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Implications of SARS-CoV-2 Infection in Systemic Juvenile Idiopathic Arthritis
Laura Marinela Ailioaie1, Constantin Ailioaie1, Gerhard Litscher2
1Department of Medical Physics, Alexandru Ioan Cuza University, 11 Carol I Boulevard, 700506 Iasi, Romania.
Abstract:
Systemic juvenile idiopathic arthritis (sJIA) is a serious multifactorial autoinflammatory disease with a significant mortality rate due to macrophage activation syndrome (MAS). Recent research has deepened the knowledge about the pathophysiological mechanisms of sJIA-MAS, facilitating new targeted treatments, and biological disease-modifying antirheumatic drugs (bDMARDs), which significantly changed the course of the disease and prognosis. This review highlights that children are less likely to suffer severe COVID-19 infection, but at approximately 2-4 weeks, some cases of multisystem inflammatory syndrome in children (MIS-C) have been reported, with a fulminant course. Previous established treatments for cytokine storm syndrome (CSS) have guided COVID-19 therapeutics. sJIA-MAS is different from severe cases of COVID-19, a unique immune process in which a huge release of cytokines will especially flood the lungs. In this context, MIS-C should be reinterpreted as a special MAS, and long-term protection against SARS-CoV-2 infection can only be provided by the vaccine, but we do not yet have sufficient data. COVID-19 does not appear to have a substantial impact on rheumatic and musculoskeletal diseases (RMDs) activity in children treated with bDMARDs, but the clinical features, severity and outcome in these patients under various drugs are not yet easy to predict. Multicenter randomized controlled trials are still needed to determine when and by what means immunoregulatory products should be administered to patients with sJIA-MAS with a negative corticosteroid response or contraindications, to optimize their health and safety in the COVID era.
Insights
Systemic juvenile idiopathic arthritis (sJIA) with macrophage activation syndrome (MAS) requires new treatments. This review discusses sJIA-MAS, COVID-19, and multisystem inflammatory syndrome in children (MIS-C), highlighting treatment needs.
Area of Science:
- Pediatric Rheumatology
- Infectious Diseases
- Immunology
Background:
- Systemic juvenile idiopathic arthritis (sJIA) is a severe autoinflammatory disease with high mortality from macrophage activation syndrome (MAS).
- Biological disease-modifying antirheumatic drugs (bDMARDs) have improved sJIA prognosis.
- Multisystem inflammatory syndrome in children (MIS-C) shares features with MAS and can have a severe course.
Purpose of the Study:
- To review current understanding of sJIA-MAS pathophysiology and treatment.
- To compare sJIA-MAS with COVID-19-associated MIS-C.
- To discuss the impact of COVID-19 on pediatric rheumatic diseases and identify future research needs.
Main Methods:
- Literature review of sJIA, MAS, COVID-19, and MIS-C.
- Analysis of pathophysiological mechanisms and treatment strategies.
- Synthesis of current evidence on disease interactions and management.
Main Results:
- sJIA-MAS and severe COVID-19 involve distinct cytokine storm mechanisms.
- MIS-C can be viewed as a specific form of MAS.
- COVID-19 has a limited impact on pediatric rheumatic diseases treated with bDMARDs, but outcomes are unpredictable.
Conclusions:
- New targeted therapies and bDMARDs have improved sJIA outcomes.
- Further research, including multicenter trials, is needed to optimize immunoregulatory treatment for sJIA-MAS, especially in the context of COVID-19.
- Vaccination is crucial for long-term SARS-CoV-2 protection, though data are limited.
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