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:Case Report: Bispecific CD20/CD30-targeted chimeric antigen receptor T-cell therapy for non-Hodgkin's lymphoma.
第二剂作为巩固治疗给予,迄今持续无病生存超过 12 个月。
未标注:靶向CD19的CAR T细胞疗法是治疗B细胞恶性肿瘤的一项突破性免疫疗法。然而,CD19丢失介导的复发/难治性疾病仍是重大挑战,迫切需要靶向其他抗原的CAR T细胞。为解决这一问题,我们开发了一种靶向CD20的CAR T细胞,并加入额外的CD30结合结构域以增强癌细胞杀伤。本文报告一例肿块较大的转化型滤泡性淋巴瘤患者,接受靶向CD20/CD30的CAR-T细胞治疗并成功。患者在一个月间隔内接受两次抗CD20/CD30 CAR-T治疗。首次输注后1个月达到完全代谢缓解,未发生细胞因子释放综合征(CRS)或免疫效应细胞相关神经毒性综合征(ICANS)。第二次输注作为巩固治疗;截至报告时,患者无病生存已持续超过12个月。本病例凸显靶向CD20/CD30 CAR T细胞疗法的治疗潜力和安全性。临床试验注册:ClinicalTrials.gov,NCT06756321。
UNLABELLED: CD19-directed CAR T-cell therapy is a breakthrough immunotherapy for B-cell malignancies. However, CD19 loss-mediated relapsed/refractory disease continues to pose a significant challenge, highlighting the urgent need for CAR T cells targeting alternative antigens. To address this issue, we developed a CD20-directed CAR T incorporated with an additional CD30-directed binder to enhance cytotoxicity toward cancer cells. Here, we report that a patient with bulky transformed follicular lymphoma was successfully treated with CD20/CD30-directed CAR-T cells. The patient received two doses of anti-CD20/CD30-CAR-T therapy administered one month apart. Complete metabolic remission was achieved 1 month after the first infusion without evidence of cytokine release syndrome (CRS) or immune effector cell-associated neurotoxicity syndrome (ICANS). The second dose was given as a consolidation therapy with sustained disease-free survival exceeding 12 months to date. The report underscores the promising therapeutic potential and safety profile of CD20/CD30-directed CAR T-cell therapy. CLINICAL TRIAL REGISTRATION: https://www.clinicaltrials.gov, identifier NCT06756321.
MEMBER ACCOUNT
登录成功会直接打开下一页。