Vento S, Hegarty J E, Alberti A, O'Brien C J, Alexander G J, Eddleston A L, Williams R
Hepatology. 1985 Mar-Apr;5(2):192-7. doi: 10.1002/hep.1840050206.
Using a newly developed indirect T lymphocyte migration inhibition test, cell-mediated immunity to HBsAg and HBcAg was directly and simultaneously examined in a total of 21 patients with HBsAg-positive chronic liver disease (CLD), and in seven subjects whose sera contained anti-HBs (2 previous acute hepatitis B; 4 hepatitis B vaccine recipients and 1 chronic active hepatitis). T cell sensitization to HBcAg was invariably detected in the HBsAg-positive CLD patients tested (12/12), whereas T cell sensitization to HBsAg was not present in any of the patients (0/21). In contrast, T cell sensitization to HBsAg was present in all anti-HBs-positive subjects. These results support the hypothesis that the cellular immune response to HBcAg, rather than to HBsAg, is implicated in the pathogenesis of HBsAg-positive CLD. Moreover, the observation that the addition of T cells from patients with HBsAg-positive CLD to T cells from anti-HBs positive subjects in a ratio of 1 to 9 reversed their sensitization to HBsAg, suggests that a hyperactivity of HBsAg-specific suppressor T cell population may be responsible for persistent HBs antigenemia.
采用新开发的间接T淋巴细胞迁移抑制试验,对总共21例HBsAg阳性慢性肝病(CLD)患者以及7例血清中含有抗-HBs的受试者(2例既往急性乙型肝炎;4例乙型肝炎疫苗接种者和1例慢性活动性肝炎患者)的细胞介导免疫对HBsAg和HBcAg进行了直接且同步的检测。在所检测的HBsAg阳性CLD患者(12/12)中均检测到对HBcAg的T细胞致敏,而在任何患者中均未检测到对HBsAg的T细胞致敏(0/21)。相反,在所有抗-HBs阳性受试者中均存在对HBsAg的T细胞致敏。这些结果支持了这样一种假说,即对HBcAg而非对HBsAg的细胞免疫反应与HBsAg阳性CLD的发病机制有关。此外,观察到将HBsAg阳性CLD患者的T细胞与抗-HBs阳性受试者的T细胞以1比9的比例混合后,逆转了他们对HBsAg的致敏,这表明HBsAg特异性抑制性T细胞群体的过度活跃可能是持续性HBs抗原血症的原因。