Abstract

Natural killer (NK) cells play a therapeutic role in liver fibrosis (LF). We aimed to analyze NK cells in heavy drinkers without cirrhosis or decompensated liver disease and establish correlations with other related subpopulations. Data on sociodemographic characteristics, alcohol consumption, laboratory parameters, and immunophenotyping of NK (CD16+/CD56+), T (CD3+), B (CD19+), NKT (CD16+/CD56+/CD3+), and cytotoxic (CD3-CD8+) cells were collected. Fibrosis-4 (FIB-4) scores were used to compare patients without (FIB-4 < 1.45) and with (FIB-4 > 3.25) advanced LF (ALF). We included 136 patients (76% male) with a mean age of 49 years who had a 15-year alcohol use disorder (AUD) and alcohol consumption of 164 g/day. Patients with ALF (n = 25) presented significantly lower absolute total lymphocyte, T cell, B cell, and NKT cell numbers than patients without LF (n = 50; p < 0.01). However, the NK cells count was similar (208 ± 109 cells/µL vs. 170 ± 105 cells/µL) in both groups. The T cells percentage was lower (80.3 ± 5.6% vs. 77 ± 7%; p = 0.03) and the NK cells percentage was higher (9.7 ± 5% vs. 13 ± 6%; p = 0.02) in patients with ALF than in those without LF. The percentages of NK cells and T cells were inversely correlated in patients without (r = –0.65, p < 0.01) and with ALF (r = −0.64; p < 0.01). Additionally, the NK cells and CD3-CD8+ cell percentages were positively correlated in patients without (r = 0.87, p < 0.01) and with (r = 0.92; p < 0.01) ALF. Conclusions: Heavy drinkers without decompensated liver disease showed an increase in NK cells related to T cells lymphopenia and an increase in cytotoxic populations. The interaction of NK cells with other subpopulations may modify alcohol-related liver disease progression.

Highlights

  • Liver fibrosis (LF) is the main prognostic marker for the progression of alcohol liver disease (ALD) [1]

  • The natural killer (NK) cells of the patients with alcohol-related cirrhosis showed greater cytotoxicity than those of healthy individuals, as measured by the release of cytotoxic granules [16]. The discrepancies between these results suggest that alcohol may exert different effects on NK cells based on the different stages of liver disease

  • Patients Details who had an alcohol use disorder (AUD) for 15 years (IQR: 7–20) and an alcohol consumption of 163 ± 80 g/day

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Summary

Introduction

Liver fibrosis (LF) is the main prognostic marker for the progression of alcohol liver disease (ALD) [1]. The mechanisms of hepatic inflammation as a triggering factor in stellate cell activation and in the consequent development of LF have been extensively studied [2]. Immune cells are key to the progression of ALD [3]. Natural killer (NK) cells have been extensively studied for their potential antifibrotic effects and as therapeutic targets [4]. In addition to inhibiting hepatic stellate cells and preventing the progression of LF, NK cells have antiviral and antitumor effects through the secretion of regulatory cytokines and the release of cytotoxic granules [5]. NK cells represent 5–20% of peripheral lymphocytes and up to 50% of resident lymphocytes in the liver; their phenotype and function vary widely depending on their location [6]

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