Clonal vaccinia virus grown in cell culture as a new smallpox vaccine
Center for Infectious Disease and Vaccine Research; Department of Medicine, Division of Infectious Diseases and Immunology
Immunity | Immunology and Infectious Disease | Immunology of Infectious Disease | Infectious Disease
Although the smallpox virus was eradicated over 20 years ago, its potential release through bioterrorism has generated renewed interest in vaccination. To develop a modern smallpox vaccine, we have adapted vaccinia virus that was derived from the existing Dryvax vaccine for growth in a human diploid cell line. We characterized six cloned and one uncloned vaccine candidates. One clone, designated ACAM1000, was chosen for development based on its comparability to Dryvax when tested in mice, rabbits and monkeys for virulence and immunogenicity. By most measures, ACAM1000 was less virulent than Dryvax. We compared ACAM1000 and Dryvax in a randomized, double-blind human clinical study. The vaccines were equivalent in their ability to produce major cutaneous reactions ('takes') and to induce neutralizing antibody and cell-mediated immunity against vaccinia virus.
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Citation: Nat Med. 2003 Sep;9(9):1125-30. Epub 2003 Aug 17. doi:10.1038/nm916. Link to article on publisher's site
Weltzin, Richard; Liu, Jian; Pugachev, Konstantin V.; Myers, Gwendolyn A.; Coughlin, Brie; Blum, Paul S.; Nichols, Richard; Johnson, Casey; Cruz, John; Kennedy, Jeffrey S.; Ennis, Francis A.; and Monath, Thomas P., "Clonal vaccinia virus grown in cell culture as a new smallpox vaccine" (2003). Infectious Diseases and Immunology Publications and Presentations. 271.