通过整合优化的 CAR 内结构域和 iNKT 衔接器增强 iNKT 细胞免疫治疗
Enhancing iNKT cell immunotherapy through the integration of optimized CAR endodomains and iNKT engagers.
iNKT细胞正逐渐成为一种极具前景的癌症免疫治疗平台。
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Enhancing iNKT cell immunotherapy through the integration of optimized CAR endodomains and iNKT engagers.
iNKT细胞正逐渐成为一种极具前景的癌症免疫治疗平台。
Anti-BCMA/GPRC5D CAR T cells in patients with relapsed or refractory multiple myeloma who have extraosseous extramedullary disease.
这些发现支持抗 BCMA/GPRC5D 双特异性 CAR T 细胞在伴骨外 EMD 的复发/难治性多发性骨髓瘤(RRMM)患者中诱导了高缓解率,且安全性可控。
Dual-antigen-targeting T-cell immunotherapies in MM: circumventing tumor heterogeneity and preventing antigen escape.
双靶向最终应在大规模 III 期试验中,与靶点转换的单靶向药物序贯治疗这一经典方案进行比较。
Correction: BCMA/GPRC5D bispecific CAR T-cell therapy for relapsed/refractory multiple myeloma with extramedullary disease: a single-center, single-ar
BCMA/GPRC5D bispecific CAR T-cell therapy for relapsed/refractory multiple myeloma with extramedullary disease: a single-center, single-arm, phase 1 t
这些发现共同凸显了针对侵袭性多发性骨髓瘤患者、尤其是伴髓外疾病患者的 BCMA/GPRC5D 双靶向 CAR T 细胞疗法的潜在治疗策略,并支持在更大规模的多中心临床研究中进一步探索和验证的必要性。
Preclinical development of three novel CARs targeting CD79b for the treatment of non-Hodgkin's lymphoma and characterization of the loss of the target
基于特异性、疗效和靶抗原丢失,CARLY3 代表了一种针对非霍奇金淋巴瘤的潜在新型 CAR 治疗。
ARI0003: Co-transduced CD19/BCMA dual-targeting CAR-T cells for the treatment of non-Hodgkin lymphoma.
CD19 CAR-T 疗法在复发/难治性非霍奇金淋巴瘤(NHL)中已取得显著缓解。
Anti-BCMA/GPRC5D bispecific CAR T cells in patients with relapsed or refractory multiple myeloma: a single-arm, single-centre, phase 1 trial.
抗BCMA/GPRC5D双特异性CAR T细胞在复发或难治性多发性骨髓瘤患者中显示出良好的安全性特征和令人鼓舞的活性。
Anti-BCMA/GPRC5D bispecific CAR T cells for relapsed or refractory multiple myeloma: is 1 + 1 greater than 2?
Bispecific CAR T cell therapy targeting BCMA and CD19 in relapsed/refractory multiple myeloma: a phase I/II trial.
我们的研究表明,双特异性 BC19 CAR T 细胞治疗 R/R MM 患者可行、安全且有效。
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