T细胞受体
生物
嵌合抗原受体
T细胞
免疫疗法
分子生物学
癌症免疫疗法
土拨鼠肝炎病毒
Jurkat细胞
细胞毒性T细胞
免疫系统
病毒学
癌症研究
病毒
免疫学
乙型肝炎病毒
七鳃鳗科
体外
生物化学
作者
Shalini Pullarkat,Graeme C. Black,Marie Bleakley,Denise Buenrostro,Aude G. Chapuis,Alexandre V. Hirayama,Carla A. Jaeger-Ruckstuhl,Erik L. Kimble,Bo M. Lee,David G. Maloney,Jerald P. Radich,Brandon Seaton,Jennifer M. Specht,Cameron J. Turtle,David W. Woolston,Jocelyn H. Wright,Cecilia C.S. Yeung
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2024-06-06
卷期号:19 (6): e0303057-e0303057
标识
DOI:10.1371/journal.pone.0303057
摘要
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.
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