Evidence map›Paper›PMID 39066790›Full record

ReviewSeminars in immunopathology2024

Early-life risk factors which govern pro-allergic immunity.

Catherine Ptaschinski, Bernhard F Gibbs

Abstract readReview
In one paragraph

Review in Seminars in immunopathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

2 authors.

Catherine PtaschinskiDepartment of Pathology, University of Michigan, Ann Arbor, USA.ORCID 0000-0002-2098-8373
Bernhard F GibbsSchool of Psychology and Life Sciences, Canterbury Christ Church University, North Holmes Road, Canterbury, Kent, CT1 1QU, UK. bernhard.gibbs@canterbury.ac.uk.ORCID 0000-0002-0537-228X

Funding

Role of epithelial barrier function in food-induced anaphylaxisR01AI167957 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Catherine Mary Ptaschinski · 2023 to 2026
$1.6M
NIAID NIH HHS R01 AI167957NIH HHS R01AI167957
6 · The paper itself

Abstract

Allergic diseases affect up to 40% of the global population with a substantial rise in food allergies, in particular, over the past decades. For the majority of individuals with allergy fundamental programming of a pro-allergic immune system largely occurs in early childhood where it is crucially governed by prenatal genetic and environmental factors, including their interactions. These factors include several genetic aberrations, such as filaggrin loss-of-function mutations, early exposure to respiratory syncytial virus, and various chemicals such as plasticizers, as well as the influence of the gut microbiome and numerous lifestyle circumstances. The effects of such a wide range of factors on allergic responses to an array of potential allergens is complex and the severity of these responses in a clinical setting are subsequently not easy to predict at the present time. However, some parameters which condition a pro-allergic immune response, including severe anaphylaxis, are becoming clearer. This review summarises what we currently know, and don't know, about the factors which influence developing pro-allergic immunity particularly during the early-life perinatal period.

Indexed as

Filaggrin ProteinsHypersensitivityAllergensAnimalsDisease SusceptibilityEnvironmental ExposureGastrointestinal MicrobiomeHumansPregnancyPrenatal Exposure Delayed EffectsRisk FactorsAllergensFilaggrin ProteinsFLG protein, humanAllergyAnaphylaxisFood allergyMicrobiomePerinatal

Identifiers

PMID39066790
PMCPMC11283399

What OpenQuestion holds

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LicenceCC BY
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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.