4.7 Article

Expression of H3N2 nucleoprotein in maize seeds and immunogenicity in mice

期刊

PLANT CELL REPORTS
卷 34, 期 6, 页码 969-980

出版社

SPRINGER
DOI: 10.1007/s00299-015-1758-0

关键词

Nucleoprotein; H3N2; Plant-based vaccine; Antigens; Transgenic maize

资金

  1. U.S. Department of Agriculture National Institute of Food and Agriculture [IOW05162]
  2. Plant Sciences Institute of Iowa State University
  3. Charoen Pokphand Indonesia

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Key message Oral administration of maize-expressed H3N2 nucleoprotein induced antibody responses in mice showing the immunogenicity of plant-derived antigen and its potential to be utilized as a universal flu vaccine. Abstract Influenza A viruses cause influenza epidemics that are devastating to humans and livestock. The vaccine for influenza needs to be reformulated every year to match the circulating strains due to virus mutation. Influenza virus nucleoprotein (NP) is a multifunctional RNA-binding protein that is highly conserved among strains, making it a potential candidate for a universal vaccine. In this study, the NP gene of H3N2 swine origin influenza virus was expressed in maize endosperm. Twelve transgenic maize lines were generated and analyzed for recombinant NP (rNP) expression. Transcript analysis showed the main accumulation of rNP in seed. Protein level of rNP in T1 transgenic maize seeds ranged from 8.0 to 35 mu g of NP/g of corn seed. The level increased up to 70 mu g of NP/g in T3 seeds. A mouse study was performed to test the immunogenicity of one line of maize-derived rNP (MNP). Mice were immunized with MNP in a prime-boost design. Oral gavage administration showed that a humoral immune response was elicited in the mice treated with MNP indicating the immunogenicity of MNP. NP-specific antibody responses in the MNP group showed comparable antibody titer with the groups receiving positive controls such as Vero cell-derived NP (VNP) or alphavirus replicon particle-derived NP (ANP). Cytokine analysis showed antigen-specific stimulation of IL-4 cytokine elicited in splenocytes from mice treated with MNP further confirming a TH2 humoral immune response induced by MNP administration.

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