In this analysis, we introduce a new categorization of HLA DR alleles
which are important members of HLA class II genes encoding cell surfac
e glycoproteins that function to present antigenic peptides to T cells
. We have grouped all HLA DR molecules into seven different functional
categories on the basis of their ability to bind and present antigeni
c peptides to T cells and their association with susceptibility or res
istance to disease. This novel categorization of DR alleles on the bas
is of function allows for the prediction of seven similar subregion st
ructures (supertypes or supermotifs) within pocket 4 of HLA DR peptide
binding groove as the molecular basis for grouping these alleles. The
physicochemical characteristics of HLA DR supertype residues, charge
in particular, may influence the selectivity for binding peptide, domi
nate promiscuous T-cell recognition of antigenic peptides, and affect
HLA DR disease associations. To rationalize the functional categories
of DR alleles, we have further combined the seven DR supertype pattern
s into three groups based on the charges of residues within the supert
ypes. Grouping HLA DR alleles into functional categories may assist in
understanding the mechanistic basis of autoimmunity, resolving curren
t paradoxes in HLA disease associations, and developing new immunother
apy strategies.