Evidence map›Paper›PMID 34944105›Full record

ReviewCells2021

Early Life Inflammation and the Developing Hematopoietic and Immune Systems: The Cochlea as a Sensitive Indicator of Disruption.

Kelly S Otsuka, Christopher Nielson, Matthew A Firpo, Albert H Park, Anna E Beaudin

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. 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
1.1field-weighted citation impact, top 27% 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, 11 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

5 authors at 1 institution in 1 country.

Kelly S OtsukaDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Christopher NielsonDivision of Otolaryngology-Head and Neck Surgery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.ORCID 0000-0001-7495-223X
Matthew A FirpoDepartment of Surgery, University of Utah, Salt Lake City, UT 84112, USA.
Albert H ParkDivision of Otolaryngology-Head and Neck Surgery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Anna E BeaudinDivision of Hematology and Hematologic Malignancies, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
University of Utah · US

Funding

Regulation of tissue resident macrophage development by IL-7R signalingR01HL147081 · NHLBI · UNIVERSITY OF UTAH · PI BEAUDIN, ANNA E · 2019 to 2023
$1.8M
Cross-disciplinary Training in Immunology, Inflammation and Infectious DiseaseT32AI138945 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Tracey Jane Lamb, Matthew A Williams · 2018 to 2026
$1.6M
University of Pittsburgh Training Program in Antimicrobial ResistanceT32AI138954 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRISON, LEE H · 2019 to 2023
$971k
Contributio of a novel developmentally-restricted hematopoietic stem cellK01HL130753 · NHLBI · UNIVERSITY OF UTAH · PI BEAUDIN, ANNA E · 2016 to 2020
$891k
NHLBI NIH HHS K01 HL130753NHLBI NIH HHS R01 HL147081NIAID NIH HHS T32 AI138945NIAID NIH HHS T32 AI138954
6 · The paper itself

Abstract

Emerging evidence indicates that perinatal infection and inflammation can influence the developing immune system and may ultimately affect long-term health and disease outcomes in offspring by perturbing tissue and immune homeostasis. We posit that perinatal inflammation influences immune outcomes in offspring by perturbing (1) the development and function of fetal-derived immune cells that regulate tissue development and homeostasis, and (2) the establishment and function of developing hematopoietic stem cells (HSCs) that continually generate immune cells across the lifespan. To disentangle the complexities of these interlinked systems, we propose the cochlea as an ideal model tissue to investigate how perinatal infection affects immune, tissue, and stem cell development. The cochlea contains complex tissue architecture and a rich immune milieu that is established during early life. A wide range of congenital infections cause cochlea dysfunction and sensorineural hearing loss (SNHL), likely attributable to early life inflammation. Furthermore, we show that both immune cells and bone marrow hematopoietic progenitors can be simultaneously analyzed within neonatal cochlear samples. Future work investigating the pathogenesis of SNHL in the context of congenital infection will therefore provide critical information on how perinatal inflammation drives disease susceptibility in offspring.

Indexed as

HematopoiesisAnimalsCochleaFetusHearing Loss, SensorineuralHumansImmune SystemInflammationcochleacongenital infectioncytomegalovirusfetal-derived immune cellshematopoiesishematopoietic stem and progenitor cellsinflammationsensorineural hearing loss

Identifiers

PMID34944105
PMCPMC8700005
OpenAlexW4200122181

What OpenQuestion 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 OpenQuestion graph.