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Enhancement of dendritic cells with melanoma-associated antigen 3 for inducing cytotoxicity by cytotoxic T lymphocytes on bladder cancer BIU-87 cells. | LitMetric

AI Article Synopsis

  • The study aimed to evaluate the effectiveness of dendritic cells (DCs) sensitized with MAGE-3 peptides in activating lymphocytes against BIU-87 bladder cancer cells.
  • MAGE-3-sensitized DCs were found to significantly enhance T cell proliferation and cytotoxic activity against tumor cells compared to controls.
  • The research also indicated that these sensitized DCs could inhibit tumor growth in a mouse model, suggesting their potential as a vaccine for bladder cancer immunotherapy.

Article Abstract

To determine the cytotoxic effect of lymphocytes activated by melanoma-associated antigen 3 (MAGE-3)-sensitized dendritic cells (DCs) on BIU-87 tumor cells, and to evaluate the possibility of MAGE-3-peptide-pulsed DCs as a vaccine in bladder cancer immunotherapy, the proliferation of T cells and the activity of cytotoxic T lymphocytes (CTLs) were examined by the MTT method. CTLs were induced by MAGE-3-sensitized DCs, or by ovalbumin (OVA) peptide and non-sensitized DCs as controls, respectively. The results indicated that MAGE-3-sensitized DCs have the ability to promote the proliferation of T cells as well as the cytotoxic activity of CTLs on bladder cancer cells in comparison with OVA peptide and non-sensitized DCs. In other words, DCs sensitized by the MAGE-3 antigen peptide could obviously upregulate the proliferation of T cells, which resulted in the growth inhibition of bladder cancer BIU-87 cells. In addition, MAGE-3-sensitized DCs played an important role in inhibiting the growth of human BIU-87 tumor xenografts in nude mice.

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Source
http://dx.doi.org/10.4238/gmr.15039001DOI Listing

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