Abstract
The only vaccine currently available for the prevention of tuberculosis in man is a live attenuated vaccine, bacille Calmette-Guerin (BCG), derived from Mycobacterium bovis. Concerns over the lack of the universal efficacy and safety of BCG have resulted in efforts to develop a new generation of TB vaccines. Historically, killed whole-cell preparations of mycobacteria have been ineffective vaccines. We revisited the potential of killed whole-cell vaccines by comparing their efficacy with live BCG Pasteur in a guinea pig challenge model. BCG Pasteur was inactivated with a low concentration of formalin and showed to be non-viable in culture or severe combined immunodeficient mice. Formalin-inactivated BCG was mixed with non-phospholipid liposome adjuvants (Novasomes™) and administered to guinea pigs as a single subcutaneous inoculation. All formulations were well tolerated and one conferred a significant survival advantage against lethal aerogenic challenge with M. bovis. Crown Copyright © 2003 Published by Elsevier Ltd. All rights reserved.
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CITATION STYLE
Chambers, M. A., Wright, D. C., Brisker, J., Williams, A., Hatch, G., Gavier-Widén, D., … Hewinson, R. G. (2004). A single dose of killed Mycobacterium bovis BCG in a novel class of adjuvant (NovasomeTM) protects guinea pigs from lethal tuberculosis. Vaccine, 22(8), 1063–1071. https://doi.org/10.1016/j.vaccine.2003.05.002
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