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:Mechanisms for resistance to BCMA-targeted immunotherapies in multiple myeloma.
Mechanisms for resistance to BCMA-targeted immunotherapies in multiple myeloma.
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多发性骨髓瘤(MM)仍然无法治愈,患者最终面临复发/难治的困境。靶向B细胞成熟抗原(BCMA)的免疫治疗方法在复发/难治性MM患者中显示出巨大疗效,主要包括CAR-T 细胞、双特异性T细胞衔接器(TCEs)和抗体药物偶联物(ADCs)。然而,它们对长期生存的影响仍有待确定。尽管如此,对这些新疗法的耐药仍然不可避免,这在实验室研究和临床实践中都提出了我们从未遇到的挑战。在这种情况下,旨在增强和延长BCMA靶向治疗抗MM活性的研究正在迅速扩展。尽管我们对其耐药机制的理解存在相当大的不确定性,但这些机制主要归因于抗原依赖性、T细胞驱动因素和(免疫)肿瘤微环境。在这篇综述中,我们总结了目前对BCMA靶向免疫治疗耐药机制的理解,并讨论了克服它的潜在策略。
Multiple myeloma (MM) remains incurable and patients eventually face the relapse/refractory dilemma. B cell maturation antigen (BCMA)-targeted immunotherapeutic approaches have shown great effectiveness in patients with relapsed/refractory MM, mainly including chimeric antigen receptor T cells (CAR-T), bispecific T cell engagers (TCEs), and antibody-drug conjugates (ADCs).
However, their impact on long-term survival remains to be determined. Nonetheless, resistance to these novel therapies is still inevitable, raising a challenge that we have never met in both laboratory research and clinical practice. In this scenario, the investigation aiming to enhance and prolong the anti-MM activity of BCMA-targeted therapies has been expanding rapidly.
Despite considerable uncertainty in our understanding of the mechanisms for their resistance, they have mainly been attributed to antigen-dependency, T cell-driven factors, and (immune) tumor microenvironment. In this review, we summarize the current understanding of the mechanisms for resistance to BCMA-targeted immunotherapies and discuss potential strategies for overcoming it.
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