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Dendritic cells induce specific cytotoxic T lymphocytes against prostate cancer TRAMP-C2 cells loaded with freeze- thaw antigen and PEP-3 peptide.

Abstract
Prostate cancer is the most common cancer in men. In this study, we investigated immune responses of cytotoxic T lymphocytes (CTLs) against TRAMP-C2 prostate cancer cells after activation by dendritic cells (DCs) loaded with TRAMP-C2 freeze-thaw antigen and/or PEP-3 peptide in vitro. Bone marrow-derived DC from the bone marrow of the C57BL/6 were induced to mature by using the cytokine of rhGM-CSF and rhIL-4, and loaded with either the freeze-thaw antigen or PEP-3 peptide or both of them. Maturation of DCs was detected by flow cytometry. The killing efficiency of the CTLs on TRAMP-C2 cells were detected by flow cytometry, CCK8, colony formation, transwell migration, and wound-healing assay. The levels of the IFN-γ, TNF-β and IL-12 were measured by enzyme-linked immunosorbent assay (ELISA). Compared with the unloaded DCs, the loaded DCs had significantly increased expression of several phenotypes related to DC maturation. CTLs activated by DCs loaded with freeze-thaw antigen and PEP-3 peptide had more evident cytotoxicity against TRAMP-C2 cells in vitro. The secretion levels of IFN-γ, TNF-β and IL-12, secreted by DCs loaded with antigen and PEP-3 and interaction with T cells, were higher than in the other groups. Our results suggest that the CTLs activated by DCs loaded with TRAMP-C2 freeze-thaw antigen and PEP-3 peptide exert a remarkable killing efficiency against TRAMP-C2 cells in vitro.
AuthorsXiao-Qi Liu, Rong Jiang, Si-Qi Li, Jing Wang, Fa-Ping Yi
JournalAsian Pacific journal of cancer prevention : APJCP (Asian Pac J Cancer Prev) Vol. 16 Issue 2 Pg. 571-8 ( 2015) ISSN: 2476-762X [Electronic] Thailand
PMID25684489 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Neoplasm
  • Cytokines
  • Pep-3 peptide
  • Peptides
Topics
  • Animals
  • Antigens, Neoplasm (immunology, metabolism)
  • Apoptosis
  • Blotting, Western
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Cytokines (metabolism)
  • Dendritic Cells (immunology, metabolism, pathology)
  • Flow Cytometry
  • Freezing
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Peptides (immunology, metabolism)
  • Prostatic Neoplasms (immunology, metabolism, pathology)
  • T-Lymphocytes, Cytotoxic (immunology, metabolism, pathology)
  • Wound Healing
  • Xenograft Model Antitumor Assays

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