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:Precision Immunotherapy Utilizing Adapter CAR-T Cells (AdCAR-T) in Metastatic Breast Cancer Leads to Target Specific Lysis.
我们的结果表明,MPE来源的类器官可作为可靠工具,以患者个体化方式评估AdCAR-T对转移性BC的疗效。
转移性乳腺癌(BC)的常见症状之一是恶性胸腔积液(MPE)的形成,其中含有来源于原发肿瘤部位的恶性细胞。转移性BC中MPE的不良预后表明,需要可靠的精准肿瘤学以及能够代表转移性BC异质性的模型。在本研究中,我们利用类器官技术从四名晚期BC患者的MPE中培养了转移性肿瘤细胞。我们通过流式细胞术(FC)评估了MPE来源类器官系上肿瘤相关抗原的表达。基于个体抗原表达模式,患者来源类器官分别接受了适配体CAR-T细胞(AdCAR-T)以及靶向CD276、HER2、EGFR、TROP2或EpCAM的生物素化单克隆抗体处理。共培养实验显示,AdCAR-T对类器官的特异性裂解取决于个体抗原表达模式。我们的结果表明,MPE来源类器官可作为可靠工具,以患者个体化方式评估AdCAR-T对转移性BC的疗效。该方法有望应用于临床前环境,以指导治疗决策。此外,我们的研究证明了利用AdCAR-T靶向患者个体化抗原模式进行精准免疫治疗的可行性。
A frequent symptom of metastasized breast cancer (BC) includes the development of malignant pleural effusion (MPE), which contains malignant cells derived from the primary tumor site. The poor prognosis of MPE in metastasized BC indicates the necessity for dependable precision oncology and the importance of models representing the heterogenous nature of metastatic BC. In this study, we cultured MPE-derived metastatic tumor cells from four advanced BC patients using organoid technology. We assessed the expression of tumor-associated antigens on MPE-derived organoid lines by flow cytometry (FC). Based on an individual antigen expression pattern, patient-derived organoids were treated with adapter CAR-T cells (AdCAR-T) and biotinylated monoclonal antibodies targeting CD276, HER2, EGFR, TROP2, or EpCAM. Co-culture assays revealed specific organoid lysis by AdCAR-T depending on individual antigen expression patterns. Our results demonstrate that MPE-derived organoids can serve as a reliable tool for assessing the efficacy of AdCAR-T on metastatic BC in a patient-individualized manner. This approach could potentially be applied in a preclinical setting to instruct therapy decisions. Further, our study demonstrates the feasibility of precision immunotherapy utilizing AdCAR-T to target patient-individualized antigen patterns.
MEMBER ACCOUNT
登录成功会直接打开下一页。