DEC-205—Targeted Antigen Delivery Enhances T Cell Immunity in a Murine Model of West Nile Virus Encephalitis 2260788
Abstract
Abstract Introduction Targeted immunotherapies aimed at enhancing antiviral T cell responses are of particular interest for treating neurotropic viral infections such as West Nile Virus (WNV), which lacks a licensed human vaccine. Previous studies have shown that DEC-205+ dendritic cells (DCs) in the central nervous system (CNS) play a role in reactivating antiviral immunity during WNV infection. Methods Methods to investigate this: a hybrid scFv antibody targeting DEC-205 and conjugated to a peptide from the WNV NS4b protein was administered to mice infected with WNV-TX. Poly I:C was co-delivered as an adjuvant to promote DC maturation. Immunological outcomes were assessed by quantifying co-stimulatory molecule expression (CD40, CD80, CD86) on DCs and evaluating T cell activation markers and cytokine profiles. Results Mice receiving the DEC-205—NS4b scFv showed increased expression of activation markers and higher levels of pro-inflammatory cytokines, suggesting enhanced antiviral immunity. Conclusion These findings support targeted DC-based strategies as a promising approach for future WNV vaccine development. Funding Source Cal Poly Pomona Project Hatchery Topic Categories Immune Response Regulation: Cellular Mechanisms (IRC)
Article Details
Journal Info
The Journal of Immunology
American Association of Immunologists
Authors (4)
Manuel Ramirez
Cal Poly, Pomona
Joshua Herzler
Cal Poly Pomona
Michaela Montinola
Cal Poly Pomona
Douglas Durrant
Cal Poly Pomona