Impaired recovery of Epstein-Barr virus (EBV)-specific CD8+ T lymphocytes after partially T-depleted allogeneic stem cell transplantation may identify patients at very high risk for progressive EBV reactivation and lymphoproliferative disease

被引:113
作者
Meij, P
van Esser, JWJ
Niesters, HGM
van Baarle, D
Miedema, F
Blake, N
Rickinson, AB
Leiner, I
Pamer, E
Löwenberg, B
Cornelissen, JJ
Gratama, JW
机构
[1] Erasmus MC Daniel Den Hoed, Lab Clin & Tumor Immunol, Dept Internal Oncol, NL-3008 AE Rotterdam, Netherlands
[2] Erasmus MC Daniel Den Hoed, Dept Virol, NL-3008 AE Rotterdam, Netherlands
[3] Sanquin Res CLB, Dept Clin Viroimmunol, Amsterdam, Netherlands
[4] Landsteiner Lab AMC, Amsterdam, Netherlands
[5] Univ Liverpool, Dept Med Microbiol, Liverpool L69 3BX, Merseyside, England
[6] Univ Birmingham, CRC, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
[7] Mem Sloan Kettering Canc Ctr, Ctr Infect Dis, New York, NY 10021 USA
关键词
D O I
10.1182/blood-2002-10-3001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epstein-Barr virus (EBV)-specific cytotoxic T lymphocytes are considered pivotal to prevent lymphoproliferative disease (LPD) in allogeneic stem cell transplantation (SCT) recipients. We evaluated the recovery of EBV-specific CD8(+) T cells after partially T-cell-depleted SCT and studied the interaction between EBV-specific CD8(+) T cells, EBV reactivation, and EBV-LPD. EBV-specific CD8(+) T cells were enumerated using 12 class, I HLA tetramers presenting peptides derived from 7 EBV proteins. Blood samples were taken at regular intervals after SCT in 61 patients, and EBV DNA,levels Were assessed by real-time polymerase chain reaction. Forty-five patients showed EBV reactivation, including 25 With high-level reactivation (le, more than 1000 genome equivalents [geq] per milliliter). Nine of these 25 patients progressed to EBV-LPD. CD8(+) cells specific for latent or lytic EBV epitopes repopulated the peripheral blood at largely similar rates. In most patients, EBV-specific CD8(+) T-cell counts had returned to normal levels within 6 months after SCT. Concurrently, the incidence of EBV reactivations, clearly decreased. Patients with insufficient EBV-specific CD8(+) T-cell recovery were at high risk for EBV reactivation in the first 6 months after SCT. Failure to detect EBV-specific CD8(+) T cells in patients with high-level reactivation was associated With the subsequent development of EBV-LPD (P = .048). Consequently, the earlier defined positive predictive value of approximately 40%, based on high-level EBV reactivation. only, increased to 100% in patients without detectable EBV-specific CD8(+) T cells. Thus, impaired recovery of EBV-specific CD8(+) T cells in patients with high-level EBV reactivation may identity a subgroup at very high risk for EBV-LPD and supports that EBV-specific CD8(+) T cells protect SCT recipients from progressive, EBV. reactivation and EBV-LPD. (C) 2003 by The American Society of Hematology.
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收藏
页码:4290 / 4297
页数:8
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