Human herpesvirus-6 infection: A prospective study evaluating HHV-6 DNA levels in liver from children with acute liver failure

被引:29
作者
Chevret, Laurent [1 ]
Boutolleau, David [2 ,6 ]
Halimi-Idri, Nadia [2 ]
Branchereau, Sophie [7 ]
Baujard, Catherine [3 ]
Fabre, Monique [4 ]
Gautheret-Dejean, Agnes [6 ]
Debray, Dominique [5 ]
机构
[1] CHU Bicetre, AP HP, Pediat Intens Care Unit, F-94275 Le Kremlin Bicetre, France
[2] CHU Bicetre, AP HP, Virol Lab, Le Kremlin Bicetre, France
[3] CHU Bicetre, AP HP, Pediat Anesthesiol Unit, Le Kremlin Bicetre, France
[4] CHU Bicetre, AP HP, Anatomopathol Unit, Le Kremlin Bicetre, France
[5] CHU Bicetre, AP HP, Pediat Hepatol Unit, Le Kremlin Bicetre, France
[6] Hop La Pitie Salpetriere, AP HP, Virol Lab, Paris, France
[7] CHU Bicetre, AP HP, Pediat Surg, Le Kremlin Bicetre, France
关键词
human herpesvirus 6; acute liver failure; diagnosis; real-time PCR; children;
D O I
10.1002/jmv.21143
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aim of this prospective study was to investigate the role of HHV-6 infection in children with acute onset of liver failure using real-time quantitative PCR. Twenty-three children (median age, 24 months) were included: 6 cases of fulminant hepatic failure of undetermined cause (group 1); 4 cases of fulminant hepatic failure of recognized cause (group 2); 3 cases of acute decompensation of chronic liver disease (group 3); and 10 cases of chronic liver disease (group 4). HHV-6 genomic DNA was detected and quantified using real-time PCR in plasma and livers obtained at the time of transplantation. HHV6-DNA detection rate was significantly higher among groups 1, 2, and 3 compared to group 4 (76.9% vs. 20% P=0.02). Viral loads ranged from 6 to 32,500 copies/106 cells. Significantly higher viral loads were found in 4 of 9 children with acute onset of liver failure of unknown origin (group 1, n = 3; group 3, n = 1) and 1 child with fulminant autoimmune hepatitis (group 2) (P=0.03). These results strongly support the hypothesis that HHV-6 may cause fulminant hepatic failure and acute decompensation of chronic liver disease in children. Nevertheless, a threshold viral load value still remains to be determined.
引用
收藏
页码:1051 / 1057
页数:7
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