Adoptive cellular immunotherapy using ex vivo expanded allogeneic gamma-delta (Vγ9Vδ2) T lymphocytes that recognize phosphoantigens via BTN3A1/BTN2A1 and stress ligands via NKG2D to mediate HLA-independent cytotoxicity.
Ex vivo expanded allogeneic Vγ9Vδ2 T cells that recognize tumor-associated phosphoantigens via BTN3A1/BTN2A1 and stress-induced ligands via NKG2D, enabling HLA-independent cytotoxicity through perforin/granzyme release and cytokine production.
Allogeneic Vγ9Vδ2 T cells recognize phosphoantigen-induced BTN3A1/BTN2A1 complexes on target cells via their TCR and directly lyse them through perforin/granzyme release (with supportive cytokine-mediated cytotoxicity).
Adoptive cellular immunotherapy using ex vivo expanded allogeneic gamma-delta (Vγ9Vδ2) T lymphocytes that recognize phosphoantigens via BTN3A1/BTN2A1 and stress ligands via NKG2D to mediate HLA-independent cytotoxicity.
Ex vivo expanded allogeneic Vγ9Vδ2 T cells that recognize tumor-associated phosphoantigens via BTN3A1/BTN2A1 and stress-induced ligands via NKG2D, enabling HLA-independent cytotoxicity through perforin/granzyme release and cytokine production.
Vγ9Vδ2 T cells engage the BTN3A1/BTN2A1 complex induced by phosphoantigens on target cells, activating HLA‑independent cytotoxicity and killing via perforin/granzyme (and death‑receptor) pathways.
Adoptive cellular immunotherapy using ex vivo expanded allogeneic gamma-delta (Vγ9Vδ2) T lymphocytes that recognize phosphoantigens via BTN3A1/BTN2A1 and stress ligands via NKG2D to mediate HLA-independent cytotoxicity.
Ex vivo expanded allogeneic Vγ9Vδ2 T cells that recognize tumor-associated phosphoantigens via BTN3A1/BTN2A1 and stress-induced ligands via NKG2D, enabling HLA-independent cytotoxicity through perforin/granzyme release and cytokine production.
MICA is an NKG2D ligand; allogeneic Vγ9Vδ2 T cells bind MICA via NKG2D and directly kill target cells through perforin/granzyme release (and death receptor pathways).
Adoptive cellular immunotherapy using ex vivo expanded allogeneic gamma-delta (Vγ9Vδ2) T lymphocytes that recognize phosphoantigens via BTN3A1/BTN2A1 and stress ligands via NKG2D to mediate HLA-independent cytotoxicity.
Ex vivo expanded allogeneic Vγ9Vδ2 T cells that recognize tumor-associated phosphoantigens via BTN3A1/BTN2A1 and stress-induced ligands via NKG2D, enabling HLA-independent cytotoxicity through perforin/granzyme release and cytokine production.
Vγ9Vδ2 T cells engage MICB via NKG2D, triggering degranulation and killing target cells through perforin/granzyme-mediated cytotoxicity.
Adoptive cellular immunotherapy using ex vivo expanded allogeneic gamma-delta (Vγ9Vδ2) T lymphocytes that recognize phosphoantigens via BTN3A1/BTN2A1 and stress ligands via NKG2D to mediate HLA-independent cytotoxicity.
Ex vivo expanded allogeneic Vγ9Vδ2 T cells that recognize tumor-associated phosphoantigens via BTN3A1/BTN2A1 and stress-induced ligands via NKG2D, enabling HLA-independent cytotoxicity through perforin/granzyme release and cytokine production.
Vγ9Vδ2 T cells express NKG2D, which binds ULBP1 on target cells, triggering activation and direct killing via perforin/granzyme-mediated cytotoxicity (and death receptor pathways).