IndraLab

Statements


| 5

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"Interestingly, we found that TLR2 reduces RV induced STAT1 and STAT2 activation indicating TLR2 may inhibit amplification of IFNs that involves JAK and STAT signaling pathway."

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"In these situations, discovering novel therapeutic modalities that can dampen IFN signaling is potentially valuable.Other RV strategies have also been identified that are directed at disrupting STAT1 signaling during infection."
| PMC

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"Although viral factors responsible for this inhibitory effect downstream of STAT1 activation have not yet been identified, it is possible that redundancy in RV inhibition of the STAT1 pathway exists, perhaps indicative of the vital role of inhibiting IFN signaling in enabling RV replication.The ability of the RV NSP1 protein to target IRFs for proteasomal degradation extends to IRF7 and IRF9, two additional factors that are critical for the optimal amplification of IFN-dependent antiviral responses [40], [42]."
| PMC

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"RV has also been shown to inhibit the function of STAT1 and STAT2 by an unknown mechanism and thus, can potentially inhibit all types of IFN responses [XREF_BIBR]."

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"Furthermore, RV infection was observed to block the migration of STAT1, STAT2 and NF-kappaB to the nucleus, thus preventing host cell immune responses [XREF_BIBR]."