Study objectives: The incidence of posttransplant lymphoproliferative disor
der (PTLD) has been reported to range from 6.4 to 20% in lung transplant (L
T) recipients. Postulated contributing factors include Epstein-Barr virus (
EBV) infection and the use of immunosuppression, particularly muromonab-CD3
(OKT3)(Orthoclone OKT-3; Ortho Biotech; Raritan, NJ). We sought to examine
these PTLD risk factors in 109 LT recipients at our institution who surviv
ed >1 month.
Design: Retrospective review of EBV serology of all LT recipients at our in
stitution. Our standard transplant protocol includes OKT3 for induction and
refractory rejection, as well as lifelong acyclovir for herpes prophylaxis
, We do not perform EBV donor-recipient matching.
Setting: A university-based LT center.
Results: We found that 5 of 109 patients were serologically negative for EB
V prior to lung transplantation, and all of these patients converted follow
ing lung transplantation, The mean time to conversion was 151 days (range,
11 to 365 days). One fatal case of PTLD was documented in an EBV seroconver
ter (one of five patients) 12 weeks status posttransplantation for lymphang
ioleiomyomatosis. One nonfatal extrathoracic PTLD was documented in a serop
ositive patient (1 of 104 patients) 33 months posttransplantation.
Conclusions: We conclude the following: (1) PTLD in LT recipients may have
a lower incidence (2 of 109 patients; 1.8%) than previously reported, despi
te an aggressive immunosuppressive regimen; and (2) the incidence of PTLD i
s higher in patients with primary EBV infection (20% vs 1%).