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Published on: March 12, 2018
Infliximab treatment for refractory Kawasaki disease with coronary artery aneurysm
Taku Oishi1, Mikiya Fujieda, Taisuke Shiraishi
1Department of Pediatrics, Kochi National Hospital, Kochi, Japan.
Insights
Tumor necrosis factor-alpha (TNF-alpha) plays a role in Kawasaki disease (KD) with coronary artery aneurysms (CA). Infliximab, an anti-TNF-alpha agent, successfully treated a young patient with refractory KD and CA.
Area of Science:
- Immunology
- Pediatrics
- Cardiology
Background:
- Kawasaki disease (KD) is an acute febrile vasculitis primarily affecting young children.
- Coronary artery aneurysms (CA) are a serious complication of KD, linked to inflammatory processes.
- Elevated levels of Tumor Necrosis Factor-alpha (TNF-alpha) are observed in KD patients with CA.
Observation:
- A 1-month-old infant presented with refractory KD complicated by CA.
- The patient received treatment with infliximab, an anti-TNF-alpha biologic agent.
- Clinical assessment focused on the resolution of CA and control of KD symptoms.
Findings:
- Infliximab administration led to the improvement of coronary artery aneurysms.
- The patient's Kawasaki disease was effectively controlled following treatment.
- Symptom resolution and absence of complications were noted 20 months post-onset.
Implications:
- This case suggests TNF-alpha inhibition is a potential therapeutic strategy for refractory KD with CA.
- Targeting TNF-alpha may prevent or reverse vascular damage in KD.
- Further research into anti-TNF-alpha agents for KD management is warranted.
Abstract:
Tumor necrosis factor-alpha (TNF-alpha) is considered to be 1 of the factors that induce vasculitis, including coronary artery aneurysm (CA), in Kawasaki disease (KD), because the blood concentration of TNF-alpha is higher in patients with CA compared with those without. Therefore, an anti-TNF-alphaagent (infliximab) was administered to a 1-month-old girl with refractory KD complicated by CA and subsequently, the CA improved and KD was controlled without complications 20 months after the onset.
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