Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2011 Aug;3(8):1004-19.
doi: 10.3390/toxins3081004. Epub 2011 Aug 15.

Monoclonal antibody therapies against anthrax

Affiliations
Review

Monoclonal antibody therapies against anthrax

Zhaochun Chen et al. Toxins (Basel). 2011 Aug.

Abstract

Anthrax is a highly lethal infectious disease caused by the spore-forming bacterium Bacillus anthracis. It not only causes natural infection in humans but also poses a great threat as an emerging bioterror agent. The lethality of anthrax is primarily attributed to the two major virulence factors: toxins and capsule. An extensive effort has been made to generate therapeutically useful monoclonal antibodies to each of the virulence components: protective antigen (PA), lethal factor (LF) and edema factor (EF), and the capsule of B. anthracis. This review summarizes the current status of anti-anthrax mAb development and argues for the potential therapeutic advantage of a cocktail of mAbs that recognize different epitopes or different virulence factors.

Keywords: Bacillus anthracis; a cocktail of mAbs; anti-EF mAbs; anti-LF mAbs; anti-PA mAbs; anti-capsule mAbs; post-exposure treatment of anthrax.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Comprehensive protection could be achieved by a combination of anti-PA, anti-LF, anti-EF and anti-PGA mAbs that target major steps of the infection process.

References

    1. Jernigan D.B., Raghunathan P.L., Bell B.P., Brechner R., Bresnitz E.A., Butler J.C., Cetron M., Cohen M., Doyle T., Fischer M., et al. Investigation of bioterrorism-related anthrax, United States, 2001: epidemiologic findings. Emerg. Infect. Dis. 2002;8:1019–1028. - PMC - PubMed
    1. Inglesby T.V., O’Toole T., Henderson D.A., Bartlett J.G., Ascher M.S., Eitzen E., Friedlander A.M., Gerberding J., Hauer J., Hughes J., et al. Anthrax as a biological weapon, 2002: updated recommendations for management. J. Am. Med. Assoc. 2002;287:2236–2252. - PubMed
    1. van der Goot G., Young J.A. Receptors of anthrax toxin and cell entry. Mol. Aspects Med. 2009;30:406–412. - PMC - PubMed
    1. Duesbery N.S., Webb C.P., Leppla S.H., Gordon V.M., Klimpel K.R., Copeland T.D., Ahn N.G., Oskarsson M.K., Fukasawa K., Paull K.D., et al. Proteolytic inactivation of MAP-kinase-kinase by anthrax lethal factor. Science. 1998;280:734–737. - PubMed
    1. Vitale G., Bernardi L., Napolitani G., Mock M., Montecucco C. Susceptibility of mitogen-activated protein kinase kinase family members to proteolysis by anthrax lethal factor. Biochem. J. 2000;352:739–745. - PMC - PubMed

Publication types

MeSH terms