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©The Author(s) 2017.
World J Gastroenterol. Feb 7, 2017; 23(5): 817-829
Published online Feb 7, 2017. doi: 10.3748/wjg.v23.i5.817
Published online Feb 7, 2017. doi: 10.3748/wjg.v23.i5.817
Figure 1 Cells obtained represented typical morphological characteristic of primary tumor cells and mature dendritic cells.
Cells were derived from five pancreatic cancer (PC) patients and with similar shape of target cells. A: Most of the cultured primary tumor cells (over 90%) showed a DcR3-positive expression (magnification × 200); B: After cultured for 7 d, matured dendritic cells (DCs) were transfected without RNA and assembled into non-cohesive colonies, and the ablated cell showed a distinctive villiform process (magnification × 200). DCs transfected with total tumor RNA alone (C) or together with anti-DcR3 mAb mRNA (D) showed similar cell morphology to DCs transfected without RNA (C: magnification × 400; D: scanning electron microscope, bar represents 10 μm).
- Citation: Chen J, Guo XZ, Li HY, Zhao JJ, Xu WD. Dendritic cells engineered to secrete anti-DcR3 antibody augment cytotoxic T lymphocyte response against pancreatic cancer in vitro. World J Gastroenterol 2017; 23(5): 817-829
- URL: https://www.wjgnet.com/1007-9327/full/v23/i5/817.htm
- DOI: https://dx.doi.org/10.3748/wjg.v23.i5.817