Login / Signup

Characterization of humoral responses to Nipah virus infection in the Syrian Hamster model of disease.

Florine E M ScholteSergio E RodriguezStephen R WelchKatherine A DaviesSarah C GenzerJoAnn D Coleman-McCrayJessica R HarmonTeresa E SorvilloMichael K LoElif KaraaslanEric BergeronJoel M MontgomeryJessica R SpenglerChristina F Spiropoulou
Published in: The Journal of infectious diseases (2023)
Nipah virus (NiV) is a highly pathogenic paramyxovirus. The Syrian hamster model recapitulates key features of human NiV disease and is a critical tool for evaluating antivirals and vaccines. Here we describe longitudinal humoral immune responses in NiV-infected Syrian hamsters. Samples were obtained 1-28 days after infection and analyzed by ELISA, neutralization, and Fc-mediated effector function assays. NiV infection elicited robust antibody responses against the nucleoprotein and attachment glycoprotein. Levels of neutralizing antibodies were modest and only detectable in surviving animals. Fc-mediated effector functions were mostly observed in nucleoprotein-targeting antibodies. Antibody levels and activities positively correlated with challenge dose.
Keyphrases
  • immune response
  • dendritic cells
  • endothelial cells
  • regulatory t cells
  • high throughput
  • cancer therapy
  • drug delivery
  • inflammatory response
  • monoclonal antibody
  • single cell