During the past year, a plethora of structural information has provided det
ailed insights into the interactions between classical MHC class I molecule
s and their cognate receptors on T cells. Likewise, there have been major a
dvances in our knowledge of the structures and functions of five nonclassic
al MHC-like molecules: HLA-DM (murine H2-M), HLA-E, HFE, ZAG and MIC-A.