# Evaluating the Efficacy of Probiotics on Inflammatory Cytokines in Alcoholic Liver Disease: A Focus on IL-6 and IL-10

**Authors:** Jiadila Bahetiyaer, Jie Cui, Wenhui Li, Jian Zhang, Ye Sun, Chunqing Ai, Shuying Liu, Shuaiming Jiang, Chengcheng Zhang, Jinchi Jiang

PMC · DOI: 10.3390/nu18040666 · 2026-02-18

## TL;DR

This study finds that probiotics can reduce IL-6 and increase IL-10 in patients with alcoholic liver disease, suggesting potential therapeutic benefits.

## Contribution

The study provides novel evidence on the differential effects of probiotics on specific inflammatory cytokines in alcoholic liver disease.

## Key findings

- Probiotics significantly reduced IL-6 levels in patients with alcoholic liver disease.
- Probiotics significantly increased IL-10 levels but had no significant effect on IL-1β or TNF-α.
- The effect on IL-6 was stronger in Asian populations, male subjects, and with solid dosage forms.

## Abstract

Background: While probiotics may offer therapeutic benefits for alcoholic liver disease (ALD), their impact on inflammatory markers in ALD patients is still uncertain. Objective: This study aims to investigate the effects of probiotic supplementation on inflammatory biomarkers in patients with alcoholic liver disease, particularly examining its role in modulating interleukin-6 (IL-6) levels. Methods: A comprehensive search was performed across PubMed, Embase, and Web of Science to identify randomized controlled trials investigating probiotic interventions in patients with alcoholic liver disease. Seven independent comparisons were chosen for meta-analysis to evaluate probiotics’ effects on inflammatory markers, with subgroup analyses examining the impact of region, formulation type, and gender. Results: The findings demonstrated that probiotics led to a significant reduction in IL-6 levels (SMD = −0.68, 95% CI [−1.15; −0.20], p = 0.005). No statistically significant effect of probiotics on interleukin-1β (IL-1β) (SMD = −0.35, 95% CI [−0.87, 0.17], p = 0.18) or tumor necrosis factor alpha (TNF-α) levels (SMD = −0.73, 95% CI [−1.68, 0.21], p = 0.13) was observed. Notably, probiotics were associated with a significant increase in interleukin-10 (IL-10) levels (SMD = 0.93,95% CI [−0.02; 1.87], p = 0.05). Subgroup analyses further revealed that the efficacy of probiotics in reducing IL-6 levels was more pronounced in studies characterized by higher proportions of Asian participants, solid dosage forms, and male subjects. Conclusions: Probiotics have notably reduced IL-6 levels by altering the gut microbiota and increased IL-10 levels, with limited impact on IL-1β and TNF-α. These results suggest probiotics could be used to treat ALD and emphasize the need for personalized probiotic approaches for different populations.

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL1B (interleukin 1 beta), TNF (tumor necrosis factor), IL10 (interleukin 10)
- **Diseases:** alcoholic liver disease (MONDO:0043693)

## Full-text entities

- **Genes:** FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, TREM1 (triggering receptor expressed on myeloid cells 1) [NCBI Gene 54210] {aka CD354, TREM-1}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, NR1H4 (nuclear receptor subfamily 1 group H member 4) [NCBI Gene 9971] {aka BAR, FXR, HRR-1, HRR1, PFIC5, RIP14}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** Alcoholic Fatty Liver (MESH:D005235), Fatty Liver (MESH:D005234), ALD (MESH:D008108), hepatocyte dysfunction (MESH:D006331), liver injury (MESH:D017093), necrosis (MESH:D009336), liver cancer (MESH:D006528), injury to (MESH:D014947), impairment of liver function (MESH:D008107), Inflammatory (MESH:D007249), Alcoholic (MESH:D000437), Alcoholic cirrhosis (MESH:D008104), Alcoholic hepatitis (MESH:D006519), Alcoholic liver fibrosis (MESH:D008103)
- **Chemicals:** prebiotic (MESH:D056692), LPS (MESH:D008070), alcohol (MESH:D000438), Acetaldehyde (MESH:D000079), SCFAs (MESH:D005232), ROS (MESH:D017382), bile acid (MESH:D001647), butyrate (MESH:D002087)
- **Species:** Lactiplantibacillus plantarum (species) [taxon 1590], Streptococcus (genus) [taxon 1301], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Lacticaseibacillus rhamnosus (species) [taxon 47715]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943775/full.md

---
Source: https://tomesphere.com/paper/PMC12943775