Abstract |
We have vaccinated cats with fixed autologous FIV infected PBMC to determine whether autologous presentation of antigen is capable of inducing a protective immune response against homologous challenge. To this end autologous PBMC were infected with a FIV molecular clone (19k1). When infection was established, cells were inactivated by dialysis against paraformaldehyde. Upon vaccination, cats developed a virus specific immune response as measured by ELISA against the Gag protein of FIV. No antibodies against the envelope protein were detected with a peptide ELISA. Virus neutralizing antibodies however could be detected with a neutralization assay based on infection of CrFK cells, but not in an assay based on infection of primary T-cells. Although vaccination led to the induction of these virus-specific immune responses, vaccinated cats were not protected against homologous challenge but showed an accelerated viraemia upon infection. This was shown both by PCR and cell-associated viral load. The possible mechanisms underlying this observation are discussed in this paper.
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Authors | J A Karlas, K H Siebelink, M A v Peer, W Huisman, G F Rimmelzwaan, A D Osterhaus |
Journal | Veterinary immunology and immunopathology
(Vet Immunol Immunopathol)
Vol. 65
Issue 2-4
Pg. 353-65
(Oct 23 1998)
ISSN: 0165-2427 [Print] Netherlands |
PMID | 9839884
(Publication Type: Journal Article)
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Chemical References |
- Antibodies, Viral
- DNA Primers
- DNA, Viral
- Viral Vaccines
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Topics |
- Animals
- Antibodies, Viral
(analysis)
- Blood Component Transfusion
- Blood Transfusion, Autologous
- Cats
- DNA Primers
(chemistry)
- DNA, Viral
(analysis)
- Feline Acquired Immunodeficiency Syndrome
(immunology, prevention & control)
- Immunodeficiency Virus, Feline
(genetics, immunology)
- Polymerase Chain Reaction
(veterinary)
- T-Lymphocytes
(immunology, virology)
- Vaccination
(veterinary)
- Viral Load
- Viral Vaccines
(administration & dosage)
- Viremia
(etiology, immunology)
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