Monitoring of oral cytomegalovirus DNA shedding for the prediction of viral DNAemia in allogeneic hematopoietic stem cell transplant recipients

被引:4
作者
Pascual, Tania [1 ]
Solano, Carlos [2 ,3 ]
Torres, Ignacio [1 ]
Talaya, Alberto [1 ]
Gimenez, Estela [1 ]
Vinuesa, Victor [1 ]
Pinana, Jose L. [2 ]
Hernandez-Boluda, Juan C. [2 ]
Perez, Ariadna [2 ]
Navarro, David [1 ,4 ]
机构
[1] Hosp Clin Univ, Inst Res INCLIVA, Microbiol Serv, Valencia, Spain
[2] Hosp Clin Univ, Inst Res INCLIVA, Hematol Serv, Valencia, Spain
[3] Univ Valencia, Sch Med, Dept Med, Valencia, Spain
[4] Univ Valencia, Sch Med, Dept Microbiol, Valencia, Spain
关键词
allogeneic hematopoietic stem cell transplantation; CMV oral shedding; Cytomegalovirus (CMV); plasma CMV DNAemia; saliva; MARROW-TRANSPLANTATION; DISEASE; INFECTION; GANCICLOVIR; LOAD;
D O I
10.1002/jmv.25185
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Preemptive antiviral therapy based on detecting cytomegalovirus (CMV) DNAemia above a preestablished threshold is the mainstay strategy for the prevention of CMV disease in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients; nevertheless, CMV DNAemia, even at low levels, may increase mortality. We investigated whether surveillance of saliva for the presence of CMV DNA may anticipate the occurrence of CMV DNAemia. This was a prospective observational study with 53 consecutively enrolled allo-HSCT recipients. Saliva and plasma specimens were collected on a weekly basis from Day 0 to Day 100 after transplantation. CMV DNA was quantified in both specimen types using the Abbott Real-Time PCR assay (Abbott Molecular, Des Plaines, IL). CMV DNA was quantifiable in 44 (83%) patients: either in saliva (n=1) or plasma (n=12) only, or in both specimen types (n=31). CMV oral shedding preceded the occurrence of CMV DNAemia in eight patients (18.2%), while the opposite pattern was observed in 21 patients (47.7%). The CMV DNA loads quantified in saliva and plasma correlated modestly (P=0.33; P=0.013) and did not differ in magnitude (P=0.527). No transplantation factors, other than recipient CMV seropositivity, were associated with oral CMV DNA shedding; serum CMV IgG levels were comparable, regardless of the timing of the detection of CMV DNA at both sites. In summary, screening of saliva specimens for the presence of CMV DNA appear to be of limited value for anticipating the occurrence of CMV DNAemia in allo-HSCT recipients.
引用
收藏
页码:1375 / 1382
页数:8
相关论文
共 20 条
[1]   Comparison of the new Abbott Real Time CMV assay and the Abbott CMV PCR Kit for the quantitation of plasma cytomegalovirus DNAemia [J].
Angeles Clari, Maria ;
Bravo, Dayana ;
Costa, Elisa ;
Munoz-Cobo, Beatriz ;
Solano, Carlos ;
Jose Remigia, Maria ;
Gimenez, Estela ;
BenMarzouk-Hidalgo, Omar J. ;
Perez-Romero, Pilar ;
Navarro, David .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2013, 75 (02) :207-209
[2]   A LONGITUDINAL FOLLOW-UP OF SALIVARY SECRETION IN BONE-MARROW TRANSPLANT PATIENTS [J].
CHAUSHU, G ;
ITZKOVITZCHAUSHU, S ;
YEFENOF, E ;
SLAVIN, S ;
OR, R ;
GARFUNKEL, AA .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1995, 79 (02) :164-169
[3]   Herpesviruses excretion in saliva of pediatric transplant recipients [J].
Correa Sierra, Consuelo Beatriz ;
Cardella, Vivian Kouri ;
Perez Santos, Lissette ;
Silverio, Cesar E. ;
Hondal, Norma ;
Florin, Jose .
TRANSPLANT INFECTIOUS DISEASE, 2017, 19 (06)
[4]   Saliva as a source of HCMV DNA in allogeneic stem cell transplantation patients [J].
Correia-Silva, J. F. ;
Bruna-Romero, O. ;
Resende, R. G. ;
Miranda, L. P. M. ;
Oliveira, F. E. ;
Costa, F. O. ;
Xavier, S. G. ;
Figueiredo-Neves, S. P. ;
Almeida, H. C. ;
Bittencourt, H. ;
Gomez, R. S. .
ORAL DISEASES, 2010, 16 (02) :210-216
[5]   Cytomegalovirus shedding in the oral cavity of allogeneic haematopoietic stem cell transplant patients [J].
Correia-Silva, Jde F. ;
Victoria, J. M. N. ;
Guimaraes, A. L. S. ;
Salomao, U. E. ;
de Abreu, M. H. N. G. ;
Bittencourt, H. ;
Gomez, R. S. .
ORAL DISEASES, 2007, 13 (02) :163-169
[6]   A collaborative study to establish the 1st WHO International Standard for human cytomegalovirus for nucleic acid amplification technology [J].
Fryer, Jacqueline F. ;
Heath, Alan B. ;
Minor, Philip D. .
BIOLOGICALS, 2016, 44 (04) :242-251
[7]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[8]   EARLY TREATMENT WITH GANCICLOVIR TO PREVENT CYTOMEGALOVIRUS DISEASE AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
GOODRICH, JM ;
MORI, M ;
GLEAVES, CA ;
DUMOND, C ;
CAYS, M ;
EBELING, DF ;
BUHLES, WC ;
DEARMOND, B ;
MEYERS, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (23) :1601-1607
[9]   Cytomegalovirus viral load and mortality after haemopoietic stem cell transplantation in the era of pre-emptive therapy: a retrospective cohort study [J].
Green, Margaret L. ;
Leisenring, Wendy ;
Xie, Hu ;
Mast, T. Christopher ;
Cui, Yadong ;
Sandmaier, Brenda M. ;
Sorror, Mohamed L. ;
Goyal, Sonia ;
Oezkoek, Sezen ;
Yi, Jessica ;
Sahoo, Farah ;
Kimball, Louise E. ;
Jerome, Keith R. ;
Marks, Morgan A. ;
Boeckh, Michael .
LANCET HAEMATOLOGY, 2016, 3 (03) :E119-E127
[10]   ANALYSIS OF INCOMPLETE DATA [J].
HARTLEY, HO ;
HOCKING, RR .
BIOMETRICS, 1971, 27 (04) :783-&