Evidence map›Paper›PMID 40777327›Full record

ArticlebioRxiv : the preprint server for biology2025

A Microphysiologic Model of the Cervical Epithelium Recapitulates Microbial, Immunologic, and Pathogenic Properties of Sexually Transmitted Infections.

Katherine M Nelson, Daniel J Minahan, Vonetta L Edwards, Ian J Glomski, David J Delgado Diaz, Keena Thomas, Forrest C Walker, Patrik M Bavoil, Isabelle Derré, Alison K Criss and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Katherine M NelsonDepartment of Biomedical Engineering, University of Delaware, Newark, DE.ORCID 0000-0002-1070-1551
Daniel J MinahanDepartment of Biomedical Engineering, University of Delaware, Newark, DE.ORCID 0000-0003-3065-055X
Vonetta L EdwardsCenter for Advanced Microbiome Research and Innovation, Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Ian J GlomskiDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA.ORCID 0009-0006-3738-3430
David J Delgado DiazDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA.ORCID 0000-0001-5982-7641
Keena ThomasDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA.
Forrest C WalkerDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA.ORCID 0000-0003-4503-8734
Patrik M BavoilDepartment of Microbial Pathogenesis, University of Maryland, Baltimore, MD.ORCID 0000-0002-7340-5741
Isabelle DerréDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA.ORCID 0000-0002-7055-4346
Alison K CrissDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA.ORCID 0000-0001-7738-3757
Jacques RavelCenter for Advanced Microbiome Research and Innovation, Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0002-0851-2233
Jason P GleghornDepartment of Biomedical Engineering, University of Delaware, Newark, DE.ORCID 0000-0003-1283-2966

Funding

The Effects of Sex Hormones on Chlamydia InfectionU19AI158930 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CRISS, ALISON K · 2021 to 2025
$7.7M
NIAID NIH HHS U19 AI158930
6 · The paper itself

Abstract

Sexually transmitted infections (STIs) of the cervicovaginal mucosa are among the most common global infections. Clinical studies have revealed that susceptibility to STIs and the subsequent host responses they elicit are frequently associated with vaginal microbiota compositions that facilitate infection. Current monolayer cell culture and animal models fail to reproduce the multilevel complexity required to investigate these relationships simultaneously and/or with sufficient physiological relevance. To address this limitation, we have developed a microphysiologic system (MPS) that models human cervical tissue, its microbiota, and is susceptible to infection by two prominent genital pathogens, Chlamydia trachomatis and Neisseria gonorrhoeae. Significantly, this MPS platform recapitulates essential dynamic, polymicrobial, immune, and pathogenic features of chlamydial and gonococcal infections as they occur in humans. The low-cost MPS device requires no specialized equipment or specific expertise and was experimentally validated for both chlamydial and gonococcal infections across multiple non-engineering, remotely located laboratories, demonstrating its transferability and reproducibility. The MPS platform described herein provides a novel tool for expanded research into genital infections in a reconstituted system that closely mimics the cervical epithelium, a significant advance over existing models.

Indexed as

cervixchlamydiagonorrheahost-pathogen interactionsmicrobiomeMicrophysiologic modelorgan on a chip

Identifiers

PMID40777327
PMCPMC12330506

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.