Hepatitis B flares in chronic hepatitis B: Pathogenesis, natural course, and management

被引:250
作者
Chang, Ming-Ling [1 ]
Liaw, Yun-Fan [1 ]
机构
[1] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp, Liver Res Unit, Taipei 105, Taiwan
关键词
Alpha-fetoprotein; Chemotherapy; Cirrhosis; Hepatitis B virus; Hepatocellular carcinoma; Immune clearance; Immune restoration; Interferona-alpha; Nucleos(t)ide analogue; Pregnancy; E-ANTIGEN SEROCONVERSION; SPONTANEOUS HBEAG SEROCONVERSION; VIRUS HBV REACTIVATION; ACUTE EXACERBATION; LAMIVUDINE THERAPY; ADEFOVIR DIPIVOXIL; ANTIVIRAL THERAPY; CORE ANTIGEN; PEGINTERFERON ALPHA-2A; TRANSAMINASE LEVEL;
D O I
10.1016/j.jhep.2014.08.033
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis B flare, defined as an event with abrupt rise of alanine aminotransferase (ALT) levels to >5 times the upper limit of normal during chronic hepatitis B virus (HBV) infection, is considered to be the result of a human leukocyte antigen-I restricted, cytotoxic T lymphocyte mediated immune response against HBV and its downstream mechanisms. It may occur spontaneously, during or after antiviral therapy and in the setting of immunosuppression and/or chemotherapy. The clinical spectrum of hepatitis B flares varies from asymptomatic to symptomatic and typical overt acute hepatitis, even with hepatic decompensation or failure. Flares may also occur in viraemic patients with cirrhosis with higher incidence of decompensation/mortality, hence requiring immediate antiviral therapy. An upsurge of serum HBV DNA and hepatitis B surface antigen levels usually precedes the abrupt rise of ALT levels. Rising or stable and high HBV DNA during flares represent ineffective immune clearance and further hepatocytolysis, even hepatic decompensation, may occur. Such patients require immediate antiviral therapy. In contrast, bridging hepatic necrosis and/or alpha-fetoprotein levels >100 ng/ml or decreasing HBV DNA during flares represent a more effective immune clearance and frequently leads to seroclearance of HBV DNA and/or hepatitis B e antigen with remission. If patients are non-cirrhotic and there is no concern of developing decompensation, patients may be observed for 3-6 months before deciding on the need of antiviral therapy. Severe and repeated flares are prone to develop into decompensation or lead to the development of cirrhosis, thus a timely treatment to prevent the hepatitis B flare is better than to cope with the flare. Screening, monitoring and prophylactic or pre-emptive antiviral therapy is mandatory for patients who are going to receive immunosuppressants or chemotherapy. (C) 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1407 / 1417
页数:11
相关论文
共 96 条
[1]   Immune cell responses are not required to induce substantial hepatitis B virus antigen decline during pegylated interferon-alpha administration [J].
Allweiss, Lena ;
Volz, Tassilo ;
Luetgehetmann, Marc ;
Giersch, Katja ;
Bornscheuer, Till ;
Lohse, Ansgar W. ;
Petersen, Joerg ;
Ma, Han ;
Klumpp, Klaus ;
Fetcher, Simon P. ;
Dandri, Maura .
JOURNAL OF HEPATOLOGY, 2014, 60 (03) :500-507
[2]   IFN-α inhibits HBV transcription and replication in cell culture and in humanized mice by targeting the epigenetic regulation of the nuclear cccDNA minichromosome [J].
Belloni, Laura ;
Allweiss, Lena ;
Guerrieri, Francesca ;
Pediconi, Natalia ;
Volz, Tassilo ;
Pollicino, Teresa ;
Petersen, Joerg ;
Raimondo, Giovanni ;
Dandri, Maura ;
Levrero, Massimo .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (02) :529-537
[3]   Transient restoration of anti-viral T cell responses induced by lamivudine therapy in chronic hepatitis B (vol 39, pg 595, 2003) [J].
Boni, C ;
Penna, A ;
Bertoletti, A ;
Lamonaca, V ;
Rapti, I ;
Missale, G ;
Pilli, M ;
Urbani, S ;
Cavalli, A ;
Cerioni, S ;
Panebianco, R ;
Jenkins, J ;
Ferrari, C .
JOURNAL OF HEPATOLOGY, 2004, 40 (06) :1053-1054
[4]   Chronic hepatitis B e antigen (HBeAg) negative, anti-HBe positive hepatitis B: an overview [J].
Bonino, F ;
Brunetto, MR .
JOURNAL OF HEPATOLOGY, 2003, 39 :S160-S163
[5]   A comparison of entecavir and lamivudine for HBeAg-positive chronic hepatitis B [J].
Chang, TT ;
Gish, RG ;
de Man, R ;
Gadano, A ;
Sollano, J ;
Chao, YC ;
Lok, AS ;
Han, KH ;
Goodman, Z ;
Zhu, J ;
Cross, A ;
DeHertogh, D ;
Wilber, R ;
Colonno, R ;
Apelian, D .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (10) :1001-1010
[6]   Age-Specific Prognosis Following Spontaneous Hepatitis B e Antigen Seroconversion in Chronic Hepatitis B [J].
Chen, Yi-Cheng ;
Chu, Chia-Ming ;
Liaw, Yun-Fan .
HEPATOLOGY, 2010, 51 (02) :435-444
[7]   Steroid-free chemotherapy decreases risk of hepatitis B virus (HBV) reactivation in HBV-carriers with lymphoma [J].
Cheng, AL ;
Hsiung, CA ;
Su, IJ ;
Chen, PJ ;
Chang, MC ;
Tsao, CJ ;
Kao, WY ;
Uen, WC ;
Hsu, CH ;
Tien, HF ;
Chao, TY ;
Chen, LT ;
Whang-Peng, J .
HEPATOLOGY, 2003, 37 (06) :1320-1328
[8]   Determinants for sustained HBeAg response to lamivudine therapy [J].
Chien, RN ;
Yeh, CT ;
Tsai, SL ;
Chu, CM ;
Liaw, YF .
HEPATOLOGY, 2003, 38 (05) :1267-1273
[9]   Pretherapy alanine transaminase level as a determinant for hepatitis B e antigen seroconversion during lamivudine therapy in patients with chronic hepatitis B [J].
Chien, RN ;
Liaw, YF ;
Atkins, M .
HEPATOLOGY, 1999, 30 (03) :770-774
[10]   Intrahepatic Distribution of Hepatitis B Surface and Core Antigens in Chronic Hepatitis B Virus Infection Hepatocyte With Cytoplasmic/Membranous Hepatitis B Core Antigen as a Possible Target for Immune Hepatocytolysis [J].
Chu, Chia-Ming ;
Liaw, Yun-Fan .
GASTROENTEROLOGY, 1987, 92 (01) :220-225