Evidence map›Paper›PMID 17202369›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

Oral vaccination with salmonella simultaneously expressing Yersinia pestis F1 and V antigens protects against bubonic and pneumonic plague.

Xinghong Yang, B Joseph Hinnebusch, Theresa Trunkle, Catharine M Bosio, Zhiyong Suo, Mike Tighe, Ann Harmsen, Todd Becker, Kathryn Crist, Nancy Walters and 2 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
–field-weighted citation impact
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

44 citing papers in PubMed.

  1. Genetic engineering ofEcoSal Plus · 2024
    Review
  2. Article
  3. Review
  4. Plague Vaccines: Status and Future.Advances in experimental medicine and biology · 2016
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Progress inFrontiers in biology · 2013
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Developing live vaccines against plague.Journal of infection in developing countries · 2011
    Review
  18. Article
  19. Article
  20. Article
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

12 authors.

Xinghong YangVeterinary Molecular Biology, Montana State University, Bozeman, MT 59717, USA.
B Joseph Hinnebusch
Theresa Trunkle
Catharine M Bosio
Zhiyong Suo
Mike Tighe
Ann Harmsen
Todd Becker
Kathryn Crist
Nancy Walters
Recep Avci
David W Pascual

Funding

Immunity to Pulmonary InfectionsZIAAI001013 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BOSIO, CATHARINE · 2009 to 2025
$18.9M
VIRUSES: FROM PARTICLES TO PROTEOMICSP20RR020185 · NCRR · MONTANA STATE UNIVERSITY - BOZEMAN · PI MEISSNER, NICOLE · 2004 to 2011
$17.0M
Animal Models to Study Plague Infection and ImmunityZIAAI000919 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HINNEBUSCH, B J · 2009 to 2023
$8.3M
Immunity to Pneumonic TularemiaZ01AI001013 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI BOSIO, CATHARINE · 2007 to 2008
$2.8M
Rodent Models To Study Pathogenesis Of Bubonic And SeptiZ01AI000919 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI HINNEBUSCH, BERNARD JOSEPH · 2002 to 2008
$1.6M
Mucosal Vaccines for PlagueR01AI056286 · NIAID · MONTANA STATE UNIVERSITY - BOZEMAN · PI PASCUAL, DAVID W · 2004 to 2006
$1.3M
NCRR NIH HHS P20 RR 020185NCRR NIH HHS P20 RR020185NIAID NIH HHS AI 56286NIAID NIH HHS R01 AI056286NIAID NIH HHS U54 AI 06537
6 · The paper itself

Abstract

The gut provides a large area for immunization enabling the development of mucosal and systemic Ab responses. To test whether the protective Ags to Yersinia pestis can be orally delivered, the Y. pestis caf1 operon, encoding the F1-Ag and virulence Ag (V-Ag) were cloned into attenuated Salmonella vaccine vectors. F1-Ag expression was controlled under a promoter from the caf1 operon; two different promoters (P), PtetA in pV3, PphoP in pV4, as well as a chimera of the two in pV55 were tested. F1-Ag was amply expressed; the chimera in the pV55 showed the best V-Ag expression. Oral immunization with Salmonella-F1 elicited elevated secretory (S)-IgA and serum IgG titers, and Salmonella-V-Ag(pV55) elicited much greater S-IgA and serum IgG Ab titers than Salmonella-V-Ag(pV3) or Salmonella-V-Ag(pV4). Hence, a new Salmonella vaccine, Salmonella-(F1+V)Ags, made with a single plasmid containing the caf1 operon and the chimeric promoter for V-Ag allowed the simultaneous expression of F1 capsule and V-Ag. Salmonella-(F1+V)Ags elicited elevated Ab titers similar to their monotypic derivatives. For bubonic plague, mice dosed with Salmonella-(F1+V)Ags and Salmonella-F1-Ag showed similar efficacy (>83% survival) against approximately 1000 LD(50) Y. pestis. For pneumonic plague, immunized mice required immunity to both F1- and V-Ags because the mice vaccinated with Salmonella-(F1+V)Ags protected against 100 LD(50) Y. pestis. These results show that a single Salmonella vaccine can deliver both F1- and V-Ags to effect both systemic and mucosal immune protection against Y. pestis.

Indexed as

Administration, OralAnimalsAntibodiesAntigens, BacterialImmunogeneticsMiceMice, Inbred BALB CMucous MembranePlagueSalmonellaSalmonella InfectionsSalmonella VaccinesSurvival RateYersinia InfectionsYersinia pestisAntibodiesAntigens, BacterialSalmonella Vaccines

Identifiers

PMID17202369
PMCPMC9809976

What OpenQuestion holds

Textmetadata
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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.