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:Cell therapy for a rare disease- hairy cell leukemia variant.
Cell therapy for a rare disease- hairy cell leukemia variant.
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毛细胞白血病变异型(HCL-v)是一种罕见的克隆性成熟B细胞恶性肿瘤,病程呈慢性进展。HCL-v患者常对作为一线治疗的嘌呤核苷类似物耐药。为解决当前HCL-v治疗的不足,我们研究了一种基于BAFF配体的CAR-T 细胞,该配体能够结合全部三种BAFF受体:BAFF受体、TACI和BCMA。研究显示,HCL-v患者来源细胞高表达全部三种BAFF受体;BAFF CAR-T 细胞在体外可对细胞系及HCL-v患者细胞诱导显著细胞毒作用。与HCL-v细胞共孵育后,CAR-T 细胞显著活化、脱颗粒并释放促炎细胞因子,与上述细胞毒作用相符。研究还成功从一例HCL-v患者直接制备BAFF CAR-T 细胞,并观察到这些细胞在体外可直接自体杀伤患者肿瘤细胞。该患者来源CAR-T 细胞还有效杀伤了Hair-M细胞系和另一名HCL-v患者来源肿瘤细胞。
最后,研究建立了两种HCL小鼠异种移植模型:皮下Bonna-12模型和静脉注射Hair-M模型。治疗后肿瘤负荷下降、生存期延长,且未见显著毒性。
总之,本研究显示BAFF CAR-T 细胞在体外和体内均可对多种细胞系及患者来源HCL-v样本发挥抗肿瘤作用,可能成为HCL-v患者的一种有效治疗策略。
Hairy cell leukemia variant (HCL-v) is a rare malignancy of clonal mature B-cells that follows a chronic disease course. HCL-v patients are often resistant to purine nucleoside analogs, which are the first-line therapy. To address the shortcomings of current therapy for HCL-v, we investigated the activity of a BAFF ligand-based CAR-T cell which binds to all three BAFF receptors, BAFF-receptor, TACI, and BCMA.
Here, we demonstrate that HCLv patient-derived cells highly express all three BAFF receptors and that BAFF CAR-T cells induce significant cytotoxicity in vitro against both cell lines and HCL-v patient cells. This cytotoxicity corresponds with significant CAR-T cell activation, degranulation, and release of pro-inflammatory cytokines after co-incubation with HCLv cells.
Furthermore, we successfully generated BAFF CAR-T cells directly from an HCLv patient and observed direct autologous killing against patient tumor cells in vitro. These HCLv patient-derived CAR-T cells were also effective in killing the Hair-M cell line and tumor cells derived from a different HCLv patient. Lastly, we also developed two mouse xenograft models for HCL, a subcutaneous Bonna-12 model and intravenous Hair-M xenograft model.
We observed decreases in tumor burden and prolonged overall survival without significant toxicity.
In conclusion, here we show that BAFF CAR-T cells exert anti-tumor effects in vitro and in vivo against multiple cell lines and patient-derived HCL-v samples and may be a successful therapeutic strategy for HCLv patients.
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