Cummings Kara L, Rosen Hugo R, Hahn Young S
Beirne Carter Center for Immunology Research and Department of Microbiology, University of Virginia, Charlottesville, VA 22908, USA.
Clin Immunol. 2009 Sep;132(3):401-11. doi: 10.1016/j.clim.2009.05.002. Epub 2009 May 26.
CD4+ T cell responses are impaired in chronic HCV infection. To determine factor(s) involved in CD4+ T cell dysregulation, we examined the effect of extracellular core on the alteration of CD4+ T cell responses and the cell surface level of core-binding protein, gC1qR on CD4+ T cells from acute HCV patients with resolved and chronic infection. During the acute phase of infection, the frequency of gC1qR+CD4+ T cells increased in both resolved and chronic HCV infection compared to healthy controls. Notably, 6 months later, the frequency of gC1qR+CD4+ T cells maintained elevated in chronic patients compared to that in resolved patients. In addition, TCR stimulation increased the frequency of gC1qR+CD4+ T cells, resulting in core-induced inhibition of T cell responses in both resolved and chronic patients. These results suggest that HCV infection expands gC1qR+CD4+ T cells, which increase the susceptibility to core-mediated immune dysregulation and facilitate the establishment of HCV persistency.
在慢性丙型肝炎病毒(HCV)感染中,CD4 + T细胞反应受损。为了确定参与CD4 + T细胞失调的因素,我们研究了细胞外核心蛋白对急性HCV感染已缓解患者和慢性感染患者CD4 + T细胞反应改变以及CD4 + T细胞表面核心结合蛋白gC1qR水平的影响。在感染急性期,与健康对照相比,已缓解和慢性HCV感染患者中gC1qR + CD4 + T细胞的频率均增加。值得注意的是,6个月后,与已缓解患者相比,慢性患者中gC1qR + CD4 + T细胞的频率仍保持升高。此外,TCR刺激增加了gC1qR + CD4 + T细胞的频率,导致已缓解和慢性患者中核心蛋白诱导的T细胞反应受到抑制。这些结果表明,HCV感染会使gC1qR + CD4 + T细胞扩增,这增加了对核心蛋白介导的免疫失调的易感性,并促进了HCV持续性感染的建立。