Objectives: Granulomas contain multinucleated giant cells (MGCs), the function of which remains largely unknown. In patients with autoimmune granulomatous disease, the granulomas can be resolved during treatment with glucocorticosteroid (GCS). However, little is known about the influence of GCSs on the formation of MGCs.
Methods: Monocytes isolated from buffy coats were stimulated with IFN-γ and Concanavalin A to form MGCs either in presence or absence of TNF-α, methylprednisolone (MP), adalimumab or human immunoglobulin G. The concentrations of IL-1β, IL-6, IL-10, IL-12p70 and TNF-α in the culture supernatants were measured after 18 h of stimulation.
Results: MP, at a concentration of 0.1 µM, inhibited monocyte fusion (P < 0.05), and abrogated the formation of MGCs completely at higher concentrations. The production of IL-1β, IL-6 and TNF-α that accompanied MGC formation was reduced significantly by 10 µM MP. Recombinant TNF-α, at a concentration of 50 ng/ml, increased the number of formed MGCs and counteracted the inhibitory effect of 0.1 µM MP, while higher concentrations of MP still blocked MGC formation completely. Blockade of TNF-α with adalimumab within 16 h after stimulation significantly reduced the number MGCs formed (P < 0.05).
Conclusion: MP inhibits the fusion of monocytes into MGCs, as well as the monocyte production of pro-inflammatory cytokines, which may be an important aspect of its beneficial effect in chronic granulomatous disorders. MCG formation can be promoted by TNF-α and inhibited by TNF-α blockade.
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http://dx.doi.org/10.1093/rheumatology/keq213 | DOI Listing |
Pol J Pathol
January 2025
Department of Dermatology, Medical University of Warsaw, Warsaw, Poland.
Multinucleate cell angiohistiocytoma (MCAH) is a rare benign cutaneous entity. It classically presents as slowly progressive erythematous to violaceous papules on the distal extremities of middle-aged or elderly women. The entity may clinically resemble granuloma annulare, lichen planus, and several cutaneous vascular proliferations.
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Department of Pathobiology and Population Medicine, Mississippi State University, 240 Wise Center Drive, Mississippi State, Mississippi 39762, USA.
Histoplasmosis is a rarely reported clinical disease of equids in North America and is historically attributed to Histoplasma capsulatum var. capsulatum. This report details a case of intestinal histoplasmosis with lymphadenitis in an American Mammoth Jackstock donkey from Mississippi.
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Research Center for Genome & Medical Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Objectives: GCA is a granulomatous vasculitis affecting large vessels, leading to intimal occlusion accompanied by the accumulation of myofibroblasts. Histopathologically, GCA is characterized by destruction of the tunica media and hypertrophy of the intima with invasion of activated CD4+ T cells, macrophages and multinucleated giant cells (MNGCs). Despite these well-defined histopathological features, the molecular pathology of GCA has largely remained elusive.
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NeuroMarkers, Houston, Texas, USA.
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View Article and Find Full Text PDFFront Bioeng Biotechnol
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Clinic and Policlinic for Dermatology and Venereology, University Medical Center Rostock, Rostock, Germany.
This study investigates the mechanical properties as well as and cyto- and biocompatibility of collagen membranes cross-linked with glutaraldehyde (GA), proanthocyanidins (PC), hexamethylendiisocyanate (HMDI) and 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EC/NHS). A non-crosslinked membrane was used as reference control (RF). The initial cytotoxic analyses revealed that the PC, EC, and HMDI crosslinked membranes were cytocompatible, while the GA crosslinked membrane was cytotoxic and thus selected as positive control in the further study.
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