Evidence map›Paper›PMID 28889999›Full record

ArticleImmunobiology2017

Humoral immune responses during asthma and influenza co-morbidity in mice.

Laura A Doorley, Kim S LeMessurier, Amy R Iverson, Maneesha Palipane, Amali E Samarasinghe

Open access · greenAbstract read
In one paragraph

Article in Immunobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. 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.

Laura A DoorleyCollege of Graduate Health Sciences, University of Tennessee Health Science Center, Memphis, TN 38103, United States; Children's Foundation Research Institute, Memphis, TN 38103, United States.
Kim S LeMessurierChildren's Foundation Research Institute, Memphis, TN 38103, United States; Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN 38103, United States.
Amy R IversonDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, United States.
Maneesha PalipaneChildren's Foundation Research Institute, Memphis, TN 38103, United States; Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN 38103, United States.
Amali E SamarasingheCollege of Graduate Health Sciences, University of Tennessee Health Science Center, Memphis, TN 38103, United States; Children's Foundation Research Institute, Memphis, TN 38103, United States; Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN 38103, United States. Electronic address: asamaras@uthsc.edu.
University of Tennessee Health Science Center · USSt. Jude Children's Research Hospital · US

Funding

Eosinophils as Regulators of Host Immunity against Influenza InfectionsR01AI125481 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SAMARASINGHE, AMALI · 2017 to 2021
$1.9M
NIAID NIH HHS N01 AI070005NIAID NIH HHS R01 AI125481
6 · The paper itself

Abstract

Humoral immunity serve dual functions of direct pathogen neutralization and enhancement of leukocyte function. Antibody classes are determined by antigen triggers, and the resulting antibodies can contribute to disease pathogenesis and host defense. Although asthma and influenza are immunologically distinct diseases, since we have found that allergic asthma exacerbation promotes antiviral host responses to influenza A virus, we hypothesized that humoral immunity may contribute to allergic host protection during influenza. C57BL/6J mice sensitized and challenged with Aspergillus fumigatus (or not) were infected with pandemic influenza A/CA/04/2009 virus. Negative control groups included naïve mice, and mice with only 'asthma' or influenza. Concentrations of antibodies were quantified by ELISA, and in situ localization of IgA- and IgE-positive cells in the lungs was determined by immunohistochemistry. The number and phenotype of B cells in spleens and mediastinal lymph nodes were determined by flow cytometry at predetermined timepoints after virus infection until viral clearance. Mucosal and systemic antibodies remained elevated in mice with asthma and influenza with prominent production of IgE and IgA compared to influenza-only controls. B cell expansion was prominent in the mediastinal lymph nodes of allergic mice during influenza where most cells produced IgG

Indexed as

AnimalsAntibodies, ViralAspergillosisAspergillus fumigatusAsthmaB-LymphocytesFemaleHumansImmunity, HumoralImmunoglobulin AImmunoglobulin EInfluenza A virusInfluenza, HumanMiceMice, Inbred C57BLOrthomyxoviridae InfectionsAntibodies, ViralImmunoglobulin AImmunoglobulin EAntibodyFungal allergyHost-pathogen interactionsLungPandemic influenza

Identifiers

PMID28889999
PMCPMC5650545
OpenAlexW2752291315

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.