DNA-mediated immunization in a transgenic mouse model of the hepatitis B surface antigen chronic carrier state

被引:137
作者
Mancini, M
Hadchouel, M
Davis, HL
Whalen, RG
Tiollais, P
Michel, ML
机构
[1] INSERM,UNITE RECOMBINAIS & EXPRESS GENET,U163,F-75724 PARIS 15,FRANCE
[2] INST PASTEUR,DEPT BIOL MOL,F-75724 PARIS 15,FRANCE
[3] INSERM,CTR RECH,U347,F-94276 LE KREMLIN BICETR,FRANCE
[4] OTTAWA CIVIC HOSP,LOEB MED RES INST,OTTAWA,ON K1Y 4E9,CANADA
[5] UNIV OTTAWA,FAC HLTH SCI,OTTAWA,ON K1H 8M5,CANADA
[6] UNIV OTTAWA,FAC MED,OTTAWA,ON K1H 8M5,CANADA
关键词
D O I
10.1073/pnas.93.22.12496
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transgenic mice expressing the sequences coding for the envelope proteins of the hepatitis B virus (HBV) in the liver have been used as a model of the HBV chronic carrier state. We evaluated the possibility of inducing a specific immune response to the viral envelope antigens and thus potentially controlling chronic HBV infection, Using HBV-specific DNA-mediated immunization in this transgenic model, we show that the immune response induced after a single intramuscular injection of DNA resulted in the complete clearance of circulating hepatitis B surface antigen and in the long-term control of transgene expression in hepatocytes. This response does not involve a detectable cytopathic effect in the liver, Adoptive transfer of fractionated primed spleen cells from DNA-immunized mice shea that T cells are responsible for the down-regulation of HBV mRNA in the liver of transgenic mice. To our knowledge, this is the first demonstration of a potential immunotherapeutic application of DNA-mediated immunization against an infectious disease and raises the possibility of designing more effective ways of treating HBV chronic carriers.
引用
收藏
页码:12496 / 12501
页数:6
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