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qPCR 检测法用于检测 CAR-T 和 TCR-T 细胞中的 Woodchuck Hepatitis Virus Post-Transcriptional Regulatory Elements 在新鲜和福尔马林固定组织中的表达。

qPCR assay for detection of Woodchuck Hepatitis Virus Post-Transcriptional Regulatory Elements from CAR-T and TCR-T cells in fresh and formalin-fixed tissue.

机构信息

Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.

出版信息

PLoS One. 2024 Jun 6;19(6):e0303057. doi: 10.1371/journal.pone.0303057. eCollection 2024.

Abstract

As adoptive cellular therapies become more commonplace in cancer care, there is a growing need to monitor site-specific localization of engineered cells-such as chimeric antigen receptor T (CAR-T) cells and T-cell receptor T (TCR-T) cells-in patients' tissues to understand treatment effectiveness as well as associated adverse events. Manufacturing CAR-T and TCR-T cells involves transduction with viral vectors commonly containing the WPRE gene sequence to enhance gene expression, providing a viable assay target unique to these engineered cells. Quantitative PCR (qPCR) is currently used clinically in fresh patient tissue samples and blood with target sequences specific to each immunotherapy product. Herein, we developed a WPRE-targeted qPCR assay that is broadly applicable for detection of engineered cell products in both fresh and archival formalin-fixed paraffin embedded (FFPE) tissues. Using both traditional PCR and SYBR Green PCR protocols, we demonstrate the use of this WPRE-targeted assay to successfully detect two CAR-T cell and two TCR-T cell products in FFPE tissue. Standard curve analysis reported a reproducible limit of detection at 100 WPRE copies per 20μL PCR reaction. This novel and inexpensive technique could provide better understanding of tissue abundance of engineered therapeutic T cells in both tumor and second-site toxicity tissues and provide quantitative assessment of immune effector cell trafficking in archival tissue.

摘要

随着过继性细胞疗法在癌症治疗中变得越来越普遍,越来越需要监测工程细胞(如嵌合抗原受体 T(CAR-T)细胞和 T 细胞受体 T(TCR-T)细胞)在患者组织中的特定部位定位,以了解治疗效果以及相关的不良事件。制造 CAR-T 和 TCR-T 细胞涉及使用通常包含 WPRE 基因序列的病毒载体进行转导,以增强基因表达,为这些工程细胞提供独特的可行检测靶点。定量聚合酶链反应(qPCR)目前在新鲜患者组织样本和血液中用于临床,具有针对每种免疫疗法产品的特定靶序列。在此,我们开发了一种针对 WPRE 的 qPCR 检测方法,该方法广泛适用于检测新鲜和存档福尔马林固定石蜡包埋(FFPE)组织中的工程细胞产品。我们使用传统 PCR 和 SYBR Green PCR 方案,证明了该 WPRE 靶向检测方法可成功检测 FFPE 组织中的两种 CAR-T 细胞和两种 TCR-T 细胞产品。标准曲线分析报告称,在 20μL PCR 反应中,100 个 WPRE 拷贝的重现性检测限可重复性良好。这种新颖且廉价的技术可以更好地了解肿瘤和第二部位毒性组织中工程治疗性 T 细胞的组织丰度,并对存档组织中免疫效应细胞的迁移进行定量评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620f/11156344/782c5f72224d/pone.0303057.g001.jpg

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