KMID : 1188320200140020265
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Gut and Liver 2020 Volume.14 No. 2 p.265 ~ p.268
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Ex Vivo T Cell Cytokine Expression Predicts Survival in Patients with Severe Alcoholic Hepatitis
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Dhanda Ashwin D.
Yates Euan Schewitz-Bowers Lauren P. Lait Philippa J. Lee Richard W. J. Cramp Matthew E.
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Abstract
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Alcoholic hepatitis (AH) is an acute inflammatory liver condition with high early mortality rate. Steroids improve short-term survival but nonresponders have the worst outcomes. There is a clinical need to identify these high-risk individuals at the time of presentation. T cells are implicated in AH and steroid responsiveness. We measured ex vivo T cell cytokine expression as a candidate biomarker of outcomes in patients with AH. Consecutive patients (bilirubin >80 ¥ìmol/L and ratio of aspartate aminotransferase to alanine aminotransferase >1.5 who were heavy alcohol consumers with discriminant function [DF] ¡Ã32), were recruited from University Hospitals Plymouth NHS Trust. T cells were obtained and stimulated ex vivo. Cytokine expression levels were determined by flow cytometry and protein multiplex analysis. Twenty-three patients were recruited (10 male; median age 51 years; baseline DF 67; 30% 90-day mortality). Compared to T cells from nonsurvivors at day 90, T cells from survivors had higher baseline baseline intracellular interleukin (IL)-10:IL-17A ratio (0.43 vs 1.20, p=0.02). Multiplex protein analysis identified interferon ¥ã (IFN¥ã) and tumor necrosis factor-¥á (TNF-¥á) as independent predictors of 90-day mortality (p=0.04, p=0.01, respectively). The ratio of IFN¥ã to TNF-¥á was predictive of 90-day mortality (1.4 vs 0.2, p=0.03). These data demonstrate the potential utility of T cell cytokine release assays performed on pretreatment blood samples as biomarkers of survival in patients with severe AH. Our key findings were that intracellular IL-10:IL-17A and IFN¥ã:TNF-¥á in culture supernatants were predictors of 90-day mortality. This offers the promise of developing T cell-based diagnostic tools for risk stratification.
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KEYWORD
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Hepatitis, alcoholic, T cells, Cytokines, Biomarker
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