The impact of the non‐classical MHC proteins HLA‐DM and HLA‐DO on loading of MHC class II molecules

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Abstract
Summary: Peptide binding to classical major histocompatibility complex (MHC) class II molecules is known to be determined by the properties of the class ii peptide binding groove but recently it turned out to be co‐controlled by the activity of the non‐classical MHC molecules HLA‐DM and HLA‐DO: HLA‐DM functions as a mediator of peptide exchange. In addition, HLA‐DM is a chaperone for MHC class II molecules in endosomal and lysosomal loading compartments because it stabilizes the empty MHC class Ii peptide binding groove and keeps it receptive for peptide loading until appropriate peptide ligands are captured. Since HLA‐DM favors the generation of high‐stability peptide‐MHC class Ii complexes by releasing low‐stability peptide ligands, DM activity affects the peptide repertoire presented on the ceil surface of antigen‐presenting cells. HLA‐DO is expressed mainly in B cells and binds tightly to HLA‐DM thereby modulating its activity Together, HLA‐DM and HLA‐DO are critical factors in shaping the MHC class Il‐associated self or foreign peptide repertoire of antigen presenting cells and, hence, govern initiation or prevention of an immune response.