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Published on: December 26, 2017
[Kawasaki disease. Treatment with intravenous gammaglobulins]
1Laboratoire d'Immunologie, Faculté de Médecine, Tours.
Insights
High-dose intravenous immunoglobulins rapidly resolved Kawasaki disease symptoms in 30 French children. This treatment effectively prevented coronary artery aneurysms, highlighting its value in immune-related diseases.
Area of Science:
- Pediatrics
- Immunology
- Cardiology
Background:
- Kawasaki disease is an acute febrile illness primarily affecting young children.
- Coronary artery abnormalities, including aneurysms, are a significant complication.
- Intravenous immunoglobulin (IVIG) is a standard treatment, but modified forms are being explored.
Purpose of the Study:
- To evaluate the efficacy of plasmin-modified immunoglobulins in treating acute Kawasaki disease.
- To assess the impact of this treatment on clinical symptoms, laboratory markers, and coronary artery outcomes.
Main Methods:
- Thirty French children with acute Kawasaki disease received high-dose intravenous plasmin-modified immunoglobulins (1-2.5 g/kg).
- Clinical symptoms, laboratory parameters (hyperfibrinogenemia, leukocytosis, thrombocytosis), and immunological markers were monitored.
- Echocardiography and coronary arteriography were used to assess coronary artery status.
Main Results:
- Rapid resolution of clinical symptoms was observed in all patients.
- Hyperfibrinogenemia, hyperleukocytosis, and thrombocytosis regressed within 1-3 weeks.
- Only one child showed transient left coronary artery dilatation; coronary arteriography was normal at 6 months, indicating prevention of aneurysms.
Conclusions:
- High-dose intravenous plasmin-modified immunoglobulins are effective in treating acute Kawasaki disease.
- This therapy appears to prevent the development of coronary artery aneurysms.
- The immunoregulatory properties of immunoglobulins underpin their therapeutic value in immune-mediated conditions.
Abstract:
Thirty French children (18 males, 12 females; mean age 20 +/- 18 months) presenting with Kawasaki disease were treated with high-dose intravenous plasmin-modified immunoglobulins (Veinoglobulines Institut Mérieux, France) during the acute phase of the disease. The total dose ranged from 1 to 2.5 g/kg (mean 1.88 +/- 0.50) administered in 1 to 5 infusions. In every case the clinical symptoms disappeared rapidly. Hyperfibrinaemia and hyperleucocytosis with granulocytosis regressed within one week, and high platelet counts within 2 to 3 weeks. the disappearance of immunological abnormalities paralleled that of clinical signs. Three-dimensional echocardiography showed dilatation of the left coronary artery in only one of the 30 children at 1 and 6 months, but coronary arteriography performed during the 6th month gave normal results. Intravenous immunoglobulin therapy seems to be effective in preventing the development of coronary aneurysms in patients with Kawasaki disease. The immunoregulatory function of immunoglobulins accounts for this effectiveness and for their value in immune diseases.
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