Evidence map›Paper›PMID 37790838›Full record

ArticleNewborn (Clarksville, Md.)

Linked Th17 and Calgranulin Responses in Maternal-cord Blood Dyads of Preterm Gestations with Histologic Chorioamnionitis.

Christopher Q Buchanan, Megan L Lawlor, Chukwuebuka Okafor, Shannon R Kurian, Andrea E Philip, Abigael E Finkle, Jay J McQuillan, Seema Haridas, Joyce M Koenig

Open access · bronzeAbstract read
In one paragraph

Article in Newborn (Clarksville, Md.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 71% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

9 authors at 1 institution in 1 country.

Christopher Q BuchananDepartment of Obstetrics, Gynecology and Women's Health, Division of Maternal-Fetal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Megan L LawlorDepartment of Obstetrics, Gynecology and Women's Health, Division of Maternal-Fetal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Chukwuebuka OkaforDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Shannon R KurianDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Andrea E PhilipDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Abigael E FinkleDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Jay J McQuillanDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Seema HaridasDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Joyce M KoenigDepartment of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Saint Louis University · US

Funding

T Regulatory Cells and Neonatal Innate ImmunityR21AI094478 · NIAID · SAINT LOUIS UNIVERSITY · PI KOENIG, JOYCE MARIE, PENG, GUANGYONG · 2012 to 2013
$413k
NIAID NIH HHS R21 AI094478
6 · The paper itself

Abstract

Introduction: Maternal-fetal immune crosstalk mechanisms are increasingly identified in the pathogenesis of gestational disorders, including histologic chorioamnionitis (HCA). Although an inflammatory Th17 immune phenotype has been described in preterm neonates with HCA, the associated maternal Th17 response is relatively unknown. To refine our understanding of Th17 biology in this context, we examined Th17 responses in maternal-cord blood dyads of preterm gestations. Materials and methods: Paired maternal and cord blood (CB) samples were prospectively collected from preterm gestations (23-34 weeks) with HCA or controls. Th17-linked cell frequencies and plasma calgranulin (S100A8, S100A12) levels were determined by flow cytometry and enzyme-linked immunoassay, respectively. Results: Analyses of 47 maternal-cord blood pairs showed striking parallel increases in Th17 cell frequencies as well as plasma calgranulin levels in the presence of fetal inflammation. Cord blood S100A12 levels were directly correlated with Th17 cell frequencies. In CB cultures, rh-S100A12 promoted Conclusions: Maternal and CB Th17-linked responses are dually amplified in gestations with HCA, supporting a biological role for maternal-fetal interactions in this disorder. In addition to advancing current knowledge of neonatal Th17 mechanisms, these data shed new light on their association with maternal inflammation.

Indexed as

Fetal inflammationGamma–delta T cellsMaternal inflammationS100S100A12S100A8Treg cells

Identifiers

PMID37790838
PMCPMC10547109
OpenAlexW4383551563

What OpenQuestion holds

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LicenceCC BY-NC
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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.