Evidence map›Paper›PMID 38563602›Full record

ArticleJournal of immunotoxicology2024

Lung-delivered IL-10 therapy elicits beneficial effects via immune modulation in organic dust exposure-induced lung inflammation.

Aaron D Schwab, Todd A Wyatt, Amy J Nelson, Angela Gleason, Rohit Gaurav, Debra J Romberger, Jill A Poole

Open access · goldAbstract read
In one paragraph

Article in Journal of immunotoxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-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

5 citing papers in PubMed, 5 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Aaron D SchwabDivision of Allergy and Immunology, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Todd A WyattResearch Service, Veterans Affairs Nebraska-Western Iowa Health Care System, Omaha, NE, USA.
Amy J NelsonDivision of Allergy and Immunology, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Angela GleasonDivision of Allergy and Immunology, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Rohit GauravDivision of Allergy and Immunology, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Debra J RombergerResearch Service, Veterans Affairs Nebraska-Western Iowa Health Care System, Omaha, NE, USA.
Jill A PooleDivision of Allergy and Immunology, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
University of Nebraska Medical Center · US

Funding

Surveillance of Agricultural Injuries in the Central States RegionsU54OH010162 · OH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RAUTIAINEN, RISTO HEIKKI · 2011 to 2025
$23.6M
The Role of TP-R on Alcohol-Induced Multi-Organ Damage: Liver and HeartP50AA030407 · NIAAA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Kusum K. Kharbanda · 2023 to 2026
$7.9M
Resolving Occupational Exposure-Induced Lung DiseaseR01OH012045 · OH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI POOLE, JILL A · 2021 to 2024
$2.3M
Targeting the ACOD1 immunometabolic pathway of lung myeloid cells to reduce environmental exposure-induced lung diseaseF30ES036063 · NIEHS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SCHWAB, AARON · 2024 to 2025
$76k
Reactive aldehydes and alcohol misuse in lung infectionsI01BX005886 · VA · OMAHA VA MEDICAL CENTER · PI WYATT, TODD A · 2023 to 2025
–
BLR&D Research Career Scientist ApplicationIK6BX005962 · VA · OMAHA VA MEDICAL CENTER · PI WYATT, TODD A · 2022 to 2025
–
BLRD VA I01 BX005886BLRD VA IK6 BX005962NIAAA NIH HHS P50 AA030407NIEHS NIH HHS F30 ES036063NIOSH CDC HHS R01 OH012045NIOSH CDC HHS U54 OH010162
6 · The paper itself

Abstract

Efficacious therapeutic options capable of resolving inflammatory lung disease associated with environmental and occupational exposures are lacking. This study sought to determine the preclinical therapeutic potential of lung-delivered recombinant interleukin (IL)-10 therapy following acute organic dust exposure in mice. Here, C57BL/6J mice were intratracheally instilled with swine confinement organic dust extract (ODE) (12.5%, 25%, 50% concentrations) with IL-10 (1 μg) treatment or vehicle control intratracheally-administered three times: 5 hr post-exposure and then daily for 2 days. The results showed that IL-10 treatment reduced ODE (25%)-induced weight loss by 66% and 46% at Day 1 and Day 2 post-exposure, respectively. IL-10 treatment reduced ODE (25%, 50%)-induced lung levels of TNFα (-76%, -83% [reduction], respectively), neutrophil chemoattractant CXCL1 (-51%, -60%), and lavage fluid IL-6 (-84%, -89%). IL-10 treatment reduced ODE (25%, 50%)-induced lung neutrophils (-49%, -70%) and recruited CD11c

Indexed as

Lung DiseasesPneumoniaAnimalsDustInterleukin-10LungMiceMice, Inbred C57BLSwineDustInterleukin-10immunologyinflammationlung diseaseOrganic dusttherapy

Identifiers

PMID38563602
PMCPMC11137733
OpenAlexW4393540974

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.