Association of tumour necrosis factor alpha and interleukin 6 levels with cytomegalovirus DNA detection and disease after renal transplantation

被引:33
作者
Tong, CYW
Bakran, A
Williams, H
Cuevas, LE
Peiris, JSM
Hart, CA
机构
[1] Univ Liverpool, Dept Med Microbiol, Liverpool L69 3BX, Merseyside, England
[2] Univ Liverpool, Liverpool Sch Trop Med, Stat & Epidemiol Unit, Liverpool L3 5QA, Merseyside, England
[3] Royal Liverpool Univ Hosp, Renal Transplant Unit, Liverpool, Merseyside, England
[4] Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
关键词
TNF-alpha; IL-6; CMV; renal transplantation;
D O I
10.1002/jmv.1013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Cytokines such as tumour necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6) are thought to be important in the pathogenesis of post-transplant cytomegalovirus (CMV) disease. CMV infection increases the production of TNF-alpha and IL-6. Conversely, TNF-alpha switches on the replication of CMV. To study the association of these two cytokines with CMV activity and disease, TNF-alpha and IL-6 levels were assayed in plasma samples taken serially from three groups of renal transplant recipients. Group A (n = 12) had CMV disease and syndrome; Group B (n =11) had detectable CMV DNA in plasma or peripheral blood leucocytes without disease, i.e., presumed asymptomatic CMV infection, and Group C (n = 11) had no detectable CMV DNA nor disease. The median peak TNF-alpha levels in patients with CMV disease (Group A) were significantly higher than that in Group B or Group C (P < 0.02) whereas the median peak IL-6 levels in group C patients were significantly lower than that in group A (P < 0.04) or group B (P < 0.03). A TNF-<alpha> level of above 100 pg/ ml was significantly associated with CMV disease and high plasma CMV load (> 10,000 copies/ml). IL-6 levels above 15 pg/ml were significantly associated with CMV DNA detection, but not with CMV disease or elevated CMV load. High levels of TNF-alpha or IL-6 were not associated with CMV donor/recipient serostatus, HHV-6 or HHV-7 DNA detection, immunosuppressive regimen or rejection episodes. The role of TNF-alpha in the pathogenesis of CMV disease deserves further investigation. J. Med. Virol. 64:29-34, 2001. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:29 / 34
页数:6
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