Evidence map›Paper›PMID 35173037›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2022

Age-Dependent Reduction in Asthmatic Pathology through Reprogramming of Postviral Inflammatory Responses.

Guy Hazan, Anna Eubanks, Carrie Gierasch, Jeffrey Atkinson, Carolyn Fox, Ariel Hernandez-Leyva, Anne L Rosen, Andrew L Kau, Eugene Agapov, Jennifer Alexander-Brett and 12 more

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Postnatal antibiotic exposure due to maternal group B streptococcus is associated with childhood asthma.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2025
    Article
  9. Review
  10. Article
  11. The role of innate immune system in respiratory viral infection related asthma.Frontiers in cellular and infection microbiology · 2025
    Review
  12. Multi-organ phenotypes in mice lacking latent TGFβ binding protein 2 (LTBP2).Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Review
  13. Age-dependent rebound in asthma exacerbations after COVID-19 lockdown.The journal of allergy and clinical immunology. Global · 2022
    Article
  14. 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

22 authors at 1 institution in 1 country.

Guy HazanDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Anna EubanksDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Carrie GieraschDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Jeffrey AtkinsonDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-9125-7968
Carolyn FoxDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Ariel Hernandez-LeyvaDivision of Allergy and Immunology, Department of Medicine and Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO.
Anne L RosenDivision of Allergy and Immunology, Department of Medicine and Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-7656-3382
Andrew L KauDivision of Allergy and Immunology, Department of Medicine and Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-9386-3766
Eugene AgapovDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Jennifer Alexander-BrettDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Deborah SteinbergDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Diane KelleyDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Michael WhiteDepartment of Pathology/Immunology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-5110-6567
Derek ByersDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Kangyun WuDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-8093-094X
Shamus P KeelerDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-1301-0852
Yong ZhangDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Jeffrey R KoenitzerDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Elise EidenInstitute for Informatics, Washington University School of Medicine, St. Louis, MO; and.
Neil AndersonDivision of Laboratory and Genomic Medicine, Department of Pathology, Washington University School of Medicine, St. Louis, MO.
Michael J HoltzmanDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-8750-3716
Jeffrey HaspelDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO; jhaspel@wustl.edu.ORCID 0000-0001-5839-0265
Washington University in St. Louis · US

Funding

Defining and Controlling Airway DiseaseR35HL145242 · NHLBI · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2019 to 2025
$6.6M
Clock Gene Control of Viral Infection and AsthmaR01HL135846 · NHLBI · WASHINGTON UNIVERSITY · PI HASPEL, JEFFREY ADAM · 2017 to 2021
$2.8M
Non-Classical Cytokine Secretion in Chronic Airway DiseaseR01HL152245 · NHLBI · WASHINGTON UNIVERSITY · PI ALEXANDER-BRETT, JENNIFER · 2020 to 2024
$2.8M
Circadian Signatures in Chronic Lung DiseaseR01HL152968 · NHLBI · WASHINGTON UNIVERSITY · PI HASPEL, JEFFREY ADAM · 2020 to 2023
$2.5M
The circadian clock as an age sensor in asthma resolutionR01HL172823 · NHLBI · WASHINGTON UNIVERSITY · PI Jeffrey Adam Haspel · 2024 to 2026
$2.3M
NHLBI NIH HHS R01 HL135846NHLBI NIH HHS R01 HL152245NHLBI NIH HHS R01 HL152968NHLBI NIH HHS R01 HL172823NHLBI NIH HHS R35 HL145242
6 · The paper itself

Abstract

Asthma is a chronic disease of childhood, but for unknown reasons, disease activity sometimes subsides as children mature. In this study, we present clinical and animal model evidence suggesting that the age dependency of childhood asthma stems from an evolving host response to respiratory viral infection. Using clinical data, we show that societal suppression of respiratory virus transmission during coronavirus disease 2019 lockdown disrupted the traditional age gradient in pediatric asthma exacerbations, connecting the phenomenon of asthma remission to virus exposure. In mice, we show that asthmatic lung pathology triggered by Sendai virus (SeV) or influenza A virus is highly age-sensitive: robust in juvenile mice (4-6 wk old) but attenuated in mature mice (>3 mo old). Interestingly, allergen induction of the same asthmatic traits was less dependent on chronological age than viruses. Age-specific responses to SeV included a juvenile bias toward type 2 airway inflammation that emerged early in infection, whereas mature mice exhibited a more restricted bronchiolar distribution of infection that produced a distinct type 2 low inflammatory cytokine profile. In the basal state, aging produced changes to lung leukocyte burden, including the number and transcriptional landscape of alveolar macrophages (AMs). Importantly, depleting AMs in mature mice restored post-SeV pathology to juvenile levels. Thus, aging influences chronic outcomes of respiratory viral infection through regulation of the AM compartment and type 2 inflammatory responses to viruses. Our data provide insight into how asthma remission might develop in children.

Indexed as

Age FactorsAgingAnimalsAsthmaCOVID-19CytokinesHumansInfluenza A virusInfluenza, HumanLungMiceMice, Inbred C57BLOrthomyxoviridae InfectionsRespirovirus InfectionsSARS-CoV-2Sendai virusCytokines

Identifiers

PMID35173037
PMCPMC8917060
OpenAlexW4213047832

What OpenQuestion 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 OpenQuestion graph.