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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Bortezomib enhances the efficacy of BCMA CAR-T therapy through up-regulating BCMA expression in myeloma cells.
Bortezomib enhances the efficacy of BCMA CAR-T therapy through up-regulating BCMA expression in myeloma cells.
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靶向B细胞成熟抗原(BCMA)的CAR-T(CAR-T)细胞疗法在治疗多发性骨髓瘤(MM)方面已显示出显著的临床获益。硼替佐米作为一种蛋白酶体抑制剂,获批作为MM一线药物已有二十年,已证明具有强效抗肿瘤活性。
在本研究中,我们发现硼替佐米处理可稳定BCMA的表达,并提出假设:BCMA CAR-T 疗法联合硼替佐米可增强抗MM疗效。体外实验显示,用低浓度硼替佐米预处理MM肿瘤细胞系MM1.S和强制表达BCMA的肿瘤细胞系NALM-6后,BCMA表达上调。当与BCMA CAR-T 细胞接触时,对这些经硼替佐米处理的肿瘤细胞的细胞毒性增加,表明硼替佐米诱导的BCMA上调有助于增强CAR-T 细胞的活性。
此外,在体内实验中,联合治疗显著增强了抗MM能力并延长了生存率。而且,安全性分析发现没有组织损伤或体重减轻,表明该联合策略具有良好的耐受性。
我们的研究为增强BCMA靶向CAR-T 肿瘤免疫治疗提供了一种可靠且有效的策略。
Chimeric antigen receptor T (CAR-T) cell therapy targeting B cell mature antigen (BCMA) has shown remarkable clinical benefits in treating multiple myeloma (MM). Bortezomib, a proteasome inhibitor approved as a first-line agent for MM for two decades, has demonstrated potent antitumor activity. In this study, we found that bortezomib treatment stabilizes the expression of BCMA and conceived the hypothesis that BCMA CAR-T therapy combined with bortezomib would enhance the anti-MM efficacy.
The in vitro experiments revealed that pretreatment of both MM tumor cell line MM1. S and tumor cell line NALM-6 forced expression of BCMA with low concentrations of bortezomib up-regulated BCMA expression. When encountered with BCMA CAR-T cells, the cytotoxicity to these bortezomib-treated tumor cells was increased, indicating that the up-regulated BCMA induced by bortezomib contributes to the enhanced activities of the CAR-T cells.
Further, in the in vivo experiment, the combined treatment significantly enhanced the anti-MM ability and prolonged the survival rate.
Moreover, safety analysis found that there is no tissue damage or loss of weight, suggesting the favorable tolerability of this combination strategy.
Our study provided a surety and efficacious strategy for the BCMA-targeted CAR-T cancer immunotherapy enhancement.
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