Kosman C, Steiner N, Pulyaeva H, Mitton W, Slack R, Hartzman R J, Ng J, Hurley C K
Department of Microbiology, Georgetown University Medical Center, Washington, DC 20007, USA.
Tissue Antigens. 2000 May;55(5):437-42. doi: 10.1034/j.1399-0039.2000.550506.x.
The antigen encoded by B5002 differs in sequence from that encoded by B5001 only at amino acid residue 167 (consensus tryptophan vs. serine) which results in B45 serologic reactivity. To search for B5002, the frequencies of alleles encoding the serologically defined B45 antigen were determined by sequence-based typing in 5 major U.S. populations: Caucasians, African Americans, Asians/Pacific Islanders, Hispanics, and Native Americans. The percent of serologically defined B45-positive individuals in the 5 populations ranged from 0.7-9.0%. Thirty-two B45-positive individuals were randomly chosen, when available, for sequence-based typing from each ethnic group from a database of 82,979 consecutively typed unrelated individuals. The B5002 allele was most prevalent in Hispanic (22%) and Caucasian (9%) individuals, while conspicuously absent in African Americans. In addition, a new allele associated with the B45 antigenic specificity, B4502, has been identified from an African American individual of Middle Eastern descent. In light of the continuing need to reconcile differences between relationships determined by the sequence homologies among alleles and relationships based on the serologic determinants carried by allelic products when determining the level of HLA match for hematopoietic stem cell transplantation, it is suggested that B5002 be recognized individually from other B*50 alleles when reporting HLA-B typings for clinical purposes.