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Acute Resolving Woodchuck Hepatitis Virus (WHV) Infection Is Associated with a Strong Cytotoxic T-Lymphocyte Response to a Single WHV Core Peptide▿

机译:急性解决的土拨鼠肝炎病毒(WHV)感染与对单个WHV核心肽的强烈细胞毒性T淋巴细胞反应▿

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摘要

Woodchucks infected with woodchuck hepatitis virus (WHV) are an excellent model for studying acute, self-limited and chronic hepadnaviral infections. Defects in the immunological response leading to chronicity are still unknown. Specific T-helper cell responses to WHV core and surface antigens (WHcAg and WHsAg, respectively) are associated with acute resolving infection; however, they are undetectable in chronic infection. Up to now, cytotoxic T-lymphocyte (CTL) responses could not be determined in the woodchuck. In the present study, we detected virus-specific CTL responses by a CD107a degranulation assay. The splenocytes of woodchucks in the postacute phase of WHV infection (18 months postinfection) were isolated and stimulated with overlapping peptides covering the whole WHcAg. After 6 days, the cells were restimulated and stained for CD3 and CD107a. One peptide (c96-110) turned out to be accountable for T-cell expansion and CD107a staining. Later, we applied the optimized degranulation assay to study the kinetics of the T-cell response in acute WHV infection. We found a vigorous T-cell response against peptide c96-110 with peripheral blood cells beginning at the peak of viral load (week 5) and lasting up to 15 weeks postinfection. In contrast, there was no T-cell response against peptide c96-110 detectable in chronically WHV-infected animals. Thus, with this newly established flow cytometric degranulation assay, we detected for the first time virus-specific CTLs and determined one immunodominant epitope of WHcAg in the woodchuck.
机译:感染了土拨鼠肝炎病毒(WHV)的土拨鼠是研究急性,自限性和慢性肝炎病毒感染的绝佳模型。导致慢性的免疫反应缺陷仍然未知。对WHV核心和表面抗原(分别为WHcAg和WHsAg)的特定T辅助细胞反应与急性解决感染有关;但是,在慢性感染中无法检测到它们。到目前为止,尚未在土拨鼠中确定细胞毒性T淋巴细胞(CTL)反应。在本研究中,我们通过CD107a脱粒试验检测到病毒特异性CTL反应。分离WHV感染后急性期(感染后18个月)的土拨鼠脾细胞,并用覆盖整个WHcAg的重叠肽刺激。 6天后,将细胞再刺激并针对CD3和CD107a染色。事实证明,一种肽(c96-110)负责T细胞扩增和CD107a染色。后来,我们应用优化的脱粒试验来研究急性WHV感染中T细胞反应的动力学。我们发现针对肽c96-110的强烈T细胞反应,外周血细胞始于病毒载量高峰(第5周),持续至感染后15周。相反,在慢性WHV感染的动物中没有针对肽c96-110的T细胞应答。因此,通过这种新近建立的流式细胞仪脱颗粒试验,我们首次检测到了病毒特异性CTL,并在土拨鼠中确定了WHcAg的一个免疫优势表位。

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