| Literature DB >> 30115567 |
Madalina E Carter-Timofte1, Søren R Paludan2, Trine H Mogensen3.
Abstract
In most individuals, varicella zoster virus (VZV) causes varicella upon primary infection and zoster during reactivation. However, in a subset of individuals, VZV may cause severe disease, including encephalitis. Host genetics is believed to be the main determinant of exacerbated disease manifestations. Recent studies have demonstrated that defects in the DNA sensor RNA polymerase III (POL III) confer selective increased susceptibility to VZV infection, thus providing fundamental new insight into VZV immunity. Here we describe the roles of POL III in housekeeping and immune surveillance during VZV infection. We present the latest knowledge on the role of POL III in VZV infection and discuss outstanding questions related to the role of POL III in VZV immunity, and how this insight can be translated into clinical medicine.Entities:
Keywords: DNA sensing; RNA polymerase III; interferon; varicella zoster virus
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Year: 2018 PMID: 30115567 DOI: 10.1016/j.molmed.2018.07.009
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951