Evidence map›Paper›PMID 16880389›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Monitoring the T cell response to genital tract infection.

Nadia R Roan, Todd M Gierahn, Darren E Higgins, Michael N Starnbach

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

40 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Infection and immunity · 2025
    Article
  5. Cytotoxic CD4+ T Cells Are Induced during Infection with Chlamydia trachomatis.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. T cell responses to Chlamydia.Pathogens and disease · 2021
    Review
  13. Modulation of Immune Response toFrontiers in cellular and infection microbiology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Nadia R RoanDepartment of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA 02115, USA.
Todd M Gierahn
Darren E Higgins
Michael N Starnbach
Harvard University · US

Funding

Cytotoxic T Cell Mediated Immunity to ChlamydiaR01AI039558 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI STARNBACH, MICHAEL N · 2001 to 2025
$15.6M
Single Cell Expression Profiling of Chlamydia GenesR21AI055900 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI STARNBACH, MICHAEL N · 2003 to 2004
$464k
CYTOTOXIC T CELL MEDIATED IMMUNITY TO CHLAMYDIAR29AI039558 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI STARNBACH, MICHAEL N · 1996 to 2000
$135k
NIAID NIH HHS AI039558NIAID NIH HHS AI055900NIAID NIH HHS R01 AI039558NIAID NIH HHS R21 AI055900NIAID NIH HHS R29 AI039558
6 · The paper itself

Abstract

To date, it has not been possible to study antigen-specific T cell responses during primary infection of the genital tract. The low frequency of pathogen-specific T cells in a naïve mouse makes it difficult to monitor the initial events after antigen encounter. We developed a system to examine the response of pathogen-specific T cells in the genital mucosa after intrauterine infection. We identified the protective CD4(+) T cell antigen Cta1 from Chlamydia trachomatis and generated T cell receptor (TCR) transgenic (tg) mice with specificity for this protein. By transferring TCR tg T cells into naïve animals, we determined that Chlamydia-specific T cells were activated and proliferated in the lymph nodes draining the genital tract after primary intrauterine infection. Activated T cells migrated into the genital mucosa and secreted IFN-gamma. The development of Chlamydia-specific TCR tg mice provides an approach for dissecting how pathogen-specific T cells function in the genital tract.

Indexed as

AnimalsBone Marrow CellsCD4-Positive T-LymphocytesCell ProliferationChlamydia InfectionsChlamydia trachomatisInterferon-gammaLymph NodesMiceMice, Inbred C57BLMice, TransgenicReceptors, Antigen, T-CellSpleenTumor Necrosis Factor Receptor Superfamily, Member 7Interferon-gammaReceptors, Antigen, T-CellTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID16880389
PMCPMC1567698
OpenAlexW2100920671

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.