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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.
Pullarkat, Shalini; Black, Graeme; Bleakley, Marie; Buenrostro, Denise; Chapuis, Aude G; Hirayama, Alexandre V; Jaeger-Ruckstuhl, Carla A; Kimble, Erik L; Lee, Bo M; Maloney, David G; Radich, Jerald; Seaton, Brandon W; Specht, Jennifer M; Turtle, Cameron J; Woolston, David W; Wright, Jocelyn H; Yeung, Cecilia C S.
Afiliação
  • Pullarkat S; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Black G; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Bleakley M; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Buenrostro D; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Chapuis AG; Department of Pediatrics, University of Washington, Seattle, Washington, United States of America.
  • Hirayama AV; Program in Immunology, University of Washington, Seattle, Washington, United States of America.
  • Jaeger-Ruckstuhl CA; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Kimble EL; Program in Immunology, University of Washington, Seattle, Washington, United States of America.
  • Lee BM; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Maloney DG; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Radich J; Program in Immunology, University of Washington, Seattle, Washington, United States of America.
  • Seaton BW; Department of Medicine, Division of Hematology and Oncology, University of Washington, Seattle, Washington, United States of America.
  • Specht JM; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Turtle CJ; Department of Medicine, Division of Hematology and Oncology, University of Washington, Seattle, Washington, United States of America.
  • Woolston DW; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Wright JH; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Yeung CCS; Department of Medicine, Division of Hematology and Oncology, University of Washington, Seattle, Washington, United States of America.
PLoS One ; 19(6): e0303057, 2024.
Article em En | MEDLINE | ID: mdl-38843256
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Vírus da Hepatite B da Marmota / Formaldeído Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Vírus da Hepatite B da Marmota / Formaldeído Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article