IL-10RA Mutation as a Risk Factor of Severe Influenza-Associated Encephalopathy: A Case Report

Author:

Ishige Takashi12,Igarashi Yoshiko1,Hatori Reiko1,Tatsuki Maiko1,Sasahara Yoji3,Takizawa Takumi1,Arakawa Hirokazu1

Affiliation:

1. Department of Pediatrics, Graduate School of Medicine, Gunma University, Maebashi, Japan;

2. Cell Biology Program, Inflammatory Bowel Disease Centre, The Hospital for Sick Children, Toronto, Canada; and

3. Department of Pediatrics, Graduate School of Medicine, Tohoku University, Miyagi, Japan

Abstract

Influenza-associated encephalitis and encephalopathy (IAE) is a severe complication of influenza infection with high morbidity and mortality. We present the case of a patient with IL-10RA mutation who developed encephalopathy after influenza infection. A 10-day-old boy developed recurrent fever and anal fistula. Growth failure gradually became apparent. He had been treated with antibiotics and elemental nutrition. However, the patient did not respond to the treatments. At 11 months, he suddenly developed shock with encephalopathy and multiple organ failures. He was then diagnosed with IAE. A cytokine study revealed elevated levels of IL-1 receptor antagonist, IL-2, IL-6, IL-8, IP-10, eotaxin, G-CSF, MCP-1, and IL-10. These cytokines are normally downregulated by IL-10. Genetic testing revealed a IL-10RA mutation at the 3′ end of exon 4 (c.537G→A). These findings might reflect an increased risk of severe IAE in patients with IL-10RA mutation.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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