Monitoring cytomegalovirus IE-1 and PP65-Specific CD4+ and CD8+ T-cell responses after allogeneic stem cell transplantation may identify patients at risk for recurrent CMV reactivations

被引:65
作者
Gratama, Jan W. [1 ]
Brooimans, Rik A. [1 ]
van der Holt, Bronno [2 ]
Sintnicolaas, Kees [3 ]
van Doornum, Gerard [4 ]
Niesters, Huberrus G. [4 ]
Lowenberg, Bob [5 ]
Cornelissen, Jan J. [5 ]
机构
[1] Erasmus MC, Dept Internal Oncol, Rotterdam, Netherlands
[2] Erasmus MC, Dept Trials & Stat, Rotterdam, Netherlands
[3] Sanquin Blood Bank S W Reg, Lab Histocompatibil & Immunogenet, Rotterdam, Netherlands
[4] Erasmus MC, Dept Virol, Rotterdam, Netherlands
[5] Erasmus MC, Dept Hematol, Rotterdam, Netherlands
关键词
hematopoietic stem cell transplantation; cytomegalovirus; T-cell subsets; protein-spanning peptide pools; interferon-gamma;
D O I
10.1002/cyto.b.20420
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
We studied the recovery of CMV-specific CD4(+) and CD8(+) T-cell immunity in 52 recipients of allogeneic stem cell transplantation (SCT). The proportions of IFN-gamma-producing CD4(+) and CD8(+) T cells upon in vitro activation using peptide pools representing the CMV pp65 and IE-1 proteins were assessed at multiple time points post SCT, and correlated with the occurrence of CIVIV reactivation. In a retrospective analysis, recurrent CIVIV reactivations occurred in 9 patients and were associated with low pp65-specific CD4(+) T-cell and low IE-1-specific CD8(+) T-cell reactivities, whereas patients without detectable CMV reactivation (n = 30) or a single reactivation (n = 13) showed a better recovery of these immune responses. CD4(+) T-cell responses to IE-1 were infrequent in most patients, whereas CD8(+) T-cell responses to pp65 occurred frequently, but did not correlate with protection against (recurrent) reactivation. Prospectively, CMV-specific T-cell responses could be studied prior to 14 reactivation episodes in 8 patients. CD4(+) T-cell responses to IE-1 and pp65 were positive in only 1 and 2 episodes, respectively. CD8(+) T-cell responses against IE-1 were positive in 4, but against pp65 in 12 episodes, again showing that CD8+ T-cell reactivity against pp65 did not prevent CMV reactivation. Thus, monitoring of particular CMV-specific CD4(+) and CD8(+) T-cell responses after allogeneic SCT may identify patients at risk for recurrent CMV reactivations. (C) 2008 Clinical Cytometry Society.
引用
收藏
页码:211 / 220
页数:10
相关论文
共 49 条
[1]   Long-term cytomegalovirus infection leads to significant changes in the composition of the CD8+ T-cell repertoire, which may be the basis for an imbalance in the cytokine production profile in elderly persons [J].
Almanzar, G ;
Schwaiger, S ;
Jenewein, B ;
Keller, M ;
Herndler-Brandstetter, D ;
Würzner, R ;
Schönitzer, D ;
Grubeck-Loebenstein, B .
JOURNAL OF VIROLOGY, 2005, 79 (06) :3675-3683
[2]   Cytomegalovirus in hematopoietic stem cell transplant recipients: Current status, known challenges, and future strategies [J].
Boeckh, M ;
Nichols, WG ;
Papanicolaou, G ;
Rubin, R ;
Wingard, JR ;
Zaia, Y .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2003, 9 (09) :543-558
[3]   Late cytomegalovirus disease and mortality in recipients of allogeneic hematopoietic stem cell transplants: importance of viral load and T-cell immunity [J].
Boeckh, M ;
Leisenring, W ;
Riddell, SR ;
Bowden, RA ;
Huang, ML ;
Myerson, D ;
Stevens-Ayers, T ;
Flowers, MED ;
Cunningham, T ;
Corey, L .
BLOOD, 2003, 101 (02) :407-414
[4]   Increased transplant-related morbidity and mortality in CMV-seropositive patients despite highly effective prevention of CMV disease after allogeneic T-cell-depleted stem cell transplantation [J].
Broers, AEC ;
van der Holt, R ;
van Esser, JWJ ;
Gratama, JW ;
Henzen-Logmans, S ;
Kuenen-Boumeester, V ;
Löwenberg, B ;
Cornelissen, JJ .
BLOOD, 2000, 95 (07) :2240-2245
[5]   Dynamics of cytomegalovirus (CMV)-specific T cells in HIV-1-infected individuals progressing to AIDS with CMV end-organ disease [J].
Bronke, C ;
Palmer, NM ;
Jansen, CA ;
Westerlaken, GHA ;
Polstra, AM ;
Reiss, P ;
Bakker, M ;
Miedema, F ;
Tesselaar, K ;
van Baarle, D .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (06) :873-880
[6]   Protection from cytomegalovirus after transplantation is correlated with immediate early 1-specific CD8 T cells [J].
Bunde, T ;
Kirchner, A ;
Hoffmeister, B ;
Habedank, D ;
Hetzer, R ;
Cherepnev, G ;
Proesch, S ;
Reinke, P ;
Volk, HD ;
Lehmkuhl, H ;
Kern, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (07) :1031-1036
[7]   A randomized multicenter comparison of CD34+-selected progenitor cells from blood vs from bone marrow in recipients of HLA-identical allogeneic transplants for hematological malignancies [J].
Cornelissen, JJ ;
van der Holt, B ;
Petersen, EJ ;
Vindelov, L ;
Russel, CA ;
Höglund, M ;
Maertens, J ;
Schouten, HC ;
Braakman, E ;
Steijaert, MMC ;
Zijlmans, MJM ;
Slaper-Cortenbach, I ;
Boogaerts, MA ;
Löwenberg, B ;
Verdonck, LF .
EXPERIMENTAL HEMATOLOGY, 2003, 31 (10) :855-864
[8]   Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation [J].
Cwynarski, K ;
Ainsworth, J ;
Cobbold, M ;
Wagner, S ;
Mahendra, P ;
Apperley, J ;
Goldman, J ;
Craddock, C ;
Moss, PAH .
BLOOD, 2001, 97 (05) :1232-1240
[9]  
Dwyer J., 1992, STAT MODELS LONGITUD, P3
[10]   Infusion of cytomegalovirus (CMV)-specific T cells for the treatment of CMV infection not responding to antiviral chemotherapy [J].
Einsele, H ;
Roosnek, E ;
Rufer, N ;
Sinzger, C ;
Riegler, S ;
Löffler, J ;
Grigoleit, U ;
Moris, A ;
Rammensee, HG ;
Kanz, L ;
Kleihauer, A ;
Frank, F ;
Jahn, G ;
Hebart, H .
BLOOD, 2002, 99 (11) :3916-3922