CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Next-generation BCMA-targeted chimeric antigen receptor CARTemis-1: the impact of manufacturing procedure on CAR T-cell features.
Next-generation BCMA-targeted chimeric antigen receptor CARTemis-1: the impact of manufacturing procedure on CAR T-cell features.
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CARTemis-1 经过合理设计,旨在提高抗肿瘤疗效、克服 sBCMA 抑制并整合安全基因的表达。CARTemis-1 的制备已在 GMP 标准下成功验证。将开展针对多发性骨髓瘤患者的 I/II 期临床试验(EuCT 号 2022-503063-15-00)。
靶向BCMA的CAR疗法正在作为多发性骨髓瘤的治疗方法进行研究。然而,鉴于大多数研究中缺乏平台期,探索更有效的替代方案势在必行。我们展示了一种新型优化抗BCMA CAR(CARTemis-1)的临床前和临床验证。此外,我们探讨了制造工艺如何影响CAR-T 细胞产品的质量和适应性。
CARTemis-1的优化在临床前水平进行了体外和体内评估。CARTemis-1的制备在GMP条件下得到验证,研究了从白细胞分离术到最终产品的免疫表型动态变化。在此,我们研究了生产工艺对CAR-T 细胞的影响,以确定最佳细胞培养方案和扩增时间,从而提高产品的适应性。
比较了两种不同间隔区的CARTemis-1版本。较长版本显示出增强的细胞毒性。将安全基因EGFRt整合到CARTemis-1结构中可作为监测标记物。CARTemis-1未受到可溶性BCMA的抑制,并在体外和体内均表现出强效抗肿瘤作用。比较了使用IL-2或IL-7/IL-15的扩增,结果显示使用IL-7/IL-15时增殖更多、分化更少、耗竭更少。在GMP指南下连续生产了三批CARTemis-1,均符合所有要求的规格。在GMP条件下生产的CARTemis-1细胞显示出记忆亚群增加、耗竭标志物减少,并对MM细胞系和原代骨髓瘤细胞具有选择性抗肿瘤效力。获得最佳适配产品的最佳释放时间点为> 6天且< 10天(第8-10天)。
CAR therapy targeting BCMA is under investigation as treatment for multiple myeloma. However, given the lack of plateau in most studies, pursuing more effective alternatives is imperative. We present the preclinical and clinical validation of a new optimized anti-BCMA CAR (CARTemis-1). In addition, we explored how the manufacturing process could impact CAR-T cell product quality and fitness.
CARTemis-1 optimizations were evaluated at the preclinical level both, in vitro and in vivo. CARTemis-1 generation was validated under GMP conditions, studying the dynamics of the immunophenotype from leukapheresis to final product. Here, we studied the impact of the manufacturing process on CAR-T cells to define optimal cell culture protocol and expansion time to increase product fitness.
Two different versions of CARTemis-1 with different spacers were compared. The longer version showed increased cytotoxicity. The incorporation of the safety-gene EGFRt into the CARTemis-1 structure can be used as a monitoring marker. CARTemis-1 showed no inhibition by soluble BCMA and presents potent antitumor effects both in vitro and in vivo. Expansion with IL-2 or IL-7/IL-15 was compared, revealing greater proliferation, less differentiation, and less exhaustion with IL-7/IL-15. Three consecutive batches of CARTemis-1 were produced under GMP guidelines meeting all the required specifications. CARTemis-1 cells manufactured under GMP conditions showed increased memory subpopulations, reduced exhaustion markers and selective antitumor efficacy against MM cell lines and primary myeloma cells. The optimal release time points for obtaining the best fit product were > 6 and < 10 days (days 8-10).
CARTemis-1 has been rationally designed to increase antitumor efficacy, overcome sBCMA inhibition, and incorporate the expression of a safety-gene. The generation of CARTemis-1 was successfully validated under GMP standards. A phase I/II clinical trial for patients with multiple myeloma will be conducted (EuCT number 2022-503063-15-00).
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