Evidence map›Paper›PMID 37766409›Full record

ArticleAmerican journal of reproductive immunology (New York, N.Y. : 1989)2023

Modeling an ascending infection by Ureaplasma parvum and its cell signaling and inflammatory response at the feto-maternal interface.

Giovana Fernanda Cosi Bento, Lauren S Richardson, Márcia Guimarães da Silva, Ourlad Alzeus G Tantengco, Ramkumar Menon

Open access · bronzeAbstract read
In one paragraph

Article in American journal of reproductive immunology (New York, N.Y. : 1989), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.7field-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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Detection ofFrontiers in cellular and infection microbiology · 2025
    Article
  6. Review
  7. Review
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

5 authors at 3 institutions in 3 countries.

Giovana Fernanda Cosi BentoDepartment of Pathology, Botucatu Medical School, São Paulo State University, São Paulo, Brazil.ORCID 0000-0003-3868-2935
Lauren S RichardsonDivision of Basic Science and Translational Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Texas, USA.
Márcia Guimarães da SilvaDepartment of Pathology, Botucatu Medical School, São Paulo State University, São Paulo, Brazil.
Ourlad Alzeus G TantengcoDepartment of Physiology, College of Medicine, University of the Philippines Manila, Manila, Philippines.
Ramkumar MenonDivision of Basic Science and Translational Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Texas, USA.ORCID 0000-0001-9213-6105
The University of Texas Medical Branch at Galveston · USUniversidade Estadual Paulista (Unesp) · BRUniversity of the Philippines Manila · PH

Funding

UTMB WOMEN'S HEALTH RESEARCH SCHOLARS PROGRAMK12HD052023 · NICHD · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI BERENSON, ABBEY B · 2005 to 2023
$8.1M
UTMB Women's Health Research Scholars ProgramK12AR084228 · NIAMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI ABBEY B BERENSON · 2023 to 2026
$2.7M
Intercellular interactions define cell migrations and transitions that maintain fetal membrane homeostasisR01HD100729 · NICHD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HAN, ARUM, MENON, RAMKUMAR · 2020 to 2024
$2.6M
Developing extracellular vesicle based therapeutics against pre-term birth through the use of maternal-fetal interface on a chipUH3TR003283 · NCATS · TEXAS ENGINEERING EXPERIMENT STATION · PI HAN, ARUM, MENON, RAMKUMAR · 2023 to 2025
$2.3M
Developing extracellular vesicle based therapeutics against pre-term birth through the use of maternal-fetal interface on a chipUG3TR003283 · NCATS · TEXAS ENGINEERING EXPERIMENT STATION · PI HAN, ARUM, MENON, RAMKUMAR · 2020 to 2021
$1.5M
NCATS NIH HHS UG3 TR003283NCATS NIH HHS UH3 TR003283NIAMS NIH HHS K12 AR084228NICHD NIH HHS K12 HD052023NICHD NIH HHS R01 HD100729
6 · The paper itself

Abstract

problemAscending bacterial infection is associated with ∼ 40% of spontaneous preterm birth (PTB), and Ureaplasma spp. is one of the most common bacteria isolated from the amniotic fluid. Developing novel in vitro models that mimic in vivo uterine physiology is essential to study microbial pathogenesis. We utilized the feto-maternal interface organ-on-chip (FMi-OOC) device and determined the propagation of Ureaplasma parvum, and its impact on cell signaling and inflammation. METHOD OF STUDY: FMi-OOC is a microphysiologic device mimicking fetal membrane/decidua interconnected through microchannels. The impact of resident decidual CD45

resultsU. parvum transversed the chorion and reached the amnion epithelium after 72 hours but did not induce cell signaling kinases (p38MAPK and JNK) activation, or cellular transition (epithelial-mesenchymal), regardless of the presence of immune cells. The inflammatory response was limited to the choriodecidual interface and did not promote inflammation in the amnion layer.

conclusionsOur data suggest that U. parvum is poorly immunogenic and does not produce massive inflammatory changes at the feto-maternal interface. We speculate that the presence of U. parvum may still compromise the feto-maternal interface making it susceptible to other pathogenic infection.

Indexed as

Premature BirthUreaplasmaAmnionFemaleHumansInfant, NewbornInflammationSignal Transductiondeciduafetal membraneinfectioninflammationorgan-on-chippregnancypreterm birth

Identifiers

PMID37766409
PMCPMC10571092
OpenAlexW4386418694

What OpenQuestion holds

Textmetadata
LicenceTDM
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.