Engagement of surface Compound Library datasheet receptors other than TCR also contributes to the induction or regulation of Vγ9Vδ2 T-cell responses. Vγ9Vδ2 T cells express several types of NK cell receptors (NKRs), which can increase (i.e. NKR-P1A) or decrease (i.e. ILT2 or NKG2A/CD94) TCR activation 21–23, whereas other surface receptors (i.e. CD16, CD224) can directly trigger a Vγ9Vδ2 T-cell response

24, 25. NKG2D, a homodimeric C-type lectin-like receptor, has this ability to directly trigger Vγ9Vδ2 T-cell functions 26. Particularly, anti-tumor cytotoxic activity of Vγ9Vδ2 T cells is triggered and regulated not only upon TCR-dependent antigen recognition but also through the ligation of NKG2D by its ligands 27. BGB324 purchase In humans, the ligands of NKG2D are the MHC class I-related chain proteins A and B (MICA/B) and UL16-binding proteins (ULBP) 1–4. Their expression is induced or upregulated on tumor and virus-infected cells 28. Nevertheless, while evidence of NKG2D contribution has been demonstrated in the anti-tumor response of Vγ9Vδ2 T cells 27, no direct role in their anti-infectious response has yet been reported. Moreover, the upregulation of MICA at the surface of Mycobacterium tuberculosis-infected DCs results

in a significant increase of the TCR-dependent Vγ9Vδ2 T-cell effector functions 29. However, the role played by the interaction of NKG2D with its ligands during anti-infectious activity of Vγ9Vδ2 T cells remains to be clarified. To further address this issue, we analyzed the role of NKG2D recruitment in a bacterial infection model. First, we demonstrated that NKG2D ligands (such as ULBP1 and ULBP2) trigger TNF-α and IFN-γ production and the release of lytic granules through their interaction with NKG2D and the triggering Cepharanthine of PI3K-dependent

intracellular signaling pathways. Moreover, concomitant TCR and NKG2D engagement led to stronger effector functions of Vγ9Vδ2 T cells. In vitro, the impairment of NKG2D recruitment decreases the anti-infectious activity of Vγ9Vδ2 T cells, leading to a higher development of Brucella in infected macrophages. ULBP1 is the main NKG2D ligand expressed by Brucella-infected macrophages and is involved in the impairment of intramacrophagic bacterial development. Altogether, these results provide evidence that NKG2D and its ligands are involved, at least in part, in the anti-infectious effect of Vγ9Vδ2 T cells. To study the role of NKG2D in Vγ9Vδ2 T-cell functions, we used two fusion proteins ULBP1-leucine zipper (LZ) and ULBP2-LZ composed of the ULBP1 or ULBP2 soluble part (two NKG2D ligands) and a LZ domain previously described in 30. While UL16-LZ, a control protein that is not a NKG2D ligand shows no detectable binding to Vγ9Vδ2 T cells, ULBP1-LZ and ULBP2-LZ do. This interaction is completely blocked by the presence of a blocking anti-NKG2D mAb (M585) (Fig. 1A).