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HLA-Ig Based Artificial Antigen Presenting Cells for Efficient ex vivo Expansion of Human CTL
Published on: April 11, 2011
Enhancing DNA immunization by targeting ASFV antigens to SLA-II bearing cells.
J M Argilaguet1, E Pérez-Martín, C Gallardo
1Centre de Recerca en Sanitat Animal (CReSA), UAB-IRTA, Campus de la UAB, 08193 Bellaterra, Barcelona, Spain.
Targeting African swine fever virus antigens to immune cells improved DNA vaccine responses in pigs, but did not prevent lethal challenge. This research informs future vaccine development for swine diseases.
Area of Science:
- Veterinary Immunology
- Molecular Biology
- Vaccinology
Background:
- DNA vaccines often show poor immunogenicity in large animals, including pigs.
- A plasmid DNA vaccine (pCMV-PQ) encoding African swine fever virus (ASFV) genes failed to elicit immune responses in pigs, unlike in mice.
Purpose of the Study:
- To enhance immune responses in pigs against ASFV using DNA vaccination.
- To investigate the efficacy of targeting antigens to antigen-presenting cells (APCs) in swine.
Main Methods:
- Construction of a novel DNA vaccine (pCMV-APCH1PQ) encoding ASFV genes fused to a single-chain variable fragment targeting swine leukocyte antigen II (SLA II).
- Immunization of pigs with pCMV-APCH1PQ and assessment of immune responses.
- Evaluation of vaccine efficacy through lethal ASFV challenge.
Main Results:
- Targeting antigens to APCs significantly enhanced immune responses in pigs compared to the non-targeted vaccine.
- Despite enhanced immune responses, the vaccine did not confer protection against lethal ASFV challenge.
- Viremia exacerbation was observed in vaccinated pigs, correlated with non-neutralizing antibodies and SLA II-restricted T-cell responses.
Conclusions:
- Targeting antigens to APCs is a viable strategy to boost DNA vaccine immunogenicity in pigs.
- Further research is needed to develop protective vaccines against ASFV, potentially by improving antigen presentation or inducing neutralizing antibodies.
- These findings have implications for developing vaccines against ASFV and other swine pathogens.
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