Evidence map›Paper›PMID 30996135›Full record

ArticleJCI insight2019

The effect of BPIFA1/SPLUNC1 genetic variation on its expression and function in asthmatic airway epithelium.

Niccolette Schaefer, Xingnan Li, Max A Seibold, Nizar N Jarjour, Loren C Denlinger, Mario Castro, Andrea M Coverstone, W Gerald Teague, Jonathan Boomer, Eugene R Bleecker and 13 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Genome-wide Association Study IdentifiesAllergy, asthma & immunology research · 2026
    Article
  2. Review
  3. Article
  4. House dust mite allergens, store-operated CaThe Journal of physiology · 2024
    Review
  5. Airway Serous Cells: A Comparative Study of Spatial Distribution and Abundance among Species.Journal of respiratory biology and translational medicine · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Phenotype overlap in the natural history of asthma.European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. SPLUNC1 α6 Peptidomimetic: A Novel Therapeutic for Asthma.American journal of respiratory cell and molecular biology · 2022
    Article
  17. A SPLUNC1 Peptidomimetic Inhibits Orai1 and Reduces Inflammation in a Murine Allergic Asthma Model.American journal of respiratory cell and molecular biology · 2022
    Article
  18. Article
  19. SPLUNC1: a novel marker of cystic fibrosis exacerbations.The European respiratory journal · 2021
    Article
  20. 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

23 authors at 9 institutions in 1 country.

Niccolette SchaeferNational Jewish Health, Denver, Colorado, USA.
Xingnan LiUniversity of Arizona, Tucson, Arizona, USA.
Max A SeiboldNational Jewish Health, Denver, Colorado, USA.
Nizar N JarjourUniversity of Wisconsin-Madison, Madison, Wisconsin, USA.
Loren C DenlingerUniversity of Wisconsin-Madison, Madison, Wisconsin, USA.
Mario CastroWashington University in St. Louis, St. Louis, Missouri, USA.
Andrea M CoverstoneWashington University in St. Louis, St. Louis, Missouri, USA.
W Gerald TeagueUniversity of Virginia, Charlottesville, Virginia, USA.
Jonathan BoomerWashington University in St. Louis, St. Louis, Missouri, USA.
Eugene R BleeckerUniversity of Arizona, Tucson, Arizona, USA.
Deborah A MeyersUniversity of Arizona, Tucson, Arizona, USA.
Wendy C MooreWake Forest University, Winston-Salem, North Carolina, USA.
Gregory A HawkinsWake Forest University, Winston-Salem, North Carolina, USA.
John FahyUCSF, San Francisco, California, USA.
Brenda R PhillipsUCSF, San Francisco, California, USA.
David T MaugerPennsylvania State University, Centre County, Pennsylvania, USA.
Azzeddine DakhamaNational Jewish Health, Denver, Colorado, USA.
Shaan GellatlyNational Jewish Health, Denver, Colorado, USA.
Nicole PavelkaNational Jewish Health, Denver, Colorado, USA.
Reena BermanNational Jewish Health, Denver, Colorado, USA.
Y Peter DiUniversity of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Sally E WenzelUniversity of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Hong Wei ChuNational Jewish Health, Denver, Colorado, USA.
National Jewish Health · USUniversity of Arizona · USWashington University in St. Louis · USCity College of San Francisco · USUniversity of Pittsburgh · USUniversity of Wisconsin–Madison · USWake Forest University · USPennsylvania State University · USUniversity of Virginia · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
PEDIATRIC ASTHMA NETWORK DATA COORDINATING CENTERU10HL064313 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MAUGER, DAVID T. · 1999 to 2008
$18.3M
Transcriptomic and Genetic Endotyping of Exacerbation-Prone AsthmaticsP01HL132821 · NHLBI · NATIONAL JEWISH HEALTH · PI SEIBOLD, MAX A · 2017 to 2021
$9.0M
Clinical Coordinating Center for the Severe Asthma Research Program (SARP)U10HL109086 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MAUGER, DAVID T. · 2011 to 2017
$8.1M
Stability of Severe Asthma Phenotypes: Impact of ExacerbationsU10HL109168 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI JARJOUR, NIZAR N · 2011 to 2016
$3.9M
Genes, air pollution, and asthma severity in minority childrenR01MD010443 · NIMHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SEIBOLD, MAX A, ZIV, ELAD · 2016 to 2020
$3.8M
Severe Asthma Research Program (SARP)-Washington UniversityU10HL109257 · NHLBI · WASHINGTON UNIVERSITY · PI CASTRO, MARIO · 2011 to 2016
$3.8M
Genetic Control of Airway Epithelium Gene Expression in Childhood AsthmaticsR01HL128439 · NHLBI · NATIONAL JEWISH HEALTH · PI SEIBOLD, MAX A · 2015 to 2019
$3.1M
Novel antimicrobial agents to overcome antibiotic resistant Pseudomonas and MRSA respiratory infectionR01AI133351 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DI, YUANPU PETER · 2017 to 2021
$2.6M
SPLUNC1 in Severe AsthmaR01HL125128 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, HONG W, DI, YUANPU PETER · 2015 to 2018
$1.9M
NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002345NHLBI NIH HHS P01 HL132821NHLBI NIH HHS R01 HL125128NHLBI NIH HHS R01 HL128439NHLBI NIH HHS U10 HL064313NHLBI NIH HHS U10 HL109086NHLBI NIH HHS U10 HL109168NHLBI NIH HHS U10 HL109257NIAID NIH HHS R01 AI133351NIMHD NIH HHS R01 MD010443
6 · The paper itself

Abstract

Bacterial permeability family member A1 (BPIFA1), also known as short palate, lung, and nasal epithelium clone 1 (SPLUNC1), is a protein involved in the antiinflammatory response. The goal of this study was to determine whether BPIFA1 expression in asthmatic airways is regulated by genetic variations, altering epithelial responses to type 2 cytokines (e.g., IL-13). Nasal epithelial cells from patients with mild to severe asthma were collected from the National Heart, Lung, and Blood Institute Severe Asthma Research Program centers, genotyped for rs750064, and measured for BPIFA1. To determine the function of rs750064, cells were cultured at air-liquid interface and treated with IL-13 with or without recombinant human BPIFA1 (rhBPIFA1). Noncultured nasal cells with the rs750064 CC genotype had significantly less BPIFA1 mRNA expression than the CT and TT genotypes. Cultured CC versus CT and TT cells without stimulation maintained less BPIFA1 expression. With IL-13 treatment, CC genotype cells secreted more eotaxin-3 than CT and TT genotype cells. Also, rhBPIFA1 reduced IL-13-mediated eotaxin-3. BPIFA1 mRNA levels negatively correlated with serum IgE and fractional exhaled nitric oxide. Baseline FEV1% levels were lower in the asthma patients with the CC genotype (n = 1,016). Our data suggest that less BPIFA1 in asthma patients with the CC allele may predispose them to greater eosinophilic inflammation, which could be attenuated by rhBPIFA1 protein therapy.

Indexed as

AdolescentAdultAgedAllelesAsthmaCells, CulturedChemokine CCL26ChildEosinophilsEpithelial CellsFemaleForced Expiratory VolumeGene Expression RegulationGenetic Predisposition to DiseaseGlycoproteinsHumansBPIFA1 protein, humanCCL26 protein, humanChemokine CCL26GlycoproteinsInterleukin-13PhosphoproteinsRecombinant ProteinsAsthmaInflammationTh2 response

Identifiers

PMID30996135
PMCPMC6538329
OpenAlexW2935810127

What OpenQuestion holds

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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.