Early Treatment Consideration in Patients with Hepatitis B 'e' Antigen-Positive Chronic Infection: Is It Time for a Paradigm Shift?

被引:9
作者
Koffas, Apostolos [1 ]
Mak, Lung-Yi [1 ,2 ]
Gill, Upkar S. [1 ]
Kennedy, Patrick T. F. [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizard Inst, Barts Liver Ctr,Ctr Immunobiol, London E1 2AT, England
[2] Univ Hong Kong, Sch Clin Med, Dept Med, Hong Kong, Peoples R China
来源
VIRUSES-BASEL | 2022年 / 14卷 / 05期
关键词
HBeAg-positive chronic hepatitis B; HBeAg-positive chronic infection; immune tolerant disease phase; CLINICAL-PRACTICE GUIDELINES; IMMUNE-TOLERANT-PHASE; HEPATOCELLULAR-CARCINOMA; T-CELLS; COST-EFFECTIVENESS; SURFACE-ANTIGEN; VIRUS INFECTION; DNA; LIVER; SERUM;
D O I
10.3390/v14050900
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chronic hepatitis B (CHB) is associated with significant morbidity and mortality, due to the adverse sequelae of cirrhosis and hepatocellular carcinoma (HCC). To date, antiviral therapy has been reserved for patients with ostensibly active liver disease, fibrosis or cirrhosis, and/or increased risk of HCC. Historically, patients with hepatitis B 'e' antigen (HBeAg)-positive chronic infection, were not offered antiviral therapy. Nevertheless, there has been compelling evidence emerging in recent years, demonstrating that this disease phase is in fact not characterized by immunological tolerance. HBV integration into the human genome is a frequent event found in these patients. Additionally, it may well be associated with active inflammation and fibrosis, even in the presence of persistently normal liver enzymes. Likewise, it appears that the mechanisms of hepatocarcinogenesis are already present during this early stage of the disease. This was reflected in the European Association for the Study of the Liver (EASL) guidelines, where treating patients above the age of 30 years with HBeAg-positive chronic infection was proposed. Lowering the treatment threshold to broaden treatment eligibility is likely to slow disease progression and reduce the risk of developing HCC. The current review discusses the reasons to consider early antiviral therapy in HBeAg-positive chronic infection.
引用
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页数:12
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共 55 条
[1]   Integration of tumour and viral genomic characterisations in HBV-related hepatocellular carcinomas [J].
Amaddeo, Giuliana ;
Cao, Qian ;
Ladeiro, Yannick ;
Imbeaud, Sandrine ;
Nault, Jean-Charles ;
Jaoui, Daphne ;
Mathe, Yann Gaston ;
Laurent, Christophe ;
Laurent, Alexis ;
Bioulac-Sage, Paulette ;
Calderaro, Julien ;
Zucman-Rossi, Jessica .
GUT, 2015, 64 (05) :820-829
[2]   Chronic hepatitis B virus carriers in the immunotolerant phase of infection:: Histologic findings and outcome [J].
Andreani, Tony ;
Serfaty, Lawrence ;
Mohand, Djamila ;
Dernaika, Salem ;
Wendum, Dominique ;
Chazouilleres, Olivier ;
Poupon, Raoul .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2007, 5 (05) :636-641
[3]   Adaptive immunity in HBV infection [J].
Bertoletti, Antonio ;
Ferrari, Carlo .
JOURNAL OF HEPATOLOGY, 2016, 64 :S71-S83
[4]   Hepatitis B virus infection and the immune response: The big questions [J].
Boeijen, Lauke L. ;
Hoogeveen, Ruben C. ;
Boonstra, Andre ;
Lauer, Georg M. .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2017, 31 (03) :265-272
[5]   Characterization of hepatitis B virus (HBV)-specific T-cell dysfunction in chronic HBV infection [J].
Boni, Carolina ;
Fisicaro, Paola ;
Valdatta, Caterina ;
Amadei, Barbara ;
Di Vincenzo, Paola ;
Giuberti, Tiziana ;
Laccabue, Diletta ;
Zerbini, Alessandro ;
Cavalli, Albertina ;
Missale, Gabriele ;
Bertoletti, Antonio ;
Ferrari, Carlo .
JOURNAL OF VIROLOGY, 2007, 81 (08) :4215-4225
[6]  
Burton AR, 2018, J CLIN INVEST, V128, P4588, DOI [10.1172/jci121960, 10.1172/JCI121960]
[7]   Effects of Tenofovir Disoproxil Fumarate in Hepatitis B e Antigen-Positive Patients With Normal Levels of Alanine Aminotransferase and High Levels of Hepatitis B Virus DNA [J].
Chan, Henry L. Y. ;
Chan, Chi Kuen ;
Hui, Aric Josun ;
Chan, Sing ;
Poordad, Fred ;
Chang, Ting-Tsung ;
Mathurin, Philippe ;
Flaherty, John F. ;
Lin, Lanjia ;
Corsa, Amy ;
Gaggar, Anuj ;
Subramanian, G. Mani ;
McHutchison, John G. ;
Lee, Sam ;
Gane, Edward J. .
GASTROENTEROLOGY, 2014, 146 (05) :1240-1248
[8]   A novel nomogram to predict evident histological liver injury in patients with HBeAg-positive chronic hepatitis B virus infection [J].
Chang, Xiujuan ;
Wang, Jing ;
Chen, Yan ;
Long, Qinghua ;
Song, Laicheng ;
Li, Qin ;
Liu, Huabao ;
Shang, Qinghua ;
Yu, Zujiang ;
Jiang, Li ;
Xiao, Guangming ;
Li, Li ;
Chen, Liang ;
Wang, Xiaodong ;
Li, Zhiqin ;
Chen, Da ;
Dong, Zheng ;
An, Linjing ;
Tan, Lin ;
Chen, Yongping ;
Yang, Yongping .
EBIOMEDICINE, 2021, 67
[9]   Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level [J].
Chen, CJ ;
Yang, HI ;
Su, J ;
Jen, CL ;
You, SL ;
Lu, SN ;
Huang, GT ;
Iloeje, UH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (01) :65-73
[10]   Increasing on-treatment hepatocellular carcinoma risk with decreasing baseline viral load in HBeAg-positive chronic hepatitis B [J].
Choi, Won-Mook ;
Kim, Gi-Ae ;
Choi, Jonggi ;
Han, Seungbong ;
Lim, Young-Suk .
JOURNAL OF CLINICAL INVESTIGATION, 2022, 132 (10)