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Persistent LCMV infection is controlled by blockade of type I interferon signaling.


ABSTRACT: During persistent viral infections, chronic immune activation, negative immune regulator expression, an elevated interferon signature, and lymphoid tissue destruction correlate with disease progression. We demonstrated that blockade of type I interferon (IFN-I) signaling using an IFN-I receptor neutralizing antibody reduced immune system activation, decreased expression of negative immune regulatory molecules, and restored lymphoid architecture in mice persistently infected with lymphocytic choriomeningitis virus. IFN-I blockade before and after establishment of persistent virus infection resulted in enhanced virus clearance and was CD4 T cell-dependent. Hence, we demonstrate a direct causal link between IFN-I signaling, immune activation, negative immune regulator expression, lymphoid tissue disorganization, and virus persistence. Our results suggest that therapies targeting IFN-I may help control persistent virus infections.

SUBMITTER: Teijaro JR 

PROVIDER: S-EPMC3640797 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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Persistent LCMV infection is controlled by blockade of type I interferon signaling.

Teijaro John R JR   Ng Cherie C   Lee Andrew M AM   Sullivan Brian M BM   Sheehan Kathleen C F KC   Welch Megan M   Schreiber Robert D RD   de la Torre Juan Carlos JC   Oldstone Michael B A MB  

Science (New York, N.Y.) 20130401 6129


During persistent viral infections, chronic immune activation, negative immune regulator expression, an elevated interferon signature, and lymphoid tissue destruction correlate with disease progression. We demonstrated that blockade of type I interferon (IFN-I) signaling using an IFN-I receptor neutralizing antibody reduced immune system activation, decreased expression of negative immune regulatory molecules, and restored lymphoid architecture in mice persistently infected with lymphocytic chor  ...[more]

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