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CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic vaccinia Virus VET3-TGI

Term · Oncology and biomedicine · MLC-T-ONC-012847

An oncolytic vaccinia virus (VV) genetically engineered to express C-X-C chemokine receptor type 3 (CXCR3), the human pro-inflammatory cytokine interleukin-12 (IL-12), and an inhibitor of transforming growth factor (TGF)-beta 1 (TGFb1; TGF-b1), with potential immunomodulating and antineoplastic activities. Upon administration of CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic VV VET3-TGI, the virus preferentially targets, infects and replicates in tumor cells, particularly tumor cells expressing CXCR3 ligands, causing oncolysis. In turn, the lysed tumor cells release various tumor-associated antigens (TAAs), which induce an immune response against the tumor cells. In addition, CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic VV VET3-TGI promotes the secretion of IL-12 and the TGFb1 inhibitor in the tumor microenvironment (TME). IL-12 activates natural killer cells (NKs), induces the secretion of interferon-gamma (IFNg) and promotes CD8 cytotoxic T-lymphocyte (CTL) responses against tumor cells, which may result in immune-mediated tumor cell death and inhibition of tumor cell proliferation. The inhibition of TGFb1 prevents TGFb1-mediated signaling. This abrogates TGFb1-mediated immunosuppression, enhances anti-tumor immunity in the TME and further promotes CTL-mediated immune response against tumor cells. The TGF-beta signaling pathway is often deregulated in tumors and plays a key role in immunosuppression in the TME. TGFb1 is the predominant isoform in many tumors.

Table 1. Record
IdentifierMLC-T-ONC-012847
FieldOncology and biomedicine
SynonymsCXCR3/IL-12/TGF-beta inhibitor engineered oncolytic vaccinia virus VET3-TGI; CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic VV VET3-TGI
ReferencesNational Cancer Institute Thesaurus (CC BY 4.0)
Record as JSON
{
  "id": "MLC-T-ONC-012847",
  "term": "CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic vaccinia Virus VET3-TGI",
  "field": "Oncology and biomedicine",
  "definition": "An oncolytic vaccinia virus (VV) genetically engineered to express C-X-C chemokine receptor type 3 (CXCR3), the human pro-inflammatory cytokine interleukin-12 (IL-12), and an inhibitor of transforming growth factor (TGF)-beta 1 (TGFb1; TGF-b1), with potential immunomodulating and antineoplastic activities. Upon administration of CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic VV VET3-TGI, the virus preferentially targets, infects and replicates in tumor cells, particularly tumor cells expressing CXCR3 ligands, causing oncolysis. In turn, the lysed tumor cells release various tumor-associated antigens (TAAs), which induce an immune response against the tumor cells. In addition, CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic VV VET3-TGI promotes the secretion of IL-12 and the TGFb1 inhibitor in the tumor microenvironment (TME). IL-12 activates natural killer cells (NKs), induces the secretion of interferon-gamma (IFNg) and promotes CD8 cytotoxic T-lymphocyte (CTL) responses against tumor cells, which may result in immune-mediated tumor cell death and inhibition of tumor cell proliferation. The inhibition of TGFb1 prevents TGFb1-mediated signaling. This abrogates TGFb1-mediated immunosuppression, enhances anti-tumor immunity in the TME and further promotes CTL-mediated immune response against tumor cells. The TGF-beta signaling pathway is often deregulated in tumors and plays a key role in immunosuppression in the TME. TGFb1 is the predominant isoform in many tumors.",
  "synonyms": [
    "CXCR3/IL-12/TGF-beta inhibitor engineered oncolytic vaccinia virus VET3-TGI",
    "CXCR3/IL-12/TGFb1 inhibitor engineered oncolytic VV VET3-TGI"
  ],
  "references": [
    "National Cancer Institute Thesaurus"
  ],
  "url": "https://mlchart.com/terminology/oncology/cxcr3-il-12-tgfb1-inhibitor-engineered-oncolytic-vaccinia-virus-vet3-tgi/"
}

Record 5,544 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.