Complications of systemic juvenile idiopathic arthritis: risk factors and management recommendations.


Autoria(s): Woerner A.; von Scheven-Gête A.; Cimaz R.; Hofer M.
Data(s)

2015

Resumo

Systemic juvenile idiopathic arthritis (SJIA) is an inflammatory condition characterized by fever, lymphadenopathy, arthritis, rash and serositis. Systemic inflammation has been associated with dysregulation of the innate immune system, suggesting that SJIA is an autoinflammatory disorder. IL-1 and IL-6 play a major role in the pathogenesis of SJIA, and treatment with IL-1 and IL-6 inhibitors has shown to be highly effective. However, complications of SJIA, including macrophage activation syndrome, limitations in functional outcome by arthritis and long-term damage from chronic inflammation, continue to be a major issue in SJIA patients' care. Translational research leading to a profound understanding of the cytokine crosstalk in SJIA and the identification of risk factors for SJIA complications will help to improve long-term outcome.

Identificador

http://serval.unil.ch/?id=serval:BIB_D6430B56221B

isbn:1744-8409 (Electronic)

pmid:25843554

doi:10.1586/1744666X.2015.1032257

isiid:000353239000004

Idioma(s)

en

Fonte

Expert Review of Clinical Immunology, vol. 11, no. 5, pp. 575-588

Tipo

info:eu-repo/semantics/review

article