We have determined accompanying events and reviewed the management and
outcome of late acute cellular rejection episodes in 384 consecutive
liver recipients. A significant proportion of patients experienced con
comitant viral infection (group 1, n=15 [41%]), with CMV infection com
prising the largest group and smaller contributions from other viruses
(CMV, 30%; HSV, 5%; EBV, 3%; varicella zoster virus, 3%). Thirteen (3
5%) patients (group 2) developed late rejection associated with low ma
intenance immunosuppression, and in a further 10 patients (group 3), n
o accompanying factor could be identified. Refractory rejection was hi
gher in late compared with early rejection episodes in our series (29%
vs. 9.2%, P<0.05). Antiviral chemotherapy administered in rejection e
pisodes with concomitant viral infection, either as sole treatment in
cases with accompanying hepatitis or as adjunctive therapy to further
supplemental immunosuppression in episodes of steroid-resistant reject
ion, controlled the rejection process in all treated patients.