Evidence map›Paper›PMID 21937985›Full record

ArticleMucosal immunology2012

Protective role of Toll-like receptor 4 in experimental gonococcal infection of female mice.

M Packiam, H Wu, S J Veit, N Mavrogiorgos, A E Jerse, R R Ingalls

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Long-term survival ofMicrobiology spectrum · 2025
    Article
  2. Experimental Urethral Infection with Neisseria gonorrhoeae.Current topics in microbiology and immunology · 2024
    Review
  3. Microbiology spectrum · 2023
    Article
  4. Antimicrobial agents and chemotherapy · 2021
    Article
  5. Article
  6. Review
  7. Pharmacokinetic Data Are Predictive ofAntimicrobial agents and chemotherapy · 2019
    Article
  8. Review
  9. Quantitative Proteomics of the 2016 WHOMolecular & cellular proteomics : MCP · 2019
    Article
  10. Review
  11. Article
  12. Pathogenesis ofFrontiers in immunology · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  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

6 authors at 2 institutions in 1 country.

M PackiamDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
H Wu
S J Veit
N Mavrogiorgos
A E Jerse
R R Ingalls
Uniformed Services University of the Health Sciences · USBoston University · US

Funding

Trichomonas Typing SystemU19AI031496 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SPARLING, PHILIP FREDERICK · 1995 to 2014
$24.9M
The TLR4/MD-2 signaling pathway in gonoccocal diseaseU19AI084048 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RICE, PETER A. · 2009 to 2013
$13.1M
GONOCOCCAL INFECTION AND GENE EXPRESSION IN FEMALE MICER01AI042053 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI JERSE, ANN E. · 1999 to 2014
$3.8M
ROLE OF LOS AND ITS RECEPTORS IN GONOCOCCAL PATHEGENEISR01AI046613 · NIAID · BOSTON MEDICAL CENTER · PI INGALLS, ROBIN R · 2000 to 2009
$2.5M
NIAID NIH HHS R01 AI042053NIAID NIH HHS R01 AI046613NIAID NIH HHS R01 AI42053NIAID NIH HHS R01 AI46613NIAID NIH HHS U19 AI031496NIAID NIH HHS U19 AI084048NIAID NIH HHS U19 AI31496
6 · The paper itself

Abstract

Neisseria gonorrhoeae is a common bacterial sexually transmitted infection. Like all Gram-negative bacteria, the outer membrane of the gonococcus is rich in endotoxin, a known ligand for Toll-like receptor (TLR)4. However, the role of endotoxin and that of its cognate receptor TLR4 in the mucosal response to acute gonococcal infection in the genital tract of women is unclear. To test this, we examined the course of infection after vaginal inoculation of N. gonorrhoeae in mice carrying the Lps(d) mutation in Tlr4, which renders them unresponsive to endotoxin. Although there was no difference in the duration of colonization, Lps(d) mice had a significantly higher peak bacterial burden which coincided with a massive polymorphonuclear cell influx and concomitant upregulation of a subset of inflammatory cytokine and chemokine markers. Notably, infected Lps(d) mice showed a decrease in interleukin-17, suggesting that Th17 responses are more dependent on TLR4 signaling in vivo. Defective polymorphonuclear cell-mediated and complement-independent serum killing of gonococci in Lps(d) mice was also observed and may account for the increased bacterial burden. This is the first in vivo evidence that TLR4-regulated factors modulate early inflammatory responses to gonococcal infection in the female reproductive tract and control bacterial replication.

Indexed as

AnimalsCell MovementCells, CulturedCytokinesCytotoxicity, ImmunologicDisease Models, AnimalFemaleGonorrheaHumansInflammation MediatorsMiceMice, Inbred BALB CMice, Inbred C3HMice, Mutant StrainsMutationNeisseria gonorrhoeaeCytokinesInflammation MediatorsToll-Like Receptor 4

Identifiers

PMID21937985
PMCPMC3240729
OpenAlexW1974423099

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.