Abstract
Healthy synovial tissue includes a lining layer of synovial fibroblasts and
macrophages. The influx of leucocytes during active rheumatoid arthritis (RA)
includes monocytes that differentiate locally into proinflammatory macrophages,
and these produce pathogenic tumour necrosis factor. During sustained remission,
the synovial tissue macrophage numbers recede to normal. The constitutive
presence of tissue macrophages in the lining layer of the synovial membrane in
healthy donors and in patients with RA during remission suggests that this
macrophage population may have a role in maintaining and reinstating synovial
tissue homeostasis respectively. Recent appreciation of the different origins and
functions of tissue-resident compared with monocyte-derived macrophages has
improved the understanding of their relative involvement in organ homeostasis in
mouse models of disease. In this review, informed by mouse models and human data,
we describe the presence of different functional subpopulations of human synovial
tissue macrophages and discuss their distinct contribution to joint homeostasis
and chronic inflammation in RA.
Lingua originale | English |
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pagine (da-a) | e000527-N/A |
Rivista | RMD Open |
Volume | 3 |
DOI | |
Stato di pubblicazione | Pubblicato - 2017 |
Keywords
- arthritis
- inflammation
- synovitis