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Generation of Tumor-activated T cells Using Electroporation.
Alinezhadbalalami, Nastaran; Graybill, Philip M; Imran, Khan Mohammad; Verbridge, Scott S; Allen, Irving C; Davalos, Rafael V.
Afiliación
  • Alinezhadbalalami N; Department of Biomedical Engineering and Mechanics, Virginia Tech, 325 Stanger Street, Blacksburg, VA 24061, USA; Institute for Critical Technology and Applied Sciences, Virginia Tech, Kelly Hall, Blacksburg, VA 24061, USA. Electronic address: nalinezh@vt.edu.
  • Graybill PM; Department of Mechanical Engineering, Virginia Tech, Goodwin Hall, 635 Prices Fork Road, Blacksburg, VA 24061, USA; Institute for Critical Technology and Applied Sciences, Virginia Tech, Kelly Hall, Blacksburg, VA 24061, USA. Electronic address: pmg1@vt.edu.
  • Imran KM; Graduate Program in Translational Biology, Medicine and Health, Virginia Tech, 1 Riverside Circle, Roanoke, VA 24016, USA; Institute for Critical Technology and Applied Sciences, Virginia Tech, Kelly Hall, Blacksburg, VA 24061, USA. Electronic address: imrankhan@vt.edu.
  • Verbridge SS; Department of Biomedical Engineering and Mechanics, Virginia Tech, 325 Stanger Street, Blacksburg, VA 24061, USA; Institute for Critical Technology and Applied Sciences, Virginia Tech, Kelly Hall, Blacksburg, VA 24061, USA. Electronic address: sverb@vt.edu.
  • Allen IC; Department of Biomedical Sciences and Pathobiology, Virginia Tech, 205 Duck Pond Drive, Blacksburg, VA 24061, USA; Institute for Critical Technology and Applied Sciences, Virginia Tech, Kelly Hall, Blacksburg, VA 24061, USA. Electronic address: icallen@vt.edu.
  • Davalos RV; Department of Biomedical Engineering and Mechanics, Virginia Tech, 325 Stanger Street, Blacksburg, VA 24061, USA; Department of Mechanical Engineering, Virginia Tech, Goodwin Hall, 635 Prices Fork Road, Blacksburg, VA 24061, USA; Institute for Critical Technology and Applied Sciences, Virginia Tech,
Bioelectrochemistry ; 142: 107886, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34303065
Expansion of cytotoxic T lymphocytes (CTLs) is a crucial step in almost all cancer immunotherapeutic methods. Current techniques for expansion of tumor-reactive CTLs present major limitations. This study introduces a novel method to effectively produce and expand tumor-activated CTLs using high-voltage pulsed electric fields. We hypothesize that utilizing high-voltage pulsed electric fields may be an ideal method to activate and expand CTLs due to their non-thermal celldeath mechanism. Tumor cells were subjected to high-frequency irreversible electroporation (HFIRE) with various electric field magnitudes (1250, 2500 V/cm) and pulse widths (1, 5, and 10 µs), or irreversible electroporation (IRE) at 1250 V/cm. The treated tumor cells were subsequently cocultured with CD4+ and CD8+ T cells along with antigen-presenting cells. We show that tumor-activated CTLs can be produced and expanded when exposed to treated tumor cells. Our results suggest that CTLs are more effectively expanded when pulsed with HFIRE conditions that induce significant cell death (longer pulse widths and higher voltages). Activated CD8+ T cells demonstrate cytotoxicity to untreated tumor cells suggesting effector function of the activated CTLs. The activated CTLs produced with our technique could be used for clinical applications with the goal of targeting and eliminating the tumor.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfocitos T Citotóxicos / Electroporación / Glioblastoma Límite: Humans Idioma: En Revista: Bioelectrochemistry Asunto de la revista: BIOQUIMICA Año: 2021 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfocitos T Citotóxicos / Electroporación / Glioblastoma Límite: Humans Idioma: En Revista: Bioelectrochemistry Asunto de la revista: BIOQUIMICA Año: 2021 Tipo del documento: Article