Evidence map›Paper›PMID 41863394›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2026

Temporal variation in markers of immune signaling and wound repair in primary human airway epithelial cells following acute versus repeated woodsmoke condensate exposure.

Elise Hickman, Chloe K Chou, Cole Seifert, Jessie Chappel, Yong Ho Kim, Elizabeth Corteselli, Julia E Rager

Abstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Elise HickmanCurriculum in Toxicology and Environmental Medicine, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, United States.ORCID 0000-0001-6152-050X
Chloe K ChouCurriculum in Toxicology and Environmental Medicine, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, United States.ORCID 0009-0007-8037-1715
Cole SeifertDepartment of Environmental Sciences and Engineering, Gillings School of Global Public Health, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, United States.ORCID 0009-0003-2914-2002
Jessie ChappelCurriculum in Toxicology and Environmental Medicine, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, United States.ORCID 0009-0005-1492-118X
Yong Ho KimCenter for Public Health and Environmental Assessment, United States Environmental Protection Agency, Research Triangle Park, NC 27711, United States.ORCID 0000-0001-7527-0134
Elizabeth CorteselliCurriculum in Toxicology and Environmental Medicine, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, United States.ORCID 0000-0003-3646-0730
Julia E RagerCurriculum in Toxicology and Environmental Medicine, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, United States.ORCID 0000-0002-2882-5042

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HONG JIN KIM · 1985 to 2026
$201.5M
NCI NIH HHS P30 CA016086NIH HHS
6 · The paper itself

Abstract

Wildfire smoke (WFS) exposures are becoming more common, and firefighters and community members are often exposed to WFS for days to weeks. Controlled studies assessing the effects of repeated exposure to WFS and woodsmoke (WS; as a surrogate for WFS) or compared acute versus repeated exposure have evaluated a limited number of timepoints and endpoints using rodent models. Here, we leveraged differentiated primary human bronchial epithelial cells (HBECs) to test the hypothesis that different molecular responses occur upon acute versus repeat exposures to WS. HBECs (n = 4 donors) were exposed to 22 µg/cm2 red oak WS condensate for an acute, 4-h exposure, or repeat exposures of 4 h/d, 3 d/wk, across 2 wk. Membrane permeability, cell viability, and transcriptional responses were measured at the end of each exposure paradigm, and secreted proteins were measured throughout the repeat exposure. Acute exposure significantly increased expression of genes involved in fibrosis and immune response, whereas repeated exposure significantly decreased expression of genes involved in tissue repair and remodeling. Secreted protein responses were similar to transcriptomic responses and demonstrated temporal variation in response to exposure. This study supports the feasibility of using HBECs to evaluate acute and repeat WS exposures and indicates differential responses from these exposures with direct relevance to pulmonary disease processes, including those involved in fibrosis, asthma, and chronic obstructive pulmonary disease. These findings highlight the need for future studies to better understand molecular responses to repeated smoke exposures.

Indexed as

BronchiEpithelial CellsSignal TransductionSmokeWound HealingBiomarkersCells, CulturedCell SurvivalHumansTime FactorsWildfiresBiomarkersSmokeinterindividual responseslung cellsproteomicstemporaltranscriptomicswildfire

Identifiers

PMID41863394
PMCPMC13120886

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.