Evidence map›Paper›PMID 38394609›Full record

ArticleThe Journal of infectious diseases2024

Interferon-γ Responses to Chlamydia trachomatis Vaccine Candidate Proteins in Women With Different Chlamydia Outcomes.

Jacob Dziadula, Steffanie Sabbaj, Kanupriya Gupta, Gary Cutter, Hong Yu, Robert C Brunham, William M Geisler

Open access · greenAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Jacob DziadulaDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Steffanie SabbajDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Kanupriya GuptaDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Gary CutterDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Hong YuBritish Columbia Centre for Disease Control, University of British Columbia, Vancouver, British Columbia, Canada.
Robert C BrunhamBritish Columbia Centre for Disease Control, University of British Columbia, Vancouver, British Columbia, Canada.
William M GeislerDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0000-0002-0603-2404
University of Alabama at Birmingham · USUniversity of British Columbia · CA

Funding

National Dissemination of I-Corps@NCATS: Accelerating Translation through CommercializationUL1TR003096 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GUTIERREZ, ORLANDO M, KIMBERLY, ROBERT P. · 2019 to 2023
$43.6M
Mechanisms and Correlates of Immune Protection against Genital Chlamydia in HumansR01AI093692 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GEISLER, WILLIAM M · 2012 to 2023
$4.5M
Host Immune Responses to Chlamydia trachomatis Candidate Vaccine Antigens and their Association with Clinical Correlates of Protective Immunity in WomenR01AI148359 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GEISLER, WILLIAM M · 2020 to 2024
$3.2M
Midcareer Mentoring Award for Patient-Oriented Research in Chlamydia trachomatis InfectionK24AI125685 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WILLIAM M GEISLER · 2016 to 2026
$1.3M
National Institute of Allergy and Infectious DiseasesNCATS NIH HHSNCATS NIH HHS UL1 TR003096NIAID NIH HHS K24 AI125685NIAID NIH HHS R01 AI093692NIAID NIH HHS R01 AI148359NIH HHS 1R01AI148359
6 · The paper itself

Abstract

backgroundChlamydia trachomatis testing and treatment strategies have not decreased infection rates, justifying need for a chlamydia vaccine. A murine study showed that a vaccine consisting of major outer membrane protein (MOMP) and polymorphic membrane proteins (Pmps) E, F, G, and H elicited protective immunity; studies on human cellular immune responses to Pmps are sparse.

methodsInterferon gamma (IFN-γ) responses to these 5 proteins were measured by ELISPOT in peripheral blood mononuclear cells from women returning for treatment of a positive chlamydia test. Responses were compared in those with spontaneous chlamydia clearance versus persisting infection at baseline and no reinfection versus reinfection at a 3-month follow-up visit.

resultsIFN-γ response to 1 or more proteins was detected in 39% at baseline and 51.5% at follow-up, most often to PmpE and MOMP. IFN-γ responses to MOMP were detected less often at follow-up versus baseline in women with reinfection, but were maintained in those without reinfection. Women with spontaneous clearance had a higher magnitude of IFN-γ response to PmpE and MOMP.

conclusionsIFN-γ responses to these 5 C. trachomatis vaccine candidate proteins were heterogenous and primarily directed against MOMP and PmpE. Spontaneous chlamydia clearance and absence of reinfection may be clinical correlates of protection.

Indexed as

Bacterial VaccinesChlamydia InfectionsChlamydia trachomatisInterferon-gammaLeukocytes, MononuclearAdolescentAdultBacterial Outer Membrane ProteinsBacterial ProteinsEnzyme-Linked Immunospot AssayFemaleHumansReinfectionYoung AdultBacterial Outer Membrane ProteinsBacterial ProteinsBacterial VaccinesInterferon-gammachlamydiainterferon-γspontaneous clearancevaccine

Identifiers

PMID38394609
PMCPMC11420703
OpenAlexW4392092794

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.