4.5 Review

Circulating neutrophil anti-pathogen dysfunction in cirrhosis

Journal

JHEP REPORTS
Volume 5, Issue 11, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhepr.2023.100871

Keywords

neutrophils; cirrhosis; phagocytosis; ROS; chemotaxis; NETs

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Neutrophil dysfunction in patients with cirrhosis impairs their ability to fight bacterial infections, leading to negative prognosis and survival. The causes of neutrophil function changes in cirrhosis are not completely understood, hindering the development of effective therapeutic strategies.
Neutrophils are the largest population of leucocytes and are among the first cells of the innate immune system to fight against intruding pathogens. In patients with cirrhosis, neutrophils exhibit altered functionality, including changes in phagocytic ability, bacterial killing, chemotaxis, degranulation, reactive oxygen species production and NET (neutrophil extracellular trap) forma-tion. This results in their inability to mount an adequate antibacterial response and protect the individual from infection. Prognosis and survival in patients with cirrhosis are greatly influenced by the development of infectious complications. Multidrug-resistant bacterial infections in patients with cirrhosis are currently a growing problem worldwide; therefore, alternative methods for the prevention and treatment of bacterial infections in cirrhosis are urgently needed. The prevention and treatment of neutrophil dysfunction could be a potential way to protect patients from bacterial infections. However, the reasons for changes in neutrophil function in cirrhosis are still not completely understood, which limits the development of efficient therapeutic strategies. Both cellular and serum factors have been proposed to contribute to the functional impairment of neutrophils. Herein, we review the current knowledge on features and proposed causes of neutrophil dysfunction in cirrhosis, with a focus on current knowledge gaps and limitations, as well as opportunities for future investigations in this field. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL). This is an open access article under the CC BY license (http://creativecommons.org/licenses/ by/4.0/).

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