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Updated: Aug 27, 2025

Influenza A Virus Studies in a Mouse Model of Infection
Published on: September 7, 2017
Host Responses to Live-Attenuated ASFV (HLJ/18-7GD)
Yuqin Fan1, Weiye Chen1, Chenggang Jiang1
1State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
The African swine fever virus vaccine candidate HLJ/18-7GD effectively protects pigs by boosting specific antibodies and T lymphocyte responses. This study elucidates the immune mechanisms behind the vaccine
Area of Science:
- Veterinary Immunology
- Virology
- Vaccinology
Background:
- African swine fever (ASF) is a devastating viral disease impacting swine populations globally.
- The novel vaccine candidate HLJ/18-7GD, lacking multigene families and the CD2v gene, has shown promise in preliminary safety and efficacy trials.
- Understanding the precise immune mechanisms of HLJ/18-7GD is crucial for its successful deployment.
Purpose of the Study:
- To investigate the immune-protective mechanisms of the African swine fever vaccine candidate HLJ/18-7GD.
- To analyze the humoral and cellular immune responses in pigs following immunization with HLJ/18-7GD.
- To compare the immune response induced by HLJ/18-7GD with that of the parent virus.
Main Methods:
- Pigs were immunized with a single dose of HLJ/18-7GD (10^6 TCID50).
- Humoral immunity was assessed by measuring specific antibody levels.
- Cellular immunity was evaluated by analyzing T lymphocyte subsets (Th, CTL, DP-T cells) and cytokine production (GM-CSF, IFN-γ, TNF-α) in peripheral blood mononuclear cells (PBMCs) after immunization and challenge with virulent virus.
- In vitro assays were performed to assess PBMC responses to the HLJ/18 strain.
Main Results:
- HLJ/18-7GD immunization induced high levels of specific antibodies in pigs.
- A transient increase in T lymphocyte subsets (Th, CTL, DP-T cells) was observed in PBMCs post-immunization.
- Following challenge with virulent HLJ/18, immunized pigs showed significantly elevated Th, CTL, and DP-T cell percentages.
- Upregulation of GM-CSF, IFN-γ, and TNF-α was noted at 7 days post-inoculation, contrasting with results from parent virus infection.
- PBMCs from immunized pigs promoted higher CD8+ T cell responses against the HLJ/18 strain in vitro.
Conclusions:
- The vaccine candidate HLJ/18-7GD elicits robust specific antibody and T lymphocyte responses.
- The observed immune responses, including cytokine production, contribute to the protective effects of HLJ/18-7GD.
- These findings provide a theoretical foundation for the use of HLJ/18-7GD as a safe and effective vaccine against African swine fever.
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