Evidence map›Paper›PMID 25964469›Full record

ArticleInfection and immunity2015

Generation of a Novel Staphylococcus aureus Ghost Vaccine and Examination of Its Immunogenicity against Virulent Challenge in Rats.

Nagarajan Vinod, Sung Oh, Hyun Jung Park, Jung Mo Koo, Chang Won Choi, Sei Chang Kim

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. 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
2.9field-weighted citation impact, top 9% 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, 70 citations in OpenAlex.

  1. Article
  2. Bacterial ghosts (BGs): A promising approach as candidate vaccine.World journal of microbiology & biotechnology · 2026
    Review
  3. A Chemically InducedVaccines · 2026
    Article
  4. Article
  5. Pathogens (Basel, Switzerland) · 2025
    Review
  6. Immunogenicity evaluation of altSonflex1-2-3Frontiers in immunology · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Protective Immunity againstInternational journal of molecular sciences · 2022
    Article
  16. Heat-killedFrontiers in microbiology · 2022
    Article
  17. Hydrochloric acid-treatedMolecular & cellular toxicology · 2022
    Article
  18. Review
  19. Article
  20. Review
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

6 authors at 1 institution in 1 country.

Nagarajan VinodDepartment of Biology & Medicinal Science, Pai Chai University, Daejeon, South Korea.
Sung OhDepartment of Biology & Medicinal Science, Pai Chai University, Daejeon, South Korea.
Hyun Jung ParkDepartment of Biology & Medicinal Science, Pai Chai University, Daejeon, South Korea.
Jung Mo KooDepartment of Biology & Medicinal Science, Pai Chai University, Daejeon, South Korea.
Chang Won ChoiDepartment of Biology & Medicinal Science, Pai Chai University, Daejeon, South Korea choicw@pcu.ac.kr kimsc@pcu.ac.kr.
Sei Chang KimDepartment of Biology & Medicinal Science, Pai Chai University, Daejeon, South Korea choicw@pcu.ac.kr kimsc@pcu.ac.kr.
Pai Chai University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus is a Gram-positive pathogen that causes a wide range of infections in humans and animals. Bacterial ghosts are nonliving, empty cell envelopes and are well represented as novel vaccine candidates. In this study, we examined the immunogenicity and protective efficacy of S. aureus ghosts (SAGs) against a virulent challenge in rats. Nonliving SAGs were generated by using the MIC of sodium hydroxide. The formation of a transmembrane lysis tunnel structure in SAGs was visualized by scanning electron microscopy. To investigate these SAGs as a vaccine candidate, rats were divided into four groups, A (nonimmunized control), B (orally immunized), C (subcutaneously immunized), and D (intravenously immunized). The IgG antibody responses were significantly stronger in the SAG-immunized groups than in the nonimmunized control group (P < 0.05). Moreover, a significant increase in the populations of CD4(+) and CD8(+) T cells was observed in all three immunized groups (P < 0.05). We also found that serum bactericidal antibodies were significantly elicited in the SAG-immunized groups (P < 0.05). Most importantly, the bacterial loads in the immunized groups were significantly lower than those in the nonimmunized control group (P < 0.01). These results suggest that immunization with SAGs induces immune responses and provides protection against a virulent S. aureus challenge.

Indexed as

Administration, OralAnimalsAntibodies, BacterialBacterial LoadBlood Bactericidal ActivityCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDisease Models, AnimalElectronsImmunoglobulin GInjections, IntravenousInjections, SubcutaneousMaleMicroscopy, Electron, ScanningRats, Sprague-DawleySodium HydroxideAntibodies, BacterialImmunoglobulin GSodium HydroxideStaphylococcal VaccinesVaccines, Inactivated

Identifiers

PMID25964469
PMCPMC4468543
OpenAlexW2201776864

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.