Biochemical experiments have established that the metabolism of inositol ph
ospholipids by phosphoinositide 3-kinases (PI3Ks) and lipid-phosphatases is
triggered by many receptors that control T lymphocyte function, including
antigen-receptors, costimulatory molecules, cytokines and chemokines. Novel
effectors of P13K have been identified in the immune system and shown to b
e important in the control of lymphocyte activation. Moreover, key lipid-ph
osphatases have been identified that act to terminate or modulate P13K sign
alling in cells of the immune system.