下一代肿瘤不可知靶点即将出现
Next-generation tumor-agnostic targets on the horizon.
肿瘤不可知药物开发将肿瘤学重新聚焦于共享的分子依赖性而非组织来源,从而能够针对跨肿瘤的罕见可操作驱动因素进行高效开发。
英文原题:Rapid identification of antigen-specific TCRs for cancer immunotherapy.
T 细胞受体(TCR)可识别由主要组织相容性复合体(MHC)分子——在人类中称为 HLA——提呈的肽段,从而实现对表达特定抗原的肿瘤细胞的靶向清除。
T 细胞受体(TCR)能够识别主要组织相容性复合体(MHC)分子呈递的肽段;在人类中,MHC 称为 HLA。该特性使研究者能够靶向清除表达特定抗原的肿瘤细胞。近年来,TCR 工程化 T 细胞(TCR-T)疗法在靶向实体瘤的临床试验中取得显著进展。值得注意的是,美国 FDA 于 2024 年 8 月批准了首个用于晚期滑膜肉瘤的 TCR-T 药物,成为该领域的重要里程碑。开发 TCR-T 疗法的关键是识别肿瘤相关抗原表位和功能强效的 TCR。本文提出一套完整方案,介绍如何识别免疫原性表位,以及如何从 HLA 转基因小鼠中高效筛选抗原特异性 TCR。该方案还包括 TCR-T 细胞制备及其体外功能评估方法。这些方法为推动肿瘤特异性 TCR 的开发和 TCR-T 疗法的临床转化提供了可靠框架。
T cell receptors (TCRs) can recognize peptides presented by major histocompatibility complex (MHC) molecules, referred to as HLA in humans, which enables the targeted eradication of tumor cells expressing specific antigens. In recent years, TCR-engineered T cell (TCR-T) cell therapy has demonstrated substantial advancements in clinical trials targeting solid tumors. Notably, in August 2024, the U.S. FDA approved the first TCR-T drug for the treatment of advanced synovial sarcoma, representing a pivotal milestone in the field. For the development of TCR-T therapy, identifying tumor-associated antigen epitopes and high-functional TCRs are critical. Here, we present a comprehensive protocol outlining the process of identification of immunogenic epitopes and the efficient screening of antigen-specific TCRs from HLA transgenic mice. Additionally, the protocol encompasses methodologies for TCR-T cell preparation and their functional evaluation in vitro . These approaches provide a robust framework for advancing the development of tumor-specific TCRs and fostering the clinical translation of TCR-T therapies.
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