MLchartDataset catalogue

Autologous anti-MUC16 CAR-mbIL15-safety switch T cells PRGN-3005

Term · Oncology and biomedicine · MLC-T-ONC-011481

A preparation of autologous T lymphocytes that have been genetically modified to co-express three transgenes using the Sleeping Beauty (SB) transposon system and include a chimeric antigen receptor (CAR) targeting the unshed portion of the tumor-associated antigen (TAA) human mucin 16 (MUC16, cancer antigen 125; CA125; FLJ14303), a membrane-bound IL-15 (mbIL15) and a safety/kill switch, with potential immunostimulating and antineoplastic activities. Upon introduction of the autologous anti-MUC16 CAR-mbIL15-safety switch T cells PRGN-3005 into the patient, the T cells target and bind to MUC16-expressing tumor cells, thereby inducing selective toxicity in MUC16-expressing tumor cells. MUC16, a member of the mucin family of glycoproteins, is overexpressed on a variety of cancer cell types. IL-15 is a pro-survival cytokine that is required for the maintenance of long-lived CD8+ memory T cells and use of mbIL15 preserves T stem-cell memory (TSCM) through sustained IL-15 signaling, improves T-cell persistence and potentiates the immune response against tumor cells. The safety switch can promote selective elimination of the CAR-T cells. The SB system permits integration of the CAR, the IL-15 fusion variant and safety switch transgenes into T cells without the need for viral vectors and accelerates the manufacturing process.

Table 1. Record
IdentifierMLC-T-ONC-011481
FieldOncology and biomedicine
SynonymsTGFbR1 inhibitor PF-06952229; autologous CAR-T cells PRGN 3005; autologous PRGN-3005 UltraCAR-T cells; PRGN-3005 UltraCAR-T cells; autologous anti-MUC16 CAR-T cells PRGN-3005
ReferencesNational Cancer Institute Thesaurus (CC BY 4.0)
Record as JSON
{
  "id": "MLC-T-ONC-011481",
  "term": "Autologous anti-MUC16 CAR-mbIL15-safety switch T cells PRGN-3005",
  "field": "Oncology and biomedicine",
  "definition": "A preparation of autologous T lymphocytes that have been genetically modified to co-express three transgenes using the Sleeping Beauty (SB) transposon system and include a chimeric antigen receptor (CAR) targeting the unshed portion of the tumor-associated antigen (TAA) human mucin 16 (MUC16, cancer antigen 125; CA125; FLJ14303), a membrane-bound IL-15 (mbIL15) and a safety/kill switch, with potential immunostimulating and antineoplastic activities. Upon introduction of the autologous anti-MUC16 CAR-mbIL15-safety switch T cells PRGN-3005 into the patient, the T cells target and bind to MUC16-expressing tumor cells, thereby inducing selective toxicity in MUC16-expressing tumor cells. MUC16, a member of the mucin family of glycoproteins, is overexpressed on a variety of cancer cell types. IL-15 is a pro-survival cytokine that is required for the maintenance of long-lived CD8+ memory T cells and use of mbIL15 preserves T stem-cell memory (TSCM) through sustained IL-15 signaling, improves T-cell persistence and potentiates the immune response against tumor cells. The safety switch can promote selective elimination of the CAR-T cells. The SB system permits integration of the CAR, the IL-15 fusion variant and safety switch transgenes into T cells without the need for viral vectors and accelerates the manufacturing process.",
  "synonyms": [
    "TGFbR1 inhibitor PF-06952229",
    "autologous CAR-T cells PRGN 3005",
    "autologous PRGN-3005 UltraCAR-T cells",
    "PRGN-3005 UltraCAR-T cells",
    "autologous anti-MUC16 CAR-T cells PRGN-3005"
  ],
  "references": [
    "National Cancer Institute Thesaurus"
  ],
  "url": "https://mlchart.com/terminology/oncology/autologous-anti-muc16-car-mbil15-safety-switch-t-cells-prgn-3005/"
}

Record 2,813 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.