Evidence map›Paper›PMID 36376214›Full record

ArticleVaccine2022

Immunization with a tri-antigen syphilis vaccine significantly attenuates chancre development, reduces bacterial load, and inhibits dissemination of Treponema pallidum.

Sheila A Lukehart, Barbara Molini, Alloysius Gomez, Charmie Godornes, Rebecca Hof, Mark C Fernandez, Ragan A Pitner, Sean A Gray, Darrick Carter, Lorenzo Giacani and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The Global Syphilis Epidemic: Turning the Tide.Sexually transmitted diseases · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Frontiers in immunology · 2026
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. B-Cell Epitope Mapping of theDiagnostics (Basel, Switzerland) · 2025
    Article
  15. Article
  16. Time-course transcriptomics reveals the impact ofFrontiers in microbiology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Evaluation of a minimal array ofMicrobiology spectrum · 2024
    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

11 authors at 3 institutions in 2 countries.

Sheila A LukehartDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA; Department of Global Health, University of Washington, Seattle, WA, USA.
Barbara MoliniDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA.
Alloysius GomezDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada.
Charmie GodornesDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA.
Rebecca HofDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada.
Mark C FernandezDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA.
Ragan A PitnerPAI Life Sciences, Seattle, WA, USA.
Sean A GrayPAI Life Sciences, Seattle, WA, USA.
Darrick CarterPAI Life Sciences, Seattle, WA, USA.
Lorenzo GiacaniDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA.
Caroline E CameronDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA; Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada. Electronic address: caroc@uvic.ca.
University of Washington · USPAI Life Sciences (United States) · USUniversity of Victoria · CA

Funding

University of Washington (UW) Sexually Transmitted Infections (STI) Cooperative Research Center (CRC) - Syphilis Vaccine to Protect against Local and Disseminated T. pallidum InfectionU19AI144133 · NIAID · UNIVERSITY OF WASHINGTON · PI GIACANI, LORENZO · 2019 to 2023
$10.6M
TREPONEMA PALLIDUM PATHOGENESIS ASSOCIATED MOLECULESR01AI042143 · NIAID · UNIVERSITY OF WASHINGTON · PI LUKEHART, SHEILA A. · 1998 to 2015
$5.4M
Project 4: Antigenic variation of TprKR01AI063940 · NIAID · UNIVERSITY OF WASHINGTON · PI LUKEHART, SHEILA A. · 2004 to 2013
$3.3M
PROTECTIVE IMMUNITY AGAINST SYPHILISP01AI034616 · NIAID · UNIVERSITY OF WASHINGTON · PI LUKEHART, SHEILA A. · 1993 to 2003
$2.5M
Innovative approaches to syphilis vaccine designR01AI123196 · NIAID · UNIVERSITY OF WASHINGTON · PI CAMERON, CAROLINE E, LUKEHART, SHEILA A. · 2016 to 2019
$2.3M
Extracellular Matrix Adhesins of Treponema pallidumR37AI051334 · NIAID · UNIVERSITY OF VICTORIA · PI CAROLINE E CAMERON · 2019 to 2026
$2.3M
NIAID NIH HHS P01 AI034616NIAID NIH HHS R01 AI042143NIAID NIH HHS R01 AI063940NIAID NIH HHS R01 AI123196NIAID NIH HHS R37 AI051334NIAID NIH HHS U19 AI144133
6 · The paper itself

Abstract

Syphilis continues to be a significant public health concern worldwide. The disease is endemic in many low- and middle-income countries, and rates have risen sharply in high-income countries over the last decade. The continued prevalence of infectious and congenital syphilis worldwide highlights the need for the development of an effective syphilis vaccine to complement public health measures for syphilis control. The complex, multi-stage course of syphilis infection necessitates a holistic approach to the development of an effective vaccine, in which immunization prevents both the localized stage of infection (typified by the highly infectious chancre) and the disseminated stages of infection (typified by the secondary rash, neurosyphilis, and destructive tertiary lesions, as well as congenital syphilis). Inhibiting development of the infectious chancre would reduce transmission thus providing community- level protection, while preventing dissemination would provide individual-level protection by reducing serious sequelae and may also provide community level protection by reducing shedding during secondary syphilis. In the current study we build upon prior investigations which demonstrated that immunizations with individual, well characterized T. pallidum TprK, TprC, and Tp0751 peptides elicits partial protection against infection in the animal model. Specifically, we show here that immunization with a TprC/TprK/Tp0751 tri-antigen cocktail protects animals from progressive syphilis lesions and substantially inhibits dissemination of the infection.

Indexed as

ChancreSyphilisSyphilis, CongenitalAnimalsBacterial LoadBacterial VaccinesImmunizationTreponema pallidumBacterial VaccinesBacteriumSyphilisTreponema pallidumVaccine

Identifiers

PMID36376214
PMCPMC10318934
OpenAlexW4309098868

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.