Absence of initial viral replication and long-term high dose immunoglobulin administration improve results of hepatitis B virus recurrence prophylaxis after liver transplantation

1997 ◽  
Vol 29 (1-2) ◽  
pp. 517-518 ◽  
Author(s):  
J. Gugenheim ◽  
E. Baldini ◽  
D. Ouzan ◽  
J. Mouiel
2016 ◽  
Vol 30 (5) ◽  
pp. 579-588 ◽  
Author(s):  
Po-Hung Chen ◽  
Berkeley N. Limketkai ◽  
Panagiotis Trilianos ◽  
Muge Pirtini-Cetingul ◽  
Tinsay A. Woreta ◽  
...  

2008 ◽  
Vol 40 (6) ◽  
pp. 1961-1964 ◽  
Author(s):  
A.W. Avolio ◽  
E. Nure ◽  
M. Pompili ◽  
R. Barbarino ◽  
M. Basso ◽  
...  

2015 ◽  
Vol 99 (7) ◽  
pp. 1321-1334 ◽  
Author(s):  
Bruno Roche ◽  
Anne Marie Roque-Afonso ◽  
Frederik Nevens ◽  
Didier Samuel

2017 ◽  
Vol 61 (9) ◽  
Author(s):  
Takuro Uchida ◽  
Michio Imamura ◽  
C. Nelson Hayes ◽  
Nobuhiko Hiraga ◽  
Hiromi Kan ◽  
...  

ABSTRACT Nucleot(s)ide analogues and peginterferon (PEG-IFN) treatment are the only approved therapies for chronic hepatitis B virus (HBV) infection. However, complete eradication of the virus, as indicated by persistent loss of hepatitis B surface antigen (HBsAg), is rare among treated patients. This is due to long-term persistence of the HBV genome in infected hepatocytes in the form of covalently closed circular DNA (cccDNA). In this study, we investigated whether administration of a large dose of a nucleoside analogue in combination with PEG-IFN can achieve long-term loss of HBsAg in human hepatocyte chimeric mice. Mice were treated with a high dose of entecavir and/or PEG-IFN for 6 weeks. High-dose combination therapy with both drugs resulted in persistently negative HBV DNA in serum. Although small amounts of HBV DNA and cccDNA (0.1 and 0.01 copy/cell, respectively) remained in the mouse livers, some of the mice remained persistently negative for serum HBV DNA at 13 weeks after cessation of the therapy. Serum HBsAg and hepatitis B core-related antigen (HBcrAg) continued to decrease and eventually became negative at 12 weeks after cessation of the therapy. Analysis of the HBV genome in treated mice showed accumulation of G-to-A hypermutation and CpG III island methylation. Persistent loss of serum HBV DNA and loss of HBV markers by high-dose entecavir and PEG-IFN combination treatment in chimeric mice suggests that control of HBV can be achieved even in the absence of a cellular immune response.


2008 ◽  
Vol 9 (4) ◽  
pp. 215-218
Author(s):  
Viola Sacchi

Hepatitis B is the most common serious liver infection in the world, with about 350 million people who are infected with the hepatitis B virus (HBV) and about 1 million deaths annually.Hepatitis B is characterized by an acute and a chronic phase, if the subject fails to produce adequate immune response.About 5-10% of adults infected with HBV go on to develop chronic infection and become chronic carriers (CHB); moreover, the liver damage, if not stopped, continues until cirrhosis or hepatocellular carcinoma. In the natural history of HBV infection, the most important event is HBeAg seroconversion, characterized by loss of HBeAg (a specific antigen of the virus) and development of anti-HBe antibodies (HBeAg-positive patients). If the seroconversion has occurred early (when liver damage is not already significant) and is maintained, long-term prognosis is excellent. The disease can follow a more aggressive course if active viral replication persists despite anti-HBe positivity. This state, characterized by continuing viral replication, has been termed as HBeAg-negative CHB, and is the most prevalent form in Italy. At the moment, there are 4 approved antiviral drug classes, with different antiviral efficacy, for the treatment of chronic hepatitis B: interferons, nucleoside analogues, nucleotide analogues, and cyclopents.The primary target of the treatment is a prolonged suppression of viral replication, in order to avoid long term complications and increase survival.


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