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      Evaluation of adaptive immune responses and heterologous protection induced by inactivated bluetongue virus vaccines.

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          Abstract

          Eradication of bluetongue virus is possible, as has been shown in several European countries. New serotypes have emerged, however, for which there are no specific commercial vaccines. This study addressed whether heterologous vaccines would help protect against 2 serotypes. Thirty-seven sheep were randomly allocated to 7 groups of 5 or 6 animals. Four groups were vaccinated with commercial vaccines against BTV strains 2, 4, and 9. A fifth positive control group was given a vaccine against BTV-8. The other 2 groups were unvaccinated controls. Sheep were then challenged by subcutaneous injection of either BTV-16 (2 groups) or BTV-8 (5 groups). Taken together, 24/25 sheep from the 4 experimental groups developed detectable antibodies against the vaccinated viruses. Furthermore, sheep that received heterologous vaccines showed significantly reduced viraemia and clinical scores for BTV-16 when compared to unvaccinated controls. Reductions in clinical signs and viraemia among heterologously vaccinated sheep were not as common after challenge with BTV-8. This study shows that heterologous protection can occur, but that it is difficult to predict if partial or complete protection will be achieved following inactivated-BTV vaccination.

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          Author and article information

          Journal
          Vaccine
          Vaccine
          Elsevier BV
          1873-2518
          0264-410X
          Jan 15 2015
          : 33
          : 4
          Affiliations
          [1 ] ANSES, UMR 1161 Virologie ANSES-INRA-ENVA, 23 avenue du Général de Gaulle, 94704 Maisons-Alfort, France. Electronic address: emmanuel.breard@anses.fr.
          [2 ] Université Paris-Est, Ecole Nationale Vétérinaire d'Alfort, Unité de Pathologie du Bétail, 7 avenue du Général de Gaulle, 94704 Maisons-Alfort, France.
          [3 ] ANSES, UMR 1161 Virologie ANSES-INRA-ENVA, 23 avenue du Général de Gaulle, 94704 Maisons-Alfort, France.
          [4 ] Vector-Borne Diseases Programme, The Pirbright Institute, Pirbright, Woking, Surrey GU24 0NF, United Kingdom.
          [5 ] CODA-CERVA, Department of Virology, Ukkel, Belgium.
          [6 ] MERIAL S.A.S., 254 Rue Marcel Mérieux, 69007 Lyon, France.
          [7 ] MERIAL S.A.S., P.I. Plaine de l'Ain, Allée des Cyprès, 01150 Saint-Vulbas, France.
          [8 ] Université Paris-Est, Ecole Nationale Vétérinaire d'Alfort, Centre de recherche biomédicale, 7 avenue du Général de Gaulle, 94704 Maisons-Alfort, France.
          [9 ] ANSES, unité Epidémiologie, 23 avenue du Général de Gaulle, 94704 Maisons-Alfort, France.
          Article
          S0264-410X(14)01610-7
          10.1016/j.vaccine.2014.11.053
          25500308
          6c90dacd-5a8a-4184-9e88-378d58671917
          History

          Bluetongue virus disease,Experimental infection,Heterologous challenges,Inactivated vaccines,Sheep

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