Allogeneic CD123CAR-CD28-CD3zeta-EGFRt-expressing T lymphocytes
Term · Oncology and biomedicine · MLC-T-ONC-009839
A preparation of genetically modified allogeneic T cells transduced with a replication-incompetent, self-inactivating lentiviral vector expressing a hinge-optimized, chimeric antigen receptor (CAR), comprised of a CD28 co-stimulatory signaling domain fused to CD3 zeta, the single-chain variable fragment of CD123 antigen (interleukin-3 receptor alpha chain or IL3RA), and a truncated form of the human epidermal growth factor receptor (EGFRt), with potential immunostimulating and antineoplastic activities. Upon intravenous administration, allogeneic CD123CAR-CD28-CD3zeta-EGFRt-expressing T lymphocytes are directed to and induce selective toxicity in CD123-expressing tumor cells. CD123 is normally expressed on committed blood progenitor cells in the bone marrow; its overexpression is associated with increased leukemic cell proliferation and aggressiveness. Devoid of both ligand binding domains and tyrosine kinase activity, EGFRt both facilitates detection of the administered T cells in vivo and can promote elimination of those cells following a cetuximab-induced antibody-dependent cellular cytotoxicity (ADCC) response. The costimulatory signaling domain enhances both proliferation of T cells and antitumor activity. Hinge optimization prevents recognition of the CAR by Fc receptors (FcRs).
| Identifier | MLC-T-ONC-009839 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | allogeneic CD123R(EQ)28zeta/EGFRt+ T cells |
| References | National Cancer Institute Thesaurus (CC BY 4.0) |
Record as JSON
{
"id": "MLC-T-ONC-009839",
"term": "Allogeneic CD123CAR-CD28-CD3zeta-EGFRt-expressing T lymphocytes",
"field": "Oncology and biomedicine",
"definition": "A preparation of genetically modified allogeneic T cells transduced with a replication-incompetent, self-inactivating lentiviral vector expressing a hinge-optimized, chimeric antigen receptor (CAR), comprised of a CD28 co-stimulatory signaling domain fused to CD3 zeta, the single-chain variable fragment of CD123 antigen (interleukin-3 receptor alpha chain or IL3RA), and a truncated form of the human epidermal growth factor receptor (EGFRt), with potential immunostimulating and antineoplastic activities. Upon intravenous administration, allogeneic CD123CAR-CD28-CD3zeta-EGFRt-expressing T lymphocytes are directed to and induce selective toxicity in CD123-expressing tumor cells. CD123 is normally expressed on committed blood progenitor cells in the bone marrow; its overexpression is associated with increased leukemic cell proliferation and aggressiveness. Devoid of both ligand binding domains and tyrosine kinase activity, EGFRt both facilitates detection of the administered T cells in vivo and can promote elimination of those cells following a cetuximab-induced antibody-dependent cellular cytotoxicity (ADCC) response. The costimulatory signaling domain enhances both proliferation of T cells and antitumor activity. Hinge optimization prevents recognition of the CAR by Fc receptors (FcRs).",
"synonyms": [
"allogeneic CD123R(EQ)28zeta/EGFRt+ T cells"
],
"references": [
"National Cancer Institute Thesaurus"
],
"url": "https://mlchart.com/terminology/oncology/allogeneic-cd123car-cd28-cd3zeta-egfrt-expressing-t-lymphocytes/"
}
Record 725 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.