ADNA Vaccine That Encodes an Antigen-Presenting Cell-Specific Heterodimeric Protein Protects against Cancer and Influenza

被引:16
作者
Braathen, Ranveig [1 ,2 ]
Spang, Heidi Cecilie Larsen [1 ,2 ]
Hinke, Daniela Maria [1 ,2 ]
Blazevski, Jana [1 ,2 ]
Bobic, Sonja [1 ,2 ]
Fossum, Even [1 ,2 ]
Bogen, Bjarne [1 ,2 ]
机构
[1] Univ Oslo, Inst Clin Med, KG Jebsen Ctr Influenza Vaccines Res, N-0027 Oslo, Norway
[2] Oslo Univ Hosp, N-0027 Oslo, Norway
关键词
T-CELL; DNA VACCINES; CLASS-II; IN-VITRO; MOLECULES; RECEPTOR; IMMUNOGENICITY; EXPRESSION; EFFICACY; ELECTROPORATION;
D O I
10.1016/j.omtm.2020.01.007
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Immunogenicity of DNA vaccines can be increased by constructing the DNA in such a way that it encodes secreted homodimeric fusion proteins that target antigen-presenting cells (APCs). In this study, we have developed novel APC-targeting vaccine molecules with an increased flexibility due to introduction of a heterodimerization motif. The heterodimeric proteins permit four different fusions within a single molecule, thus allowing expression of two different APC-targeting moieties and two different antigens. Two types of heterodimeric fusion proteins were developed that employed either the ACID/BASE or the Barnase/Barstar motifs, respectively. The ACID/BASE heterodimeric vaccines conferred protection against challenges with either influenza virus or tumor cells in separate preclinical models. The ACID/BASE motif was flexible since a large number of different targeting moieties and antigens could be introduced with maintenance of specificity, antigenicity, and secretion. APC-targeting ACID/BASE vaccines expressing two different antigens induced antibody and T cell responses against either of the two antigens. Heterodimeric ACID/BASE DNA vaccines were of approximately the same potency as previously reported homodimeric DNA vaccines. The flexibility and potency of the ACID/BASE format suggest that it could be a useful platform for DNA vaccines that encode APC-targeting fusion proteins.
引用
收藏
页码:378 / 392
页数:15
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