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自身炎症性骨病,重点关注慢性复发性多灶性骨髓炎(CRMO)。

Autoinflammatory bone disorders with special focus on chronic recurrent multifocal osteomyelitis (CRMO).

机构信息

Division of Pediatric Rheumatology and Immunology, Children's Hospital Dresden, University Medical Center Carl Gustav Carus, TU Dresden, Dresden, Germany.

出版信息

Pediatr Rheumatol Online J. 2013 Dec 23;11(1):47. doi: 10.1186/1546-0096-11-47.

Abstract

Sterile bone inflammation is the hallmark of autoinflammatory bone disorders, including chronic nonbacterial osteomyelitis (CNO) with its most severe form chronic recurrent multifocal osteomyelitis (CRMO). Autoinflammatory osteopathies are the result of a dysregulated innate immune system, resulting in immune cell infiltration of the bone and subsequent osteoclast differentiation and activation. Interestingly, autoinflammatory bone disorders are associated with inflammation of the skin and/or the intestine. In several monogenic autoinflammatory bone disorders mutations in disease-causing genes have been reported. However, regardless of recent developments, the molecular pathogenesis of CNO/CRMO remains unclear.Here, we discuss the clinical presentation and molecular pathophysiology of human autoinflammatory osteopathies and animal models with special focus on CNO/CRMO. Treatment options in monogenic autoinflammatory bone disorders and CRMO will be illustrated.

摘要

无菌性骨炎症是自身炎症性骨病的标志,包括慢性非细菌性骨髓炎(CNO)及其最严重形式慢性复发性多灶性骨髓炎(CRMO)。自身炎症性骨病是由于先天免疫系统失调导致免疫细胞浸润骨骼,随后破骨细胞分化和激活的结果。有趣的是,自身炎症性骨病与皮肤和/或肠道炎症有关。在几种单基因自身炎症性骨病中,已报道了致病基因的突变。然而,无论最近的研究进展如何,CNO/CRMO 的分子发病机制仍不清楚。在这里,我们讨论了人类自身炎症性骨病的临床表现和分子病理生理学,以及特别关注 CNO/CRMO 的动物模型。将举例说明单基因自身炎症性骨病和 CRMO 的治疗选择。

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