Marrow transplants from human leukocyte antigen (HLA)-compatible unrel
ated volunteer donors have become feasible for more than 30% of patien
ts without a family match and have allowed long-term, disease-free sur
vival in 15-65% of patients with a variety of hematological disorders.
However, unrelated donor transplants have a higher incidence of graft
failure and graft versus host disease (GVHD) than do HLA-matched sibl
ing transplants. This increase may be due to disparities between donor
and recipient for undetected HLA determinants or for non-HLA histocom
patibility genes. Because of the large number of HLA loci and their hi
gh degree of polymorphism fully compatible donors will not be found fo
r most patients, Fortunately, a limited degree of HLA mismatch does no
t necessarily impair long-term survival in patients with hematologic m
alignancy. Current studies ai-e defining the risk associated with mism
atching for each histocompatibility locus and are developing methods f
or marrow transplantation that can decrease morbidity and improve surv
ival despite genetic disparity between donor and recipient.