HEPATITIS-B VIRUS-DNA IN PERIPHERAL-BLOOD LEUKOCYTES - A COMPARISON BETWEEN HEPATOCELLULAR-CARCINOMA AND OTHER HEPATITIS-B VIRUS-RELATED CHRONIC LIVER-DISEASES
Nwy. Leung et al., HEPATITIS-B VIRUS-DNA IN PERIPHERAL-BLOOD LEUKOCYTES - A COMPARISON BETWEEN HEPATOCELLULAR-CARCINOMA AND OTHER HEPATITIS-B VIRUS-RELATED CHRONIC LIVER-DISEASES, Cancer, 73(4), 1994, pp. 1143-1148
Background. Hepatitis B virus (HBV) DNA has been detected in the perip
heral blood leukocytes (PBL) during acute and chronic HBV infection. P
ossible pathobiologic significance includes infectivity and altered im
munity. There are few data relating PBL HBV-DNA with severity of the l
iver disease, in particular with hepatocellular carcinoma (HCC). Metho
ds. HBV-DNA was detected by dot-spot hybridization technique in PBL se
parated from venous blood samples of 209 hepatitis B surface antigen-p
ositive patients (28 healthy carriers and 95 chronic hepatitis, 29 cir
rhotic, and 57 HCC patients). Serum HBV-DNA and hepatitis B e-antigen
(HBeAg) were also measured.Results. Thirty percent of HCC patients wer
e hepatitis e-antigen-positive compared to 50%, 84% (P < 0.0001), and
69% (P < 0.00001) of healthy carriers and chronic hepatitis and cirrho
tic patients, respectively. Furthermore, only 11% of HCC patients had
detectable serum HBV-DNA compared to 39% (P < 0.001), 58% (P < 0.001),
and 31% (P < 0.05) of these respective patient groups. Despite low vi
ral replication among HCC patients, 58% had PBL HBV-DNA. Corresponding
figures for healthy carriers and for chronic hepatitis and cirrhotic
patients were 39%, 58%, and 56%. Fifty-two percent of HCC patients had
positive PBL HBV-DNA in the absence of serum HBV-DNA, compared with 2
5% in healthy carriers (P < 0.05) and 22% in chronic hepatitis (P < 0.
001) and 35% in cirrhotic patients (P = NS). Conclusion. The high dete
ction rate of PBL HBV-DNA among HCC patients may reflect certain patho
genetic processes of HBV infection and indicate a higher risk of devel
opment of HCC.