COMING SOON! PQDT Open is getting a new home!

ProQuest Open Access Dissertations & Theses will remain freely available as part of a new and enhanced search experience at

Questions? Please refer to this FAQ.

Dissertation/Thesis Abstract

Identification of B-cell epitopes on domain 4 of anthrax protective antigen
by Kelly-Cirino, Cassandra D., Ph.D., State University of New York at Albany, 2009, 148; 3356377
Abstract (Summary)

Protective Antigen (PA) is the receptor binding subunit common to both Lethal (LT) and Edema (ET) toxins, which contribute to the mortality associated with Bacillus anthracis infection. While recombinant PA (rPA) is likely to be an important constituent of second generation anthrax vaccines, evaluating the effectiveness of candidate vaccines is currently difficult, because the specific B cell epitopes involved in toxin neutralization have not been completely defined. The only well characterized antibody, 14B7, has been shown to disrupt the association of PA with the anthrax toxin receptors (ATR) by binding to domain 4 of PA. I hypothesized that other domain 4 epitopes play a critical role in eliciting a protective immune response to anthrax. To test this hypothesis I first identified a novel rPA immunogen capable of eliciting a protective immune response in goats and mice. I next established an LT challenge mouse model to evaluate the ability of antibodies to disrupt the intoxication pathway in vivo. To identify neutralizing epitopes on domain 4 of PA, I screened a collection of murine B cell hybridomas for monoclonal antibodies (MAbs) that reacted with the native PA protein as well as linear peptides within domain 4. Two IgG1 MAbs, 1-F1 and 2-B12, were identified that recognize distinct domain 4 linear epitopes. 1-F1 recognized residues 692-703, part of the ATR recognition region. 1-F1 blocked PA’s ability to associate with ATR in an in vitro solid phase binding assay, and neutralized LT in vitro. 2-B12 recognized residues 716-727, a region not previously known to be a target of neutralizing antibodies. 2-B12 was as effective as 1-F1 in neutralizing LT in vitro , although it only partially inhibited PA binding to ATR. Mice passively administered 1-F1 or 2-B12 were protected against LT challenge. This data confirm that several epitopes on domain 4 of PA contribute to the protective immune response against anthrax intoxication. The identification of neutralizing MAbs recognizing linear peptides provides us with a powerful tool for identifying the specific epitopes involved in the protective immune response to anthrax and advances our fundamental understanding of the mechanisms by which antibodies neutralize anthrax toxin.

Indexing (document details)
Advisor: Mantis, Nicholas J.
Commitee: Bernard, Kristen, Collier, R. John, Egan, Christina, McDonough, Kathleen
School: State University of New York at Albany
Department: Biomedical Sciences
School Location: United States -- New York
Source: DAI-B 70/05, Dissertation Abstracts International
Subjects: Microbiology, Immunology
Keywords: Anthrax, B-cell epitopes, Domain 4, Immunity, Monoclonal antibodies, Protective antigens
Publication Number: 3356377
ISBN: 978-1-109-16621-7
Copyright © 2021 ProQuest LLC. All rights reserved. Terms and Conditions Privacy Policy Cookie Policy