Evidence map›Paper›PMID 16239559›Full record

ArticleInfection and immunity2005

Comparison of immune responses to gonococcal PorB delivered as outer membrane vesicles, recombinant protein, or Venezuelan equine encephalitis virus replicon particles.

Weiyan Zhu, Christopher E Thomas, Ching-Ju Chen, Cornelius N Van Dam, Robert E Johnston, Nancy L Davis, P Frederick Sparling

Registry-linked trialOpen access · greenAbstract readComparative Study
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07758972 (A First in Human Phase I Randomized and Controlled Trial to Test Safety and Immunogenicity of a Multivalent Vaccine Against Neisseria Gonorrhoeae), which is not on this map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.0field-weighted citation impact, top 25% 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.

NCT07758972 phase1recruitingnot on this mapstarted 2026, after this paper: background citation

A First in Human Phase I Randomized and Controlled Trial to Test Safety and Immunogenicity of a Multivalent Vaccine Against Neisseria Gonorrhoeae

TypeinterventionalSponsorLimmaTech Biologics AGRan2026 to 2027Enrolled142ConditionsNeisseria GonorrheaArmsLTB-NG6, Sodium Chloride 0.9%
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Protection againstFrontiers in immunology · 2025
    Article
  4. Article
  5. Review
  6. Clinical microbiology reviews · 2024
    Review
  7. Sweet complexity:Frontiers in cellular and infection microbiology · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Recent Progress Towards a Gonococcal Vaccine.Frontiers in cellular and infection microbiology · 2022
    Review
  12. Article
  13. Review
  14. Exploitation ofFrontiers in immunology · 2019
    Review
  15. Article
  16. Review
  17. Gonorrhea - an evolving disease of the new millennium.Microbial cell (Graz, Austria) · 2016
    Review
  18. Article
  19. Enhancement of protein expression by alphavirus replicons by designing self-replicating subgenomic RNAs.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

7 authors at 2 institutions in 1 country.

Weiyan ZhuUniversity of North Carolina at Chapel Hill, Department of Medicine, Division of Infectious Disease Research, 8341 Medical Biomolecular Research Bldg., 103 Mason Farm Road, CB# 7031, Chapel Hill, NC 27599, USA.
Christopher E Thomas
Ching-Ju Chen
Cornelius N Van Dam
Robert E Johnston
Nancy L Davis
P Frederick Sparling
Office of Infectious Diseases · USUniversity of North Carolina at Chapel Hill · US

Funding

Trichomonas Typing SystemU19AI031496 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HOBBS, MARCIA METZGAR · 1995 to 2014
$24.9M
LACTOFERRIN RECEPTOR AND GONOCOCCAL PATHOGENESISR01AI026837 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI SPARLING, PHILIP FREDERICK · 1999 to 2003
$1.4M
MICROBIAL PATHOGEN GENOME PROJECT--NEISSERIA GONORRHOEAER01AI038399 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DYER, DAVID W. · 1995 to 1998
–
NIAID NIH HHS 5 R01 AI26837NIAID NIH HHS 5 U19 AI31496NIAID NIH HHS AI38399NIAID NIH HHS R01 AI026837NIAID NIH HHS U19 AI031496
6 · The paper itself

Abstract

Porin (PorB) is a major outer membrane protein produced by all Neisseria gonorrhoeae strains and has been a focus of intense interest as a vaccine candidate. In this study, the immunogenicity of PorB in mice was investigated after several immunization regimens. Outer membrane vesicles (OMV), recombinant renatured PorB (rrPorB), and PorB-expressing Venezuelan equine encephalitis (VEE) virus replicon particles (PorB VRP) were delivered intranasally (i.n.) or subcutaneously (s.c.) into the dorsal area or the hind footpad in three-dose schedules; the PorB VRP-immunized mice were given a single additional booster dose of rrPorB in Ribi adjuvant. Different delivery systems and administration routes induced different immune responses. Mice immunized s.c. with rrPorB in Ribi had the highest levels of PorB-specific serum immunoglobulin G (IgG) by enzyme-linked immunosorbent assay. Surprisingly, there was an apparent Th1 bias, based on IgG1/IgG2a ratios, after immunization with rrPorB in Ribi in the footpad while the same vaccine given in the dorsal area gave a strongly Th2-biased response. PorB VRP-immunized mice produced a consistent Th1 response with a high gamma interferon response in stimulated splenic lymphocytes and very low IgG1/IgG2a ratios. Immunization by OMV delivered i.n. was the only regimen that resulted in a serum bactericidal response, and it generated an excellent mucosal IgA response. Serum from mice immunized with rrPorB preferentially recognized the surface of whole gonococci expressing a homologous PorB, whereas serum from PorB VRP-immunized mice had relatively low whole-cell binding activity but recognized both heterologous and homologous PorB equally. The data resulting from this direct comparison suggested that important aspects of the immune response can be manipulated by altering the form of the antigen and its delivery. This information coupled with an understanding of protective antigonococcal immune responses will enable the design of the optimal vaccine for N. gonorrhoeae.

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialBacterial VaccinesCell LineCytokinesEncephalitis Virus, Venezuelan EquineFemaleGonorrheaImmunity, MucosalImmunoglobulin GMiceMice, Inbred BALB CPorinsRecombinant ProteinsRepliconAntibodies, BacterialAntigens, BacterialBacterial VaccinesCytokinesImmunoglobulin Gporin protein, NeisseriaPorinsRecombinant Proteins

Identifiers

PMID16239559
PMCPMC1273881
OpenAlexW2165961690

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.