Tian Yuan, Zhang Heng-Hui, Wei Lai, Du Shao-Cai, Chen Hong-Song, Fei Ran, Liu Feng
Hepatology Institute, Peking University People's Hospital, Beijing, China.
Viral Immunol. 2007 Dec;20(4):553-61. doi: 10.1089/vim.2007.0064.
Hepatitis C virus (HCV) nonstructural (NS) genes are relatively conserved and play critical roles in cellular immune responses against HCV. The aim of the study was to evaluate the immunogenicity of the different HCV NS genes through transduction of DCs and presentation to T cells. Monocyte-derived DCs from healthy donors were infected with the recombinant adenovirus (Ad) harboring HCV NS3 (AdNS3), NS4 (NS4A and NS4B; AdNS4), NS5 (NS5A and NS5B; AdNS5), NS3/NS4 (AdNS3/NS4), and NS4/NS5 (AdNS4/NS5) genes, and then used to stimulate autologous lymphocytes in vitro. Antigen-specific cellular immune responses were detected by interferon-gamma (IFN-gamma), interleukin 4 (IL-4), and Granzyme B (GrB) enzyme-linked immunospot assays (ELISPOT). DCs expressing different HCV NS genes all induced positive immune responses. Furthermore, DCs transfected with AdNS3/NS4 were superior to DCs infected with AdNS3 or AdNS4 in inducing HCV-specific immunity. The same results were obtained when we compared DCs infected with AdNS4/NS5 to AdNS4 or AdNS5. DCs transduced with NS3/NS4 or NS4/NS5 had similar ability to elicit specific immune responses to HCV.
丙型肝炎病毒(HCV)非结构(NS)基因相对保守,在针对HCV的细胞免疫反应中起关键作用。本研究的目的是通过树突状细胞(DC)的转导及向T细胞的呈递来评估不同HCV NS基因的免疫原性。将来自健康供体的单核细胞衍生DC用携带HCV NS3(AdNS3)、NS4(NS4A和NS4B;AdNS4)、NS5(NS5A和NS5B;AdNS5)、NS3/NS4(AdNS3/NS4)和NS4/NS5(AdNS4/NS5)基因的重组腺病毒感染,然后用于体外刺激自体淋巴细胞。通过干扰素-γ(IFN-γ)、白细胞介素4(IL-4)和颗粒酶B(GrB)酶联免疫斑点试验(ELISPOT)检测抗原特异性细胞免疫反应。表达不同HCV NS基因的DC均诱导出阳性免疫反应。此外,用AdNS3/NS4转染的DC在诱导HCV特异性免疫方面优于用AdNS3或AdNS4感染的DC。当我们将用AdNS4/NS5感染的DC与AdNS4或AdNS5进行比较时,也得到了相同的结果。用NS3/NS4或NS4/NS5转导的DC引发针对HCV的特异性免疫反应的能力相似。