Surveillance of cytomegalovirus (CMV) DNAemia in pediatric allogeneic stem cell transplantation: incidence and outcome of CMV infection and disease

被引:30
作者
Bordon, V. [1 ]
Bravo, S. [2 ]
Van Renterghem, L. [3 ]
de Moerloose, B. [1 ]
Benoit, Y. [1 ]
Laureys, G. [1 ]
Dhooge, C. [1 ]
机构
[1] Ghent Univ Hosp, B-9000 Ghent, Belgium
[2] Free Univ Brussels, Brussels, Belgium
[3] Ghent Univ Hosp, Clin Biol Lab, B-9000 Ghent, Belgium
关键词
cytomegalovirus; DNAemia; children; hematopoietic stem cell transplantation;
D O I
10.1111/j.1399-3062.2007.00242.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytomegalovirus (CMV) remains a serious problem after hematopoietic stem cell transplantation (HSCT). To investigate the incidence of CMV infection and outcome we retrospectively analyzed 70 consecutive pediatric allogeneic HSCTs monitored by CMV polymerase chain reaction (PCR), with at least 1-year follow-up or until death. All patients at risk for CMV infection (CMV-seropositive patients and CMV-seronegative recipients transplanted from CMV-seropositive donors) received hyperimmune anti-CMV globulins whereas in the group of HSCT patients with both donor and recipient CMV negativity, polyvalent immunoglobulins were given, both at a dose of 400 mg/kg. All patients received acyclovir at prophylactic doses for at least 6 months. Patients were monitored twice a week by CMV PCR. Patients with 2 positive results for CMV DNAemia received ganciclovir for 14 days and continued until 2 consecutive negative results were obtained. The incidence of CMV DNAemia was 12.8% (9/70) in the whole group, with significant higher risk for patients with CMV-seropositive recipient status, 8 out of 22 (36%), vs. patients with seronegative status, 1 out of 48 (2%) (P=0.0002). Three out of 9 patients with DNAemia developed CMV disease despite adequate preemptive treatment. The transplant-related mortality was higher in the CMV-seropositive recipient group (P=0.05). Age, use of hyperimmune anti-CMV globulins at a high dose, and the low incidence of graft-versus-host disease might be contributing factors to this low incidence.
引用
收藏
页码:19 / 23
页数:5
相关论文
共 27 条
[1]  
BACIGALUPO A, 1992, HAEMATOLOGICA, V77, P507
[2]   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
[3]   Cytomegalovirus pp65 antigenemia-guided early treatment with ganciclovir versus ganciclovir at engraftment after allogeneic marrow transplantation: A randomized double-blind study [J].
Boeckh, M ;
Gooley, TA ;
Myerson, D ;
Cunningham, T ;
Schoch, G ;
Bowden, RA .
BLOOD, 1996, 88 (10) :4063-4071
[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]  
Chou S, 1999, Transpl Infect Dis, V1, P105, DOI 10.1034/j.1399-3062.1999.010204.x
[6]   Valgandiclovir - A review of its use in the management of CMV infection and disease in immunocompromised patients [J].
Cvetkovic, RS ;
Wellington, K .
DRUGS, 2005, 65 (06) :859-878
[7]   PREVALENCE OF RESISTANCE IN PATIENTS RECEIVING GANCICLOVIR FOR SERIOUS CYTOMEGALOVIRUS-INFECTION [J].
DREW, WL ;
MINER, RC ;
BUSCH, DF ;
FOLLANSBEE, SE ;
GULLETT, J ;
MEHALKO, SG ;
GORDON, SM ;
OWEN, WF ;
MATTHEWS, TR ;
BUHLES, WC ;
DEARMOND, B .
JOURNAL OF INFECTIOUS DISEASES, 1991, 163 (04) :716-719
[8]  
DYKEWICZ CA, 2000, MMWR-MORBID MORTAL W, V49, P1
[9]  
EINSELE H, 1995, BLOOD, V86, P2815
[10]   Risk factors for treatment failures in patients receiving PCR-based preemptive therapy for CMV infection [J].
Einsele, H ;
Hebart, H ;
Kauffman-Schneider, C ;
Sinzger, C ;
Jahn, G ;
Bader, P ;
Klingebiel, T ;
Dietz, K ;
Löffler, J ;
Bokemeyer, C ;
Müller, CA ;
Kanz, L .
BONE MARROW TRANSPLANTATION, 2000, 25 (07) :757-763