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UK Anthrax Vaccine (also known as Anthrax Vaccine Precipitated or AVP) is an acellular, monovalent vaccine licensed in the United Kingdom for active immunization against anthrax, caused by *Bacillus anthracis*. It is manufactured by Porton Biopharma on behalf of the UK Government for occupational health and biodefense purposes. The vaccine is prepared from a sterile filtrate of an alum-precipitated culture supernatant of the avirulent, non-encapsulated Sterne strain (34F2) of *B. anthracis*. Unlike the US-licensed Anthrax Vaccine Adsorbed (AVA), which primarily contains protective antigen (PA), AVP contains all three components of the anthrax toxin complex: protective antigen (PA, ~65%), lethal factor (LF, ~8%), and edema factor (EF, ~3%). It is adjuvanted with aluminium potassium sulphate and administered via intramuscular injection in a primary course of four doses followed by annual boosters.
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