HLA polymorphism varies among different racial origins. Certain antige
ns are restricted to a particular ethnic group, suggesting that geneti
c events might have generated further unique polymorphism following ra
cial diversification. In this study, we have identified and characteri
zed a novel HLA-A allele, officially designated A8001. The class I mo
lecule, HLA-AXBG, encoded by this allele could not be defined by commo
nly available HLA antisera. We have identified two alloantisera that a
ppear to be monospecific for this new antigen. The observed frequency
of AXBG antigen specificity is 2% in African Americans among the total
of 254 tested, but it has not been found in 305 Caucasians tested. IE
F and cDNA sequencing analyses on multiple individuals revealed that A
XBG antigen defined by the two antisera are encoded by an identical HL
A-A8001 allele and it has a number of unique amino acid residues that
have not been observed among other HLA-A alleles but are known to occ
ur in certain human nonclassic class I genes and nonhuman primate clas
s I genes. The ability to identify the new HLA-AXBG antigen will impro
ve the precision of HLA-A typing in black populations and enable us to
match a patient with a donor for this otherwise undefined antigen in
transplantation.