Predictive negative value of persistent low Epstein-Barr virus viral load after intestinal transplantation in children

被引:68
作者
Green, M
Bueno, J
Rowe, D
Mazariegos, G
Qu, LR
Abu-Almagd, K
Reyes, J
机构
[1] Childrens Hosp Pittsburgh, Dept Pediat, Div Allergy Immunol & Infect Dis, Pittsburgh, PA 15213 USA
[2] Childrens Hosp Pittsburgh, Dept Surg, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Thomas Starzl Transplantat Inst, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Grad Sch Publ Hlth, Pittsburgh, PA 15213 USA
关键词
D O I
10.1097/00007890-200008270-00010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The correlation between an elevated Epstein-Barr virus (EBV) viral load in the peripheral blood and the subsequent development of EBV-associated posttransplant lymphoproliferative disease (PTLD) is the basis for strategies using serial measurements of the EBV viral load to guide preemptive therapy (PT). Neither the frequency, duration of monitoring, nor the predictive negative value of viral load monitoring for asymptomatic patients with persistent low or nondetectable viral loads against the development of PTLD has been established. Methods, Since April 1994, children undergoing intestinal transplantation (ITx) underwent serial monitoring of the EBV viral load in their peripheral blood using a quantitative competitive EBV polymerase chain reaction assay (PCR). Samples were obtained every 2 weeks for the first 3 months and then every 1-3 months depending on the patients clinical condition. EBV viral loads greater than or equal to 40 (for patients who were EBV seronegative pre-ITx) and greater than or equal to 200 (for those who were seropositive) genome copies/10(5) peripheral blood lymphocytes were felt to identify patients at increased risk for PTLD and generally prompted PT. Results. A total of 30 ITx recipients were compliant with our monitoring protocol; 23/30 are alive 6-59 months post-ITx. A total of 12/30 never had a viral load >40 and did not receive PT. In contrast, 18/30 had greater than or equal to 1 high viral load (greater than or equal to 200); the first high viral load was measured a median of 59 days post-ITx (range 1-440). A late rise (>6 months post-ITx) was seen in only 2/18 children. A total of 0/12 patients with persistently low viral loads received PT and none developed PTLD. In contrast, 5/18 with greater than or equal to 1 one high viral load (including 2/14 who received and 3/4 who did not receive PT) developed PTLD. All five children with PTLD were EBV seropositive pre-ITx and experienced their first high EBV PCB within the first 3 months after ITx, Conclusions. The predictive negative value of persistently low or nondetectable EBV viral loads was 100% in this study. Patients with nondetectable or low viral loads for the first 6 months after ITx did not develop PTLD regardless of their pretransplant EBV serological status. The frequency of viral load monitoring can be safely decreased for patients whose viral loads remain low for the first 6 months ITx.
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页码:593 / 596
页数:4
相关论文
共 19 条
[1]  
Abedi MR, 1997, INT J CANCER, V71, P624, DOI 10.1002/(SICI)1097-0215(19970516)71:4<624::AID-IJC19>3.0.CO
[2]  
2-B
[3]  
Barkholt LM, 1996, TRANSPL INT, V9, P439
[4]   Epstein-Barr virus infections in children after transplantation of the small intestine [J].
Finn, L ;
Reyes, J ;
Bueno, J ;
Yunis, E .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (03) :299-309
[5]  
GREEN M, 1999, CURR OPIN ORGAN TRAN, V4, P292
[6]  
Green SF, 1998, PATHOL LAB MED, V3, P143
[7]   EPSTEIN-BARR-VIRUS DNA IN PERIPHERAL-BLOOD LEUKOCYTES OF PATIENTS WITH POSTTRANSPLANT LYMPHOPROLIFERATIVE DISEASE [J].
KENAGY, DN ;
SCHLESINGER, Y ;
WECK, K ;
RITTER, JH ;
GAUDREAULTKEENER, MM ;
STORCH, GA .
TRANSPLANTATION, 1995, 60 (06) :547-554
[8]   Quantitative analysis of Epstein-Barr virus load by using a real-time PCR assay [J].
Kimura, H ;
Morita, M ;
Yabuta, Y ;
Kuzushima, K ;
Kato, K ;
Kojima, S ;
Matsuyama, T ;
Morishima, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (01) :132-136
[9]   Semiquantitative Epstein-Barr virus polymerase chain reaction analysis of peripheral blood from organ transplant patients and risk for the development of lymphoproliferative disease [J].
Lucas, KG ;
Filo, R ;
Heilman, DK ;
Lee, CH ;
Emanuel, DJ .
BLOOD, 1998, 92 (10) :3977-3978
[10]   Prevention and preemptive therapy of posttransplant lymphoproliferative disease in pediatric liver recipients [J].
McDiarmid, SV ;
Jordan, S ;
Lee, GS ;
Toyoda, M ;
Goss, JA ;
Vargas, JH ;
Martin, MG ;
Bahar, R ;
Maxfield, AL ;
Ament, ME ;
Busutti, RW .
TRANSPLANTATION, 1998, 66 (12) :1604-1611