Evidence map›Paper›PMID 18987167›Full record

ArticleClinical and vaccine immunology : CVI2009

Flagellin-F1-V fusion protein is an effective plague vaccine in mice and two species of nonhuman primates.

Steven B Mizel, Aaron H Graff, Nammalwar Sriranganathan, Sean Ervin, Cynthia J Lees, Mark O Lively, Roy R Hantgan, Michael J Thomas, James Wood, Brian Bell

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
5.3field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

82 citing papers in PubMed, 137 citations in OpenAlex.

  1. An adenoviral-vectored vaccine protects mice against aerosol challenge with Yersinia pestis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Novel Bivalent mRNA-LNP Vaccine for Highly Effective Protection against Pneumonic Plague.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Review
  9. Article
  10. Delivery ofmSphere · 2024
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Flagellin fromTropical life sciences research · 2022
    Article
  17. Review
  18. Review
  19. Article
  20. Article

22 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Steven B MizelDepartment of Microbiology and Immunology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157-1064, USA. smizel@wfubmc.edu
Aaron H Graff
Nammalwar Sriranganathan
Sean Ervin
Cynthia J Lees
Mark O Lively
Roy R Hantgan
Michael J Thomas
James Wood
Brian Bell
Wake Forest University · USVirginia–Maryland College of Veterinary Medicine · USVirginia Tech · US

Funding

Preclinical Development of Flagellin as a Mucosal Adjuvant in Biodefense VaccinesU01AI070440 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MIZEL, STEVEN B. · 2006 to 2009
$3.4M
NIAID NIH HHS U01 AI070440
6 · The paper itself

Abstract

A number of studies have clearly demonstrated that flagellin is a potent adjuvant that promotes robust immune responses when it is given with a protein antigen. In view of the potential biological and practical benefits of a recombinant protein vaccine composed of a single fusion protein containing flagellin and antigen, we have evaluated the efficacy of a fusion protein composed of flagellin and two protective antigens of Yersinia pestis (F1 and V) in eliciting protection against respiratory challenge with Y. pestis. Flagellin-F1-V was produced and purified in high yield under good manufacturing practices conditions. The fusion protein retains full Toll-like receptor 5-stimulating activity in vitro. Using a prime-boost immunization protocol, we found that flagellin-F1-V elicits robust antigen-specific humoral immunity in mice and two species of nonhuman primates. Immune mice were fully protected against intranasal challenge with 150 mean tolerated doses of Y. pestis CO92. In immune mice, the bacteria were completely cleared within 3 days after challenge. Flagellin-F1-V exhibited full stability for at least 297 days at 4 degrees C and at least 168 days at 25 degrees C. At between 29 and 84 days at 37 degrees C, the protein exhibited a loss of biological activity that appeared to be associated with a substantial change in protein diameter, possibly due to oligomerization. On the basis of our results, we believe that flagellin-F1-V is an outstanding candidate for evaluation in studies with humans.

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialBacterial ProteinsChlorocebus aethiopsDrug StabilityDrug StorageFemaleFlagellinImmunization, SecondaryMacaca fascicularisMaleMiceMice, Inbred BALB CPlague VaccinePore Forming Cytotoxic ProteinsAntibodies, BacterialAntigens, BacterialBacterial Proteinscaf1 protein, Yersinia pestisFlagellinLcrV protein, YersiniaPlague VaccinePore Forming Cytotoxic ProteinsRecombinant Fusion ProteinsToll-Like Receptor 5Virulence Factors

Identifiers

PMID18987167
PMCPMC2620661
OpenAlexW2163816719

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.