Feline Immunodeficiency Virus
Margaret J. Hosie
Search for more papers by this authorMargaret J. Hosie
Search for more papers by this authorMarjory B. Brooks DVM, DACVIM
Director, Comparative Coagulation Section
Animal Health Diagnostic Center, Cornell University, Ithaca, New York, USA
Search for more papers by this authorKendal E. Harr DVM, MS, DACVP
URIKA, LLC, Mukilteo, Washington, USA
Search for more papers by this authorDavis M. Seelig DVM, PhD, DACVP
Associate Professor, Clinical Pathology
Department of Veterinary Clinical Sciences, University of Minnesota, College of Veterinary Medicine, St. Paul, Minnesota, USA
Search for more papers by this authorK. Jane Wardrop DVM, MS, DACVP
Professor and Director, Clinical Pathology Laboratory
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, USA
Search for more papers by this authorDouglas J. Weiss DVM, PhD, DACVP
Emeritus Professor
College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota, USA
Search for more papers by this authorSummary
Feline immunodeficiency virus (FIV), discovered in 1987, shares a similar structure, genetic organization, lymphocyte tropism, and pathogenesis to the human immunodeficiency virus (HIV). During the acute phase of experimental FIV infection, mild lymphopenia and later lymphopenia and severe neutropenia have been described. The most frequent hematologic abnormalities include anemia, neutropenia, lymphopenia, and monocytosis. After infection, cats readily develop high titers of antibodies recognizing different FIV components. Antibodies can be detected by immunofluorescence assays, ELISAs, or immunochromatography tests. FIV infection can be diagnosed either directly, by detecting the virus, or indirectly, by demonstrating the presence of antibodies. Symptomatic treatment of infected cats should be directed at the clinical signs that arise from secondary infections.
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