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:Cerebral Spinal Fluid Parameters Following CD19-Targeted Therapies in Children and Young Adults.
Cerebral Spinal Fluid Parameters Following CD19-Targeted Therapies in Children and Young Adults.
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急性淋巴细胞白血病患者脑脊液中出现白细胞可能提示中枢神经系统复发。CD19靶向免疫治疗可能增加血脑屏障通透性,导致神经毒性并浸润CNS。我们研究了71例连续接受CD19CAR-T 细胞或blinatumomab治疗患者的CSF细胞和蛋白含量。应答患者在blinatumomab或CAR-T 细胞治疗后,细胞增多症的发生率分别为66%和61%。CSF参数与毒性或既往CNS疾病无关。应考虑在免疫治疗后进行常规CSF流式细胞术,以区分T细胞浸润与CNS复发。
The presence of leukocytes in the cerebral spinal fluid (CSF) of patients with acute lymphoblastic leukemia may indicate a relapse in the central nervous system. CD19-directed immunotherapy may increase the blood-brain barrier permeability, leading to neurologic toxicity and infiltrate the CNS.
We studied the CSF cell and protein content in 71 consecutive patients who received either CD19 chimeric antigen receptor T cells or blinatumomab. Responding patients had an incidence of 66% and 61% of pleocytosis following blinatumomab or chimeric antigen receptor T cells, respectively. CSF parameters did not correlate with toxicity or prior CNS disease. Routine CSF flow cytometry following immunotherapy to distinguish T-cell infiltration from CNS relapse should be considered.
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