A mouse model of human adaptive immune functions:: HLA-A2.1-/HLA-DR1-transgenic H-2 class I-/class II-knockout mice

被引:119
作者
Pajot, A
Michel, ML
Fazilleau, N
Pancré, V
Auriault, C
Ojcius, DM
Lemonnier, FA
Lone, YC
机构
[1] Inst Pasteur, Unite Immun Cellulaire Antivirale, Dept Immunol, F-75724 Paris 15, France
[2] Inst Pasteur, Unite Carcinogenese Hepat & Virol Mol, INSERM, U370,Dept Med Mol, Paris, France
[3] Inst Pasteur, Dept Immunol, Unite Biol Mol Gene, Paris, France
[4] Inst Biol Lille, CNRS, UMR 8527, Lab Immunopathol Cellulare Malad Infect, Lille, France
[5] Univ Calif, Sch Nat Sci, Merced, CA USA
关键词
human vaccine evaluation; HLA class I and II transgenic mice; H-2 class I and IIKO mice; CTL/HTL; human immune response;
D O I
10.1002/eji.200425463
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HLA-A2.1-/HLA-DR1 -transgenic H-2 class I-/class II-knockout mice were created and their immunological potential evaluated in response to hepatitis B DNA vaccine. Every single immunized mouse developed hepatitis B virus-specific antibodies, HLA-DR1-restricted helper, and HLA-A2.1-restricted cytolytic Tcell responses directed at the same immunodominant epitopes as those identified in naturally infected or vaccinated humans. These mice were specifically protected against a hepatitis B-recombinant vaccinia virus infection with a 10,000-fold or more reduction of the virus load at day 4 post-challenge. These mice represent a unique in vivo experimental model for human immune function studies without any interference with mouse MHC response which dwarfed the prediction of human responses. Furthermore, they enable the complete monitoring of immune adaptative responses for preclinical screening of candidate vaccines.
引用
收藏
页码:3060 / 3069
页数:10
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