Literature DB >> 32240716

Innate immune cells in cirrhosis.

Christine Bernsmeier1, Schalk van der Merwe2, Axel Périanin3.   

Abstract

Cirrhosis is a multisystemic disease wherein inflammatory responses originating from advanced liver disease and its sequelae affect distant compartments. Patients with cirrhosis are susceptible to bacterial infections, which may precipitate acute decompensation and acute-on-chronic liver failure, both of which are associated with high short-term mortality. Innate immune cells are an essential first line of defence against pathogens. Activation of liver macrophages (Kupffer cells) and resident mastocytes generate proinflammatory and vaso-permeating mediators that induce accumulation of neutrophils, lymphocytes, eosinophils and monocytes in the liver, and promote tissue damage. During cirrhosis progression, damage- and pathogen-associated molecular patterns activate immune cells and promote development of systemic inflammatory responses which may involve different tissues and compartments. The antibacterial function of circulating neutrophils and monocytes is gradually and severely impaired as cirrhosis worsens, contributing to disease progression. The mechanisms underlying impaired antimicrobial responses are complex and incompletely understood. This review focuses on the continuous and distinct perturbations arising in innate immune cells during cirrhosis, including their impact on disease progression, as well as reviewing potential therapeutic targets.
Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ACLF; Cirrhosis; Decompensation; Dendritic cell; Eosinophil; Immunoparesis; Immunotherapy; Innate lymphoid cell; Macrophage; Monocyte; Neutrophil; Toll-like receptor

Year:  2020        PMID: 32240716     DOI: 10.1016/j.jhep.2020.03.027

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  24 in total

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3.  Granulocyte Colony-Stimulating Factor Accelerates the Recovery of Hepatitis B Virus-Related Acute-on-Chronic Liver Failure by Promoting M2-Like Transition of Monocytes.

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4.  Faecal cytokine profiling as a marker of intestinal inflammation in acutely decompensated cirrhosis.

Authors:  Antonio Riva; Elizabeth H Gray; Sarah Azarian; Ane Zamalloa; Mark J W McPhail; Royce P Vincent; Roger Williams; Shilpa Chokshi; Vishal C Patel; Lindsey A Edwards
Journal:  JHEP Rep       Date:  2020-07-30

5.  Prevalence, Predictors, and Outcomes of Esophageal Candidiasis in Cirrhosis: An Observational Study With Systematic Review and Meta-Analysis (CANDID-VIEW).

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Review 6.  Dendritic Cell and T Cell Crosstalk in Liver Fibrogenesis and Hepatocarcinogenesis: Implications for Prevention and Therapy of Liver Cancer.

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Review 7.  Innate immune cells and their interaction with T cells in hepatocellular carcinoma.

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8.  Transcriptomic Profiling of the Liver Sinusoidal Endothelium during Cirrhosis Reveals Stage-Specific Secretory Signature.

Authors:  Nicolò Manicardi; Anabel Fernández-Iglesias; Laia Abad-Jordà; Felix Royo; Mikel Azkargorta; Martí Ortega-Ribera; David Sanfeliu-Redondo; Ana Martínez-Alcocer; Felix Elortza; Amelia J Hessheimer; Constantino Fondevila; Juan José Lozano; Juan Carlos García-Pagán; Jaime Bosch; Francisco Javier Cubero; Agustín Albillos; Javier Vaquero; Juan M Falcón-Pérez; Jordi Gracia-Sancho
Journal:  Cancers (Basel)       Date:  2021-05-29       Impact factor: 6.639

9.  Reduced Energy Metabolism Impairs T Cell-Dependent B Cell Responses in Patients With Advanced HBV-Related Cirrhosis.

Authors:  Chunhong Huang; Junwei Shao; Congcong Lou; Fengtian Wu; Tiantian Ge; Hainv Gao; Xiaoping Zheng; Xuejun Dong; Lichen Xu; Zhi Chen
Journal:  Front Immunol       Date:  2021-06-23       Impact factor: 7.561

Review 10.  Neutrophils in liver diseases: pathogenesis and therapeutic targets.

Authors:  Kai Liu; Fu-Sheng Wang; Ruonan Xu
Journal:  Cell Mol Immunol       Date:  2020-11-06       Impact factor: 11.530

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