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Vγ9Vδ2 T cells

Development stage
Phase 2
Lead developer
The University of Tokyo Hospital
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

Vγ9Vδ2 T cells are a distinct subset of human γδ (gamma delta) T lymphocytes characterized by their expression of the Vγ9 and Vδ2 chains in their T cell receptor (TCR). They represent the predominant γδ T cell population in adult human peripheral blood. These cells recognize non-peptidic phosphoantigens independently of major histocompatibility complex (MHC) molecules and play a critical role in immune surveillance against infections and tumors. In cancer immunotherapy, adoptive transfer or ex vivo expansion of autologous or allogeneic Vγ9Vδ2 T cells is being explored for hematological malignancies and solid tumors. Their mechanisms include direct cytotoxicity via perforin/granzyme pathways, antibody-dependent cellular cytotoxicity (ADCC), cytokine production (e.g., IFN-γ, TNF-α), cross-presentation of tumor antigens to CD8+ αβTCR+ cytotoxic lymphocytes, and immune regulation through interactions with B-cells and dendritic cells. Clinical trials have tested zoledronate-expanded autologous or allogeneic infusions for cancers such as non-small cell lung cancer (NSCLC) and multiple myeloma; genetic engineering approaches like CAR-modified Vγ9Vδ2 are also under investigation[1][6][7].

Other names
Vgamma9Vdelta2 T cellsVgamma-9Vdelta2 T cellsVgamma 9Vdelta2 T cellshuman Vγ9Vδ2 T lymphocytes
02

Targets

FCGR3B (Fc gamma receptor III)BTN3A1 (Butyrophilin 3A1/2A1 complex)

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