Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/127073
Author(s): Alejo A
Ruiz-Argüello M
Pontejo S
Fernández De Marco M
Saraiva M
Hernáez B
Alcamí A
Title: Chemokines cooperate with TNF to provide protective anti-viral immunity and to enhance inflammation
Publisher: Nature
Issue Date: 2018
Abstract: The role of cytokines and chemokines in anti-viral defense has been demonstrated, but their relative contribution to protective anti-viral responses in vivo is not fully understood. Cytokine response modifier D (CrmD) is a secreted receptor for TNF and lymphotoxin containing the smallpox virus-encoded chemokine receptor (SECRET) domain and is expressed by ectromelia virus, the causative agent of the smallpox-like disease mousepox. Here we show that CrmD is an essential virulence factor that controls natural killer cell activation and allows progression of fatal mousepox, and demonstrate that both SECRET and TNF binding domains are required for full CrmD activity. Vaccination with recombinant CrmD protects animals from lethal mousepox. These results indicate that a specific set of chemokines enhance the inflammatory and protective anti-viral responses mediated by TNF and lymphotoxin, and illustrate how viruses optimize anti-TNF strategies with the addition of a chemokine binding domain as soluble decoy receptors.
URI: https://hdl.handle.net/10216/127073
Source: Nature Communications, vol.9(1):1790
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: http://creativecommons.org/licenses/by/4.0/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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