Treating B-cell cancer with T cells expressing anti-CD19 chimeric antigen receptors

被引:373
作者
Kochenderfer, James N. [1 ]
Rosenberg, Steven A. [1 ]
机构
[1] NCI, Expt Transplantat & Immunol Branch, Bethesda, MD 20892 USA
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; IN-VIVO PERSISTENCE; ANTITUMOR-ACTIVITY; ADOPTIVE IMMUNOTHERAPY; ALLOGENEIC TRANSPLANTATION; GENETIC-MODIFICATION; CD19; ANTIGEN; COMPLETE RESPONSES; ENHANCED SURVIVAL; CORD-BLOOD;
D O I
10.1038/nrclinonc.2013.46
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most B-cell malignancies express CD19, and a majority of patients with B-cell malignancies are not cured by current standard therapies. Chimeric antigen receptors (CARs) are fusion proteins consisting of antigen recognition moieties and T-cell activation domains. T cells can be genetically modified to express CARs, and adoptive transfer of anti-CD19 CAR T cells is now being tested in clinical trials. Effective clinical treatment with anti-CD19 CAR T cells was first reported in 2010 after a patient with advanced-stage lymphoma treated at the NCI experienced a partial remission of lymphoma and long-term eradication of normal B cells. Additional patients have subsequently obtained long-term remissions of advanced-stage B-cell malignancies after infusions of anti-CD19 CAR T cells. Long-term eradication of normal CD19(+) B cells from patients receiving infusions of anti-CD19 CAR T cells demonstrates the potent antigen-specific activity of these T cells. Some patients treated with anti-CD19 CAR T cells have experienced acute adverse effects, which were associated with increased levels of serum inflammatory cytokines. Although anti-CD19 CAR T cells are at an early stage of development, the potent antigen-specific activity observed in patients suggests that infusions of anti-CD19 CAR T cells might become a standard therapy for some B-cell malignancies.
引用
收藏
页码:267 / 276
页数:10
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