Lymphotropic herpesvirus DNA detection in patients with active CMV infection - a possible role in the course of CMV infection after hematopoietic stem cell transplantation

被引:12
|
作者
Zawilinska, Barbara [1 ]
Kopec, Jolanta [1 ]
Szostek, Slawa [1 ]
Piatkowska-Jakubas, Beata [2 ]
Skotnicki, Aleksander B. [2 ]
Kosz-Vnenchak, Magdalena [1 ,3 ]
机构
[1] Jagiellonian Univ, Coll Med, Dept Virol, Chair Microbiol, PL-31121 Krakow, Poland
[2] Jagiellonian Univ, Coll Med, Chair & Clin Hematol, PL-31121 Krakow, Poland
[3] Jagiellonian Univ, Lab Mol Genet & Virol, Fac Biochem Biophys & Biotechnol, PL-31121 Krakow, Poland
来源
MEDICAL SCIENCE MONITOR | 2011年 / 17卷 / 08期
关键词
bone marrow transplantation; CMV DNA load; herpesviruses mixed infections; CYTOMEGALOVIRUS DISEASE; RENAL-TRANSPLANTATION; SOLID-ORGAN; RECIPIENTS; DIAGNOSIS; EPIDEMIOLOGY; QUANTITATION; REACTIVATION; ASSOCIATION; COINFECTION;
D O I
10.12659/MSM.881904
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The natural history of cytomegalovirus (CMV) infection and disease in transplant recipients prompts researchers to look for other factors contributing to this infection. The ubiquity of lymphotropic herpesviruses (EBV, HHV-6, and HHV-7) and the possibility of their activation during immunosuppression may suggest their participation in progression of CMV infection in patients after hematopoietic stem cell transplantation (HSCT). Material/Methods: The presence of CMV, EBV, HHV-6 and HHV-7 was confirmed through detection of viral DNA isolated from leukocytes. Allo-HST recipients (n=55) were examined repeatedly within the average period of 14+/-7.3 months post-transplant. Results: CMV DNA was detected in 24% of samples, while EBV, HHV-6 and HHV-7 were detected in 20%, 15% and 14% of samples, respectively. Based on the presence of CMV infection at particular time-points (months) after transplantation, the recipients were divided into 3 groups: Group I (N=15) with persistent infection, Group II (N=20) with transient infection, and Group III (N=20) without CMV infection. In Group I, the mean CMV load was significantly higher than in Group II, and the clinical condition of Group I patients was poorer. All these patients manifested clinical symptoms, and all had episodes of GvHD. All Group I patients developed multiple infections; EBV in 80%, HHV-6 in 47% and HHV-7 in 87% of patients. In the remaining groups, with the exception of HHV-6 in group II, the frequency of infected patients was lower. In addition, CMV presence was often preceded by another herpesvirus. Conclusions: The results suggest that other herpesviruses, mainly HHV-7, could predispose CMV to cause chronic infection.
引用
收藏
页码:CR432 / CR441
页数:10
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