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Poly I:C adjuvanted inactivated swine influenza vaccine induces heterologous protective immunity in pigs

tetano

Editor, Senior Moderator
Vaccine. 2014 Nov 28. pii: S0264-410X(14)01573-4. doi: 10.1016/j.vaccine.2014.11.034. [Epub ahead of print]
Poly I:C adjuvanted inactivated swine influenza vaccine induces heterologous protective immunity in pigs.
Thomas M1, Wang Z1, Sreenivasan CC1, Hause BM2, Gourapura R3, Li F4, Francis DH5, Kaushik RS4, Khatri M6.
Author information
Abstract

Swine influenza is widely prevalent in swine herds in North America and Europe causing enormous economic losses and a public health threat. Pigs can be infected by both avian and mammalian influenza viruses and are sources of generation of reassortant influenza viruses capable of causing pandemics in humans. Current commercial vaccines provide satisfactory immunity against homologous viruses; however, protection against heterologous viruses is not adequate. In this study, we evaluated the protective efficacy of an intranasal Poly I:C adjuvanted UV inactivated bivalent swine influenza vaccine consisting of Swine/OH/24366/07 H1N1 and Swine/CO/99 H3N2, referred as PAV, in maternal antibody positive pigs against an antigenic variant and a heterologous swine influenza virus challenge. Groups of three-week-old commercial-grade pigs were immunized intranasally with PAV or a commercial vaccine (CV) twice at 2 weeks intervals. Three weeks after the second immunization, pigs were challenged with the antigenic variant Swine/MN/08 H1N1 (MN08) and the heterologous Swine/NC/10 H1N2 (NC10) influenza virus. Antibodies in serum and respiratory tract, lung lesions, virus shedding in nasal secretions and virus load in lungs were assessed. Intranasal administration of PAV induced challenge viruses specific-hemagglutination inhibition- and IgG antibodies in the serum and IgA and IgG antibodies in the respiratory tract. Importantly, intranasal administration of PAV provided protection against the antigenic variant MN08 and the heterologous NC10 swine influenza viruses as evidenced by significant reductions in lung virus load, gross lung lesions and significantly reduced shedding of challenge viruses in nasal secretions. These results indicate that Poly I:C or its homologues may be effective as vaccine adjuvants capable of generating cross-protective immunity against antigenic variants/heterologous swine influenza viruses in pigs.

Copyright ? 2014. Published by Elsevier Ltd.
KEYWORDS:

Inactivated swine influenza vaccines; Poly I:C; Swine influenza virus; Vaccine adjuvants

PMID:
25437101
[PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/pubmed/25437101
 
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