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

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)

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Publication Details

Journal
The Journal of Immunology
Published
2026-07-28
DOI
https://doi.org/10.1093/jimmun/vkag141.983
Primary Topic
Mosquito-borne diseases and control
Type
article
Field-Weighted Citation Impact
0.00
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article

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

Joshua Herzler, Douglas Durrant, Manuel Ramirez, Michaela Montinola
The Journal of Immunology
Mosquito-borne diseases and control
article

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

Joshua Herzler, Douglas Durrant, Manuel Ramirez, Michaela Montinola
article en

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)

The Journal of ImmunologyVol. 215(Supplement_1)
California State Polytechnic University (US)
Good health and well-being
Openalex Percentile: Top 6%
Mosquito-borne diseases and control
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