The human leukocyte antigens (HLA) encoded by genes within the major histoc
ompatibility complex display an impressive degree of polymorphism. This var
iability is apparently maintained in human populations through the need to
successfully display a wide range of processed foreign peptides to the T ce
ll antigen receptor. The large number of alleles at the Class I and Class I
I loci pose a significant problem for molecular diagnosis. Knowledge of all
ele groups and specific alleles present in individuals has important implic
ations in organ and stem cell transplantation and in disease association st
udies. Histocompatibility laboratories have transformed themselves during t
he past decade as they have adapted the techniques of molecular diagnostics
to the challenge of identifying HLA alleles.