Development of a safe and effective nanoparticle-based vaccine against porcine epidemic diarrhea virus 2308286

Abstract Introduction Porcine epidemic diarrhea virus (PEDV), introduced into the U.S. in 2013, causes severe diarrhea and nearly 100% mortality in neonatal piglets, leading to an estimated annual economic loss near $1.8 billion. Current inactivated vaccines provide only partial protection, while live-attenuated vaccines pose safety concerns. To address this, we are developing a hybrid nanoparticle (hNP)-based spike protein vaccine with enhanced safety, immunogenicity, and protective efficacy. Methods The nanovaccine incorporates the C-terminal domain (CTD) of the PEDV USA/CO/2013/29619 spike protein. CTD is expressed in E. coli, purified, and conjugated to lipid-coated poly(lactic-co-glycolic acid) nanoparticles. The hNP platform enables incorporation of molecular adjuvants within both the polymer core and lipid layer. Nanoparticles are characterized for size, polydispersity, antigen loading, and endotoxin levels. The immunogenicity of the nanovaccines is first evaluated in mice. Results Recombinant CTD was expressed at a yield of 30 mg/L in bacterial culture and purified under denaturing conditions with subsequent refolding. Endotoxin was reduced to below 1.0 EU/mL. hNPs exhibited a size under 200 nm with a polydispersity index below 0.1, reflecting high formulation uniformity. CTD was conjugated efficiently at 35 µg/mg of hNPs. Multiple formulations have been produced with various adjuvants, including CpG oligodeoxynucleotide, resiquimod, and monophosphoryl lipid A. The nanovaccines are evaluated in eliciting systemic IgG, mucosal IgA, and cellular immune responses relevant to PEDV protection. Conclusion This modular hNP platform allows precise antigen display and flexible multi-adjuvant delivery. This platform represents a valuable approach for advancing PEDV vaccine development and improving swine health outcomes. Funding Source USDA National Institute of Food and Agriculture, AFRI project 2021-08581. Topic Categories Vaccines and Immunotherapy (VAC)

Authors

Institutions

Publication Details

Journal
The Journal of Immunology
Published
2026-07-28
DOI
https://doi.org/10.1093/jimmun/vkag141.1420
Primary Topic
Animal Virus Infections Studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Development of a safe and effective nanoparticle-based vaccine against porcine epidemic diarrhea virus 2308286

Qiaoqiao Ci, Xiang‐Jin Meng, Chenming Zhang, Yuanzhi Bian
The Journal of Immunology
Animal Virus Infections Studies
article

Development of a safe and effective nanoparticle-based vaccine against porcine epidemic diarrhea virus 2308286

Qiaoqiao Ci, Xiang‐Jin Meng, Chenming Zhang, Yuanzhi Bian
article en

Abstract

Abstract Introduction Porcine epidemic diarrhea virus (PEDV), introduced into the U.S. in 2013, causes severe diarrhea and nearly 100% mortality in neonatal piglets, leading to an estimated annual economic loss near $1.8 billion. Current inactivated vaccines provide only partial protection, while live-attenuated vaccines pose safety concerns. To address this, we are developing a hybrid nanoparticle (hNP)-based spike protein vaccine with enhanced safety, immunogenicity, and protective efficacy. Methods The nanovaccine incorporates the C-terminal domain (CTD) of the PEDV USA/CO/2013/29619 spike protein. CTD is expressed in E. coli, purified, and conjugated to lipid-coated poly(lactic-co-glycolic acid) nanoparticles. The hNP platform enables incorporation of molecular adjuvants within both the polymer core and lipid layer. Nanoparticles are characterized for size, polydispersity, antigen loading, and endotoxin levels. The immunogenicity of the nanovaccines is first evaluated in mice. Results Recombinant CTD was expressed at a yield of 30 mg/L in bacterial culture and purified under denaturing conditions with subsequent refolding. Endotoxin was reduced to below 1.0 EU/mL. hNPs exhibited a size under 200 nm with a polydispersity index below 0.1, reflecting high formulation uniformity. CTD was conjugated efficiently at 35 µg/mg of hNPs. Multiple formulations have been produced with various adjuvants, including CpG oligodeoxynucleotide, resiquimod, and monophosphoryl lipid A. The nanovaccines are evaluated in eliciting systemic IgG, mucosal IgA, and cellular immune responses relevant to PEDV protection. Conclusion This modular hNP platform allows precise antigen display and flexible multi-adjuvant delivery. This platform represents a valuable approach for advancing PEDV vaccine development and improving swine health outcomes. Funding Source USDA National Institute of Food and Agriculture, AFRI project 2021-08581. Topic Categories Vaccines and Immunotherapy (VAC)

The Journal of ImmunologyVol. 215(Supplement_1)
Virginia Tech (US)
Good health and well-being
Openalex Percentile: Top 10%
Animal Virus Infections Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.