Chronic nonbacterial osteomyelitis: pathophysiological concepts and current treatment strategies

SR Hofmann, A Schnabel, A Rösen-Wolff… - The Journal of …, 2016 - jrheum.org
SR Hofmann, A Schnabel, A Rösen-Wolff, H Morbach, HJ Girschick, CM Hedrich
The Journal of rheumatology, 2016jrheum.org
Chronic nonbacterial osteomyelitis (CNO) is an autoinflammatory bone disorder, covering a
clinical spectrum with asymptomatic inflammation of single bones at the one end, and
chronic recurrent multifocal osteomyelitis (CRMO) at the other end. The exact molecular
pathophysiology of CNO remains largely unknown. Provided familial clusters and the
association with inflammatory disorders of the skin and intestine suggest a genetic
predisposition. Recently, profound dysregulation of cytokine responses was demonstrated in …
Chronic nonbacterial osteomyelitis (CNO) is an autoinflammatory bone disorder, covering a clinical spectrum with asymptomatic inflammation of single bones at the one end, and chronic recurrent multifocal osteomyelitis (CRMO) at the other end. The exact molecular pathophysiology of CNO remains largely unknown. Provided familial clusters and the association with inflammatory disorders of the skin and intestine suggest a genetic predisposition. Recently, profound dysregulation of cytokine responses was demonstrated in CRMO. Failure to produce antiinflammatory cytokines interleukin (IL)-10 and IL-19 contributes to activation of inflammasomes and subsequent IL-1β release. In IL-10–deficient and in CNO-prone chronic multifocal osteomyelitis mice, IL-1β was linked to bone inflammation. Further, alterations to the gut microbiome were suggested in contributing to IL-1β release from innate immune cells in mice, offering an interesting target in the search for molecular mechanisms in CNO. Here, we summarize clinical presentation and treatment options in CNO/CRMO, current pathophysiological concepts, available mouse models, and promising future scientific directions.
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