# Prognostic value of inflammatory cytokine levels, clinical efficacy, and prognosis of the hybrid artificial liver support system in chronic liver failure treatment

**Authors:** Lihua Liu, Xiaoling Li, Juan Wang, Jing Ma, Xueping Nan

PMC · DOI: 10.5937/jomb0-55735 · Journal of Medical Biochemistry · 2025-10-28

## TL;DR

This study shows that combining two liver support therapies improves outcomes for chronic liver failure patients by enhancing liver function, reducing inflammation, and increasing survival rates.

## Contribution

The study demonstrates the superior efficacy of combining plasma exchange and molecular adsorption in treating chronic liver failure.

## Key findings

- Combination therapy improved liver and kidney function more than single therapies.
- Combination therapy reduced inflammatory cytokines and improved one-year survival rates.
- Combination therapy had fewer adverse reactions and higher clinical efficacy.

## Abstract

This study aimed to evaluate the effectiveness and safety of the hybrid artificial liver support system (HALSS) in patients with chronic liver failure (CLF). It also sought to analyze the inflammatory response and patient prognosis.

A total of 126 CLF patients were divided into three treatment groups: plasma exchange (PEG), double plasma molecular adsorption system (DPMASG), and a combination therapy group (CG). Key parameters, including liver and kidney function, blood coagulation, T lymphocyte subgroups, and inflammatory cytokine levels (TNF-a, procalcitonin [PCT], interferon-gamma [IFN-g], IL-2, IL-6, and IL-10), were assessed before and after treatment. The clinical efficacy, adverse reactions, and short-term prognosis were compared across the groups.

Compared to PEG and DPMASG, the combination group (CG) showed significant improvement in liver and kidney function markers, including reduced ALT, AST, total bilirubin (TBil), creatinine (Cr), INR, and prothrombin time (PT). Additionally, CG demonstrated increased levels of cholinesterase (ChE), albumin, and prothrombin activity (PTA). The CG group had a higher total clinical efficacy (92.0%) compared to PEG (76.3%) and DPMASG (78.9%). It also showed a lower rate of adverse reactions (8.0%) and improved one-year survival (36.0% vs. 18.4% and 21.1%, respectively). Furthermore, CG had the most favourable effects on inflammatory cytokine levels and T lymphocyte subsets, significantly reducing TNF-a, PCT, IFN-g, IL-2, IL-6, and IL-10.

The combination of PEG and DPMAS (HALSS) demonstrated superior clinical efficacy in improving liver and kidney function, reducing inflammation, and enhancing patient prognosis compared to single therapies. These findings support HALSS as a promising adjunctive therapy for CLF patients, improving short-term outcomes and long-term survival.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL2 (interleukin 2), IL6 (interleukin 6), IL10 (interleukin 10)
- **Diseases:** chronic liver failure (MONDO:0100193)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, UROD (uroporphyrinogen decarboxylase) [NCBI Gene 7389] {aka PCT, UPD}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** blood coagulation (MESH:D001778), inflammation (MESH:D007249), CLF (MESH:D058625)
- **Chemicals:** Cr (MESH:D003404), TBil (MESH:D001663), DPMAS (MESH:C056426), DPMASG (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12639527/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12639527/full.md

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Source: https://tomesphere.com/paper/PMC12639527