COVID-19 and liver disease: mechanistic and clinical perspectives

被引:274
作者
Marjot, Thomas [1 ]
Webb, Gwilym J. [2 ]
Barritt, Alfred S. [3 ]
Moon, Andrew M. [3 ]
Stamataki, Zania [4 ]
Wong, Vincent W. [5 ]
Barnes, Eleanor [1 ]
机构
[1] Univ Oxford, Oxford Univ Hosp NHS Fdn Trust, Translat Gastroenterol Unit, Oxford Liver Unit, Oxford, England
[2] Cambridge Univ Hosp, Addenbrookes Hosp, Cambridge Liver Unit, Cambridge, England
[3] Univ North Carolina, Div Gastroenterol & Hepatol, Chapel Hill, NC 27515 USA
[4] Univ Birmingham, Inst Immunol & Immunotherapy, Birmingham, W Midlands, England
[5] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Peoples R China
基金
英国惠康基金; 美国国家卫生研究院;
关键词
IMMUNE DYSFUNCTION; TRANSPLANT RECIPIENTS; SARS-COV-2; INFECTION; CIRRHOSIS; OUTCOMES; IMPACT; EXPRESSION; VACCINE; MODEL; CARE;
D O I
10.1038/s41575-021-00426-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This Review provides mechanistic and clinical insights into COVID-19 in the context of liver disease, discussing the potential underlying biology and clinical features of SARS-CoV-2 infection in patients with pre-existing liver conditions. The management of these patients is also discussed, including SARS-CoV-2 vaccination strategies. Our understanding of the hepatic consequences of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and its resultant coronavirus disease 2019 (COVID-19) has evolved rapidly since the onset of the pandemic. In this Review, we discuss the hepatotropism of SARS-CoV-2, including the differential expression of viral receptors on liver cell types, and we describe the liver histology features present in patients with COVID-19. We also provide an overview of the pattern and relevance of abnormal liver biochemistry during COVID-19 and present the possible underlying direct and indirect mechanisms for liver injury. Furthermore, large international cohorts have been able to characterize the disease course of COVID-19 in patients with pre-existing chronic liver disease. Patients with cirrhosis have particularly high rates of hepatic decompensation and death following SARS-CoV-2 infection and we outline hypotheses to explain these findings, including the possible role of cirrhosis-associated immune dysfunction. This finding contrasts with outcome data in pharmacologically immunosuppressed patients after liver transplantation who seem to have comparatively better outcomes from COVID-19 than those with advanced liver disease. Finally, we discuss the approach to SARS-CoV-2 vaccination in patients with cirrhosis and after liver transplantation and predict how changes in social behaviours and clinical care pathways during the pandemic might lead to increased liver disease incidence and severity.
引用
收藏
页码:348 / 364
页数:17
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