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:Neurofilament light chain serum levels correlate with the severity of neurotoxicity after CAR T-cell treatment.
Neurofilament light chain serum levels correlate with the severity of neurotoxicity after CAR T-cell treatment.
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靶向CD19的嵌合抗原受体(CAR)修饰T细胞抗肿瘤疗效显著,但治疗常伴有程度不一且难以预测的免疫效应细胞相关神经毒性综合征(ICANS)。研究者在两家主要CAR-T 治疗中心纳入96例接受CAR-T 细胞治疗的难治性B细胞恶性肿瘤患者,评估神经轴索损伤标志物神经丝轻链(NfL)血清水平是否与ICANS严重程度相关。采用单分子酶联免疫吸附测定法,在CAR-T 细胞输注前后检测血清NfL,并与ICANS严重程度进行关联分析。未经调整和调整后的分析均显示,治疗前NfL水平升高与更严重的ICANS相关。多变量统计模型显示,CAR-T 细胞输注后NfL水平显著升高,且与ICANS严重程度相关。治疗前NfL水平较高所提示的既存神经轴索损伤,与后续ICANS严重程度相关。
因此,血清NfL可能作为预测ICANS严重程度的生物标志物,并有助于改进CAR-T 细胞输注后的患者监测。不过,这些初步结果仍需在更大规模的前瞻性患者队列中验证。
Antitumor therapy with CD19-targeted chimeric antigen receptor (CAR) modified T cells is highly efficient.
However, treatment is often complicated by a unique profile of unpredictable neurotoxic adverse effects of varying degrees known as immune effector cell-associated neurotoxicity syndrome (ICANS).
We examined 96 patients receiving CAR T cells for refractory B-cell malignancies at 2 major CAR T-cell treatment centers to determine whether serum levels of neurofilament light chain (NfL), a marker of neuroaxonal injury, correlate with the severity of ICANS. Serum NfL levels were measured before and after infusion of CAR T cells using a single-molecule enzyme-linked immunosorbent assay and correlated with the severity of ICANS.
Elevated NfL serum levels before treatment were associated with more severe ICANS in both unadjusted and adjusted analyses. Multivariable statistical models revealed a significant increase in NfL levels after CAR T-cell infusion, which correlated with the severity of ICANS. Preexisting neuroaxonal injury. which was characterized by higher NfL levels before CAR T-cell treatment, correlated with the severity of subsequent ICANS.
Thus, serum NfL level might serve as a predictive biomarker for assessing the severity of ICANS and for improving patient monitoring after CAR T-cell transfusion.
However, these preliminary results should be validated in a larger prospective cohort of patients.
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