Related Experiment Video
Updated: Jun 23, 2026

Mouse Footpad Inoculation Model to Study Viral-Induced Neuroinflammatory Responses
Published on: June 14, 2020
Functional impairment of PRRSV-specific peripheral CD3+CD8high cells
Sarah Costers1, David J Lefebvre, Bruno Goddeeris
1Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium. sarah.costers@ugent.be
Porcine reproductive and respiratory syndrome virus (PRRSV) infection involves immune responses beyond antibodies. This study found that while pigs infected with PRRSV show T-cell proliferation, they lack effective cytotoxic T-lymphocyte (CTL) activity against infected cells.
Area of Science:
- Veterinary Immunology
- Virology
- Cellular Immunology
Background:
- Porcine reproductive and respiratory syndrome virus (PRRSV) replication decreases before neutralizing antibodies appear, suggesting other immune mechanisms are involved.
- Alveolar macrophages are key targets for PRRSV, and their elimination by immune cells is crucial for viral clearance.
Purpose of the Study:
- To investigate the role of PRRSV Lelystad virus (LV)-specific cytotoxic T-lymphocytes (CTL) in eliminating PRRSV-infected alveolar macrophages.
- To assess the CTL response in pigs experimentally infected with PRRSV.
Main Methods:
- Cytotoxic T-lymphocyte (CTL) assays were performed using PRRSV-infected alveolar macrophages as target cells.
- Autologous peripheral blood mononuclear cells (PBMC) from PRRSV-infected pigs were used as a source of PRRSV-specific CTL.
- Assays were validated using pseudorabies virus (PRV) Begonia-infected cells and PBMC.
Main Results:
- No detectable CTL activity against PRRSV-infected macrophages was observed in freshly isolated PBMC from PRRSV-infected pigs up to 56 days post-infection (dpi).
- Restimulation of PBMC with PRRSV in vitro induced proliferation of CD3+CD8high cells from 14 dpi, but significant CTL activity was delayed until 49-56 dpi in only one pig.
- In contrast, PRV-specific CTL activity was observed robustly from 21 dpi in control pigs.
Conclusions:
- PBMC from PRRSV-infected pigs contain CD3+CD8high cells that proliferate upon in vitro restimulation.
- These PBMC, however, fail to effectively eliminate PRRSV-infected alveolar macrophages, indicating a lack of functional PRRSV-specific CTL response during the study period.
More Related Videos
08:11Assessing the Innate Sensing of HIV-1 Infected CD4+ T Cells by Plasmacytoid Dendritic Cells Using an Ex vivo Co-culture System.
Published on: September 1, 2015
13:12Transsynaptic Tracing from Peripheral Targets with Pseudorabies Virus Followed by Cholera Toxin and Biotinylated Dextran Amines Double Labeling
Published on: September 14, 2015