# The Impact of Liver Steatosis on Interleukin and Growth Factors Kinetics during Chronic Hepatitis C Treatment

**Authors:** Leona Radmanic Matotek, Snjezana Zidovec-Lepej, Nikolina Salek, Adriana Vince, Neven Papic

PMC · DOI: 10.3390/jcm13164849 · 2024-08-16

## TL;DR

This study shows that liver steatosis in hepatitis C patients affects cytokine and growth factor levels, which may influence liver regeneration and fibrosis.

## Contribution

The study identifies specific cytokine and growth factor profiles linked to liver steatosis during hepatitis C treatment.

## Key findings

- Patients with steatotic liver disease had lower IL-9, IL-10, IL-13, and IL-22 at baseline.
- SLD was associated with higher EGF, VEGF, and ANG levels and distinct cytokine kinetics during treatment.
- At SVR12, patients with SLD had significantly higher VEGF and HGF concentrations.

## Abstract

Background/Objectives: Various biological response modifiers play important roles in the immunopathogenesis of chronic hepatitis C (CHC). While serum levels of cytokines and growth factors change with the disease severity and treatment responses, the impact of concomitant liver steatosis on systemic inflammatory response is largely unknown. The aim of this study was to analyze the characteristics and kinetics of serum profiles of interleukins and growth factors in CHC patients with steatotic liver disease (SLD). Methods: Serum concentrations of 12 cytokines (IL-5, IL-13, IL-2, IL-6, IL-9, IL-10, IFN-γ, TNF-α, IL-17A, IL-17F, IL-4 and IL-22) and 6 growth factors (Angiopoietin-2, EGF, EPO, HGF, SCF, VEGF) were analyzed in 56 CHC patients at four time points (baseline, week 4, week 8 and SVR12) with bead-based flow cytometry assay. Results: At baseline, patients with SLD had significantly lower IL-9, IL-10, IL-13 and IL-22 and higher serum concentrations of EGF, VEGF and ANG. In a subgroup of patients with advanced liver fibrosis, SLD was linked with lower serum concentrations of IL-4, IL-5, IL-9, IL-10, IL-13 and IL-22 and higher concentrations of HGH and VEGF. Distinct cytokine kinetics during DAA treatment was observed, and SLD was identified as the main source of variation for IL-5, IL-9, IL-10, IL-13, IL-17A, IL-22, EGF, VEGF and ANG. Patients with SLD at SVR12 had significantly higher VEGF and HGF serum concentrations. Conclusions: SLD is associated with distinct cytokine and growth factor profiles and kinetics during CHC treatment, which might be associated with disease severity and the capacity for liver regeneration and contribute to fibrosis persistence.

## Linked entities

- **Proteins:** IL5 (interleukin 5), IL13 (interleukin 13), IL2 (interleukin 2), IL6 (interleukin 6), IL9 (interleukin 9), IL10 (interleukin 10), IFNG (interferon gamma), TNF (tumor necrosis factor), IL17A (interleukin 17A), IL17F (interleukin 17F), IL4 (interleukin 4), IL22 (interleukin 22), ANGPT2 (angiopoietin 2), EGF (epidermal growth factor), EPO (erythropoietin), HGF (hepatocyte growth factor), KITLG (KIT ligand), VEGFA (vascular endothelial growth factor A)
- **Diseases:** chronic hepatitis C (MONDO:0005231)

## Full-text entities

- **Genes:** EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, KITLG (KIT ligand) [NCBI Gene 4254] {aka DCUA, DFNA69, FPH2, FPHH, KL-1, Kitl}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, HGF (hepatocyte growth factor) [NCBI Gene 3082] {aka DFNB39, F-TCF, HGFB, HPTA, SF}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL17F (interleukin 17F) [NCBI Gene 112744] {aka CANDF6, IL-17F, ML-1, ML1}, ANGPT2 (angiopoietin 2) [NCBI Gene 285] {aka AGPT2, ANG2, LMPHM10}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, ANG (angiogenin) [NCBI Gene 283] {aka ALS9, HEL168, RAA1, RNASE4, RNASE5}
- **Diseases:** Liver Steatosis (MESH:D005234), liver fibrosis (MESH:D008103), fibrosis (MESH:D005355), SLD (MESH:D008107), CHC (MESH:D019698), inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11355301/full.md

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Source: https://tomesphere.com/paper/PMC11355301