Induction of hepatitis C virus-specific cytotoxic T lymphocytes in mice by immunization with dendritic cells transduced with replication-defective recombinant adenovirus

被引:30
|
作者
Matsui, M
Moriya, O
Abdel-Aziz, N
Matsuura, Y
Miyamura, T
Akatsuka, T [1 ]
机构
[1] Saitama Med Sch, Dept Microbiol, Moroyama, Saitama 3500495, Japan
[2] Osaka Univ, Res Ctr Emerging Infect Dis, Microbial Dis Res Inst, Osaka, Japan
[3] Natl Inst Hlth, Dept Virol 2, Shinjuku Ku, Tokyo 162, Japan
关键词
hepatitis C virus; dendritic cells; recombinant adenovirus;
D O I
10.1016/S0264-410X(02)00460-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied the potential of dendritic cells (DCs) in priming hepatitis C virus (HCV)-specific cytotoxic T lymphocytes (CTLs) in mice. Recombinant adenovirus expressing HCV core (Adex1SR3ST) was employed to express core in DCs. Core-specific CTLs are effectively elicited by injecting Adex1SR3ST-transduced DCs, whereas injection of Adex1SR3ST does not result in effective priming. Further, Adex1SR3ST-transduced DCs more efficiently prime core-specific CTLs than Adex1SR3ST-transduced macrophages, or DCs treated with an anthrax toxin fusion protein reported previously. Upon challenge with recombinant HCV-core-expressing vaccinia virus, vaccinia titers are significantly reduced in mice immunized with Adex1SR3ST-transduced DCs. Thus, adenovirus-transduced DCs may be a promising candidate for a CTL-based vaccine against HCV. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:211 / 220
页数:10
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