Efficiency and Risk Factors for CMV Transmission in Seronegative Hematopoietic Stem Cell Recipients

被引:32
作者
Pergam, Steven A. [1 ,2 ,3 ]
Xie, Hu [2 ]
Sandhu, Ravinder [2 ]
Pollack, Margaret [1 ,3 ]
Smith, Jeremy [4 ]
Stevens-Ayers, Terry [1 ]
Ilieva, Valeria [1 ]
Kimball, Louise E. [1 ]
Huang, Meei-Li [5 ]
Hayes, Tracy S. [5 ]
Corey, Lawrence [1 ,2 ,3 ,5 ]
Boeckh, Michael J. [1 ,2 ,3 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98104 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[3] Univ Washington, Dept Med, Seattle, WA USA
[4] Dartmouth Inst Hlth Policy Res & Clin Practice, Hanover, NH USA
[5] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
关键词
Cytomegalovirus; Transmission; Donor; Graft; CYTOMEGALOVIRUS PP65 ANTIGENEMIA; ALLOGENEIC MARROW TRANSPLANTATION; PERIPHERAL-BLOOD; BONE-MARROW; PREEMPTIVE TREATMENT; INFECTION; DISEASE; DONOR; LATENT; PREVENTION;
D O I
10.1016/j.bbmt.2012.02.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytomegalovirus (CMV) transmission via stem cells or marrow in CMV donor seropositive/recipient seronegative (D+/R-) hematopoietic cell transplantation (HCT) is surprisingly inefficient, and factors associated with transmission in these high-risk HCT recipients are unknown. In a retrospective cohort of D+/R- HCT recipients, cumulative incidence curve estimates were used to determine posttransplantation rates of CMV and multivariable Cox proportional models to assess risk factors associated with transmission. A total of 447 patients from 1995 to 2007 were eligible for enrollment. Overall, 85 of 447 (19.0%) acquired CMV at a median of 49 days (IQR 41-60) posttransplantation. CMV disease before day 100 occurred in 6 of 447(1.3%) patients and in 7 of 447 (1.6%) after day 100. The donor graft, specifically the total nucleated cell count (adjusted hazard ratio [HR] 2.7; 95% confidence interval [CI], 1.4-4.7, P = .0002), was the only factor associated with CMV transmission in multivariable analyses. Notably, the source stem cells (marrow versus peripheral blood stem cell [PBSC]), screening method, and graft-versus-host disease (GVHD) were not associated with transmission. Thus, a highly cellular graft was the only identifiable risk factor associated with CMV transmission, suggesting that viral genomic content of the donor graft determines transmission efficiency in D+/R- HCT recipients. Bid Blood Marrow Transplant 18: 1391-1400 (2012) (C) 2012 American Society for Blood and Marrow Transplantation
引用
收藏
页码:1391 / 1400
页数:10
相关论文
共 53 条
[1]   Transplantation of bone marrow as compared with peripheral-blood cells from HLA-identical relatives in patients with hematologic cancers. [J].
Bensinger, WI ;
Martin, PJ ;
Storer, B ;
Clift, R ;
Forman, SJ ;
Negrin, R ;
Kashyap, A ;
Flowers, MED ;
Lilleby, K ;
Chauncey, TR ;
Storb, R ;
Appelbaum, FR ;
Rowley, S ;
Heimfeld, S ;
Blume, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (03) :175-181
[2]   Recent advances in the prevention of CMV infection and disease after hematopoietic stem cell transplantation [J].
Boeckh, M ;
Fries, B ;
Nichols, WG .
PEDIATRIC TRANSPLANTATION, 2004, 8 :19-27
[3]   Optimization of quantitative detection of cytomegalovirus DNA in plasma by real-time PCR [J].
Boeckh, M ;
Huang, M ;
Ferrenberg, J ;
Stevens-Ayers, T ;
Stensland, L ;
Nichols, WG ;
Corey, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (03) :1142-1148
[4]   The impact of cytomegalovirus serostatus of donor and recipient before hematopoietic stem cell transplantation in the era of antiviral prophylaxis and preemptive therapy [J].
Boeckh, M ;
Nichols, WG .
BLOOD, 2004, 103 (06) :2003-2008
[5]   Plasma polymerase chain reaction for cytomegalovirus DNA after allogeneic marrow transplantation - Comparison with polymerase chain reaction using peripheral blood leukocytes, pp65 antigenemia, and viral culture [J].
Boeckh, M ;
GallezHawkins, GM ;
Myerson, D ;
Zaia, JA ;
Bowden, RA .
TRANSPLANTATION, 1997, 64 (01) :108-113
[6]   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
[7]  
BOECKH M, 2003, TRANSPLANT INFECT, P277
[8]   How I treat cytomegalovirus in hematopoietic cell transplant recipients [J].
Boeckh, Michael ;
Ljungman, Per .
BLOOD, 2009, 113 (23) :5711-5719
[9]   A COMPARISON OF FILTERED LEUKOCYTE-REDUCED AND CYTOMEGALOVIRUS (CMV) SERONEGATIVE BLOOD PRODUCTS FOR THE PREVENTION OF TRANSFUSION-ASSOCIATED CMV INFECTION AFTER MARROW TRANSPLANT [J].
BOWDEN, RA ;
SLICHTER, SJ ;
SAYERS, M ;
WEISDORF, D ;
CAYS, M ;
SCHOCH, G ;
BANAJI, M ;
HAAKE, R ;
WELK, K ;
FISHER, L ;
MCCULLOUGH, J ;
MILLER, W .
BLOOD, 1995, 86 (09) :3598-3603
[10]   CYTOMEGALOVIRUS (CMV)-SPECIFIC INTRAVENOUS IMMUNOGLOBULIN FOR THE PREVENTION OF PRIMARY CMV INFECTION AND DISEASE AFTER MARROW TRANSPLANT [J].
BOWDEN, RA ;
FISHER, LD ;
ROGERS, K ;
CAYS, M ;
MEYERS, JD .
JOURNAL OF INFECTIOUS DISEASES, 1991, 164 (03) :483-487