The role of cytomegalovirus infection in allograft injury is controver
sial. A subgroup of renal graft recipients who bad histologically prov
en late-acute rejection did not respond to conventional anti-rejection
therapy (80% graft loss within 1 year). These patients showed an expa
nsion of memory-type CD8 peripheral-blood T cells that expressed inter
feron-gamma mRNA and an association with clinically symptomless cytome
galovirus infection (82% PCR positive, 42% antigenaemia). Antiviral th
erapy with ganciclovir resulted in stable improved graft function in 1
7 of 21 treated patients with cytomegalovirus-associated late-acute re
jection. The results underline the clinical relevance of cytomegalovir
us-related graft injury and offer a novel therapeutic approach.