Differential cross-matches have been proposed to allow immunised patie
nts to be grafted, whereas the dogma of a global positive cross-match
discarded them from renal transplantation. We report our one-center ex
perience considering current T positive cross-match as the only contra
-indication to grafting, as well as patients whose sera comprise speci
fic anti-donnor antibodies. A comprehensive characterization of the an
tibodies was achieved by identification of auto-antibodies and specifi
cation of IgM and IgG isotype, class I and class II specificities, as
well as HLA specificities. The differential cross-match comprised an a
uto and an allo-cross-match, against T and B lymphocytes. Historical a
nd current sera were analysed either untreated or after DTT;treatment,
at + 4 degrees C and + 22 degrees C. We performed 79 renal transplant
ations across positive crossmatches, which were 20 historical T positi
ve cross-matches, 26 historical B positive cross-matches and 33 curren
t B positive cross-matches. Results and graft survival were strictly i
dentical as those obtained in the transplantations achieved with negat
ive cross-matches throughout the same period, especially in sensitized
patients. Current positive B cell cross-matches due to IgG were assoc
iated with an increased risk for early graft failure. We conclude that
differential cross-match is a safe strategy permitting immunised pati
ents to be grafted.