Human β-herpesvirus interactions in solid organ transplant recipients

被引:132
作者
Mendez, JC
Dockrell, DH
Espy, MJ
Smith, TF
Wilson, JA
Harmsen, WS
Ilstrup, D
Paya, CV
机构
[1] Mayo Clin & Mayo Fdn, Div Infect Dis, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Div Clin Microbiol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Transplant Ctr, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Dept Med Stat, Rochester, MN 55905 USA
关键词
D O I
10.1086/317929
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The replication of beta -herpesviruses-cytomegalovirus (CMV), human herpesvirus (HHV)-6, and HHV-7-and their association with CMV disease and response to antiviral therapy were prospectively investigated in 33 liver transplant recipients not given antiviral prophylaxis. CMV, HHV-6, and HHV-7 DNA were detected within 8 weeks after transplantation in 70%, 33%, and 42% of the patients, respectively. The univariate association between CMV disease and the 3 beta -herpesviruses was more significant by virus load quantitation than by qualitative detection of DNA. This association with high levels of CMV, HHV-6, and HHV-7 (P <.001 .022, and .001, respectively) occurred mainly in CMV-seronegative recipients of transplants from CMV-seropositive donors. Antiviral therapy with ganciclovir (Gcv) reduced the load of CMV and HHV-6 and HHV-7. These results suggest that CMV disease in transplant recipients is related to the unique interaction of the 3 <beta>-herpesviruses and is ultimately reduced after intravenous Gcv treatment.
引用
收藏
页码:179 / 184
页数:6
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