Literature DB >> 15180457

Vaccine therapy for hepatitis B virus carrier.

Sk Md Fazle Akbar1, Shinya Furukawa, Norio Horiike, Morikazu Onji.   

Abstract

Despite the presence of an effective prophylactic vaccine since 1982, more than 350 million people of the world are now chronically infected with hepatitis B virus (HBV). In one scenario, a considerable numbers of chronic HBV carrier would eventually develop serious complications like liver cirrhosis and hepatocellular carcinoma. In another, chronic HBV carriers would be permanent sources of HBV infection and transmit HBV to uninfected healthy individuals. Taken together, chronic HBV infection represents a major global public health problem, especially in the developing nations of the Asia and Africa, where most of the chronic HBV-carriers reside. Unfortunately, there is no good curative therapy approach for these patients. The prospect of treatment of chronic HBV infection by antiviral agents like type-1 interferons and lamivudine is not satisfactory due to their low efficacy, considerable side effects and high costs. Vaccine therapy, an immune therapy, has recently shown considerable optimism for treating patients with chronic HBV infection. In this review, we will first describe the pathogenesis of chronic HBV carrier state to provide scientific and ethical rationales of vaccine therapy in chronic HBV carriers. Next, we will summarize the information that has been compiled from ongoing clinical trials of vaccine therapy in chronic HBV carrier. Finally, we will discuss the mechanism of action of vaccine therapy in patients with chronic HBV infection and HBV transgenic mice, a murine model of chronic HBV carrier state. This information will be valuable for developing next generation therapeutic vaccines for the management of chronic HBV infection.

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Year:  2004        PMID: 15180457     DOI: 10.2174/1568005043340885

Source DB:  PubMed          Journal:  Curr Drug Targets Infect Disord        ISSN: 1568-0053


  5 in total

1.  Mutations in the S gene region of hepatitis B virus genotype D in Golestan Province-Iran.

Authors:  Abdolvahab Moradi; Sareh Zhand; Amir Ghaemi; Naeme Javid; Alijan Tabarraei
Journal:  Virus Genes       Date:  2012-01-25       Impact factor: 2.332

2.  Hepatitis B virus (HBV) antigen-pulsed monocyte-derived dendritic cells from HBV-associated hepatocellular carcinoma patients significantly enhance specific T cell responses in vitro.

Authors:  M Shi; S Qian; W-W Chen; H Zhang; B Zhang; Z-R Tang; Z Zhang; F-S Wang
Journal:  Clin Exp Immunol       Date:  2007-02       Impact factor: 4.330

3.  Impaired functional capacities of liver dendritic cells from murine hepatitis B virus (HBV) carriers: relevance to low HBV-specific immune responses.

Authors:  A Hasebe; S M F Akbar; S Furukawa; N Horiike; M Onji
Journal:  Clin Exp Immunol       Date:  2005-01       Impact factor: 4.330

4.  HBVsvp-Pulsed Dendritic Cell Immunotherapy Induces Th1 Polarization and Hepatitis B Virus-Specific Cytotoxic T Lymphocytes Production.

Authors:  Mohamed M S Farag; Reda A Suef; Ghada M Al-Toukhy; Mohamed A Selim; Mostafa A Elbahnasawy; Nahla El Sharkawy; Sameera Ezzat; Nashwa Shebl; Mohamed T M Mansour
Journal:  Infect Drug Resist       Date:  2020-08-05       Impact factor: 4.003

5.  Osteopontin promotes dendritic cell maturation and function in response to HBV antigens.

Authors:  Guangying Cui; Jianing Chen; Jianqin He; Chong Lu; Yingfeng Wei; Lin Wang; Xuejun Xu; Lanjuan Li; Toshimitsu Uede; Hongyan Diao
Journal:  Drug Des Devel Ther       Date:  2015-06-12       Impact factor: 4.162

  5 in total

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