不可逆电穿孔增强 CAR-T 细胞对实体瘤的浸润与选择性癌细胞裂解
Irreversible Electroporation Enhances Solid Tumor Infiltration and Selective Cancer Cell Lysis by CAR T Cells.
通过利用一种双用途转化策略——直接的癌细胞靶向细胞毒性和增强的 CAR-T 细胞浸润——sIRE 能够减轻肿瘤负荷,同时保持并增强 CAR-T 细胞功能。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Expression of TILs and Patterns of Gene Expression from Paired Samples of Malignant Pleural Mesothelioma (MPM) Patients.
Expression of TILs and Patterns of Gene Expression from Paired Samples of Malignant Pleural Mesothelioma (MPM) Patients.
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MPM 是一种具有免疫抑制性肿瘤微环境的侵袭性疾病,探索免疫治疗在该疾病中的兴趣日益增加。在一线治疗中,nivolumab 联合 ipilimumab 显示出较化疗改善生存。TILs 的存在已被认为是实体瘤中对化疗抗肿瘤免疫反应的标志物。我们研究的目的是确定治疗对 MPM 中免疫细胞和免疫基因谱的影响。我们使用免疫组织化学和基因表达分析,对 10 例人类 MPM 配对肿瘤组织中的 TILs 表达变化进行了研究,样本来自配对的未治疗和治疗后样本。在这个小系列中,我们证明在疾病未经任何治疗的自然演变过程中,肿瘤样本中的炎症成分增加。全身治疗后,TILs 数量减少。我们观察到,在全身治疗或疾病进展后,免疫基因特征受到抑制。我们对配对样本的免疫谱和 MPM 基因组变化的整合分析表明,在疾病演变过程中,免疫系统倾向于转换,并随治疗而关闭。
MPM is an aggressive disease with an immunosuppressive tumor microenvironment, and interest in exploring immunotherapy in this disease has been increasing. In the first line of treatment, the combination of nivolumab and ipilimumab demonstrated an improvement in survival over chemotherapy. The presence of TILs has been recognized as a marker of antitumor immune response to chemotherapy in solid tumors. The aim of our study is to identify the effect of treatment on immune cells and the immune gene profile in MPM.
We investigated the changes in expression of TILs in 10 human MPM paired tumor tissues using immunohistochemistry and gene expression analysis from paired untreated and treated samples. In this small series, we demonstrated that during the evolution of disease without any treatment there was an increase in the inflammatory component in tumor samples. After systemic treatment there was a decrease in the number of TILs.
We observed that after systemic treatment or disease progression immune gene signatures were suppressed.
Our integrated analysis of paired samples with immune profile and genomic changes on MPM suggested that during the evolution of the disease the immune system tends to switch, turning off with treatment.
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