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:Ex vivo mesenchymal progenitor cell-based cord blood cell expansion and exofucosylation to enhance transplant engraftment.
Ex vivo mesenchymal progenitor cell-based cord blood cell expansion and exofucosylation to enhance transplant engraftment.
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脐带血(CB)移植相比其他同种异体移植物,受限于植入较慢和失败率较高。我们假设,使用间充质祖细胞(MPC)对CB进行体外扩增,并通过外岩藻糖基化强制表达介导骨趋向性的sLeX,将缩短植入时间。6例血液系统恶性肿瘤患者接受了两个CB单位(CBU)的移植。5例接受了一个未处理的CBU和一个MPC扩增、外岩藻糖基化的CBU。中性粒细胞植入、血小板>20,000/ L和血小板>50,000/ L的中位时间分别为29、45和55天。第6例接受了一个外岩藻糖基化CBU和一个MPC扩增CBU,分别在34、53和57天实现中性粒细胞植入、血小板>20,000/ L和血小板>50,000/ L。4/6例患者发生急性GVHD,包括1例III/IV级。3例在移植后中位43.6个月时存活且无疾病复发。3例患者死亡原因分别为复发、COVID和GVHD。因此,这些方法是安全的,但并未改善植入。
Umbilical cord blood (CB) transplantion is limited by slower engraftment and higher failure rates compared to other allografts.
We hypothesized that ex vivo expansion of CB using mesenchymal progenitor cells (MPCs) and exofucosylation to enforce expression of osteotropism-mediating sLeX would shorten engraftment time. Six patients with hematologic malignancies underwent transplantation with two CB units (CBUs). Five received one unmanipulated CBU and one MPC-expanded, exofucosylated CBU. Median neutrophil engraftment, platelets >20,000/ L, and platelets >50,000/ L were 29, 45, and 55 days, respectively.
A sixth received one exofucosylated CBU and one MPC-expanded CBU, achieving neutrophil engraftment, platelets >20,000/ L, and platelets >50,000/ L in 34, 53, and 57 days, respectively. Acute GVHD occurred in 4/6 patients, including one grade III/IV case. Three were alive without disease relapse at a median of 43. 6 months post-transplant. Deaths in three patients were due to relapse, COVID, and GVHD.
Thus, these approaches were safe, but did not improve engraftment.
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