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Domizio JD et al. - The expression, controlled by STAT1 phosphorylation, was independent of type I IFN. STAT1 activation was found to be strictly dependent on the PI3K-p38MAPK pathway, demonstrating a new signaling pathway leading to rapid expression of IFN-inducible genes after TLR7 triggering. Thus pDCs, through this unusual TLR7 signaling, have the capacity to promptly respond to viral infection during the early phases of the innate immune response.



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