Author: Caddy, Sarah L; Vaysburd, Marina; Papa, Guido; Wing, Mark; O’Connell, Kevin; Stoycheva, Diana; Foss, Stian; Terje Andersen, Jan; Oxenius, Annette; James, Leo C
Title: Viral nucleoprotein antibodies activate TRIM21 and induce T cell immunity Cord-id: 2i4bga0f Document date: 2020_12_1
ID: 2i4bga0f
Snippet: Nucleoprotein (N) is an immunodominant antigen in many enveloped virus infections. While the diagnostic value of antiâ€N antibodies is clear, their role in immunity is not. This is because while they are nonâ€neutralising, they somehow clear infection by coronavirus, influenza and LCMV in vivo. Here, we show that antiâ€N immune protection is mediated by the cytosolic Fc receptor and E3 ubiquitin ligase TRIM21. Exploiting LCMV as a model system, we demonstrate that TRIM21 uses antiâ€N antibod
Document: Nucleoprotein (N) is an immunodominant antigen in many enveloped virus infections. While the diagnostic value of antiâ€N antibodies is clear, their role in immunity is not. This is because while they are nonâ€neutralising, they somehow clear infection by coronavirus, influenza and LCMV in vivo. Here, we show that antiâ€N immune protection is mediated by the cytosolic Fc receptor and E3 ubiquitin ligase TRIM21. Exploiting LCMV as a model system, we demonstrate that TRIM21 uses antiâ€N antibodies to target N for cytosolic degradation and generate cytotoxic T cells (CTLs) against N peptide. These CTLs rapidly eliminate Nâ€peptideâ€displaying cells and drive efficient viral clearance. These results reveal a new mechanism of immune synergy between antibodies and T cells and highlights N as an important vaccine target.
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