决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Evidence for early, clinically silent medial temporal lobe inflammation after CAR-T cell therapy.
这些数据提示 MTL 存在早期、临床沉默的炎症反应,可能对长期认知功能产生影响,尚需进一步研究。
免疫效应细胞相关神经毒性综合征(ICANS)是嵌合抗原受体(CAR)-T 细胞治疗后最常见的神经系统并发症。即使在缺乏临床神经毒性的情况下,长期认知影响仍存有争议。CAR-T 细胞相关神经毒性常累及内侧颞叶(MTL),然而常规结构磁共振成像(MRI)往往仍显示正常。目前需要能够预测长期认知结局的亚临床神经毒性标志物。
因此,我们建立了一个影像学方案,整合了接受CAR-T细胞治疗的B细胞恶性肿瘤患者MTL的3 Tesla(T)和7 T灌注及功能连接MRI。本文展示了四例患者的纵向数据。
4例患者中有2例发生ICANS(1级和3级),这些患者还出现了轻度细胞因子释放综合征(CRS,1级)。在基线时或随访期间均未检测到MTL的结构异常。CAR-T细胞扩增在患者之间差异显著。无论是否出现ICANS、CRS或CAR-T细胞扩增,患者均表现出MTL灌注和功能连接增加,在10-14天最为明显。
OBJECTIVE: Immune effector cell-associated neurotoxicity syndrome (ICANS) is the most frequent neurological complication following chimeric antigen receptor (CAR)-T cell therapy. Long-term cognitive effects remain controversial, even in the absence of clinical neurotoxicity. CAR-T cell-associated neurotoxicity often involves the medial temporal lobe (MTL), yet conventional structural magnetic resonance imaging (MRI) frequently remains normal. There is a need for markers of subclinical neurotoxicity that may predict long-term cognitive outcomes. METHODS: Therefore, we established an imaging protocol integrating 3 Tesla (T) and 7 T perfusion and functional connectivity MRI of the MTL in patients receiving CAR-T cells for B cell malignancies. Longitudinal data from four patients is presented here. RESULTS: Two of the four patients developed ICANS (grade 1 and grade 3), and these patients also experienced mild cytokine release syndrome (CRS, grade 1). No structural abnormalities of the MTL were detected at baseline or during follow-up. CAR-T cell expansion varied markedly between patients. Regardless of ICANS, CRS, or CAR-T cell expansion, patients showed increased MTL perfusion and functional connectivity, most prominently at days 10-14. CONCLUSION: These data suggest an early, clinically silent inflammatory response in the MTL with potential implications for long-term cognitive function, which requires further investigation.
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