Evidence map›Paper›PMID 40396174›Full record

ArticleFrontiers in immunology2025

Differential activation of monocytes and PMNs in orofacial granulomatosis patients induced by bacterial and non-bacterial stimuli.

Francesco Palestra, Luca Modestino, Annagioia Ventrici, Arianna Monteforte, Gina Memoli, Anne Lise Ferrara, Leonardo Cristinziano, Remo Poto, Francesca Wanda Rossi, Gilda Varricchi and 6 more

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Article in Frontiers in immunology, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Francesco Palestra *Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Luca Modestino *Department of Internal Medicine and Clinical Immunology, University Hospital of Naples Federico II, Naples, Italy.
Annagioia VentriciDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Arianna MonteforteDepartment of Internal Medicine and Clinical Immunology, University Hospital of Naples Federico II, Naples, Italy.
Gina MemoliDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Anne Lise FerraraDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Leonardo CristinzianoCenter for Basic and Clinical Immunology Research (CISI), WAO Center of Excellence, University of Naples Federico II, Naples, Italy.
Remo PotoDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Francesca Wanda RossiDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Gilda VarricchiDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Amato De PaulisDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Gianni MaroneDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Giuseppe SpadaroDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Angelica PetraroliDepartment of Internal Medicine and Clinical Immunology, University Hospital of Naples Federico II, Naples, Italy.
Stefania Loffredo *Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Maria Rosaria Galdiero *Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Orofacial Granulomatosis (OFG) is a rare chronic inflammatory disorder characterized by persistent or recurrent swelling of the lips and oral mucosa, often accompanied by granulomatous inflammation in the orofacial region with limited effective treatment options available. Emerging evidence suggests an immune dysregulation in the development and progression of OFG. Immune cells, including monocytes and neutrophils (PMNs), are involved in autoimmune and inflammatory diseases by releasing pro-inflammatory and immunomodulatory molecules. Methods: Considering that microbial agents have been suggested as potential triggers for OFG, in this study we evaluated the effect of LPS, fMLP and PMA on the activation of monocytes and PMNs purified by 11 OFG patients and 11 sex-and age-matched healthy donors (HDs). Results: Upon stimulation, OFG-derived monocytes displayed a higher release of pro-inflammatory cytokines (CXCL8/IL-8, IL-6, TNF-α, IL-33) compared to HDs. Conversely, OFG-derived monocytes showed a lower release of IL-10, IFN-γ compared to HDs. Upon stimulation, peripheral PMNs from OFG patients released large amounts of TNF-α and MPO compared to HDs. In addition, OFG-derived PMNs showed high percentages of activated PMNs (CD62L Discussion: These preliminary data suggest that in presence of various stimuli, monocytes and PMNs of OFG patients displayed an activated phenotype compared to HDs. Unraveling the interplay between bacterial triggers and immune cell function in OFG will be necessary to elucidate mechanisms driving this complex disease and identify novel therapeutic targets for improved management of OFG patients.

Indexed as

Granulomatosis, OrofacialMonocytesNeutrophilsAdultCytokinesFemaleHumansInflammation MediatorsLipopolysaccharidesMaleMiddle AgedReactive Oxygen SpeciesYoung AdultCytokinesInflammation MediatorsLipopolysaccharidesReactive Oxygen Speciesbacterial stimulicytokines/chemokinesimmunopathogenesisinflammationNETsROS

Identifiers

PMID40396174
PMCPMC12088978

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