Kawanishi H
Arch Pathol Lab Med. 1979 Apr;103(4):157-64.
To study the morphologic interrelation of hepatocytes with the replication of hepatitis B vius (HBV) and immunocompetent cells in chronic active liver disease(CALD), organ cultures were prepared from liver biopsy specimens. Replication of hepatitis B core antigen (HBcAg) appears to occur in the nucleus of the hepatocyte in close association with intranuclear electron-dense strands and sometimes intranucleolar matrixes (likely HBcAg genomes), and cytoplasmic maturation of the HBcAg takes place in the preautolytic condition of host hepatocytes. Immunocompetent cells became progressively autolyzed in the early period of cultures. No difference in progression of hepatocyte injury in tissues from normal subjects and from hepatitis B surface antigen (HBsAg)-positive and HBsAg-negative patients with CALD may suggest that intracellular synthesis of HBV alone is not cytopathic to host hepatocytes. This model is promising for the study of HBV replication and development, and also for testing the efficacy of new antiviral agents against the virus.
为研究慢性活动性肝病(CALD)中肝细胞形态与乙型肝炎病毒(HBV)复制及免疫活性细胞之间的相互关系,我们用肝活检标本制备了器官培养物。乙型肝炎核心抗原(HBcAg)的复制似乎发生在肝细胞的细胞核内,与核内电子致密链以及有时与核仁内基质(可能是HBcAg基因组)密切相关,并且HBcAg的胞质成熟发生在宿主肝细胞的自溶前期。免疫活性细胞在培养早期逐渐自溶。正常受试者以及CALD的乙型肝炎表面抗原(HBsAg)阳性和HBsAg阴性患者组织中肝细胞损伤进展没有差异,这可能表明仅HBV的细胞内合成对宿主肝细胞没有细胞病变作用。该模型对于研究HBV复制和发展以及测试新型抗病毒药物对该病毒的疗效很有前景。