Jt. Flynn et al., INTRAVENOUS IMMUNOGLOBULIN PROPHYLAXIS OF CYTOMEGALOVIRUS-INFECTION IN PEDIATRIC RENAL-TRANSPLANT RECIPIENTS, American journal of nephrology, 17(2), 1997, pp. 146-152
Cytomegalovirus (CMV), the most significant infectious cause of morbid
ity following renal transplantation, may be a greater problem for chil
dren than for adults due to their relative lack of experience with thi
s virus. Therefore, we prospectively gave Gammagard(R) as prophylaxis
to CMV-negative children who received CMV-positive allografts and comp
ared the results to our experience with similar high-risk recipients t
ransplanted prior to our use of intravenous immunoglobulin G (IvIgG).
Symptomatic CMV disease developed in 17% of the IvIgG recipients as co
mpared with 71% of the untreated patients (p = 0.01). The CMV infectio
ns that did occur in IvIgG recipients developed significantly later th
an in untreated children (median time of onset after transplantation 2
.60 vs. 1.35 months; p < 0.05) and generally were less severe, althoug
h 1 IvIgG recipient died despite prophylaxis. IvIgG administration did
not affect the frequency of rejection or graft or patient survival. W
e conclude that IvIgG administration to high-risk pediatric renal tran
splant recipients may protect against posttransplantation CMV disease
and may lessen the severity of infections that do develop in patients
who receive it.