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Systemic juvenile idiopathic arthritis: New insights into pathogenesis and cytokine directed therapies
Abstract
Systemic juvenile idiopathic arthritis (sJIA) is considered as a polygenic autoinflammatory disease. The prominent systemic clinical features, the marked elevation of inflammatory markers, and the absence of autoantibodies make this disease very different from the other juvenile idiopathic arthritis (JIA) forms. Innate immune mechanisms appear to play a central role: the overproduction of inflammatory cytokines of innate immunity is a typical feature of sJIA. Increased understanding of the role of these cytokines has been translated into therapeutic approaches. Indeed, remarkable results have been observed with interleukin-1 (IL-1) and interleukin-6 (IL-6) inhibitors both in clinical trials and in real life. Other inhibitors of these cytokines will be available in the near future, thereby increasing the therapeutic armamentarium. A better understanding of the pathophysiology of sJIA is still needed to identify IL-1 or IL-6 responders, define a potential window of opportunity for early cytokine blockade, and identify a targeted treatment for macrophage activation syndrome. Additional therapeutic targets are needed for a small proportion of patients who do not respond to either IL-1 or IL-6 inhibition.
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“however, a small proportion of patients do not respond to either IL-1 or IL-6 inhibition, and a substantial number of patients develop macrophage activation syndrome under this treatment (Pardeo et al., 2017”
From Targeting Interleukin-6 Signaling in Clinic (2019) · cites this paper as Pardeo et al., 2017
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Cited by
Sorted by citations
Targeting Interleukin-6 Signaling in Clinic
Kang, S., Tanaka, T., Narazaki, M., & Kishimoto, T. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.026 · Cited by 904
Metadata
- Authors
- Pardeo, M., Bracaglia, C., & De Benedetti, F.
- Venue
- Best Practice & Research Clinical Rheumatology
- Publisher
- Elsevier BV
- Published
- 2017-08
- Volume
- 31
- Issue
- 4
- Pages
- 505-516
- ISSN
- 1521-6942
- Cited by
- 60
- References
- 6
- Language
- en
- Funders
- Gilead Sciences
- AbbVie
- Sanofi
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