Literature DB >> 15664918

A high-affinity monoclonal antibody to anthrax protective antigen passively protects rabbits before and after aerosolized Bacillus anthracis spore challenge.

Nehal Mohamed1, Michelle Clagett, Juan Li, Steven Jones, Steven Pincus, Giovanni D'Alia, Linda Nardone, Michael Babin, George Spitalny, Leslie Casey.   

Abstract

We have developed a therapeutic for the treatment of anthrax using an affinity-enhanced monoclonal antibody (ETI-204) to protective antigen (PA), which is the central cell-binding component of the anthrax exotoxins. ETI-204 administered preexposure by a single intravenous injection of a dose of between 2.5 and 10 mg per animal significantly protected rabbits from a lethal aerosolized anthrax spore challenge ( approximately 60 to 450 times the 50% lethal dose of Bacillus anthracis Ames). Against a similar challenge, ETI-204 administered intramuscularly at a 20-mg dose per animal completely protected rabbits from death (100% survival). In the postexposure setting, intravenous administration of ETI-204 provided protection 24 h (8 of 10) and 36 h (5 of 10) after spore challenge. Administration at 48 h postchallenge, when 3 of 10 animals had already succumbed to anthrax infection, resulted in the survival of 3 of 7 animals (43%) for the duration of the study (28 days). Importantly, surviving ETI-204-treated animals were free of bacteremia by day 10 and remained so until the end of the studies. Only 11 of 51 ETI-204-treated rabbits had positive lung cultures at the end of the studies. Also, rabbits that were protected from inhalational anthrax by administration of ETI-204 developed significant titers of PA-specific antibodies. Presently, the sole therapeutic regimen available to treat infection by inhalation of B. anthracis spores is a 60-day course of antibiotics that is effective only if administered prior to or shortly after exposure. Based upon results reported here, ETI-204 is an effective therapy for prevention and treatment of inhalational anthrax.

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Year:  2005        PMID: 15664918      PMCID: PMC547027          DOI: 10.1128/IAI.73.2.795-802.2005

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  40 in total

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4.  Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill.

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Journal:  J Immunol Methods       Date:  1989-05-12       Impact factor: 2.303

5.  Passive protection by polyclonal antibodies against Bacillus anthracis infection in guinea pigs.

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Journal:  Infect Immun       Date:  1997-12       Impact factor: 3.441

6.  Defining a serological correlate of protection in rabbits for a recombinant anthrax vaccine.

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Journal:  Vaccine       Date:  2004-01-02       Impact factor: 3.641

7.  Comparative efficacy of experimental anthrax vaccine candidates against inhalation anthrax in rhesus macaques.

Authors:  B E Ivins; M L Pitt; P F Fellows; J W Farchaus; G E Benner; D M Waag; S F Little; G W Anderson; P H Gibbs; A M Friedlander
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8.  Anthrax protective antigen forms oligomers during intoxication of mammalian cells.

Authors:  J C Milne; D Furlong; P C Hanna; J S Wall; R J Collier
Journal:  J Biol Chem       Date:  1994-08-12       Impact factor: 5.157

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Authors:  A M Friedlander; R Bhatnagar; S H Leppla; L Johnson; Y Singh
Journal:  Infect Immun       Date:  1993-01       Impact factor: 3.441

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Authors:  A M Friedlander
Journal:  J Biol Chem       Date:  1986-06-05       Impact factor: 5.157

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  55 in total

1.  Characterization of a permissive epitope insertion site in adenovirus hexon.

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2.  APEx 2-hybrid, a quantitative protein-protein interaction assay for antibody discovery and engineering.

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-09       Impact factor: 11.205

3.  Efficacy of ETI-204 monoclonal antibody as an adjunct therapy in a New Zealand white rabbit partial survival model for inhalational anthrax.

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5.  Human IgG Fc domain engineering enhances antitoxin neutralizing antibody activity.

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Review 7.  Targeting virulence not viability in the search for future antibacterials.

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Review 8.  An overview of investigational toxin-directed therapies for the adjunctive management of Bacillus anthracis infection and sepsis.

Authors:  Lernik Ohanjanian; Kenneth E Remy; Yan Li; Xizhong Cui; Peter Q Eichacker
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10.  Controlled release of an anthrax toxin-neutralizing antibody from hydrolytically degradable polyethylene glycol hydrogels.

Authors:  Yingkai Liang; Megan V Coffin; Slobodanka D Manceva; Jessica A Chichester; R Mark Jones; Kristi L Kiick
Journal:  J Biomed Mater Res A       Date:  2015-08-13       Impact factor: 4.396

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