AI Article Synopsis

  • Host protection against cutaneous herpes simplex virus 1 (HSV-1) infection depends on a strong adaptive immune response, influenced by Nav sensory neurons.
  • The removal of these neurons leads to severe skin damage and increased inflammatory response, indicating their role in controlling inflammation post-infection.
  • The study highlights how the sensory nervous system affects immune responses, suggesting potential new treatment approaches for viral infections.

Article Abstract

Host protection against cutaneous herpes simplex virus 1 (HSV-1) infection relies on the induction of a robust adaptive immune response. Here, we show that Nav sensory neurons, which are involved in pain perception, control the magnitude of CD8 T cell priming and expansion in HSV-1-infected mice. The ablation of Nav-expressing sensory neurons is associated with extensive skin lesions characterized by enhanced inflammatory cytokine and chemokine production. Mechanistically, Nav sensory neurons are required for the downregulation of neutrophil infiltration in the skin after viral clearance to limit the severity of tissue damage and restore skin homeostasis, as well as for eliciting robust CD8 T cell priming in skin-draining lymph nodes by controlling dendritic cell responses. Collectively, our data reveal an important role for the sensory nervous system in regulating both innate and adaptive immune responses to viral infection, thereby opening up possibilities for new therapeutic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131384PMC
http://dx.doi.org/10.1038/s41467-021-22841-6DOI Listing

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