Literature DB >> 9097277

New therapies for chronic hepatitis B.

J H Hoofnagle1, D Lau.   

Abstract

Currently, the only therapy of proven benefit in chronic hepatitis B is interferon-alpha which leads to a long-term benefit in only one-third of patients. New therapies for hepatitis B fall into three categories; antiviral chemotherapy, immunomodulation with cell-based therapies, vaccines or cytokines, and gene therapy such as with antisense oligonucleotides, ribozymes or viral mutants. The most promising immediate approach to therapy is with the new nucleoside antivirals--lamivudine and famciclovir. These drugs are well absorbed orally, result in profound inhibition of circulating hepatitis B virus, and, in some cases, loss of hepatitis B e antigen and improvement in serum aminotransferases. Controlled trials of long-term famciclovir and lamivudine therapy currently underway aim to show whether these drugs are safe and can provide sustained inhibition of viral replication and attentant improvement in liver disease.

Entities:  

Mesh:

Year:  1997        PMID: 9097277     DOI: 10.1111/j.1365-2893.1997.tb00159.x

Source DB:  PubMed          Journal:  J Viral Hepat        ISSN: 1352-0504            Impact factor:   3.728


  5 in total

Review 1.  Treatment of chronic hepatitis B: new antiviral therapies.

Authors:  F Yao; R G Gish
Journal:  Curr Gastroenterol Rep       Date:  1999 Feb-Mar

2.  CpG oligodeoxynucleotides with hepatitis B surface antigen (HBsAg) for vaccination in HBsAg-transgenic mice.

Authors:  E Malanchère-Brès; P J Payette; M Mancini; P Tiollais; H L Davis; M L Michel
Journal:  J Virol       Date:  2001-07       Impact factor: 5.103

Review 3.  Novel approaches towards conquering hepatitis B virus infection.

Authors:  Guo-Yi Wu; Hong-Song Chen
Journal:  World J Gastroenterol       Date:  2007-02-14       Impact factor: 5.742

Review 4.  RNA interference technologies and therapeutics: from basic research to products.

Authors:  Marta López-Fraga; Tamara Martínez; Ana Jiménez
Journal:  BioDrugs       Date:  2009       Impact factor: 5.807

5.  Targeting TLR9 agonists to secondary lymphoid organs induces potent immune responses against HBV infection.

Authors:  Irina Ushach; Ren Zhu; Elen Rosler; Rajendra K Pandey; N Tilani S De Costa; Soheil Pourshahian; Qinglin Han; Chris Li; Leonid Beigelman; Sergei M Gryaznov; Theodore Yun
Journal:  Mol Ther Nucleic Acids       Date:  2022-02-01       Impact factor: 8.886

  5 in total

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