Abstract
T cells genetically engineered to express tumour-targeting receptors are attractive anti-cancer therapeutic agents. Human T cells engrafted with a chimeric receptor specific for the B-cell lymphoma antigen CD19 fused to the CD3ζ receptor (aCD19z) are functional in vitro. Current successful clinical protocols targeting melanoma use pre-conditioning chemotherapy in combination with T cells. This study demonstrated that interleukin-2 expanded aCD19z T cells combined with cyclophosphamide effectively treated five-day established Raji B-cell lymphoma in an immunocompromised model system with 50% of mice surviving >100 days. This observation strongly supports the combination of antibody targeted T cells with chemotherapy as a novel approach for the therapy of CD19+ B-cell malignancies. © 2008 The Authors.
Original language | English |
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Pages (from-to) | 65-68 |
Number of pages | 3 |
Journal | British Journal of Haematology |
Volume | 142 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jul 2008 |
Keywords
- Adoptive transfer
- Chimeric receptor
- Cyclophosphamide
- Immunotherapy
- Lymphoma