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Opsono-Adherence Assay to Evaluate Functional Antibodies in Vaccine Development Against Bacillus anthracis and Other Encapsulated Pathogens
Published on: May 19, 2020
Anthrax Vaccine Precipitated Induces Edema Toxin-Neutralizing, Edema Factor-Specific Antibodies in Human Recipients
Eric K Dumas1,2, Timothy Gross1, Jason Larabee2
1Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation (OMRF), Oklahoma City, Oklahoma, USA.
Anthrax vaccine precipitated (AVP) elicits higher edema factor (EF) antibodies than anthrax vaccine adsorbed (AVA). While protective antigen (PA) antibodies are key for neutralizing anthrax edema toxin (ET), EF antibodies from AVP can neutralize ET.
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Edema toxin (ET) from Bacillus anthracis, comprising edema factor (EF) and protective antigen (PA), is a key virulence factor.
- Anthrax vaccine precipitated (AVP) contains low levels of EF and can induce EF-specific antibodies.
Purpose of the Study:
- To compare humoral responses to ET in recipients of AVP versus anthrax vaccine adsorbed (AVA).
- To determine if EF antibodies elicited by AVP contribute to ET neutralization.
Main Methods:
- Comparative analysis of antibody titers (IgG) against EF and PA in human vaccine recipients.
- Luciferase-based cyclic AMP reporter assay for ET neutralization.
- Analysis of antibody binding to EF decapeptides.
Main Results:
- AVP induced significantly higher incidence and titers of EF antibodies compared to AVA.
- PA IgG levels and ET neutralization capacity were comparable between AVP and AVA groups.
- Purified EF antibodies from AVP sera demonstrated ET neutralization capabilities.
Conclusions:
- While PA antibodies are the primary neutralizers of ET, EF antibodies elicited by AVP can also neutralize ET.
- The presence of EF in AVP contributes to its immunogenicity.
- Further investigation into incorporating EF components could enhance next-generation PA-based anthrax vaccines.
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