Altering T-cell activation by targeting the multidomain tyrosine kinase Itk

The Tec family non-receptor tyrosine kinase Itk is expressed in T cells, natural killer (NK) cells and mast cells. The role of this multidomain kinase in T cells has been linked to T-cell receptor–CD3 (TCR–CD3) signaling and Itk regulates and amplifies signals through the costimulatory receptors CD28 and CD2. Itk binds a specific subset of membrane inositol phospholipids through its pleckstrin homology (PH) domain; it forms functional molecular complexes with a variety of signaling proteins through its Tec homology (TH), Src homology 3 (SH3) and SH2 domains; and it phosphorylates several protein substrates on tyrosine residues in cells. Among >500 protein kinases expressed in the human proteome, we propose that Itk is a validated T-cell target suitable for pharmaceutical intervention. Targeted disruption of protein–protein interactions between Itk and some of its binding partners, and inhibition of the intrinsic kinase activity of Itk, could provide platforms through which to alter T-cell activation in immunological and inflammatory disorders.