Continuous CD8+ T-Cell Priming by Dendritic Cell Cross-Presentation of Persistent Antigen following Adeno-Associated Virus-Mediated Gene Delivery

被引:13
作者
Xu, Dan [1 ,2 ]
Walker, Christopher M. [1 ,3 ]
机构
[1] Nationwide Childrens Hosp, Res Inst, Ctr Vaccines & Immun, Columbus, OH 43205 USA
[2] Ohio State Univ, Coll Med, Integrated Biomed Sci Grad Program, Columbus, OH 43210 USA
[3] Ohio State Univ, Coll Med, Dept Pediat, Columbus, OH 43210 USA
关键词
TRANSGENE PRODUCTS; IMMUNE-RESPONSES; PLASMID DNA; LYMPHOCYTES; INDUCTION; ACTIVATION; DIRECTS;
D O I
10.1128/JVI.05375-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recombinant adeno-associated virus (rAAV) vectors establish persistent transgene expression in the skeletal muscle of mice. How dendritic cells acquire encoded antigens for CD8(+) T-cell priming is unknown. Here we document CD8(+) T-cell priming after lethal irradiation and bone marrow reconstitution of mice treated with an AAV vector several weeks earlier. Temporal separation of vector delivery and successful class I antigen presentation indicated that T-cell priming does not necessarily require antigen synthesis in AAV-transduced dendritic cells. An apparent cross-presentation of antigen acquired from muscle suggests that strategies to limit transgene expression in dendritic cells will not prevent unwanted CD8(+) T-cell responses.
引用
收藏
页码:12083 / 12086
页数:4
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