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Mucosal immunization against ovine lentivirus using PEI–DNA complexes and modified vaccinia Ankara encoding the gag and/or env genes

Abstract Sheep were immunized against Visna/Maedi virus (VMV) gag and/or env genes via the nasopharynx-associated lymphoid tissue (NALT) and lung using polyethylenimine (PEI)–DNA complexes and modified vaccinia Ankara, and challenged with live virus via the lung. env immunization enhanced humoral re...

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Bibliographic Details
Published in:Vaccine 2008-08, Vol.26 (35), p.4494-4505
Main Authors: Reina, R, Barbezange, C, Niesalla, H, de Andrés, X, Arnarson, H, Biescas, E, Mazzei, M, Fraisier, C, McNeilly, T.N, Liu, C, Perez, M, Carrozza, M.L, Bandecchi, P, Solano, C, Crespo, H, Glaria, I, Huard, C, Shaw, D.J, de Blas, I, de Andrés, D, Tolari, F, Rosati, S, Suzan-Monti, M, Andrésdottir, V, Torsteinsdottir, S, Petursson, G, Lujan, L, Pepin, M, Amorena, B, Blacklaws, B, Harkiss, G.D
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Language:English
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Summary:Abstract Sheep were immunized against Visna/Maedi virus (VMV) gag and/or env genes via the nasopharynx-associated lymphoid tissue (NALT) and lung using polyethylenimine (PEI)–DNA complexes and modified vaccinia Ankara, and challenged with live virus via the lung. env immunization enhanced humoral responses prior to but not after VMV challenge. Systemic T cell proliferative and cytotoxic responses were generally low, with the responses following single gag gene immunization being significantly depressed after challenge. A transient reduction in provirus load in the blood early after challenge was observed following env immunization, whilst the gag gene either alone or in combination with env resulted in significantly elevated provirus loads in lung. However, despite this, a significant reduction in lesion score was observed in animals immunized with the single gag gene at post-mortem. Inclusion of IFN-γ in the immunization mixture in general had no significant effects. The results thus showed that protective effects against VMV-induced lesions can be induced following respiratory immunization with the single gag gene, though this was accompanied by an increased pulmonary provirus load.
ISSN:0264-410X
1873-2518
0264-410X
DOI:10.1016/j.vaccine.2008.06.065