# mRNA Vaccination for COVID-19 Lowers the Risk for Pulmonary Fibrosis Through GIP-10/Gal-3/HIF-1 Downregulation

**Authors:** Maha R Al-Sammarraie, Fatma D Azaiez, Hejer Litaiem

PMC · DOI: 10.7759/cureus.84269 · 2025-05-17

## TL;DR

This study shows that the Pfizer vaccine reduces the risk of pulmonary fibrosis in COVID-19 patients by lowering levels of specific inflammatory markers.

## Contribution

The study identifies GIP-10, Gal-3, and HIF-1 as key biomarkers and demonstrates the Pfizer vaccine's role in downregulating them in PF-associated COVID-19.

## Key findings

- Vaccinated patients had significantly lower levels of GIP-10, Gal-3, and HIF-1 compared to non-vaccinated patients.
- GIP-10, Gal-3, and HIF-1 are strong predictors of PF in COVID-19 patients.
- The Pfizer vaccine helps control inflammation by managing GIP-10 levels.

## Abstract

Background

Pulmonary fibrosis (PF) is associated with coronavirus disease 2019 (COVID-19) through the occurrence of acute respiratory distress syndrome (ARDS). The overall sequence results in the elevation of the inflammation profile of infected individuals. The risk of PF onset in COVID-19 patients is not limited to the infection course but extends to post-infection periods. Gamma-inducible protein-10 (GIP-10) is a chemokine; its production and release are induced by interferon-gamma (IFN-γ).

Objectives

In this study, we aimed to investigate the role of GIP-10, Galectin-3 (Gal-3), and hypoxia inducible factor 1 (HIF-1) in PF-associated COVID-19 and the effectiveness of the Pfizer vaccine against the progression of PF and inflammation through evaluating these three biomarkers and their correlation with a few hematological parameters.

Design & methods

The study included 120 subjects (34-68 years) from Ibn Al-Nafees Hospital (Baghdad, Iraq). Three groups of 40 subjects were designed for our investigation as control, non-vaccinated COVID-19, and vaccinated COVID-19 patients. The presence of PF was evaluated in each participant. The COVID-19 patients with chronic kidney disease, liver cirrhosis, cancer, and pregnant women were excluded from this study. The GIP-10, Gal-3, and HIF-1 were evaluated in the subjects’ serum using Sandwich ELISA technology.

Results

The results have shown significantly elevated levels of GIP-10, Gal-3, and HIF-1 in vaccinated and non-vaccinated PF-associated COVID-19 patients compared to the control, but the vaccinated patients exhibited significantly (p<0.05) lower levels of GIP-10, Gal-3, and HIF-1 compared to non-vaccinated patients. Moreover, in non-vaccinated PF-associated COVID-19 patients, GIP-10 did not correlate significantly with any parameter, while in vaccinated patients, it was correlated positively with age, WBC, RBC, and ESR. All of GIP-10, Gal-3, and HIF-1 expressed Odds ratios (OR) 1< as risks for PF in COVID-19 patients and can be used excellently to predict PF-associated COVID-19.

Conclusions

The Pfizer vaccine for COVID-19 has a positive role in managing GIP-10 and, therefore, better controls patients' inflammation profiles.

## Linked entities

- **Proteins:** CXCL10 (C-X-C motif chemokine ligand 10), LGALS3 (galectin 3), HIF1A (hypoxia inducible factor 1 subunit alpha), IFNG (interferon gamma)
- **Diseases:** pulmonary fibrosis (MONDO:0002771), coronavirus disease 2019 (MONDO:0100096), acute respiratory distress syndrome (MONDO:0006502), chronic kidney disease (MONDO:0005300), cancer (MONDO:0004992)

## Full-text entities

- **Genes:** CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, LGALS3 (galectin 3) [NCBI Gene 3958] {aka CBP35, GAL3, GALBP, GALIG, L31, LGALS2}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}
- **Diseases:** ARDS (MESH:D012128), inflammation (MESH:D007249), COVID-19 (MESH:D000086382), infected (MESH:D007239), cancer (MESH:D009369), liver cirrhosis (MESH:D008103), PF (MESH:D011658), chronic kidney disease (MESH:D051436)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12168844/full.md

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Source: https://tomesphere.com/paper/PMC12168844