Interferon as a Mucosal Adjuvant for an Influenza Vaccine in Pigs.
Lirong LiuWenhui FanHe ZhangShuang ZhangLiang CuiMeng WangXiaoyuan BaiWenxian YangLei SunLimin YangWenjun LiuJing LiPublished in: Virologica Sinica (2019)
Interferon, a natural protein that is produced by a variety of cells during viral infection, activates the transcription of multiple functional genes in cells, regulates synergy among various signaling pathways, and mediates many biological functions such as antiviral activity, immune regulation, and cell growth. However, clinical research on interferon in livestock is lacking. In this study, recombinant porcine interferon (PoIFNα) was used as an adjuvant, in combination with inactivated influenza virus, to vaccinate 6-week-old pigs via nasal infusion. The transcription of target genes was then monitored and the functions of PoIFNα were determined with respect to the activation of mucosal immunity. We found that a combination of low-dose PoIFNα and inactivated influenza virus could significantly up-regulate the expression of immunoregulatory cytokines such as IL-2, IL-18, IFN-γ, IL-6, and IL-10 by real-time PCR, suggesting the induction of a strong mucosal innate immune response after administration. In addition, low-dose PoIFNα can significant enhancing the transcription of genes encoding homing factors including CCR9 and CCR10 (P < 0.001), thereby resulting in the induction of higher levels of HA-specific antibodies (P < 0.05), which can be determined by ELISA and IFA. Post-immunization challenges with H1N1 virus demonstrated that PoIFNα, combined with inactivated influenza virus, could alleviate clinical signs in pigs during the early stages of viral infection. These studies reveal low-dose PoIFNα as a potential mucosal adjuvant for influenza virus in pigs.
Keyphrases
- low dose
- dendritic cells
- immune response
- induced apoptosis
- genome wide
- early stage
- high dose
- ulcerative colitis
- signaling pathway
- transcription factor
- cell cycle arrest
- regulatory t cells
- real time pcr
- genome wide identification
- bioinformatics analysis
- poor prognosis
- endoplasmic reticulum stress
- oxidative stress
- clinical trial
- binding protein
- dna methylation
- epithelial mesenchymal transition
- pi k akt
- genome wide analysis
- climate change
- toll like receptor
- cell proliferation
- small molecule
- long non coding rna
- cell death
- placebo controlled