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DESCRIPTION (provided by applicant): The National Institute of Allergy and Infectious Diseases (NIAID) is supporting efforts to develop a recombinant subunit vaccine against the Category B agent ricin toxin. The current focus is on the toxin's 267- amino acid enzymatic A subunit (RTA). To date, vaccine design has been aimed at making point mutations and site-specific deletions in RTA to attenuate its enzymatic activity so that it is safe for use in humans. Very little attention has been paid to how these mutations may affect B-cell epitopes on RTA that are critical for eliciting protective immunity. It is known that neutralizing antibodies consttute only a very small fraction of the total antibody pool elicited by RTA immunization. The overwhelming antibody response is made up of non- neutralizing and toxin-enhancing antibodies. This fact may explain the relative ineffectiveness of the current lead vaccine candidate to elicit detectable serum neutralizing activity despite high titer anti-toxin antibodies Because serum neutralizing antibody titers are the singular correlate of immunity to ricin, it is essential that RTA-based subunit vaccine stimulate measurable serum neutralizing activities. Unfortunately, in the absence of a comprehensive B-cell epitope map of RTA it is not possible to engineer derivatives RTA in which key protective B-cell epitopes are preserved, while epitopes that give rise to non-neutralizing (or even deleterious) antibodies are eliminated. This applicatio proposes to generate a comprehensive and high-resolution B-cell epitope map of RTA. This will be accomplished using a unique collection of resources, including a large panel of RTA-specific mAbs, as well as a collection of RTA derivatives with mutations in all of the known immunodominant regions of the protein. The proposed research project is significant in that the resulting B-cell epitope map will be used in conjunction with the available structural information about RTA to design novel antigens in which targets of neutralizing antibodies are preserved and presented in a context designed to most effectively elicit protective immunity. PUBLIC HEALTH RELEVANCE: The proposed project will aid in the development of a vaccine against ricin toxin, one of the most deadly toxins known to mankind, and a potential biothreat agent.
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Leveraging a transcription regulatory network to understand Salmonella invasion of host epithelial cells
  • 批准号:
    10154895
  • 项目类别:
  • 资助金额:
    $18.1万
  • 财政年份:
    2021
  • 负责人:
    Nicholas J. Mantis
  • 依托单位:
Leveraging a transcription regulatory network to understand Salmonella invasion of host epithelial cells
  • 批准号:
    10374120
  • 项目类别:
  • 资助金额:
    $20.91万
  • 财政年份:
    2021
  • 负责人:
    Nicholas J. Mantis
  • 依托单位:
Lyme Disease: B cell epitope discovery and mechanisms of antibody protection
  • 批准号:
    10677521
  • 项目类别:
  • 资助金额:
    $188.72万
  • 财政年份:
    2020
  • 负责人:
    Nicholas J. Mantis
  • 依托单位:
High-Throughput Dried Blood Spot (HT-DBS) Technologies in SARS COV-2 Serology and Vaccinology
  • 批准号:
    10855042
  • 项目类别:
  • 资助金额:
    $82.46万
  • 财政年份:
    2020
  • 负责人:
    Nicholas J. Mantis
  • 依托单位:
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