Abrignani S
IRIS, Research Centre of Chiron Vaccines, Siena, Italy.
Semin Liver Dis. 1997;17(4):319-22. doi: 10.1055/s-2007-1007208.
Although immune responses to hepatitis viruses are initiated by virus-specific T cells, there is evidence that many more intrahepatic T cells are activated than those specific for the pathogen. Recent evidence suggests that cytokine combinations, such as IL-2, IL-6, and TNF alpha, can activate both naive and memory T cells in vitro. The inflammatory cytokine milieu in the liver of patients with chronic viral hepatitis may therefore favor bystander activation of T cells. This may play an important role in enhancing effector T-cell function in the liver, and in maintaining peripheral memory T cells in the absence of antigenic stimulation, such as after virus clearance.
虽然对肝炎病毒的免疫反应是由病毒特异性T细胞启动的,但有证据表明,肝内被激活的T细胞数量比针对病原体的特异性T细胞要多得多。最近的证据表明,细胞因子组合,如白细胞介素-2、白细胞介素-6和肿瘤坏死因子α,可在体外激活初始T细胞和记忆T细胞。因此,慢性病毒性肝炎患者肝脏中的炎性细胞因子环境可能有利于T细胞的旁观者激活。这可能在增强肝脏中效应T细胞功能以及在没有抗原刺激(如病毒清除后)的情况下维持外周记忆T细胞方面发挥重要作用。