Evidence map›Paper›PMID 42819158›Full record

ArticleFrontiers in immunology2026

Inflammasome expression patterns during bone regeneration: predictive biomarkers and potential therapeutic targets in non-union formation.

Maximilian M Menger, Oguzhan Nakisli, Benedikt J Braun, Steven C Herath, Daniel A K Schäfer, Dominik Saul, Michael D Menger, Emmanuel Ampofo, Selina Wrublewsky, Matthias W Laschke and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

11 authors.

Maximilian M MengerDepartment of Trauma and Reconstructive Surgery, BG Clinic Tuebingen, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Oguzhan NakisliInstitute for Clinical and Experimental Surgery, Saarland University, PharmaScienceHub (PSH), Homburg, Germany.
Benedikt J BraunDepartment of Trauma and Reconstructive Surgery, BG Clinic Tuebingen, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Steven C HerathDepartment of Trauma and Reconstructive Surgery, BG Clinic Tuebingen, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Daniel A K SchäferDepartment of Trauma and Reconstructive Surgery, BG Clinic Tuebingen, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Dominik SaulRobert Bosch Center for Tumor Diseases (RBCT), Stuttgart, Germany.
Michael D MengerInstitute for Clinical and Experimental Surgery, Saarland University, PharmaScienceHub (PSH), Homburg, Germany.
Emmanuel AmpofoInstitute for Clinical and Experimental Surgery, Saarland University, PharmaScienceHub (PSH), Homburg, Germany.
Selina WrublewskyInstitute for Clinical and Experimental Surgery, Saarland University, PharmaScienceHub (PSH), Homburg, Germany.
Matthias W LaschkeInstitute for Clinical and Experimental Surgery, Saarland University, PharmaScienceHub (PSH), Homburg, Germany.
Tina HistingDepartment of Trauma and Reconstructive Surgery, BG Clinic Tuebingen, Eberhard Karls University Tuebingen, Tuebingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Non-union formation is one of the major complications in trauma and orthopedic surgery. The inflammatory response at the fracture site is crucial for determining the healing outcome. However, there is limited information on the expression profiles of inflammasomes during both successful fracture repair and non-union formation. Methods: Hence, we analyzed the cellular inflammatory response as well as inflammasome expression during successful bone regeneration and fracture healing failure in a standardized murine fracture and non-union model over 70 days. Bone healing was analyzed by means of X-ray, biomechanics, micro-computed tomography (µCT), histology as well as immunohistochemistry and Western blotting. Results: The analysis of the callus tissue in non-unions showed a slightly increased number of MPO-positive cells and a significantly increased number of macrophages during the early healing phase. The number of macrophages remained significantly elevated until 70 days after surgery, indicating an overshooting and prolonged inflammatory response when compared to unions. This was associated with an enhanced number of p16-positive cells. Additional Western blot analyses revealed distinct differences in the inflammasome expression profiles of unions and non-unions. In particular, non-unions presented with a higher expression of the nucleotide-binding oligomerization domain (NOD)-like receptor protein (NLRP)3 at 10 days. Furthermore, at 14 days non-unions showed a higher expression of NLRP1 whereas the expression of absent in melanoma (AIM)2 was significantly reduced. Conclusion: In a clinical setting, these distinct expression profiles may serve as predictive markers for fracture healing outcome. Moreover, in the future novel treatment approaches modulating inflammasome expression may be used to stimulate bone regeneration and eventually prevent non-union formation.

Indexed as

Bone RegenerationFracture HealingFractures, UnunitedInflammasomesAnimalsBiomarkersDisease Models, AnimalMacrophagesMaleMiceBiomarkersInflammasomesAIM2bone regenerationfracture healinginflammasomeinflammationinflammatory cellsNLRP3non-union

Identifiers

PMID42819158
PMCPMC13623699

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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.