Evidence map›Paper›PMID 41192922›Full record

ArticlePrenatal diagnosis2025

Characterization of Maternal and Fetal Immunity Following in Utero Spina Bifida Repair and Surgery-Induced Preterm Birth.

Katherine Martinez Carmona, Petra K Lothert, Bohdana Fedyshyn, Jin Sung Jang, Aparna Govindan, Percy N Pacora Portella, Maureen A Lemens, Rana Chakraborty, Rodrigo Ruano, Jose L Peiro and 3 more

Abstract read
In one paragraph

Article in Prenatal diagnosis, 2025. 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
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.

  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

13 authors.

Katherine Martinez CarmonaDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0009-0004-5833-4326
Petra K LothertDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Bohdana FedyshynDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.
Jin Sung JangDepartment of Laboratory Medicine and Pathology, Rochester, Minnesota, USA.
Aparna GovindanDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Percy N Pacora PortellaDepartment of Obstetrics and Gynecology, UTHealth, Houston, Texas, USA.
Maureen A LemensDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.
Rana ChakrabortyDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.
Rodrigo RuanoDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.
Jose L PeiroDepartment of Obstetrics and Gynecology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
Eric P BerghDepartment of Obstetrics and Gynecology, UTHealth, Houston, Texas, USA.
Mauro H SchenoneDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-2118-4852
Elizabeth Ann L EnningaDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota, USA.

Funding

Training Program in ImmunologyT32AI170478 · NIAID · MAYO CLINIC ROCHESTER · PI Virginia Smith Shapiro · 2022 to 2026
$1.4M
IMMUNE RESPONSES IN THE MOTHER-INFANT DYAD INDUCED BY FETAL SURGERY, AND ASSOCIATIONS WITH PREMATURITYR21AI151208 · NIAID · MAYO CLINIC ROCHESTER · PI ENNINGA, ELIZABETH ANN LIESER · 2020 to 2021
$437k
NIAID NIH HHS R21 AI151208NIAID NIH HHS T32 AI170478
6 · The paper itself

Abstract

objectiveFetal surgery (FS) for spina bifida (SB) repair improves infant outcomes; however, spontaneous preterm birth (sPTB) is common. We aimed to evaluate maternal and fetal immune responses following FS for SB repair.

methodPregnant participants undergoing fetoscopic SB repair at 24-26 weeks of gestational age (GA) were prospectively recruited and compared to GA matched low-risk controls. Blood samples were collected at baseline, 2-week post-surgery (POD14), and delivery. Cytokine analysis, flow cytometry, and T cell receptor (TCR) sequencing were performed.

resultssPTB occurred in 5/6 of the FS group (0/6 of controls). Maternal blood in the FS group demonstrated increased alpha-fetoprotein (AFP) and anti-inflammatory IL-1RA at baseline and POD14, increased pro-inflammatory IL-8 only post-operatively, and elevated growth factors throughout. T cell phenotypes following FS revealed reduced TH17 frequency but increased activation receptors on cytotoxic T cells. At delivery, the FS cohort had reduced Th2 and Th17 helper T cells and CD4+ memory T cells, but CD8 T cells still showed increased activation. No TCR expansion was detected post-surgery, suggesting antigen-independent activation. Cord blood in FS repaired neonates had increased AFP, IL-8, IL-1RA.

conclusionSystemic immune changes following FS, particularly T cell maturation and activation, were observed. Further characterization of these mechanisms may help predict and prevent surgery-induced PTB, improving outcomes.

Indexed as

FetoscopyPremature BirthSpinal DysraphismAdultCase-Control StudiesCytokinesFemaleFetal BloodHumansInfant, NewbornPregnancyProspective StudiesCytokines

Identifiers

PMID41192922
PMCPMC12692994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.