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:Targeting chronic lymphocytic leukemia with B-cell activating factor receptor CAR T cells.
Targeting chronic lymphocytic leukemia with B-cell activating factor receptor CAR T cells.
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疾病复发/难治(R/R)的挑战仍然是嵌合抗原受体(CAR)T细胞治疗中的一个治疗障碍,尤其是在血液系统疾病中,慢性淋巴细胞白血病(CLL)对CD19 CAR-T 细胞尤其耐药。目前,尚无获批用于CLL患者的CAR-T 细胞疗法。
在本研究中,我们旨在通过选择B细胞活化因子受体(BAFF-R)作为针对CLL的CAR设计中一个有前景的靶点,来解决这一未被满足的医疗需求。BAFF-R对B细胞存活至关重要,并在CLL肿瘤上持续表达。
我们的研究发现,BAFF-R CAR-T 细胞疗法对CLL细胞系和源自CLL患者的原代B细胞均发挥了细胞毒性作用。此外,这些CAR-T 细胞对CD19敲除的CLL细胞表现出细胞毒性,而这些细胞对CD19 CAR-T 疗法耐药。
此外,我们能够从CLL患者采集的少量血液样本中生成BAFF-R CAR-T 细胞,并随后证明了这些患者来源的CAR-T 细胞对自体肿瘤细胞的细胞毒性作用。鉴于这些有希望的结果,BAFF-R CAR-T 细胞疗法有潜力满足CLL患者对有效治疗的长期需求。
The challenge of disease relapsed/refractory (R/R) remains a therapeutic hurdle in chimeric antigen receptor (CAR) T-cell therapy, especially for hematological diseases, with chronic lymphocytic leukemia (CLL) being particularly resistant to CD19 CAR T cells.
Currently, there is no approved CAR T-cell therapy for CLL patients. In this study, we aimed to address this unmet medical need by choosing the B-cell activating factor receptor (BAFF-R) as a promising target for CAR design against CLL. BAFF-R is essential for B-cell survival and is consistently expressed on CLL tumors.
Our research discovered that BAFF-R CAR T-cell therapy exerted the cytotoxic effects on both CLL cell lines and primary B cells derived from CLL patients.
In addition, the CAR T cells exhibited cytotoxicity against CD19-knockout CLL cells that are resistant to CD19 CAR T therapy.
Furthermore, we were able to generate BAFF-R CAR T cells from small blood samples collected from CLL patients and then demonstrated the cytotoxic effects of these patient-derived CAR T cells against autologous tumor cells. Given these promising results, BAFF-R CAR T-cell therapy has the potential to meet the long-standing need for an effective treatment on CLL patients.
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