Evidence map›Paper›PMID 42675520›Full record

ArticleImmunity & ageing : I & A2026

Age- and sex-dependent heterogeneity during LPS-induced murine acute lung injury.

Chantal Crispens, Annett Wilken-Schmitz, Valentin Dern, Abd Rahman Rahimi, Enrico Madau, Nadine Chiara Frigger, Josefine Jakob, Björn Häupl, Thomas Oellerich, Andreas Weigert and 4 more

Abstract read
In one paragraph

Article in Immunity & ageing : I & A, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Chantal CrispensDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Annett Wilken-SchmitzDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Valentin DernDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Abd Rahman RahimiDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Enrico MadauDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Nadine Chiara FriggerDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Josefine JakobFrankfurt Cancer Institute, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Björn HäuplDepartment of Hematology and Oncology, Goethe University Frankfurt, University Hospital, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Thomas OellerichFrankfurt Cancer Institute, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Andreas WeigertGoethe University Frankfurt, Faculty of Medicine, Institute of Biochemistry I, Frankfurt, 60590, Germany.
Steven R TalbotHannover Medical School, Institute for Laboratory Animal Science, Carl-Neuberg-Straße 1, Hannover, 30625, Germany.
Kai ZacharowskiDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Ulrike HeinickeDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany.
Andreas von KnethenDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University Frankfurt, University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt Am Main, 60590, Germany. andreas.vonknethen@unimedizin-ffm.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute respiratory distress syndrome (ARDS) remains difficult to treat due to its heterogeneous etiology. In this study, a mouse model of intratracheal lipopolysaccharide (LPS) instillation was used to investigate age- and sex-dependent immune responses. After six hours of LPS exposure and one hour of mechanical ventilation, immune cell subtypes as well as mRNA and protein expression were analyzed. Aged mice exhibited a basal pro-inflammatory immune signature already under sham conditions, whereas young mice displayed a more balanced response with parallel pro- and anti-inflammatory mechanisms. Notably, aged female LPS treated mice exhibited an exclusively pro-inflammatory response. UMAP analysis revealed distinct clustering according to age, sex, and treatment, while aged male mice formed isolated clusters. These findings highlight the importance of considering age- and sex-specific therapeutic strategies for ARDS treatment.

Indexed as

AgeingALIARDSImmune responseInflammationMICUMouse modelSex- and age-specific differences

Identifiers

PMID42675520
PMCPMC13528014

What OpenQuestion holds

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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.