Evidence map›Paper›PMID 23620186›Full record

ArticlePathogens and disease2013

OT-1 mice display minimal upper genital tract pathology following primary intravaginal Chlamydia muridarum infection.

Srikanth Manam, Bruce J Nicholson, Ashlesh K Murthy

Open access · bronzeAbstract read
In one paragraph

Article in Pathogens and disease, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

  1. Infectivity of a pathogenicity-attenuatedInfection and immunity · 2025
    Article
  2. Viral Vector-BasedVaccines · 2024
    Article
  3. Article
  4. Article
  5. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2022
    Article
  6. Characterization of Pathogenic CD8Infection and immunity · 2022
    Article
  7. Gastrointestinal Chlamydia-Induced CD8Infection and immunity · 2021
    Article
  8. T cell responses to Chlamydia.Pathogens and disease · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Infection and immunity · 2020
    Article
  13. Article
  14. The Cryptic Plasmid ImprovesInfection and immunity · 2020
    Article
  15. Article
  16. Review
  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

3 authors at 2 institutions in 1 country.

Srikanth ManamDepartment of Pathology, Midwestern University, Downers Grove, IL 60515, USA.
Bruce J Nicholson
Ashlesh K Murthy
Midwestern University · USThe University of Texas Health Science Center at San Antonio · US

Funding

Role of CD8+ T cells in Reproductive Sequelae Induced by Chlamydia InfectionR03AI088342 · NIAID · UNIVERSITY OF TEXAS SAN ANTONIO · PI MURTHY, ASHLESH KRISHNA · 2010 to 2011
$144k
NIAID NIH HHS 1R03AI088342NIAID NIH HHS R03 AI088342
6 · The paper itself

Abstract

Chlamydia trachomatis is the most common bacterial sexually transmitted disease worldwide and leads to serious pathological sequelae in the upper genital tract (UGT) including pelvic inflammatory disease, ectopic pregnancy, and infertility. Several components of the host immune responses have been shown to contribute to the UGT pathology following genital chlamydial infection. We have shown recently that CD8(+) T cells induce the chlamydial UGT pathology via the production of TNF-α. However, those studies did not determine whether the pathology is mediated by bystander or antigen-specific CD8(+) T cells. In this study, we compared chlamydial clearance and UGT pathology in OT-1 transgenic mice and the corresponding C57BL/6J wild-type mice following primary intravaginal Chlamydia muridarum infection. All CD8(+) T cells in the OT-1 mice respond only to the Ova 257-264 peptide and are incapable of responding to other antigenic epitopes including those of Chlamydia. OT-1 mice displayed vaginal chlamydial clearance comparable to the wild-type animals. However, both oviduct and uterine horn pathology were minimal in the OT-1 mice compared with the high degree of pathology observed in the wild-type animals. These results strongly suggest that Chlamydia-specific, not bystander, CD8(+) T cells mediate the UGT pathological sequelae following genital chlamydial infection.

Indexed as

AnimalsCD8-Positive T-LymphocytesChlamydia InfectionsChlamydia muridarumFemaleMiceMice, Inbred C57BLMice, TransgenicOviductsReproductive Tract InfectionsUterus

Identifiers

PMID23620186
PMCPMC3641702
OpenAlexW2165454421

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.