Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study

Abstract Background and Aim Alcoholic hepatitis (AH), a severe complication of long‐term alcohol misuse, has a 30% 90‐day mortality. Infections are common and associated with higher mortality. There is currently no accurate method to predict infection in these patients. We aimed to test a measure of...

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Main Authors: Paula Boeira, Huey Tan, Euan Yates, Ashwin Dhanda
Format: Article
Language:English
Published: Wiley 2023-04-01
Series:JGH Open
Subjects:
Online Access:https://doi.org/10.1002/jgh3.12891
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author Paula Boeira
Huey Tan
Euan Yates
Ashwin Dhanda
author_facet Paula Boeira
Huey Tan
Euan Yates
Ashwin Dhanda
author_sort Paula Boeira
collection DOAJ
description Abstract Background and Aim Alcoholic hepatitis (AH), a severe complication of long‐term alcohol misuse, has a 30% 90‐day mortality. Infections are common and associated with higher mortality. There is currently no accurate method to predict infection in these patients. We aimed to test a measure of immune function, the QuantiFERON Monitor (QFM), in predicting clinical outcomes in patients with severe AH. Methods Peripheral blood was taken at baseline, and QFM performed according to the manufacturer's instructions. In parallel, QFM samples were analyzed with a cytokine multiplex. Clinical outcomes of mortality at 28 and 90 days and development of infection were recorded prospectively. Results Forty‐nine patients were recruited (mean age 51, 59% male and mean discriminant function 57.8). Interferon (IFN)‐γ release measured by standard QFM was significantly higher in survivors compared to non‐survivors at 28 (102 vs 16 IU/mL, P = 0.02) and 90 days (115 vs 32 IU/mL; P = 0.046). The area under the receiver operating characteristic curve (AUROC) was 0.79 for 28‐day mortality. IFN‐γ, IL‐10, and IL‐23 release measured by multiplex were significantly lower in patients who developed a subsequent infection compared to those who did not (115 vs 27 IU/mL, P = 0.037; 457 vs 202 pg/mL, P = 0.008; and 1039 vs 663 pg/mL, p = 0.01, respectively). Conclusion Immune dysfunction is associated with poorer outcomes in patients with severe AH. Measurement of IFN‐γ release by standard QFM accurately predicts early mortality, which can be applied to clinical practice as a biomarker of survival. Adaptation of the test to measure IL‐10 could be used as a biomarker of subsequent infection to guide clinical treatment decisions.
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spelling doaj.art-8184ced7070c4015bd6136b42c669b982023-04-27T11:56:03ZengWileyJGH Open2397-90702023-04-017428629010.1002/jgh3.12891Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory studyPaula Boeira0Huey Tan1Euan Yates2Ashwin Dhanda3Hepatology Research Group, Faculty of Health University of Plymouth Plymouth UKHepatology Research Group, Faculty of Health University of Plymouth Plymouth UKHepatology Research Group, Faculty of Health University of Plymouth Plymouth UKHepatology Research Group, Faculty of Health University of Plymouth Plymouth UKAbstract Background and Aim Alcoholic hepatitis (AH), a severe complication of long‐term alcohol misuse, has a 30% 90‐day mortality. Infections are common and associated with higher mortality. There is currently no accurate method to predict infection in these patients. We aimed to test a measure of immune function, the QuantiFERON Monitor (QFM), in predicting clinical outcomes in patients with severe AH. Methods Peripheral blood was taken at baseline, and QFM performed according to the manufacturer's instructions. In parallel, QFM samples were analyzed with a cytokine multiplex. Clinical outcomes of mortality at 28 and 90 days and development of infection were recorded prospectively. Results Forty‐nine patients were recruited (mean age 51, 59% male and mean discriminant function 57.8). Interferon (IFN)‐γ release measured by standard QFM was significantly higher in survivors compared to non‐survivors at 28 (102 vs 16 IU/mL, P = 0.02) and 90 days (115 vs 32 IU/mL; P = 0.046). The area under the receiver operating characteristic curve (AUROC) was 0.79 for 28‐day mortality. IFN‐γ, IL‐10, and IL‐23 release measured by multiplex were significantly lower in patients who developed a subsequent infection compared to those who did not (115 vs 27 IU/mL, P = 0.037; 457 vs 202 pg/mL, P = 0.008; and 1039 vs 663 pg/mL, p = 0.01, respectively). Conclusion Immune dysfunction is associated with poorer outcomes in patients with severe AH. Measurement of IFN‐γ release by standard QFM accurately predicts early mortality, which can be applied to clinical practice as a biomarker of survival. Adaptation of the test to measure IL‐10 could be used as a biomarker of subsequent infection to guide clinical treatment decisions.https://doi.org/10.1002/jgh3.12891alcoholic hepatitisalcohol‐related liver diseasebiomarkercytokineinfection
spellingShingle Paula Boeira
Huey Tan
Euan Yates
Ashwin Dhanda
Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study
JGH Open
alcoholic hepatitis
alcohol‐related liver disease
biomarker
cytokine
infection
title Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study
title_full Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study
title_fullStr Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study
title_full_unstemmed Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study
title_short Assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis: An exploratory study
title_sort assessment of immune function and prediction of survival and infection in patients with severe alcoholic hepatitis an exploratory study
topic alcoholic hepatitis
alcohol‐related liver disease
biomarker
cytokine
infection
url https://doi.org/10.1002/jgh3.12891
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