决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Isolated oral CD30(+)/CD4(+) CAR(+) T cell lymphoma in long-term remission after radiotherapy.
Isolated oral CD30(+)/CD4(+) CAR(+) T cell lymphoma in long-term remission after radiotherapy.
一例嵌合抗原受体(CAR)⁺CD30⁺/CD4⁺ T 细胞淋巴瘤(TCL)在以抗 CD19 CAR T 细胞为基础的 tisagenlecleucel(tisa-cel)治疗后 22 个月表现为单个口腔溃疡。
一例CAR阳性CD30阳性/CD4阳性T细胞淋巴瘤(TCL)表现为单发口腔溃疡,发生于患者接受抗CD19 CAR-T细胞疗法tisagenlecleucel(tisa-cel)治疗22个月后。该TCL检测到慢病毒整合于ANKHD1-EIF4EBP3、TET2功能丧失以及NTRK1拷贝数增加,提示与插入突变无关的遗传改变参与了淋巴瘤发生。患者接受放射治疗后已缓解2年。这是俄亥俄州立大学James综合癌症中心在288例接受CAR-T细胞治疗的患者中报告的唯一CAR阳性TCL病例。
A chimeric antigen receptor (CAR) + CD30 + /CD4 + T cell lymphoma (TCL) manifested as a single oral ulceration 22 months after treatment with tisagenlecleucel (tisa-cel), an anti-CD19 CAR T cell-based therapy. The TCL showed lentiviral integration in ANKHD1-EIF4EBP3, loss of function of TET2, and NTRK1 copy number gain, suggesting that genetic alterations unrelated to insertional mutagenesis contributed to lymphomagenesis. The patient remains in remission 2 years after radiotherapy. This is the only CAR + TCL case reported at the Ohio State University James Comprehensive Cancer Center out of 288 patients treated with CAR-T cells.
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