Quantitative correlation between the Dane particle-associated DNA polymerase and the hepatitis B e antigen. 1979

W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt

In order to evaluate the potential infectivity of blood of hepatitis B patients, the Dane particle associated DNA polymerase was determined, which is a reliable marker for the presence of complete viral particles. Enzyme activities were compared with hepatitis B e antigen (HBeAg) titers determined by radioimmunoassay. Detectable DNA polymerase activity was only present in HBeAg positive blood, preferentially in samples with high antigen titers (1 : 1000 and above). These samples therefore have to be considered as highly infectious. However, blood with low HBeAg levels and free of detectable polymerase activity can still be infectious, since the polymerase reaction is rather insensitive compared to the radioimmunological HBeAg determination.

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D004259 DNA-Directed DNA Polymerase DNA-dependent DNA polymerases found in bacteria, animal and plant cells. During the replication process, these enzymes catalyze the addition of deoxyribonucleotide residues to the end of a DNA strand in the presence of DNA as template-primer. They also possess exonuclease activity and therefore function in DNA repair. DNA Polymerase,DNA Polymerases,DNA-Dependent DNA Polymerases,DNA Polymerase N3,DNA Dependent DNA Polymerases,DNA Directed DNA Polymerase,DNA Polymerase, DNA-Directed,DNA Polymerases, DNA-Dependent,Polymerase N3, DNA,Polymerase, DNA,Polymerase, DNA-Directed DNA,Polymerases, DNA,Polymerases, DNA-Dependent DNA
D005260 Female Females
D006509 Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. Hepatitis B Virus Infection
D006511 Hepatitis B Antigens Antigens of the virion of the HEPATITIS B VIRUS or the Dane particle, its surface (HEPATITIS B SURFACE ANTIGENS), core (HEPATITIS B CORE ANTIGENS), and other associated antigens, including the HEPATITIS B E ANTIGENS. HBAg,Hepatitis B Antigen,Antigen, Hepatitis B,Antigens, Hepatitis B,B Antigen, Hepatitis,B Antigens, Hepatitis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
July 1976, The Journal of infectious diseases,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
February 1977, Journal of virology,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
January 1978, Journal of medical virology,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
February 1979, Acta pathologica et microbiologica Scandinavica. Section B, Microbiology,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
January 1977, Journal of virology,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
July 1977, The Journal of general virology,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
January 1982, Hepatology (Baltimore, Md.),
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
January 1975, Intervirology,
W Siegert, and J Grunst, and W Wilmanns, and G G Frösner, and F Deinhardt
January 1975, The American journal of the medical sciences,
Copied contents to your clipboard!