Dendritic Cell Membrane Vesicles for Activation and Maintenance of Antigen-Specific T Cells

被引:41
|
作者
Ochyl, Lukasz J. [1 ]
Moon, James J. [1 ,2 ]
机构
[1] Univ Michigan, Dept Pharmaceut Sci, Biointerfaces Inst, 2800 Plymouth Dr, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, 2800 Plymouth Dr, Ann Arbor, MI 48109 USA
关键词
membrane vesicles; peptide antigens; T cell activation; vaccines; VACCINE; MICROVESICLES; NEOANTIGENS; PEPTIDE;
D O I
10.1002/adhm.201801091
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell membranes have recently gained attention as a promising drug delivery system. Here, dendritic cell membrane vesicles (DC-MVs) are examined as a platform to promote T cell responses. Nanosized DC-MVs are derived from DCs pretreated with monophosphoryl lipid A (MPLA), a FDA-approved immunostimulatory adjuvant. These mature DC-MVs activate DCs in vitro and increase their expression of costimulatory markers. DC-MVs also promote cross-priming of antigen-specific T cells in vitro, increasing their survival and CD25 expression. In addition, these mature DC-MVs potently augment the expansion of adoptively transferred CD8+ T cells in vivo, generating twofold to fourfold higher frequency of antigen-specific T cells, compared with other control formulations, including immature DC-MVs obtained without the MPLA pretreatment. Taken together, these results suggest that DC-MVs are an effective delivery platform for T cell activation and may serve as a potential delivery system for improving adoptive T cell therapy.
引用
收藏
页数:6
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