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Published on: January 31, 2020
Anakinra therapy in a child with systemic-onset juvenile rheumatoid arthritis after human herpesvirus 6 encephalitis
Laura J Mirkinson1, David Nagle, Nadja Kadom
1Department of Rheumatology, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USA. mirkil@holycrosshealth.org
Insights
Herpesvirus 6 (HHV-6) encephalitis may trigger systemic-onset juvenile idiopathic rheumatoid arthritis (SoJIA). Interleukin-1 (IL-1) receptor therapy showed effectiveness, suggesting a link between HHV-6 and IL-1 pathways in SoJIA.
Area of Science:
- Pediatric Rheumatology
- Infectious Diseases
- Immunology
Background:
- Systemic-onset juvenile idiopathic rheumatoid arthritis (SoJIA) is a significant autoimmune condition in children.
- The etiology of SoJIA remains multifactorial, with potential triggers under investigation.
- Herpesvirus 6 (HHV-6) is a known neurotropic virus, typically causing exanthem subitum in infants.
Observation:
- A 3-year-old patient presented with biopsy-proven HHV-6 encephalitis.
- The patient subsequently developed clinical manifestations consistent with SoJIA.
- The SoJIA-like symptoms showed a positive response to interleukin-1 (IL-1) receptor antagonist therapy.
Findings:
- The clinical course suggests a potential temporal relationship between HHV-6 infection and the onset of SoJIA.
- The therapeutic response to IL-1 receptor blockade indicates the likely involvement of IL-1 in the pathogenesis of this patient's SoJIA.
- This case contributes to the understanding of IL-1 receptor antagonist therapy in SoJIA.
Implications:
- HHV-6 infection should be considered as a potential trigger for new-onset SoJIA.
- Future prospective studies on new-onset SoJIA should incorporate screening for HHV-6 infection.
- Further research may elucidate the role of viral infections in the development of autoimmune conditions like SoJIA.
Abstract:
A 3-year-old patient with biopsy-proven herpesvirus 6 (HHV-6) encephalitis developed a clinical condition consistent with systemic-onset juvenile idiopathic rheumatoid arthritis (SoJIA) and responsive to synthetic interleukin-1 (IL-1) receptor therapy. This suggested both a temporal relationship between HHV-6 infection and the development of SoJIA and the likely involvement of IL-1 in his disease. This case adds to the current experience of IL-1 receptor antagonist therapy in SoJIA. In addition, it suggests that future prospective studies in new-onset SoJIA should include an evaluation for HHV-6 infection.
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