In this review, we describe the evidence from which the existence of non-MH
C histocompatibility (H) antigens was deduced, the clinical setting of bone
marrow transplantation in which they are important targets for T-cell resp
onses, and the current understanding of their molecular identity. We list t
he peptide epitopes of the human and murine minor H antigens now identified
at the molecular level, their MHC restriction molecules and the genes enco
ding them. Identification of the peptide epitopes allows T-cell responses t
o these antigens following transplantation of MHC-matched, minor H-mismatch
ed tissues to be enumerated using tetramers and elispot assays. This will f
acilitate analysis of correlations with host-versus-graft (HVG), graft-vers
us-host (GVH) and graft-versus-leukaemia (GVL) reactions in vivo. The poten
tial to use minor H peptides to modulate in vivo responses to minor H antig
ens is discussed. Factors controlling immunodominance of T-cell responses t
o one or a few of many potential minor H antigens remain to be elucidated b
ut are important for making predictions of in vivo HVG, GVH and GVL respons
es and tailoring therapy after HLA-matched bone marrow transplantation and
donor lymphocyte infusion.