The combination of cyclophosphamide and human T cells genetically engineered to target CD19 can eradicate established B-cell lymphoma

被引:23
|
作者
Cheadle, Eleanor J. [1 ]
Gilham, David E. [1 ]
Hawkins, Robert E. [1 ]
机构
[1] Univ Manchester, Paterson Inst Canc Res, Canc Res UK Dept Med Oncol, Manchester M20 4BX, Lancs, England
关键词
immunotherapy; chimeric receptor; adoptive transfer; lymphoma; cyclophosphamide;
D O I
10.1111/j.1365-2141.2008.07145.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 CD3 zeta 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.
引用
收藏
页码:65 / 68
页数:4
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