Evidence map›Paper›PMID 30797635›Full record

ArticleVaccine2019

Non-pathogenic Borrelia burgdorferi expressing Treponema pallidum TprK and Tp0435 antigens as a novel approach to evaluate syphilis vaccine candidates.

Nikhat Parveen, Mark C Fernandez, Austin M Haynes, Rui-Li Zhang, B Charmie Godornes, Arturo Centurion-Lara, Lorenzo Giacani

Abstract read
In one paragraph

Article in Vaccine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  7. Participants inFrontiers in immunology · 2025
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  8. Hitchhiker's Guide toJournal of bacteriology · 2024
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  9. Proteomic analysis of theFrontiers in microbiology · 2024
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  10. Comprehensive Overview ofCurrent protein & peptide science · 2024
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  11. Review
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  14. Review
  15. Immunization with Tp0954, an adhesin ofFrontiers in immunology · 2023
    Article
  16. Review
  17. Review
  18. Review
  19. Notes on syphilis vaccine development.Frontiers in immunology · 2022
    Review
  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

7 authors at 3 institutions in 3 countries.

Nikhat ParveenDepartment of Microbiology, Biochemistry and Molecular Genetics, Rutgers-New Jersey Medical School, Newark, NJ 07103, United States.
Mark C FernandezDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Harborview Medical Center, Seattle, WA 98104, United States.
Austin M HaynesDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Harborview Medical Center, Seattle, WA 98104, United States.
Rui-Li ZhangDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Harborview Medical Center, Seattle, WA 98104, United States; Department of Dermatology, Affiliated Wuxi No.2 People's Hospital of Nanjing Medical University, 214002 Wuxi, China.
B Charmie GodornesDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Harborview Medical Center, Seattle, WA 98104, United States.
Arturo Centurion-LaraSchool of Public Health, Universidad Peruana Cayetano Heredia, Lima 30, Peru.
Lorenzo GiacaniDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Harborview Medical Center, Seattle, WA 98104, United States; Department of Global Health, University of Washington, Seattle, WA 98104, United States. Electronic address: giacal@u.washington.edu.
University of Washington · USRutgers, The State University of New Jersey · USUniversidad Peruana Cayetano Heredia · PE

Funding

Placental Colonization by Treponema Pallidum, Congenital Syphilis & Novel VaccineU01AI115497 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI CARCAMO, CESAR PAUL EUGENIO, GIACANI, LORENZO · 2015 to 2019
$3.1M
NIAID NIH HHS U01 AI115497
6 · The paper itself

Abstract

backgroundSyphilis is resurgent in many developed countries and still prevalent in developing nations. Current and future control campaigns would benefit from the development of a vaccine, but although promising vaccine candidates were identified among the putative surface-exposed integral outer membrane proteins of the syphilis spirochete, immunization experiments in the rabbit model using recombinant antigens have failed to fully protect animals upon infectious challenge. We speculated that such recombinant immunogens, purified under denaturing conditions from Escherichia coli prior to immunization might not necessarily harbor their original structure, and hypothesized that enhanced protection would result from performing similar immunization/challenge experiments with native antigens.

methodsTo test our hypothesis, we engineered non-infectious Borrelia burgdorferi strains to express the tp0897 (tprK) and tp0435 genes of Treponema pallidum subsp. pallidum and immunized two groups of rabbits by injecting recombinant strains intramuscularly with no adjuvant. TprK is a putative integral outer membrane protein of the syphilis agent, while tp0435 encodes the highly immunogenic T. pallidum 17-kDa lipoprotein, a periplasmic antigen that was also shown on the pathogen surface. Following development of a specific host immune response to these antigens as the result of immunization, animals were challenged by intradermal inoculation of T. pallidum. Cutaneous lesion development was monitored and treponemal burden within lesions were assessed by dark-field microscopy and RT-qPCR, in comparison to control rabbits.

resultsPartial protection was observed in rabbits immunized with B. burgdorferi expressing TprK while immunity to Tp0435 was not protective. Analysis of the humoral response to TprK antigen suggested reactivity to conformational epitopes.

conclusionsImmunization with native antigens might not be sufficient to obtain complete protection to infection. Nonetheless we showed that non-infectious B. burgdorferi can be an effective carrier to deliver and elicit a specific host response to T. pallidum antigens to assess the efficacy of syphilis vaccine candidates.

Indexed as

Gene ExpressionAnimalsAntibodies, BacterialAntigens, BacterialBacterial ProteinsBacterial VaccinesBorrelia burgdorferiEnzyme-Linked Immunosorbent AssayEpitopesFluorescent Antibody TechniqueImmunity, CellularImmunizationMass SpectrometryMicePeptidesPorinsAntibodies, BacterialAntigens, BacterialBacterial ProteinsBacterial VaccinesEpitopesmajor outer sheath protein, TreponemaPeptidesPorinsRecombinant ProteinsBorrelia burgdorferiSyphilisTp0435TprKTreponema pallidum

Identifiers

PMID30797635
PMCPMC6414260
OpenAlexW2915614468

What OpenQuestion holds

Textmetadata
LicenceTDM
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.