Rafiq S, Purdon T J, Daniyan A F, Koneru M, Dao T, Liu C, Scheinberg D A, Brentjens R J
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Molecular Pharmacology Program, Sloan Kettering Institute; Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Leukemia. 2017 Aug;31(8):1788-1797. doi: 10.1038/leu.2016.373. Epub 2016 Dec 7.
CD19-directed chimeric antigen receptor (CAR) T cells are clinically effective in a limited set of leukemia patients. However, CAR T-cell therapy thus far has been largely restricted to targeting extracellular tumor-associated antigens (TAA). Herein, we report a T-cell receptor-mimic (TCRm) CAR, termed WT1-28z, that is reactive to a peptide portion of the intracellular onco-protein Wilms Tumor 1(WT1), as it is expressed on the surface of the tumor cell in the context of HLA-A02:01. T cells modified to express WT1-28z specifically targeted and lysed HLA-A02:01+ WT1+ tumors and enhanced survival of mice engrafted with HLA-A*02:01+, WT1+ leukemia or ovarian tumors. This in vivo functional validation of TCRm CAR T cells provides the proof-of-concept necessary to expand the range of TAA that can be effectively targeted for immunotherapy to include attractive intracellular targets, and may hold great potential to expand on the success of CAR T-cell therapy.
CD19导向的嵌合抗原受体(CAR)T细胞在有限的白血病患者群体中具有临床疗效。然而,迄今为止,CAR T细胞疗法在很大程度上局限于靶向细胞外肿瘤相关抗原(TAA)。在此,我们报告一种模仿T细胞受体的CAR(TCRm CAR),称为WT1-28z,它可识别细胞内癌蛋白Wilms肿瘤1(WT1)的肽段,该肽段在肿瘤细胞表面以HLA-A02:01为背景表达。经改造表达WT1-28z的T细胞特异性靶向并裂解HLA-A02:01+WT1+肿瘤,提高了接种HLA-A*02:01+、WT1+白血病或卵巢肿瘤的小鼠的存活率。TCRm CAR T细胞的这种体内功能验证为扩大可有效靶向用于免疫治疗的TAA范围提供了概念验证,使其包括有吸引力的细胞内靶点,并且可能在扩大CAR T细胞疗法的成功方面具有巨大潜力。