Viral infection and brain inflammation with seizures in PARK7 deficiency.

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作者:Lønskov Jonas, Sünderhauf Annika, Andersen Sisse, Jeppesen Caroline Bækmann, Winzig Franziska, Hinke Daniëla Maria, Heinz Johanna L, Thomsen Kenneth, Thorup Mette B, Zillinger Thomas, Bundgaard Bettina, De Keukeleere Kerstin, Jørgensen Sofie Eg, Ek Jakob, Østergaard Elsebet, Christensen Jakob, Handrup Mette Møller, van der Sluis Renee M, Mogensen Trine H
Respiratory syncytial virus (RSV) is a major health problem worldwide, particularly in infants and young children. The infection can progress to life-threatening lower respiratory disease and, in rare cases, involves the central nervous system. We explore the pathophysiology in a child with high fever, seizures, and encephalopathy with brain inflammation during severe RSV infection. Whole-genome sequencing revealed homozygosity for a rare loss-of-function variant in the early-onset Parkinson-related gene PARK7/DJ-1. PARK7 plays a role in immune regulation, stress responses, and cell death. The patient's Peripheral blood mononuclear cells and fibroblasts exhibited increased inflammatory cytokine responses, impaired RSV-induced apoptosis, and dampened autophagy. Studies in PARK7-deficient neuronal cells recapitulated the patient's cellular phenotype, which was reversed upon PARK7 reconstitution. To our knowledge, this is the first association between PARK7 deficiency and RSV-induced brain inflammation, encephalopathy, and seizures. Collectively, our results demonstrate a role for PARK7 in regulation of inflammation and cellular homeostasis and suggest that PARK7 deficiency may aggravate infectious disease and cause immunopathology.

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