Wuensch Sherry A, Pierce Robert H, Crispe I Nicholas
David H. Smith Center for Vaccine Biology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA.
J Immunol. 2006 Aug 1;177(3):1689-97. doi: 10.4049/jimmunol.177.3.1689.
The response of T cells to liver Ags sometimes results in immune tolerance. This has been proposed to result from local, intrahepatic priming, while the expression of the same Ag in liver-draining lymph nodes is believed to result in effective immunity. We tested this model, using an exogenous model Ag expressed only in hepatocytes, due to infection with an adeno-associated virus vector. T cell activation was exclusively intrahepatic, yet in contrast to the predictions of the current model, this resulted in clonal expansion, IFN-gamma synthesis, and cytotoxic effector function. Local activation of naive CD8(+) T cells can therefore cause full CD8(+) T cell activation, and hepatocellular presentation cannot be used to explain the failure of CTL effector function against some liver pathogens such as hepatitis C.
T细胞对肝脏抗原的反应有时会导致免疫耐受。有人提出这是由肝内局部启动引起的,而相同抗原在肝引流淋巴结中的表达则被认为会导致有效的免疫反应。我们使用一种仅在肝细胞中表达的外源性模型抗原来测试该模型,该抗原是由于腺相关病毒载体感染所致。T细胞激活完全发生在肝内,但与当前模型的预测相反,这导致了克隆扩增、γ干扰素合成和细胞毒性效应功能。因此,幼稚CD8(+) T细胞的局部激活可导致完全的CD8(+) T细胞激活,并且肝细胞呈递不能用于解释针对某些肝脏病原体(如丙型肝炎)的CTL效应功能的失败。