as a novel and independent biomarker for predicting the severity of COVID-19.

## Key findings

- CC16 levels were significantly higher in patients admitted to the ICU compared to non-ICU patients.
- Elevated CC16 levels were independently associated with severe COVID-19 after adjusting for known risk factors.
- TARC levels were lower in confirmed COVID-19 patients compared to negative patients.

## Abstract

The coronavirus disease 19 (COVID-19) is a disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that invades lung epithelial cells and can lead to severe respiratory failure. In this study, we evaluated whether Clara cell 16 kDa protein (CC16), a serum marker of lung alveolar cell damage, is predictive for disease severity. Patients suspected of SARS-CoV-2 infection were included in this study. Serum levels of Clara cell 16 kDa protein (CC16), soluble Fas Ligand, cytochrome C, thymus- and activation regulated chemokine (TARC) and of oxidate stress related proteins were analyzed. Clinical patient data were extracted from the Utrecht Patient Oriented Database. COVID-19 positive patients were divided in two groups according to disease severity. The mean day difference between COVID-19 diagnosis date and sampling date was +11 days. Concentrations of TARC were lower in COVID-19 positive versus COVID-19 negative patients (unpaired t-test, p=0.002). In addition, CC16 serum levels were significantly elevated in sera taken from patients that were admitted at the intensive care unit (ICU) (p=0.0082). In a matched cohort, sera taken prior to ICU admission (-3 days) contained higher CC16 levels (paired t-test, p=0.0072). Multivariable analyses adjusted for known risk factors (age, gender, blood counts, lactate dehydrogenase, c-reactive protein, underlying disease) showed that CC16 levels were independently associated to COVID-19 severity (interquartile-range, odds ratio 1.53, p=0.0102). In conclusion, our findings highlight CC16 as a promising biomarker for early identification of severe COVID19 cases, which could improve patient management and resource allocation.

## Linked entities

- **Proteins:** SCGB1A1 (secretoglobin family 1A member 1), Cyt-c-d (Cytochrome c distal), CCL17 (C-C motif chemokine ligand 17)
- **Diseases:** COVID-19 (MONDO:0100096), severe acute respiratory syndrome coronavirus 2 (MONDO:0100096), SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** SCGB1A1 (secretoglobin family 1A member 1) [NCBI Gene 7356] {aka CC10, CC16, CCPBP, CCSP, UGB, UP-1}, CCL17 (C-C motif chemokine ligand 17) [NCBI Gene 6361] {aka A-152E5.3, ABCD-2, SCYA17, TARC}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, FASLG (Fas ligand) [NCBI Gene 356] {aka ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** lung alveolar cell damage (MESH:D055370), COVID-19 (MESH:D000086382), respiratory failure (MESH:D012131)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], 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/PMC11996771/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC11996771/full.md

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Source: https://tomesphere.com/paper/PMC11996771