Evidence map›Paper›PMID 40812430›Full record

ArticleThe Journal of allergy and clinical immunology2025

Prostaglandin I

Allison E Norlander, Masako Abney, Jian Zhang, Vasiliy V Polosukhin, Christopher M Thomas, Zachary J Ceneviva, Raghad AlMotairy, Rahi Patel, Jacqueline-Yvonne Cephus, Shinji Toki and 4 more

Abstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 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

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

14 authors.

Allison E NorlanderDepartment of Cell Biology, Anatomy, and Physiology, Indiana University School of Medicine, Indianapolis, Ind; Krannert Cardiovascular Research Center, Department of Medicine, Indiana University School of Medicine, Indianapolis, Ind; Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn. Electronic address: aenorlan@iu.edu.
Masako AbneyDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Jian ZhangDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Vasiliy V PolosukhinDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Christopher M ThomasDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Zachary J CenevivaDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Raghad AlMotairyDepartment of Cell Biology, Anatomy, and Physiology, Indiana University School of Medicine, Indianapolis, Ind.
Rahi PatelDepartment of Cell Biology, Anatomy, and Physiology, Indiana University School of Medicine, Indianapolis, Ind.
Jacqueline-Yvonne CephusDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Shinji TokiDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Weisong ZhouDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
Talal A ChatilaDivision of Immunology, Boston Children's Hospital, and the Department of Pediatrics, Harvard Medical School, Boston, Mass.
Dawn C NewcombDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn; Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, Tenn.
R Stokes PeeblesDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University School of Medicine, Nashville, Tenn; Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, Tenn; United States Department of Veterans Affairs Medical Center, Nashville, Tenn.

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI David W Clapp · 1999 to 2026
$59.3M
Viral and Host Determinants of Infant and Childhood Allergy and AsthmaU19AI095227 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Sergejs Berdnikovs · 2011 to 2026
$34.9M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
Project-005U54DK106846 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Reuben Kapur, Karen Elizabeth Pollok · 2015 to 2026
$9.7M
PGI2 augments Treg functionR01AI145265 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PEEBLES, RAY STOKES · 2019 to 2023
$2.7M
GLP-1R signaling in allergic inflammationR01AI124456 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI NISWENDER, KEVIN D, PEEBLES, RAY STOKES · 2017 to 2021
$2.2M
PGI2 restrains immunopathogenesis in hypertensionR00HL159594 · NHLBI · TRUSTEES OF INDIANA UNIVERSITY · PI NORLANDER, ALLISON ELIZABETH · 2023 to 2025
$747k
Host genetics of allergen-induced lung TSLP expression and ILC2 functionR21AI145397 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PEEBLES, RAY STOKES · 2019 to 2020
$468k
PGI2 restrains immunopathogenesis in hypertensionK99HL159594 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI NORLANDER, ALLISON ELIZABETH · 2021 to 2022
$276k
The Effect of PGI2 on T regulatory Cell Function in Allergic DiseaseF32AI143005 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI NORLANDER, ALLISON ELIZABETH · 2019 to 2020
$88k
BLRD VA I01 BX004299NCI NIH HHS P30 CA068485NCI NIH HHS P30 CA082709NHLBI NIH HHS K99 HL159594NHLBI NIH HHS R00 HL159594NIAID NIH HHS F32 AI143005NIAID NIH HHS R01 AI124456NIAID NIH HHS R01 AI145265NIAID NIH HHS R21 AI145397NIAID NIH HHS U19 AI095227NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U54 DK106846
6 · The paper itself

Abstract

backgroundT regulatory (Treg) cells dampen immune activation. Treg cells downregulate the type 2 response to innocuous environmental antigens that produce allergic airway inflammation; however, ST2-positive Treg cells promote allergic airway inflammation. Prostaglandin I

objectiveWe sought to define the mechanisms responsible for PGI

methodsTreg cell-specific IP-deficient mice, Treg cell fate-tracking IP-deficient mice, and Treg cell-specific IP- and β-catenin-deficient mice were exposed to an Alternaria alternata extract sensitization and challenge model. Bronchoalveolar lavage fluid was evaluated for cell number, cell differential, and cytokines by ELISA. Lungs were evaluated by flow cytometry and histopathology.

resultsUtilizing Treg cell-specific IP-deficient mice, we found that loss of PGI

conclusionsTogether, these data further support the importance of PGI

Indexed as

beta CateninEpoprostenolInterleukin-1 Receptor-Like 1 ProteinT-Lymphocytes, RegulatoryAnimalsMiceMice, Inbred C57BLMice, KnockoutSignal Transductionbeta CateninCTNNB1 protein, mouseEpoprostenolIl1rl1 protein, mouseInterleukin-1 Receptor-Like 1 ProteinAlternaria alternatainflammationprostaglandin I(2)ST2Treg cellβ-catenin

Identifiers

PMID40812430
PMCPMC12403991

What Socratic 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 Socratic graph.