Intracellular antibody receptor TRIM21 prevents fatal viral infection
Author(s) -
Marina Vaysburd,
Ruth Watkinson,
Helen Cooper,
Martin Reed,
Kevin O‘Connell,
Jackie L Smith,
James Cruickshanks,
Leo C. James
Publication year - 2013
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1301918110
Subject(s) - ubiquitin ligase , biology , viremia , antibody , virology , knockout mouse , immune system , hek 293 cells , viral replication , fc receptor , ubiquitin , receptor , microbiology and biotechnology , virus , immunology , genetics , gene
Host species have evolved mechanisms that can inhibit pathogen replication even after a cell has been successfully invaded. Here we show that tripartite-motif protein 21 (TRIM21), a ubiquitously expressed E3 ubiquitin ligase that targets viruses inside the cytosol, protects mice against fatal viral infection. Upon infection with mouse adenovirus-1, naive mice lacking TRIM21 succumb to encephalomyelitis within 7 d. In contrast, wild-type mice rapidly up-regulate TRIM21 and control viremia. Trim21 heterozygous mice have a haploinsufficiency phenotype in which reduced TRIM21 expression leads to a viral load that is higher than wild types but lower than knockouts. TRIM21 is a high-affinity antibody receptor that allows antibodies to operate inside an infected cell. In passive transfer experiments at high viral dose, antisera that fully protects wild-type mice fails to protect most Trim21 knockout animals. These results demonstrate that TRIM21 provides potent antiviral protection and forms an important part of the humoral immune response.
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