2018
DOI: 10.1111/micc.12498
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Mast cells and primary systemic vasculitides

Abstract: Vasculitides are characterized by inflammation and necrosis of blood vessels leading to vessel occlusion and ischemic damages of tissues. Among the inflammatory cells involved in vasculitides, neutrophils, T cells, and macrophages have been identified as the predominant cell type. This review article is focused on the role of mast cells in these chronic inflammatory processes. Mast cells are characterized by their complex plasticity. Increasing evidences document that mast cells exert both pro- and anti-inflam… Show more

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Cited by 3 publications
(1 citation statement)
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“…Supraphysiological concentrations of GCSs demonstrate the capacity to restrain fibroblast proliferation and attenuate the production of IL-1 and tumor necrosis factor (TNF)-α, demonstrating their effective anti-inflammatory action [ 149 ]. The effects on inflammatory cells include: (i) reducing the number of neutrophils in the blood, lowering the activation of neutrophils, macrophages, and mast cells, which is secondary to the inhibition of cell adhesion molecule and cytokine gene transcription [ 150 ]; (ii) lowering the overall activation rate of helper T (Th) cells, reducing T cell clonal proliferation, and initiating the transition from Th1-type immune response to Th2-type immune response [ 151 ]; (iii) reducing the functionality of fibroblasts, decreasing the production of collagen and glycosaminoglycans, and in some cases, reducing healing and repair capabilities [ 152 ].…”
Section: Mechanistic Pathways Of Gc Action In Tumor Cellsmentioning
confidence: 99%
“…Supraphysiological concentrations of GCSs demonstrate the capacity to restrain fibroblast proliferation and attenuate the production of IL-1 and tumor necrosis factor (TNF)-α, demonstrating their effective anti-inflammatory action [ 149 ]. The effects on inflammatory cells include: (i) reducing the number of neutrophils in the blood, lowering the activation of neutrophils, macrophages, and mast cells, which is secondary to the inhibition of cell adhesion molecule and cytokine gene transcription [ 150 ]; (ii) lowering the overall activation rate of helper T (Th) cells, reducing T cell clonal proliferation, and initiating the transition from Th1-type immune response to Th2-type immune response [ 151 ]; (iii) reducing the functionality of fibroblasts, decreasing the production of collagen and glycosaminoglycans, and in some cases, reducing healing and repair capabilities [ 152 ].…”
Section: Mechanistic Pathways Of Gc Action In Tumor Cellsmentioning
confidence: 99%