Evidence map›Paper›PMID 27113355›Full record

ArticleInfection and immunity2016

Early-Life Intranasal Colonization with Nontypeable Haemophilus influenzae Exacerbates Juvenile Airway Disease in Mice.

Jessica R McCann, Stanley N Mason, Richard L Auten, Joseph W St Geme, Patrick C Seed

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Journal of bacteriology · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Immunization with HMW1 and HMW2 adhesins protects against colonization by heterologous strains of nontypeableProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. The Human Microbiota and Asthma.Clinical reviews in allergy & immunology · 2019
    Review
  14. Article
  15. Article
  16. Review
  17. The Role of Regulatory T Cell in NontypeableMediators of inflammation · 2018
    Article
  18. Article
  19. Breathing Better Through Bugs: Asthma and the Microbiome.The Yale journal of biology and medicine · 2016
    Review
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

5 authors at 2 institutions in 1 country.

Jessica R McCannDuke University School of Medicine, Department of Pediatrics, Durham, North Carolina, USA jessica.mccann@duke.edu.
Stanley N MasonDuke University School of Medicine, Department of Pediatrics, Durham, North Carolina, USA.
Richard L AutenDuke University School of Medicine, Department of Pediatrics, Durham, North Carolina, USA.
Joseph W St GemeChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Patrick C SeedDuke University School of Medicine, Department of Pediatrics, Durham, North Carolina, USA.
Duke University · USChildren's Hospital of Philadelphia · US

Funding

BIOLOGY OF THE HMW2 AND HMW2 ADHESINS OF H INFLUENZAER01DC002873 · NIDCD · WASHINGTON UNIVERSITY · PI ST. GEME, JOSEPH W. · 1995 to 2014
$4.4M
MICROBIAL SUCCESSION AND ADAPTIVE IMMUNE RESPONSES IN THE PREMATURE INFANTR01GM108494 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SEED, PATRICK C. · 2014 to 2017
$1.4M
Roles of Early Life Colonization and Environmental Antigens on Childhood AsthmaR21AI121742 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SEED, PATRICK C. · 2016 to 2017
$424k
NIAID NIH HHS R21 AI121742NIDCD NIH HHS R01 DC002873NIGMS NIH HHS R01 GM108494
6 · The paper itself

Abstract

Accumulating evidence suggests a connection between asthma development and colonization with nontypeable Haemophilus influenzae (NTHi). Specifically, nasopharyngeal colonization of human infants with NTHi within 4 weeks of birth is associated with an increased risk of asthma development later in childhood. Monocytes derived from these infants have aberrant inflammatory responses to common upper respiratory bacterial antigens compared to those of cells derived from infants who were not colonized and do not go on to develop asthma symptoms in childhood. In this study, we hypothesized that early-life colonization with NTHi promotes immune system reprogramming and the development of atypical inflammatory responses. To address this hypothesis in a highly controlled model, we tested whether colonization of mice with NTHi on day of life 3 induced or exacerbated juvenile airway disease using an ovalbumin (OVA) allergy model of asthma. We found that animals that were colonized on day of life 3 and subjected to induction of allergy had exacerbated airway disease as juveniles, in which exacerbated airway disease was defined as increased cellular infiltration into the lung, increased amounts of inflammatory cytokines interleukin-5 (IL-5) and IL-13 in lung lavage fluid, decreased regulatory T cell-associated FOXP3 gene expression, and increased mucus production. We also found that colonization with NTHi amplified airway resistance in response to increasing doses of a bronchoconstrictor following OVA immunization and challenge. Together, the murine model provides evidence for early-life immune programming that precedes the development of juvenile airway disease and corroborates observations that have been made in human children.

Indexed as

AnimalsBacterial LoadCytokinesDisease Models, AnimalDisease ProgressionFemaleHaemophilus InfectionsHaemophilus influenzaeHypersensitivityMiceMucin 5ACMucusNasal MucosaReproductive Tract InfectionsCytokinesMucin 5AC

Identifiers

PMID27113355
PMCPMC4936370
OpenAlexW2343306179

What OpenQuestion holds

Textmetadata
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.