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Immune response following safer administration of recombinant Salmonella Typhimurium harboring ASFV antigens in pigs. | LitMetric

Immune response following safer administration of recombinant Salmonella Typhimurium harboring ASFV antigens in pigs.

Vet Immunol Immunopathol

College of Veterinary Medicine, Biosafety Research Institute, Chonbuk National University, 79 Gobong-ro, Iksan-city Pincode-54596, Jeollabuk-Do, Republic of Korea. Electronic address:

Published: May 2023

AI Article Synopsis

  • African swine fever virus (ASFV) is a serious threat to the pig industry in Asia and Europe, with multiple serotypes and genotypes identified, but effective vaccines are still lacking due to safety concerns.
  • Recent research explored the use of a genetically modified Salmonella Typhimurium strain (rSal-ASFV) to deliver ASFV antigens in pigs, which significantly boosted various immune cells, including helper T cells and natural killer cells.
  • The study showed that rSal-ASFV can trigger a strong immune response without side effects, indicating its potential as a safe and effective way to enhance immunity against ASFV in pigs, although more research on antigen-specific responses is needed.

Article Abstract

African swine fever virus (ASFV) is a contagious epizootic pathogen adversely affecting porcine industry in Asian and European countries. Till date, 8 serotypes and 24 genotypes of the virus have been reported. Few live attenuated virus vaccine studies have reported to provide complete protection against ASFV infection but biohazard concern still remain. Recombinant subunit antigens are capable of providing cellular and humoral immunity in porcine, but not a single vaccine has hit the market yet. In the present study, we attempted to use recombinant Salmonella Typhimurium JOL912 strain harboring ASFV antigens (rSal-ASFV) to investigate its immunostimulant effect in porcine. Post intramuscular administration, we observed significant increment in the levels of helper T cells, cytotoxic T cells, natural killer (NK) cells, and immunoglobulin (i.e. IgG, IgA, and IgM) levels in rSal-ASFV treated groups. Further RT-PCR analysis indicated the increased expression of MHC-I, MHC-II, CD80/86, NK cell receptors (NKp30, NKp44, and NKp46) and cytokines while ELIspot analysis revealed significant production of IFN-γ in rSal-ASFV treated groups. Taken together, we are able to demonstrate that rSal-ASFV could elicit a non-specific cellular as well as humoral immune response. However, additional antigen specific immunity data is needed to evaluate its efficacy. Intramuscular administration of rSal-ASFV was found to be safe and immunostimulant in nature without any side-effects and may serve as an excellent option for in-vivo antigen delivery in pigs.

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Source
http://dx.doi.org/10.1016/j.vetimm.2023.110596DOI Listing

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