Evidence map›Paper›PMID 42067150›Full record

ReviewJournal of hepatology2026

Uncovering immune dysfunction in ACLF: Cellular mechanisms, molecular pathways, and therapeutic frontiers.

Marti Ortega-Ribera, Robert Brenig, Christine Bernsmeier, Gyongyi Szabo

Abstract readReview
In one paragraph

Review in Journal of hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Marti Ortega-RiberaDepartment of Medicine, Division of Gastroenterology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Robert BrenigGastroenterology and Hepatology Department, University Centre for Gastrointestinal and Liver Diseases, University Hospital Basel, Basel, Switzerland; Translational Hepatology, Department of Biomedicine, Department of Clinical Research, University of Basel, Basel, Switzerland.
Christine BernsmeierGastroenterology and Hepatology Department, University Centre for Gastrointestinal and Liver Diseases, University Hospital Basel, Basel, Switzerland; Translational Hepatology, Department of Biomedicine, Department of Clinical Research, University of Basel, Basel, Switzerland.
Gyongyi SzaboDepartment of Medicine, Division of Gastroenterology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA; Broad Institute of Harvard and MIT, Cambridge, MA, USA. Electronic address: gszabo1@bidmc.harvard.edu.

Funding

Alcohol and Monocyte Signaling Administrative SupplementR01AA011576 · NIAAA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Gyongyi Szabo · 1998 to 2026
$9.3M
TLR4 Signaling in alcoholic liver diseaseR01AA017729 · NIAAA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SZABO, GYONGYI · 2009 to 2021
$4.3M
Innate immune dysregulation in alcohol-associated liver diseaseR01AA032418 · NIAAA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Gyongyi Szabo · 2025 to 2026
$1.4M
NIAAA NIH HHS R01 AA011576NIAAA NIH HHS R01 AA017729NIAAA NIH HHS R01 AA032418
6 · The paper itself

Abstract

Acute-on-chronic liver failure (ACLF) is a life-threatening condition characterised by acute hepatic decompensation, multi-organ failure, and high short-term mortality in patients with cirrhosis. A hallmark of ACLF is profound immune dysfunction, which contributes to excessive organ-specific inflammation and impaired host defence, predisposing patients to infection, multi-organ failure and death. This review aims to elucidate the cellular and molecular mechanisms implying systemic immune dysfunction in ACLF, highlighting key pathophysiological pathways and their clinical significance. We provide an overview of ACLF, including its global clinical impact, in the context of immune dysfunction as a central driver of disease pathogenesis. The discussion focuses on alterations in innate immunity, including impaired neutrophil and monocyte phagocytosis, excessive neutrophil extracellular trap (NET) formation, and monocyte/macrophage dysfunction, which contribute to immuneparesis and exaggerated inflammation in an organ-specific manner. Also, dysregulation of natural killer (NK) cell cytotoxicity and adaptive immune dysfunction, including changes in T-cell subpopulations and B-cell antibody production in ACLF, are adressed. We further dissect the emerging evidence of molecular pathways driving dysfunction of immune cells and their impaired ability to control infections in ACLF, emphasising the roles of pathogen- and damage-associated molecular patterns (PAMPs/DAMPs), toll-like receptor (TLR) signalling, oxidative stress, mitochondrial dysfunction, epigenetic/metabolic reprogramming and immune checkpoint molecules. In addition, the review explores immune cell communication within the innate and adaptive immune systems, as well as interactions with parenchymal and non-parenchymal cells across organs affected by ACLF. Particular attention is given to inter-organ crosstalk involving the liver, circulation, brain, gut, and kidney. Finally, we summarise recent preclinical and clinical advances in biomarkers of immune dysfunction and immunomodulatory therapeutic strategies aimed at restoring immune homeostasis in patients with ACLF.

Indexed as

Acute-On-Chronic Liver FailureAdaptive ImmunityHumansImmunity, InnateKiller Cells, NaturalSignal TransductionAdaptive immunityEnd-stage liver diseaseInnate immunityInter-organ crosstalk

Identifiers

PMID42067150
PMCPMC13417364

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.