Dysbiosis-induced IL-33 contributes to impaired antiviral immunity in the genital mucosa.
Ontology highlight
ABSTRACT: Commensal microbiota are well known to play an important role in antiviral immunity by providing immune inductive signals; however, the consequence of dysbiosis on antiviral immunity remains unclear. We demonstrate that dysbiosis caused by oral antibiotic treatment directly impairs antiviral immunity following viral infection of the vaginal mucosa. Antibiotic-treated mice succumbed to mucosal herpes simplex virus type 2 infection more rapidly than water-fed mice, and also showed delayed viral clearance at the site of infection. However, innate immune responses, including type I IFN and proinflammatory cytokine production at infection sites, as well as induction of virus-specific CD4 and CD8 T-cell responses in draining lymph nodes, were not impaired in antibiotic-treated mice. By screening
SUBMITTER: Oh JE
PROVIDER: S-EPMC4760794 | biostudies-literature | 2016 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA