Chronic Recurrent Multifocal Osteomyelitis (CRMO): Presentation, Pathogenesis, and Treatment

被引:175
|
作者
Hofmann, Sigrun R. [1 ]
Kapplusch, Franz [1 ]
Girschick, Hermann J. [2 ]
Morbach, Henner [3 ]
Pablik, Jessica [4 ]
Ferguson, Polly J. [5 ]
Hedrich, Christian M. [1 ,6 ,7 ]
机构
[1] Tech Univ Dresden, Med Fak Carl Gustav Carus, Dept Pediat, Pediat Rheumatol & Immunol, Dresden, Germany
[2] Childrens Hosp, Vivantes Klinikum Friedrichshain, Berlin, Germany
[3] Univ Wurzburg, Childrens Hosp, Pediat Rheumatol & Immunol, Wurzburg, Germany
[4] Tech Univ Dresden, Med Fak Carl Gustav Carus, Div Pathol, Dresden, Germany
[5] Univ Iowa, Stead Family Childrens Hosp, Dept Pediat, Iowa City, IA USA
[6] Univ Liverpool, Inst Translat Med Child Hlth, Dept Womens & Childrens Hlth, East Prescott Rd, Liverpool L14 5AB, Merseyside, England
[7] Alder Hey Childrens NHS Fdn Trust Hosp, Dept Pediat Rheumatol, Liverpool, Merseyside, England
来源
CURRENT OSTEOPOROSIS REPORTS | 2017年 / 15卷 / 06期
关键词
Chronic non-bacterial osteomyelitis; CNO; Chronic recurrent multifocal osteomyelitis; CRMO; Treatment; Inflammation; Cytokine; Bone; Biomarkers; CHRONIC NONBACTERIAL OSTEOMYELITIS; AUTOINFLAMMATORY BONE DISORDERS; PSTPIP2-DEFICIENT MICE; IL-10; EXPRESSION; LONG-TERM; MAJEED-SYNDROME; DISEASE; IL-1-BETA; CHILDREN; MUTATION;
D O I
10.1007/s11914-017-0405-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic non-bacterial osteomyelitis (CNO) with its most severe form chronic recurrent multifocal osteomyelitis (CRMO) is an autoinflammatory bone disorder. We summarize the clinical presentation, diagnostic approaches, most recent advances in understanding the pathophysiology, and available treatment options and outcomes in CNO/CRMO. Though the exact molecular pathophysiology of CNO/CRMO remains somewhat elusive, it appears likely that variable defects in the TLR4/MAPK/inflammasome signaling cascade result in an imbalance between pro- and anti-inflammatory cytokine expressions in monocytes from CNO/CRMO patients. In this context, we present previously unpublished data on cytokine and chemokine expression in monocytes and tissues. CNO/CRMO is an autoinflammatory bone disorder resulting from imbalanced cytokine expression from innate immune cells. Though the exact molecular pathophysiology remains unclear, variable molecular defects appear to result in inflammasome activation and pro-inflammatory cytokine expression in monocytes from CNO/CRMO patients. Recent advances suggest signaling pathways and single molecules as biomarkers for CNO/CRMO as well as future treatment targets.
引用
收藏
页码:542 / 554
页数:13
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