The combination of cyclophosphamide and human T cells genetically engineered to target CD19 can eradicate established B-cell lymphoma.
Cheadle, Eleanor J ; Gilham, David E ; Hawkins, Robert E
Cheadle, Eleanor J
Gilham, David E
Hawkins, Robert E
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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 CD3zeta 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.
Description
Date
2008-07
Publisher
Keywords
Immunotherapy
Chimeric Receptor
Adoptive Transfer
Lymphoma
Cyclophosphamide
Chimeric Receptor
Adoptive Transfer
Lymphoma
Cyclophosphamide
Type
Article
Citation
The combination of cyclophosphamide and human T cells genetically engineered to target CD19 can eradicate established B-Cell lymphoma. 2008, 142 (1):65-8 Br. J. Haematol.