Allogeneic CRISPR-edited Anti-CD19 CAR T Cells PBLTT52CAR19
Term · Oncology and biomedicine · MLC-T-ONC-009871
A preparation of allogeneic T-lymphocytes transduced with a lentiviral vector encoding a chimeric antigen receptor (CAR) specific for the tumor-associated antigen (TAA) CD19, with genetic modification of CD52 and T-cell receptor alpha constant (TRAC) loci via clustered regularly interspaced short palindromic repeats (CRISPR), with potential immunostimulating and antineoplastic activities. Upon administration, the allogeneic CRISPR-edited anti-CD19 CAR T cells PBLTT52CAR19 recognize and bind to CD19-overexpressing tumor cells. This may result in a specific cytotoxic T-lymphocyte (CTL)-mediated killing of CD19-positive tumor cells. CD19 antigen is a B-cell specific cell surface antigen expressed in all B-cell lineage malignancies. The editing of the CD52 gene may make the modified donor T-cells resistant to the anti-CD52 monoclonal antibody alemtuzumab, which is used during lymphodepletion. The editing of the TRAC may eliminate TCR expression, which may abrogate the potential induction of graft-versus-host disease (GvHD) by the donor T-cells, and may also result in uniform CAR expression and enhanced T-cell potency.
| Identifier | MLC-T-ONC-009871 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | Allogeneic CRISPR-edited Anti-CD19 CAR T-cells PBLTT52CAR19; Allogeneic CRISPR-edited Anti-CD19 CAR-T Cells PBLTT52CAR19 |
| References | National Cancer Institute Thesaurus (CC BY 4.0) |
Record as JSON
{
"id": "MLC-T-ONC-009871",
"term": "Allogeneic CRISPR-edited Anti-CD19 CAR T Cells PBLTT52CAR19",
"field": "Oncology and biomedicine",
"definition": "A preparation of allogeneic T-lymphocytes transduced with a lentiviral vector encoding a chimeric antigen receptor (CAR) specific for the tumor-associated antigen (TAA) CD19, with genetic modification of CD52 and T-cell receptor alpha constant (TRAC) loci via clustered regularly interspaced short palindromic repeats (CRISPR), with potential immunostimulating and antineoplastic activities. Upon administration, the allogeneic CRISPR-edited anti-CD19 CAR T cells PBLTT52CAR19 recognize and bind to CD19-overexpressing tumor cells. This may result in a specific cytotoxic T-lymphocyte (CTL)-mediated killing of CD19-positive tumor cells. CD19 antigen is a B-cell specific cell surface antigen expressed in all B-cell lineage malignancies. The editing of the CD52 gene may make the modified donor T-cells resistant to the anti-CD52 monoclonal antibody alemtuzumab, which is used during lymphodepletion. The editing of the TRAC may eliminate TCR expression, which may abrogate the potential induction of graft-versus-host disease (GvHD) by the donor T-cells, and may also result in uniform CAR expression and enhanced T-cell potency.",
"synonyms": [
"Allogeneic CRISPR-edited Anti-CD19 CAR T-cells PBLTT52CAR19",
"Allogeneic CRISPR-edited Anti-CD19 CAR-T Cells PBLTT52CAR19"
],
"references": [
"National Cancer Institute Thesaurus"
],
"url": "https://mlchart.com/terminology/oncology/allogeneic-crispr-edited-anti-cd19-car-t-cells-pbltt52car19/"
}
Record 757 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.