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:CAR T targets: AI takes the wheel.
识别安全有效的靶点仍是 CAR T 细胞疗法的主要瓶颈。
寻找安全且有效的靶点仍是CAR-T细胞疗法发展的主要瓶颈。本期《Cell》中,Baker及其同事开发了一种大型语言模型辅助评分框架,以简化靶点筛选流程,并据此鉴定和验证糖蛋白非转移性黑色素瘤蛋白B(GPNMB)是可用于黑色素瘤、白血病及结直肠癌的候选嵌合抗原受体(CAR)T细胞靶点。
Identifying safe and effective targets remains a major bottleneck for CAR T cell therapies. In this issue of Cell, Baker and colleagues developed a large language model (LLM)-assisted scoring framework to streamline this process and as a result identified and validated glycoprotein non-metastatic melanoma protein B (GPNMB) as a candidate chimeric antigen receptor (CAR) T target across melanoma, leukemia, and colorectal cancer.
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