靶向由多种 HLA-II 等位基因混杂呈递的胞内白血病抗原的 CAR-T 细胞
CAR T Cells Targeting an Intracellular Leukemia Antigen Promiscuously Presented by Diverse HLA-II Alleles.
UNLABELLED:嵌合抗原受体(CAR)技术使 T 细胞能够有效识别并靶向谱系特异性表面抗原,从而彻底改变了 B 细胞恶性肿瘤的治疗。
英文原题:Comparison of genomic response among patients receiving dendritic cell vaccines pulsed with two different cancer-associated antigens: A retrospective observational study.
Comparison of genomic response among patients receiving dendritic cell vaccines pulsed with two different cancer-associated antigens: A retrospective observational study.
两个治疗组之间的基因组反应存在显著差异。预先存在的肿瘤遗传学特征可影响个体化DC免疫治疗的预后,凸显了液体活检在精准肿瘤学中的作用。
液体活检在树突状细胞免疫治疗中的评估和预后价值尚未得到研究,尤其是关于Wilms瘤基因1(WT1)肽和肿瘤特异性抗原或新抗原的使用。
我们旨在通过液体活检比较和对比这两个治疗组的基因组反应。
这是一项真实世界回顾性分析,分析了55名男性和46名女性(年龄在4至91岁之间)的液体活检检测结果,这些受试者接受了负载新抗原(n = 45)或WT1联合或不联合MUC1抗原(n = 56)的DC疫苗治疗。
新抗原脉冲DC疫苗组的基线总ctDNA浓度更高(p = 0.003)。与新抗原脉冲疫苗组相比,WT1脉冲疫苗组的肿瘤突变数量(p = 0.025)、高TMB突变比例(p = 0.023)以及新突变的出现(p < 0.001)均显著更高。此外,两组之间突变数量与治疗持续时间的关系存在显著差异(p = 0.016)。
BACKGROUND: The evaluative and prognostic value of liquid biopsy in dendritic cell immunotherapy has not yet been studied, especially with respect to the use of the Wilms tumor gene 1 (WT1) peptide and tumor-specific antigens or neoantigens. OBJECTIVE: We aimed to compare and contrast the genomic responses of these two treatment groups via liquid biopsy. METHODS: This was a real-world retrospective analysis of the liquid biopsy test results of 55 men and 46 women between 4 and 91 years of age who had received DC vaccines pulsed with either neoantigens (n = 45) or WT1 with or without MUC1 antigen (n = 56). RESULTS: The baseline total ctDNA concentration was greater in the neoantigen-pulsed DC vaccine group (p = 0.003). Compared with those in the neoantigen-pulsed vaccine group, the number of tumor mutations (p = 0.025), proportion of high-TMB mutations (p = 0.023), and appearance of new mutations (p < 0.001) in the WT1-pulsed vaccine group were significantly greater. Additionally, the relationships between the number of mutations and duration of treatment were significantly different between the two groups (p = 0.016). CONCLUSIONS: Genomic responses were significantly different between the two treatment groups. Preexisting tumor genetics can affect the prognosis of personalized DC immunotherapy, highlighting the role of liquid biopsy in precision oncology.
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