4.6 Article

Immune Responses in Pigs Vaccinated with Adjuvanted and Non-Adjuvanted A(H1N1)pdm/09 Influenza Vaccines Used in Human Immunization Programmes

期刊

PLOS ONE
卷 7, 期 3, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0032400

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资金

  1. Biotechnology and Biological Sciences Research Council (BBSRC)
  2. Medical Research Council (MRC)
  3. Department for Environment, Food and Rural Affairs (Defra)
  4. Wellcome Trust [BB/H014292/1]
  5. Institute for Animal Health
  6. Department of Health
  7. Biotechnology and Biological Sciences Research Council [BB/H014292/1, BBS/E/I/00001715, BB/H014306/1, BBS/E/I/00001615, BBS/E/I/00001444] Funding Source: researchfish
  8. Medical Research Council [G0600511, MC_U122785833, G0800767, MC_G0902096] Funding Source: researchfish
  9. BBSRC [BBS/E/I/00001444, BB/H014306/1, BBS/E/I/00001615, BBS/E/I/00001715, BB/H014292/1] Funding Source: UKRI
  10. MRC [G0600511, G0800767, MC_G0902096, MC_U122785833] Funding Source: UKRI

向作者/读者索取更多资源

Following the emergence and global spread of a novel H1N1 influenza virus in 2009, two A(H1N1)pdm/09 influenza vaccines produced from the A/California/07/09 H1N1 strain were selected and used for the national immunisation programme in the United Kingdom: an adjuvanted split virion vaccine and a non-adjuvanted whole virion vaccine. In this study, we assessed the immune responses generated in inbred large white pigs (Babraham line) following vaccination with these vaccines and after challenge with A(H1N1) pdm/09 virus three months post-vaccination. Both vaccines elicited strong antibody responses, which included high levels of influenza-specific IgG1 and haemagglutination inhibition titres to H1 virus. Immunisation with the adjuvanted split vaccine induced significantly higher interferon gamma production, increased frequency of interferon gamma-producing cells and proliferation of CD4(-)CD8(+) (cytotoxic) and CD4(+)CD8(+) (helper) T cells, after in vitro re-stimulation. Despite significant differences in the magnitude and breadth of immune responses in the two vaccinated and mock treated groups, similar quantities of viral RNA were detected from the nasal cavity in all pigs after live virus challenge. The present study provides support for the use of the pig as a valid experimental model for influenza infections in humans, including the assessment of protective efficacy of therapeutic interventions.

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