Vaccination of cats experimentally infected with feline immunodeficiency virus, using a recombinant feline leukemia virus vaccine

R. Lehmann From the Department of Medicine, School of Veterinary Medicine, University of Zurich, Winterthurerstr 260, CH-8057 Zurich, Switzerland (Lehmann, Franchini Wolfensberger, Lutz) and Virbac Laboratories, 1 ère Avenue LID, 06516 Carros, France (Aubert, Cronier).

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M. Franchini From the Department of Medicine, School of Veterinary Medicine, University of Zurich, Winterthurerstr 260, CH-8057 Zurich, Switzerland (Lehmann, Franchini Wolfensberger, Lutz) and Virbac Laboratories, 1 ère Avenue LID, 06516 Carros, France (Aubert, Cronier).

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A. Aubert From the Department of Medicine, School of Veterinary Medicine, University of Zurich, Winterthurerstr 260, CH-8057 Zurich, Switzerland (Lehmann, Franchini Wolfensberger, Lutz) and Virbac Laboratories, 1 ère Avenue LID, 06516 Carros, France (Aubert, Cronier).

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C. Wolfensberger From the Department of Medicine, School of Veterinary Medicine, University of Zurich, Winterthurerstr 260, CH-8057 Zurich, Switzerland (Lehmann, Franchini Wolfensberger, Lutz) and Virbac Laboratories, 1 ère Avenue LID, 06516 Carros, France (Aubert, Cronier).

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J. Cronier From the Department of Medicine, School of Veterinary Medicine, University of Zurich, Winterthurerstr 260, CH-8057 Zurich, Switzerland (Lehmann, Franchini Wolfensberger, Lutz) and Virbac Laboratories, 1 ère Avenue LID, 06516 Carros, France (Aubert, Cronier).

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H. Lutz From the Department of Medicine, School of Veterinary Medicine, University of Zurich, Winterthurerstr 260, CH-8057 Zurich, Switzerland (Lehmann, Franchini Wolfensberger, Lutz) and Virbac Laboratories, 1 ère Avenue LID, 06516 Carros, France (Aubert, Cronier).

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Summary

A group of 15 cats experimentally infected with a Swiss isolate of feline immunodeficiency virus (fiv) and a group of 15 fiv-negative control cats were inoculated with an FeLV vaccine containing recombinant FeLV-envelope. High elisa antibody titer developed after vaccination in fiv-positive and fiv-negative cats. Vaccinated and nonvaccinated controls were later challenge exposed by intraperitoneal administration of virulent FeLV subtype A (Glasgow). Although 12 of 12 nonvaccinated controls became infected with FeLV (10 persistently, 2 transiently), only 1 of 18 vaccinated (9 fiv positive, 9 fiv negative) cats had persistent and 2 of 18 had transient viremia.

From these data and other observations, 2 conclusions were drawn: In the early phase of fiv infection, the immune system is not depressed appreciably, and therefore, cats may be successfully immunized; a recombinant FeLV vaccine was efficacious in protecting cats against intraperitoneal challenge exposure with FeLV.

Summary

A group of 15 cats experimentally infected with a Swiss isolate of feline immunodeficiency virus (fiv) and a group of 15 fiv-negative control cats were inoculated with an FeLV vaccine containing recombinant FeLV-envelope. High elisa antibody titer developed after vaccination in fiv-positive and fiv-negative cats. Vaccinated and nonvaccinated controls were later challenge exposed by intraperitoneal administration of virulent FeLV subtype A (Glasgow). Although 12 of 12 nonvaccinated controls became infected with FeLV (10 persistently, 2 transiently), only 1 of 18 vaccinated (9 fiv positive, 9 fiv negative) cats had persistent and 2 of 18 had transient viremia.

From these data and other observations, 2 conclusions were drawn: In the early phase of fiv infection, the immune system is not depressed appreciably, and therefore, cats may be successfully immunized; a recombinant FeLV vaccine was efficacious in protecting cats against intraperitoneal challenge exposure with FeLV.

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