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The early humoral immune response to Bacillus anthracis toxins in patients infected with cutaneous anthrax.

Authors :
Brenneman KE
Doganay M
Akmal A
Goldman S
Galloway DR
Mateczun AJ
Cross AS
Baillie LW
Source :
FEMS immunology and medical microbiology [FEMS Immunol Med Microbiol] 2011 Jul; Vol. 62 (2), pp. 164-72. Date of Electronic Publication: 2011 Apr 15.
Publication Year :
2011

Abstract

Bacillus anthracis, the causative agent of anthrax, produces a tripartite toxin composed of two enzymatically active subunits, lethal factor (LF) and edema factor (EF), which, when associated with a cell-binding component, protective antigen (PA), form lethal toxin and edema toxin, respectively. In this preliminary study, we characterized the toxin-specific antibody responses observed in 17 individuals infected with cutaneous anthrax. The majority of the toxin-specific antibody responses observed following infection were directed against LF, with immunoglobulin G (IgG) detected as early as 4 days after the onset of symptoms in contrast to the later and lower EF- and PA-specific IgG responses. Unlike the case with infection, the predominant toxin-specific antibody response of those immunized with the US anthrax vaccine absorbed and UK anthrax vaccine precipitated licensed anthrax vaccines was directed against PA. We observed that the LF-specific human antibodies were, like anti-PA antibodies, able to neutralize toxin activity, suggesting the possibility that they may contribute to protection. We conclude that an antibody response to LF might be a more sensitive diagnostic marker of anthrax than to PA. The ability of human LF-specific antibodies to neutralize toxin activity supports the possible inclusion of LF in future anthrax vaccines.<br /> (© 2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1574-695X
Volume :
62
Issue :
2
Database :
MEDLINE
Journal :
FEMS immunology and medical microbiology
Publication Type :
Academic Journal
Accession number :
21401726
Full Text :
https://doi.org/10.1111/j.1574-695X.2011.00800.x