A 16-year-old Sardinian girl affected by homozygous beta-thalassaemia
was submitted to allogeneic BMT using an HLA-identical, MLC-negative,
unrelated donor, The donor and the patient were homozygous for the ent
ire extended haplotype A30, Cw5, B18, F130, DRB10301, DRB3*0202, DQA1
0501, DQB1*0201 and heterozygous for DPB1*0301/DPB1*0202. The conditi
oning regimen consisted of 14 mg/kg busulphan and 160mg/kg cyclophosph
amide, Engraftment was achieved 14 days from BMT and the haematologica
l reconstitution was complete without any signs of acute or chronic GV
HD. Seven months after the transplant the patient was in excellent gen
eral condition. The hypothesis is advanced that when two HLA extended
haplotypes are shared by donors and recipients, particularly in homozy
gosity, this is a very favourable immunogenetic condition in unrelated
BMT.