Causes and Consequences of Innate Immune Dysfunction in Cirrhosis

被引:134
作者
Irvine, Katharine Margaret [1 ]
Ratnasekera, Isanka [1 ]
Powell, Elizabeth E. [2 ,3 ]
Hume, David Arthur [1 ]
机构
[1] Univ Queensland, Mater Res Inst, Translat Res Inst, Brisbane, Qld, Australia
[2] Princess Alexandra Hosp, Dept Gastroenterol & Hepatol, Brisbane, Qld, Australia
[3] Univ Queensland, Fac Med, Brisbane, Qld, Australia
关键词
innate immnuity; decompensated chirrosis; infection; monocyte; ascites; COLONY-STIMULATING FACTOR; TOLL-LIKE RECEPTORS; ASCITIC FLUID; BACTERIAL-INFECTIONS; NEUTROPHIL DYSFUNCTION; ALCOHOLIC CIRRHOSIS; OPSONIC ACTIVITY; LIVER-CIRRHOSIS; SYSTEMIC INFLAMMATION; HOSPITALIZED-PATIENTS;
D O I
10.3389/fimmu.2019.00293
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Liver cirrhosis is an increasing health burden and public health concern. Regardless of etiology, patients with cirrhosis are at risk of a range of life-threatening complications, including the development of infections, which are associated with high morbidity and mortality and frequent hospital admissions. The term Cirrhosis-Associated Immune Dysfunction (CAID) refers to a dynamic spectrum of immunological perturbations that develop in patients with cirrhosis, which are intimately linked to the underlying liver disease, and negatively correlated with prognosis. At the two extremes of the CAID spectrum are systemic inflammation, which can exacerbate clinical manifestations of cirrhosis such as hemodynamic derangement and kidney injury; and immunodeficiency, which contributes to the high rate of infection in patients with decompensated cirrhosis. Innate immune cells, in particular monocytes/macrophages and neutrophils, are pivotal effector and target cells in CAID. This review focuses on the pathophysiological mechanisms leading to impaired innate immune function in cirrhosis. Knowledge of the phenotypic manifestation and pathophysiological mechanisms of cirrhosis associated immunosuppression may lead to immune targeted therapies to reduce susceptibility to infection in patients with cirrhosis, and better biomarkers for risk stratification, and assessment of efficacy of novel immunotherapies.
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页数:14
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