# Morphological and Immunohistochemical Characteristics of Liver Inflammation in Patients with a History of COVID-19

**Authors:** Ilze Strumfa, Ludmila Viksna, Oksana Kolesova, Ieva Vanaga, Haralds Plaudis, Jelena Storozenko, Boriss Strumfs, Janis Pavulans, Romans Uljanovs

PMC · DOI: 10.3390/v18010068 · Viruses · 2026-01-02

## TL;DR

This study examines liver inflammation in patients who had COVID-19, finding increased immune cell activity and tissue regeneration compared to controls.

## Contribution

The study provides new insights into liver pathology in post-COVID-19 patients, highlighting immune cell changes and regenerative processes.

## Key findings

- Post-COVID-19 patients showed higher CD3+ lymphocyte counts and lower CD68+ macrophage counts compared to controls.
- Regenerative changes in hepatocytes and biliary epithelium were more frequent and extensive in post-COVID-19 patients.
- No significant fibrosis or vascular changes were observed in post-COVID-19 patients.

## Abstract

The COVID-19 pandemic caused more than seven million deaths, mostly via acute respiratory distress syndrome with microvascular thrombosis. Compared to the amount of information about pulmonary pathology, information about COVID-19-induced liver lesions is scarce, especially with regard to the long-term consequences. The aim of our study was to evaluate inflammatory, vascular and fibrotic changes in hepatobiliary tissues of patients with a history of COVID-19 (post-COVID-19 patients). Based on the Knodell score, moderate portal inflammation was observed in 41.2% of post-COVID-19 patients, contrasting with 14.3% of control cases (p = 0.06). Moderate periportal inflammation was present in 26.5% and 7.1% of patients, respectively (p = 0.08). Post-COVID-19 patients showed higher counts of CD3+ lymphocytes (p = 0.02) and lower counts of CD68+ macrophages (p = 0.04), as well as more frequent and extensive regenerative changes in hepatocytes and the biliary epithelium (p = 0.0007). We did not find significant fibrosis or pathological changes in blood vessels, and only mild steatosis was observed in both groups.

## Linked entities

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

## Full-text entities

- **Genes:** CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** liver lesions (MESH:D008107), deaths (MESH:D003643), COVID-19 (MESH:D000086382), Post-COVID-19 (MESH:D000094024), steatosis (MESH:D005234), Liver Inflammation (MESH:D007249), acute respiratory distress syndrome (MESH:D012128), thrombosis (MESH:D013927), fibrosis (MESH:D005355)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846597/full.md

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Source: https://tomesphere.com/paper/PMC12846597