Hepatitis C virus (HCV) is the main cause of chronic hepatitis worldwide. Chronic hepatitis ultimately results in the development of hepatocellular carcinoma (HCC). However, the mechanism of hepatocarcinogenesis in chronic HCV infection is still unclear. The ability of the core protein of HCV to modulate gene transcription, cell proliferation and cell death may be involved in the pathogenesis of HCC. Here, we report the development of HCC in two independent lines of mice transgenic for the HCV core gene, which develop hepatic steatosis early in life as a histological feature characteristic of chronic hepatitis C. After the age of 16 months, mice of both lines developed hepatic tumors that first appeared as adenomas containing fat droplets in the cytoplasm. Then HCC, a more poorly-differentiated neoplasia, developed from within the adenomas, presenting in a 'nodule-in-nodule' manner without cytoplasmic fat droplets; this closely resembled the histopathological characteristics of the early stage of HCC in patients with chronic hepatitis C. These results indicate that the HCV core protein has a chief role in the development of HCC, and that these transgenic mice provide good animal models for determining the molecular events in hepatocarcinogenesis with HCV infection.

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Hepatitis C virus (HCV) is a major cause of chronic hepatitis worldwide, which finally leads to development of hepatocellular carcinoma. Chronic hepatitis C is characterized by several histological features in the liver which discriminate it from other forms of hepatitis : bile duct damage, lymphoid follicles and steatosis (fatty change). Little is known, however, about the role of HCV or its viral proteins in the pathogenesis of hepatitis. Recently, the core protein of HCV has been suggested to have a transcriptional regulatory function, and thereby to

To define the duration of viremia in the course of acute hepatitis B, we semiquantitatively determined the levels of hepatitis B virus (HBV) DNA in the sera, using polymerase chain reaction (PCR) coupled with Southern blotting, of non-immunocompromised patients with self-limited acute hepatitis B. In the sera of 10 of 11 patients, HBV DNA, which was presumably coated with viral proteins, was detected for a long period after recovery, even at the final observation times, which ranged from 6 to 19 months after disease onset. To characterize the mode of HBV that was present in serum, we immunoprecipitated immune complexes in sera by the addition of anti-human immunoglobulin G (IgG) and determined the levels of HBV DNA separately in the supernatants and pellets. In the acute phase of hepatitis B, high levels of HBV DNA were detected both in the supernatants and pellets at comparative levels. After the convalescent phase, the amount of HBV DNA in the supernatant decreased with respect to that in the pellets. It is notable that, in most cases, serum HBV persisted as a form of immune complex even after the seroconversion to antibody to hepatitis B surface antigen (anti-HBs). These data suggest that the replication of HBV may persist in some organs, most likely in the liver or peripheral blood cells, for a long period after recovery from acute hepatitis B, and the data indicate the possible transmission of HBV from organ transplantation donors who exhibit serological markers of past infection only. (HEPATOLOGY 1998;27:1377-1382.)The duration of viremia in acute hepatitis B has been considered to cease with the clearance of the hepatitis B surface antigen (HBsAg) from serum. 1,2 However, in view of the fact that viremia in chronic hepatitis B persists after the disappearance from serum of HBsAg and the appearance of an antibody to HBsAg (anti-HBs), both of which occur in the natural course of the disease and during interferon therapy, [3][4][5][6][7][8][9] the duration of viremia in acute hepatitis B must be determined using sensitive methods to prevent the transmission of hepatitis B upon transfusion of HBsAg-negative blood [10][11][12] from patients who are recovering from acute hepatitis. Indeed, a recent study using polymerase chain reaction (PCR) has shown that hepatitis B virus (HBV) persists even in serological recovery from acute hepatitis B. 13 It is also important to determine whether HBV exists in a free or immunoglobulin (Ig)-bound form if HBV persists in serum. The extent of viremia and the modality of the virus during and after the course of acute hepatitis B, however, have not been well described. In the present study, we semiquantitatively measured the level of HBV DNA in the sera of patients in Japan, where acute hepatitis B rarely evolves into chronic infection. 14,15 PATIENTS AND METHODSPatients. We studied 11 consecutive Japanese patients (male: female ϭ 10:1) with self-limited acute hepatitis B who were admitted to our hospitals from 1991 to 1995 (Table 1). All 11 patients exhibited single-peaked ele...

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