Evidence map›Paper›PMID 41874649›Full record

ArticleEuropean journal of trauma and emergency surgery : official publication of the European Trauma Society2026

Attenuating pulmonary injury and inflammation with C5/CD14 inhibition therapy: results from a porcine polytrauma model with blunt chest trauma.

Ümit Mert, Rald V M Groven, Kang Qin, Johannes Greven, Elizabeth Rosado Balmayor, Tom Eirik Mollnes, Markus Huber-Lang, Martijn van Griensven, Frank Hildebrand, Klemens Horst

Abstract read
In one paragraph

Article in European journal of trauma and emergency surgery : official publication of the European Trauma Society, 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

10 authors.

Ümit Mert *Department of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany. uemit.baran.mert@gmail.com.ORCID http://orcid.org/0000-0001-6125-6040
Rald V M Groven *Department of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany. rgroven@ukaachen.de.ORCID http://orcid.org/0000-0001-8733-289X
Kang QinExperimental Orthopedics and Trauma Surgery, Department of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0002-7655-8663
Johannes GrevenExperimental Orthopedics and Trauma Surgery, Department of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0003-2856-4804
Elizabeth Rosado BalmayorExperimental Orthopedics and Trauma Surgery, Department of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0002-0484-4847
Tom Eirik MollnesResearch Laboratory, Nordland Hospital Bodø, Parkveien 95, Bodø, 8005, Norway.ORCID http://orcid.org/0000-0002-5785-802X
Markus Huber-LangInstitute of Clinical- and Experimental Trauma-Immunology, Ulm University Hospital, Helmholzstraße 8/1, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0003-2359-6516
Martijn van GriensvenDepartment of Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology- Inspired Regenerative Medicine, Maastricht University, Universiteitssingel 40, Maastricht, 6229 ER, The Netherlands.ORCID http://orcid.org/0000-0001-5104-9881
Frank HildebrandDepartment of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0001-7729-9838
Klemens HorstDepartment of Orthopedic, Trauma- and Reconstructive Surgery, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0002-7162-6153

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThoracic injury is prevalent among polytrauma patients, affecting up to 45% of these patients and often leading to complications such as pulmonary dysfunction up to acute respiratory distress syndrome (ARDS). This study investigates the impact of surgical invasiveness and C5/CD14 inhibition therapy on pulmonary tissue damage and the local immune response of the lungs in a porcine polytrauma model.

methodsA post hoc analysis focusing on the pulmonary consequences of blunt thoracic trauma and multiple trauma was performed in a previously published porcine trauma model, in presence or absence of immunomodulation. A control group (n = 6; CG) was used that received identical instrumentation, anesthesia, nutrition, and fluid intake, but no trauma. For the trauma model, male pigs underwent a standardized polytrauma, followed by allocation into three treatment groups: early total care (n = 8; ETC), damage control orthopedics (n = 8; DCO), and ETC with C5/CD14 inhibition (n = 4). Pulmonary histopathological changes were assessed at 72 h after trauma through lung injury scores and wet/dry ratios, while ex vivo cytokine expressions from isolated alveolar macrophages (AMs) were analyzed using enzyme-linked immunosorbent assays.

resultsHistological results revealed significant lung damage in both the ETC and DCO groups compared to the control as well as the C5/CD14 inhibition group. The addition of C5/CD14 inhibition significantly lessened lung tissue damage, as indicated by lower lung injury scores and wet/dry ratios. Cytokine assays showed that AMs from the ETC + C5/CD14 group exhibited significantly decreased levels of proinflammatory cytokines compared to the other trauma groups, while showing similar cytokine expression levels as compared to the control group.

conclusionsEarly double blockade of C5/CD14 effectively mitigates pulmonary tissue damage and post-traumatic inflammatory responses in lung tissue. This might result in reduced complications like ARDS and facilitating earlier definitive surgical interventions. These findings underscore the potential importance of immunomodulation strategies in managing post-traumatic outcomes and highlight the need for further research into their clinical applications in polytrauma settings.

Indexed as

Lipopolysaccharide ReceptorsLung InjuryMultiple TraumaThoracic InjuriesWounds, NonpenetratingAnimalsCytokinesDisease Models, AnimalMacrophages, AlveolarMaleRespiratory Distress SyndromeSwineCytokinesLipopolysaccharide ReceptorsAlveolar macrophagesComplement system inhibitionImmunomodulationInflammationLung injuryPolytraumaToll-like receptor signaling inhibition

Identifiers

PMID41874649
PMCPMC13013225

What Socratic holds

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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.