DEC-205—Targeted Antigen Delivery Enhances T Cell Immunity in a Murine Model of West Nile Virus Encephalitis 2260788

M Manuel Ramirez (Cal Poly, Pomona) J Joshua Herzler (Cal Poly Pomona) M Michaela Montinola (Cal Poly Pomona) D Douglas Durrant (Cal Poly Pomona)

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

Volume / Issue Vol. 215, Issue Supplement_1
Published August 01, 2026
ISSN 0022-1767
Publisher American Association of Immunologists

Authors (4)

M

Manuel Ramirez

Cal Poly, Pomona

J

Joshua Herzler

Cal Poly Pomona

M

Michaela Montinola

Cal Poly Pomona

D

Douglas Durrant

Cal Poly Pomona