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The genome organisation of HBV; the genes overlap. ORF S, in green, encodes HBsAg. HBsAg under a transmission electron microscope: the protein self assembles into virus-like particles. HBsAg (also known as the Australia antigen) is the surface antigen of the hepatitis B virus (HBV). Its presence in blood indicates existing hepatitis B infection.
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The recombinant vaccine is based on a Hepatitis B surface antigen gene inserted into yeast (Saccharomyces cerevisiae) cells which are free of any concerns associated with human blood products. [ 17 ] [ 65 ] This allows the yeast to produce only the noninfectious surface protein, without any danger of introducing actual viral DNA into the final ...
If the host is able to clear the infection, eventually the HBsAg will become undetectable and will be followed by IgG antibodies to the hepatitis B surface antigen and core antigen (anti-HBs and anti HBc IgG). [39] The time between the removal of the HBsAg and the appearance of anti-HBs is called the window period. A person negative for HBsAg ...
HBIG should be given within 14 days of exposure to the hepatitis B virus. [7] The half-life of HBIG is about 3 weeks. In lieu of a booster administration of HBIG, a hepatitis B vaccination is initiated at the time of the initial HBIG administration, thus providing long term protection.
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Hepatitis E is inflammation of the liver caused by infection with the hepatitis E virus (HEV); [4] [5] it is a type of viral hepatitis. [6] Hepatitis E has mainly a fecal-oral transmission route that is similar to hepatitis A, although the viruses are unrelated.
HBeAg is an antigen that can be found between the icosahedral nucleocapsid core and the lipid envelope (the outer most layer of the hepatitis b virus).However, HBeAg is considered "nonparticulate" or "secretory". [2]