Epstein-Barr virus (EBV) reactivation is a frequent event after allogeneic stem cell transplantation (SCT) and quantitatively predicts EBV-lymphoproliferative disease following T-cell-depleted SCT

被引:292
作者
van Esser, JWJ
van der Holt, B
Meijer, E
Niesters, HGM
Trenschel, R
Thijsen, SFT
van Loon, AM
Frassoni, F
Bacigalupo, A
Schaefer, UW
Osterhaus, ADME
Gratama, JW
Löwenberg, B
Verdonck, LF
Cornelissen, JJ
机构
[1] Univ Rotterdam Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Hematol, NL-3075 EA Rotterdam, Netherlands
[2] Univ Rotterdam Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Stat, NL-3075 EA Rotterdam, Netherlands
[3] Univ Rotterdam Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Virol, NL-3075 EA Rotterdam, Netherlands
[4] Univ Rotterdam Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Med & Tumor Immunol, NL-3075 EA Rotterdam, Netherlands
[5] Univ Utrecht, Med Ctr, Dept Hematol, Utrecht, Netherlands
[6] Univ Utrecht, Med Ctr, Dept Virol, Utrecht, Netherlands
[7] Univ Hosp Essen, Clin Bone Marrow Transplantat, Essen, Germany
[8] Osped San Martino Genoa, Dept Hematol, Genoa, Italy
关键词
D O I
10.1182/blood.V98.4.972
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reactivation of the Epstein-Barr virus (EBV) after allogeneic stem cell transplantation (allo-SCT) may evoke a protective cellular immune response or may be complicated by the development of EBV-lymphoproliferative disease (EBV-LPD). So far, very little is known about the incidence, recurrence, and sequelae of EBV reactivation following allo-SCT. EBV reactivation was retrospectively monitored in 85 EBV-seropositive recipients of a T-cell-depleted (TCD) allo-SCT and 65 EBV-seropositive recipients of an unmanipulated allo-SCT. Viral reactivation (more than So EBV genome equivalents [gEq]/mL) was monitored frequently by quantitative realtime plasma polymerase chain reaction until day 180 after SCT. Probabilities of developing viral reactivation were high after both unmanipulated and TCD-allogeneic SCT (31% +/- 6% versus 65% +/- 7%, respectively). A high CD34(+) cell number of the graft appeared as a novel significant predictor (P = .001) for EBV reactivation. Recurrent reactivation was observed more frequently in recipients of a TCD graft, and EBV-LPD occurred only after TCD-SCT. High-risk status, TCD, and use of antithymocyte globulin were predictive for developing EBV-LPD. Plasma EBV DNA quantitatively predicted EBV-LPD. The positive and negative predictive values of a viral load of 1000 gEq/mL were, respectively, 39% and 100% after TCD. Treatment-related mortality did not differ significantly between TCD and non-TCD transplants, but the incidence of chronic graft-versus-host disease was significantly less in TCD patients. It is concluded that EBV reactivation occurs frequently after TCD and unmanipulated allo-SCT, especially in recipients of grafts with high CD34(+) cell counts. EBV-LPD, however, occurred only after TCD, and EBV load quantitatively predicted EBV-LPD in recipients of a TCD graft. (C) 2001 by The American Society of Hematology.
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页码:972 / 978
页数:7
相关论文
共 64 条
[1]   High levels of Epstein-Barr virus DNA in blood of solid-organ transplant recipients and their value in predicting posttransplant lymphoproliferative disorders [J].
Baldanti, F ;
Grossi, P ;
Furione, M ;
Simoncini, L ;
Sarasini, A ;
Comoli, P ;
Maccario, R ;
Fiocchi, R ;
Gerna, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :613-619
[2]  
Barkholt LM, 1996, TRANSPL INT, V9, P439
[3]  
Beck R, 1999, J CLIN MICROBIOL, V37, P3430
[4]  
Cavazzana-Calvo M, 1998, BRIT J HAEMATOL, V103, P543
[5]  
CLIFT R, 1989, BONE MARROW TRANSPL, V4, P445
[6]  
Cornelissen JJ, 2000, BLOOD, V96, p507A
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]  
Curtis RE, 1999, BLOOD, V94, P2208
[9]   Reduced incidence of Epstein-Barr virus-associated posttransplant lymphoproliferative disorder using preemptive antiviral therapy [J].
Darenkov, IA ;
Marcarelli, MA ;
Basadonna, GP ;
Friedman, AL ;
Lorber, KM ;
Howe, JG ;
Crouch, J ;
Crouch, J ;
Bia, MJ ;
Kliger, AS ;
Lorber, MI .
TRANSPLANTATION, 1997, 64 (06) :848-852
[10]  
DAVIS CL, 1995, CLIN TRANSPLANT, V9, P53