protein-engineered interleukin-2 XTX202
Term · Oncology and biomedicine · MLC-T-ONC-016265
A modified form of the recombinant form of human endogenous cytokine interleukin-2 (IL-2), that is masked with a protein domain, with potential immunoregulatory and antineoplastic activities. Upon administration of protein-engineered IL-2 XTX202, IL-2 is bound to the protein and pharmacologically inactive. IL-2 does not become active until cleaved by specific proteases in the tumor microenvironment (TME). Upon proteolytic cleavage, unbound and active IL-2 locally binds to the IL-2 receptor beta (CD122) and gamma (CD132) subunits (IL2Rb/g) that are expressed on CD8+ T-effector cells and natural killer (NK) cells, thereby activating IL2R-mediated signaling within these immune cells. The activation of T cells and NK cells mediate cytolytic immune responses against tumor cells causing tumor cell destruction and inhibition of tumor cell proliferation. XTX202 does not bind to IL-2 receptor alpha (IL-2Ra) and does not cause IL-2Ra-mediated toxicities. The selective activation in the TME enhances the IL-2-mediated cytolytic responses against tumor cells while sparing the unwanted effects of systemic, peripheral immune activation.
| Identifier | MLC-T-ONC-016265 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | engineered IL-2 prodrug XTX202; modified IL-2 XTX202; protein-engineered IL-2 XTX202; tumor-selective IL-2 XTX202 |
| References | National Cancer Institute Thesaurus (CC BY 4.0) |
Record as JSON
{
"id": "MLC-T-ONC-016265",
"term": "protein-engineered interleukin-2 XTX202",
"field": "Oncology and biomedicine",
"definition": "A modified form of the recombinant form of human endogenous cytokine interleukin-2 (IL-2), that is masked with a protein domain, with potential immunoregulatory and antineoplastic activities. Upon administration of protein-engineered IL-2 XTX202, IL-2 is bound to the protein and pharmacologically inactive. IL-2 does not become active until cleaved by specific proteases in the tumor microenvironment (TME). Upon proteolytic cleavage, unbound and active IL-2 locally binds to the IL-2 receptor beta (CD122) and gamma (CD132) subunits (IL2Rb/g) that are expressed on CD8+ T-effector cells and natural killer (NK) cells, thereby activating IL2R-mediated signaling within these immune cells. The activation of T cells and NK cells mediate cytolytic immune responses against tumor cells causing tumor cell destruction and inhibition of tumor cell proliferation. XTX202 does not bind to IL-2 receptor alpha (IL-2Ra) and does not cause IL-2Ra-mediated toxicities. The selective activation in the TME enhances the IL-2-mediated cytolytic responses against tumor cells while sparing the unwanted effects of systemic, peripheral immune activation.",
"synonyms": [
"engineered IL-2 prodrug XTX202",
"modified IL-2 XTX202",
"protein-engineered IL-2 XTX202",
"tumor-selective IL-2 XTX202"
],
"references": [
"National Cancer Institute Thesaurus"
],
"url": "https://mlchart.com/terminology/oncology/protein-engineered-interleukin-2-xtx202/"
}
Record 13,765 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.