Evidence map›Paper›PMID 23133684›Full record

ArticlePLoS neglected tropical diseases2012

CT694 and pgp3 as serological tools for monitoring trachoma programs.

E Brook Goodhew, Jeffrey W Priest, Delynn M Moss, Guangming Zhong, Beatriz Munoz, Harran Mkocha, Diana L Martin, Sheila K West, Charlotte Gaydos, Patrick J Lammie

Abstract readEvaluation Study
In one paragraph

Article in PLoS neglected tropical diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
–field-weighted citation impact
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

92 citing papers in PubMed.

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  9. Article
  10. Discrepancy Between Active Trachoma and Tests of Chlamydial Infection in Alto Amazonas, Peru.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  11. Article
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  13. Differences in novelFrontiers in parasitology · 2026
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  16. Data Resource Profile: Global Trachoma Serology Data Repository.International journal of epidemiology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Article

32 more citing papers are in PubMed but not listed here.

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

10 authors.

E Brook GoodhewDivision of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Jeffrey W Priest
Delynn M Moss
Guangming Zhong
Beatriz Munoz
Harran Mkocha
Diana L Martin
Sheila K West
Charlotte Gaydos
Patrick J Lammie

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDefining endpoints for trachoma programs can be a challenge as clinical signs of infection may persist in the absence of detectable bacteria. Antibody-based tests may provide an alternative testing strategy for surveillance during terminal phases of the program. Antibody-based assays, in particular ELISAs, have been shown to be useful to document C. trachomatis genital infections, but have not been explored extensively for ocular C. trachomatis infections. METHODOLOGY/PRINCIPAL

findingsAn antibody-based multiplex assay was used to test two C. trachomatis antigens, pgp3 and CT694, for detection of trachoma antibodies in bloodspots from Tanzanian children (n = 160) collected after multiple rounds of mass azithromycin treatment. Using samples from C. trachomatis-positive (by PCR) children from Tanzania (n = 11) and control sera from a non-endemic group of U.S. children (n = 122), IgG responses to both pgp3 and CT694 were determined to be 91% sensitive and 98% specific. Antibody responses of Tanzanian children were analyzed with regard to clinical trachoma, PCR positivity, and age. In general, children with more intense ocular pathology (TF/TI = 2 or most severe) had a higher median antibody response to pgp3 (p = 0.0041) and CT694 (p = 0.0282) than those with normal exams (TF/TI = 0). However, 44% of children with no ocular pathology tested positive for antibody, suggesting prior infection. The median titer of antibody responses for children less than three years of age was significantly lower than those of older children. (p<0.0001 for both antigens). CONCLUSIONS/SIGNIFICANCE: The antibody-based multiplex assay is a sensitive and specific additional tool for evaluating trachoma transmission. The assay can also be expanded to include antigens representing different diseases, allowing for a robust assay for monitoring across NTD programs.

Indexed as

Anti-Bacterial AgentsAntibodies, BacterialAntigens, BacterialAzithromycinBacterial ProteinsChildChild, PreschoolDrug MonitoringFemaleHumansImmunoglobulin GInfantLymphogranuloma VenereumMaleSensitivity and SpecificityTanzaniaAnti-Bacterial AgentsAntibodies, BacterialAntigens, BacterialAzithromycinBacterial ProteinsCT694 protein, Chlamydia trachomatisImmunoglobulin Gpgp3 protein, Chlamydia

Identifiers

PMID23133684
PMCPMC3486877

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Registered trials

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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.