作者: Jared Evan Knickelbein
DOI:
关键词: Cytotoxic T cell 、 Granzyme B 、 Ex vivo 、 Biology 、 Herpes simplex virus 、 In vivo 、 Virology 、 HSL and HSV 、 Immediate early protein 、 Lytic cycle
摘要: Reactivation of herpes simplex virus (HSV) from neuronal latency is a common and potentially devastating cause disease worldwide. CD8 T cells can completely inhibit HSV reactivation, IFN-gamma affords portion this protection. We now show that cell lytic granules are also required for the maintenance type 1 (HSV-1) both in vivo ex cultures, their directed release into junctions with neurons latently infected ganglia does not induce apoptosis. Our findings support non-lethal mechanism viral inactivation by demonstrating granule component, granzyme B, degrades HSV-1 immediate early protein, ICP4, which essential further gene expression. These reveal novel non-apoptotic function B context inhibiting reactivation latency.