Comparison of tamarins and marmosets as hosts for GBV-B infections and the effect of immunosuppression on duration of viremia

被引:67
|
作者
Lanford, RE
Chavez, D
Notvall, L
Brasky, KM
机构
[1] SW Natl Primate Res Ctr, Dept Virol & Immunol, San Antonio, TX 78227 USA
[2] SW Fdn Biomed Res, San Antonio, TX 78227 USA
[3] SW Natl Primate Res Ctr, Dept Lab Anim Med, San Antonio, TX 78227 USA
关键词
hepatitis C virus; HCV; FK506; primary hepatocytes; nonhuman primate;
D O I
10.1016/S0042-6822(03)00193-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
GBV-B virus is a close relative to hepatitis C virus (HCV) that causes hepatitis in tamarins, and thus, is an attractive surrogate model for HCV. In this study, we demonstrate that the host range of GBV-B extends to the common marmoset with an infection profile similar to that observed for tamarins. Marmoset hepatocytes were susceptible to in vitro infection with GBV-B. Virus was efficiently secreted into the medium, and approximately 25% of hepatocytes were positive for NS3 staining. In an attempt to induce persistent infections, tamarins were immunosuppressed with FK506 and inoculated with GBV-B. Although no chronic infections were induced, the duration of viremia was increased in most animals. In one animal, the duration of viremia was extended to 46 weeks, but viral clearance occurred 18 weeks after stopping FK506 therapy. The greater availability of marmosets in comparison to tamarins will greatly facilitate future research efforts with this model. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:72 / 80
页数:9
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