Activation of antitumor cytotoxic T lymphocytes by fusions of human dendritic cells and breast carcinoma cells
Author(s) -
Jianlin Gong,
David Avigan,
Dongshu Chen,
Zekui Wu,
Shigeo Koido,
Masahiro Kashiwaba,
Donald Küfe
Publication year - 2000
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.050587197
Subject(s) - cytotoxic t cell , antigen , cancer research , breast carcinoma , antigen presenting cell , major histocompatibility complex , dendritic cell , biology , immunotherapy , immunology , t cell , breast cancer , immune system , in vitro , cancer , genetics , biochemistry
We have reported that fusions of murine dendritic cells (DCs) and murine carcinoma cells reverse unresponsiveness to tumor-associated antigens and induce the rejection of established metastases. In the present study, fusions were generated with primary human breast carcinoma cells and autologous DCs. Fusion cells coexpressed tumor-associated antigens and DC-derived costimulatory molecules. The fusion cells also retained the functional potency of DCs and stimulated autologous T cell proliferation. Significantly, the results show that autologous T cells are primed by the fusion cells to induce MHC class I-dependent lysis of autologous breast tumor cells. These findings demonstrate that fusions of human breast cancer cells and DCs activate T cell responses against autologous tumors.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom