Evidence map›Paper›PMID 37814791›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2023

Grandmaternal allergen sensitization reprograms epigenetic and airway responses to allergen in second-generation offspring.

Katie M Lebold, Madeline Cook, Alexandra B Pincus, Kimberly A Nevonen, Brett A Davis, Lucia Carbone, Gina N Calco, Aubrey B Pierce, Becky J Proskocil, Allison D Fryer and 2 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

12 authors at 2 institutions in 1 country.

Katie M LeboldDepartment of Emergency Medicine, Stanford University School of Medicine, Palo Alto, California, United States.
Madeline CookDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.ORCID 0000-0001-7448-4966
Alexandra B PincusDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.
Kimberly A NevonenKnight Cardiovascular Institute Epigenetics Consortium, Oregon Health and Science University, Portland, Oregon, United States.
Brett A DavisKnight Cardiovascular Institute Epigenetics Consortium, Oregon Health and Science University, Portland, Oregon, United States.ORCID 0000-0001-7985-1921
Lucia CarboneKnight Cardiovascular Institute Epigenetics Consortium, Oregon Health and Science University, Portland, Oregon, United States.ORCID 0000-0002-2118-107X
Gina N CalcoDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.
Aubrey B PierceDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.
Becky J ProskocilDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.ORCID 0000-0002-7803-6447
Allison D FryerDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.ORCID 0000-0003-1712-9831
David B JacobyDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.
Matthew G DrakeDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, Oregon, United States.ORCID 0000-0001-5476-0361
Oregon Health & Science University · USStanford University · US

Funding

Identifying mechanisms and reversibility of eosinophil-induced airway hyperinnervation in asthmaR01HL155623 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DRAKE, MATTHEW G. · 2021 to 2025
$3.3M
Airway Sensory Nerves in AsthmaR01HL124165 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBSEN, ELIZABETH A, JACOBY, DAVID B · 2014 to 2017
$3.1M
Prenatal control of offspring airway responsivenessR01HL144008 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2019 to 2022
$2.4M
Insulin Modulates Parasympathetic Nerve Control of LungsR01HL131525 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI FRYER, ALLISON DEBORAH · 2017 to 2020
$1.9M
Rapid Toll-like receptor 7-mediated nitric oxide production in the airwayK08HL121254 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DRAKE, MATTHEW G. · 2014 to 2018
$732k
Eosinophil-mediated Sensory Neuroplasticity in AsthmaF30HL132414 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEBOLD, KATHERINE M · 2016 to 2019
$197k
NHLBI NIH HHS F30 HL132414NHLBI NIH HHS K08 HL121254NHLBI NIH HHS R01 HL124165NHLBI NIH HHS R01 HL131525NHLBI NIH HHS R01 HL144008NHLBI NIH HHS R01 HL155623
6 · The paper itself

Abstract

Asthma susceptibility is influenced by environmental, genetic, and epigenetic factors. DNA methylation is one form of epigenetic modification that regulates gene expression and is both inherited and modified by environmental exposures throughout life. Prenatal development is a particularly vulnerable time period during which exposure to maternal asthma increases asthma risk in offspring. How maternal asthma affects DNA methylation in offspring and what the consequences of differential methylation are in subsequent generations are not fully known. In this study, we tested the effects of grandmaternal house dust mite (HDM) allergen sensitization during pregnancy on airway physiology and inflammation in HDM-sensitized and challenged second-generation mice. We also tested the effects of grandmaternal HDM sensitization on tissue-specific DNA methylation in allergen-naïve and -sensitized second-generation mice. Descendants of both allergen- and vehicle-exposed grandmaternal founders exhibited airway hyperreactivity after HDM sensitization. However, grandmaternal allergen sensitization significantly potentiated airway hyperreactivity and altered the epigenomic trajectory in second-generation offspring after HDM sensitization compared with HDM-sensitized offspring from vehicle-exposed founders. As a result, biological processes and signaling pathways associated with epigenetic modifications were distinct between lineages. A targeted analysis of pathway-associated gene expression found that Smad3 was significantly dysregulated as a result of grandmaternal allergen sensitization. These data show that grandmaternal allergen exposure during pregnancy establishes a unique epigenetic trajectory that reprograms allergen responses in second-generation offspring and may contribute to asthma risk.

Indexed as

AsthmaPrenatal Exposure Delayed EffectsAllergensAnimalsDisease SusceptibilityEpigenesis, GeneticEpigenomicsFemaleHumansMicePregnancyPyroglyphidaeAllergensairway hyperreactivityallergenasthmaepigeneticsmaternal asthma

Identifiers

PMID37814791
PMCPMC11068409
OpenAlexW4387472505

What Socratic holds

Textmetadata
LicenceCC BY
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.