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Tumor cell-derived microparticles: a new form of cancer vaccine

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Article: e1017704 | Received 05 Feb 2015, Accepted 06 Feb 2015, Published online: 30 Jun 2015

Figures & data

Figure 1. T-MPs function as novel cell-free cancer vaccines. Upon UV irradiation, tumor cells release MPs that contain tumor antigens and DNA fragments. After being taken up by DCs, DNAs of T-MPs induce the expression of type I IFN by activating the cGAS/STING pathway. Type I IFN, in turn, enhances DC maturation by upregulating CD80, CD86, and MHCII. Armed DCs then activate tumor-specific T cells, leading to cytolysis of tumor cells.

Figure 1. T-MPs function as novel cell-free cancer vaccines. Upon UV irradiation, tumor cells release MPs that contain tumor antigens and DNA fragments. After being taken up by DCs, DNAs of T-MPs induce the expression of type I IFN by activating the cGAS/STING pathway. Type I IFN, in turn, enhances DC maturation by upregulating CD80, CD86, and MHCII. Armed DCs then activate tumor-specific T cells, leading to cytolysis of tumor cells.

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