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Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition

Systemic juvenile idiopathic arthritis (SJIA) is a disease marked with arthritis and several features of systemic inflammation including fevers, rashes, hepatosplenomegaly, lymphadenopathy, and serositis. The presentation can be variable and arthritis can be a later feature. Macrophage activation sy...

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Autores principales: Grevich, Sriharsha, Shenoi, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687245/
https://www.ncbi.nlm.nih.gov/pubmed/29184458
http://dx.doi.org/10.2147/AHMT.S109495
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author Grevich, Sriharsha
Shenoi, Susan
author_facet Grevich, Sriharsha
Shenoi, Susan
author_sort Grevich, Sriharsha
collection PubMed
description Systemic juvenile idiopathic arthritis (SJIA) is a disease marked with arthritis and several features of systemic inflammation including fevers, rashes, hepatosplenomegaly, lymphadenopathy, and serositis. The presentation can be variable and arthritis can be a later feature. Macrophage activation syndrome can be a life-threatening complication of this illness and requires early recognition and prompt therapy. Advancements in understanding the biology of SJIA have led to the development of cytokine-targeted therapies, mainly interleukin-1 (IL-1) and IL-6 inhibitors that have significantly improved outcomes. In this review, we provide an update on the advances in the understanding of SJIA biology and also the therapeutic options.
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spelling pubmed-56872452017-11-28 Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition Grevich, Sriharsha Shenoi, Susan Adolesc Health Med Ther Review Systemic juvenile idiopathic arthritis (SJIA) is a disease marked with arthritis and several features of systemic inflammation including fevers, rashes, hepatosplenomegaly, lymphadenopathy, and serositis. The presentation can be variable and arthritis can be a later feature. Macrophage activation syndrome can be a life-threatening complication of this illness and requires early recognition and prompt therapy. Advancements in understanding the biology of SJIA have led to the development of cytokine-targeted therapies, mainly interleukin-1 (IL-1) and IL-6 inhibitors that have significantly improved outcomes. In this review, we provide an update on the advances in the understanding of SJIA biology and also the therapeutic options. Dove Medical Press 2017-11-09 /pmc/articles/PMC5687245/ /pubmed/29184458 http://dx.doi.org/10.2147/AHMT.S109495 Text en © 2017 Grevich and Shenoi. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Grevich, Sriharsha
Shenoi, Susan
Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition
title Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition
title_full Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition
title_fullStr Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition
title_full_unstemmed Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition
title_short Update on the management of systemic juvenile idiopathic arthritis and role of IL-1 and IL-6 inhibition
title_sort update on the management of systemic juvenile idiopathic arthritis and role of il-1 and il-6 inhibition
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687245/
https://www.ncbi.nlm.nih.gov/pubmed/29184458
http://dx.doi.org/10.2147/AHMT.S109495
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