DNA-based immunotherapy: potential for treatment of chronic viral hepatitis?

被引:22
作者
Beckebaum, S
Cicinnati, VR
Gerken, G
机构
[1] Univ Essen Gesamthsch, Dept Gastroenterol & Hepatol, D-45147 Essen, Germany
[2] Univ Essen Gesamthsch, Dept Surg, D-4300 Essen 1, Germany
关键词
D O I
10.1002/rmv.359
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Persistent HBV and HCV infection represent major causes of chronic liver disease with a high risk of progression to liver cirrhosis and hepatocellular carcinoma (HCC). Conventional protein-based vaccines are highly efficacious in preventing HBV infection; whereas in therapeutic settings with chronically infected patients, results have been disappointing. Prophylactic vaccination against HCV infection has not yet been achieved due to many impediments including frequent spontaneous mutations of the virus with escape from immune system control. Using animal models it has been demonstrated that DNA-based immunisation strategies may overcome this problem because of their potential to induce immunity against multiple viral epitopes. DNA-based vaccines mimic the effect of live attenuated viral vaccines, eliciting cell mediated immunity in addition to inducing humoral responses. Efficacy may further be improved by addition of DNA encoding immunomodulatory cytokines and more recently, direct genetic modulation of antigen-presenting cells, such as dendritic cells (DC), has been shown to increase antigen-specific immune responses. This review focuses on immunological aspects of chronic HBV and HCV infection and on the potential of DNA- and DC-based vaccines for the treatment of chronic viral hepatitis. Copyright (C) 2002 John Wiley Sons, Ltd.
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收藏
页码:297 / 319
页数:23
相关论文
共 181 条
[1]   Induction of cytokine production and proliferation of memory lymphocytes by murine liver dendritic cell progenitors: role of these progenitors as immunogenic resident antigen-presenting cells in the liver [J].
Abe, M ;
Akbar, SMF ;
Horiike, N ;
Onji, M .
JOURNAL OF HEPATOLOGY, 2001, 34 (01) :61-67
[2]   Identification and characterization of mutations in hepatitis B virus resistant to lamivudine [J].
Allen, MI ;
Deslauriers, M ;
Andrews, CW ;
Tipples, GA ;
Walters, KA ;
Tyrrell, DLJ ;
Brown, N ;
Condreay, LD .
HEPATOLOGY, 1998, 27 (06) :1670-1677
[3]   HLA AND HEPATITIS-B INFECTION [J].
ALMARRI, A ;
BATCHELOR, JR .
LANCET, 1994, 344 (8931) :1194-1195
[4]  
Alt M, 1999, EUR J CLIN INVEST, V29, P868
[5]   Impaired dendritic cell maturation in patients with chronic, but not resolved, hepatitis C virus infection [J].
Auffermann-Gratzinger, S ;
Keeffe, EB ;
Levy, S .
BLOOD, 2001, 97 (10) :3171-3176
[6]   Impaired allostimulatory function of dendritic cells in chronic hepatitis C infection [J].
Bain, C ;
Fatmi, A ;
Zoulim, F ;
Zarski, JP ;
Trépo, C ;
Inchauspé, G .
GASTROENTEROLOGY, 2001, 120 (02) :512-524
[7]  
Ballas ZK, 1996, J IMMUNOL, V157, P1840
[8]   Viral persistence, antibody to E1 and E2, and hypervariable region 1 sequence stability in hepatitis C virus-inoculated chimpanzees [J].
Bassett, SE ;
Thomas, DL ;
Brasky, KM ;
Lanford, RE .
JOURNAL OF VIROLOGY, 1999, 73 (02) :1118-1126
[9]   Routes of plasmid DNA vaccination that prime murine humoral and cellular immune responses [J].
Böhm, W ;
Mertens, T ;
Schirmbeck, R ;
Reimann, J .
VACCINE, 1998, 16 (9-10) :949-954
[10]   Lamivudine treatment can overcome cytotoxic T-cell hyporesponsiveness in chronic hepatitis B: New perspectives for immune therapy [J].
Boni, C ;
Penna, A ;
Ogg, GS ;
Bertoletti, A ;
Pilli, M ;
Cavallo, C ;
Cavalli, A ;
Urbani, S ;
Boehme, R ;
Panebianco, R ;
Fiaccadori, F ;
Ferrari, C .
HEPATOLOGY, 2001, 33 (04) :963-971