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Progressive immune dysfunction in cats experimentally infected with feline immunodeficiency virus
M Torten1, M Franchini, J E Barlough
1Department of Medicine, School of Veterinary Medicine, University of California, Davis 95616.
Journal of Virology
|May 1, 1991
Summary
Feline immunodeficiency virus (FIV) infection causes a gradual decline in T-cell function in cats. However, B-cell responses to T-independent stimuli remain unaffected, indicating a specific impact on cell-mediated immunity.
Area of Science:
- Veterinary Immunology
- Virology
- Immunodeficiency
Background:
- Feline immunodeficiency virus (FIV) is an important lentivirus affecting domestic cats.
- Understanding FIV's impact on the immune system is crucial for feline health management.
Purpose of the Study:
- To investigate the progressive effects of FIV infection on T-cell and B-cell immune functions in domestic cats.
- To characterize the timeline of immune deterioration following FIV infection.
Main Methods:
- Monitoring of specific-pathogen-free domestic cats post-infection with the Petaluma isolate of FIV.
- Assessment of circulating CD4+ and CD8+ T-lymphocyte counts and ratios.
- Evaluation of in vitro lymphocyte proliferation responses to pokeweed mitogen and concanavalin A.
- Assessment of in vivo antibody responses to T-dependent and T-independent synthetic polypeptide immunogens.
Main Results:
- Early FIV infection (within 6 months) showed decreased CD4+ lymphocytes and CD4+/CD8+ T-cell ratio, with a mild reduction in T-cell proliferation.
- By 11-12 months post-infection, a clear deficit in pokeweed mitogen response was observed.
- Later stages (25-44 months) revealed declining responses to concanavalin A and impaired antibody production to T-dependent antigens.
- Antibody responses to T-independent antigens remained intact throughout the study.
Conclusions:
- Feline immunodeficiency virus induces a slow, progressive impairment of T-cell mediated immunity.
- The B-cell capacity to respond to T-independent antigens is preserved during FIV infection.
- These findings highlight the specific impact of FIV on cellular immunity while humoral immunity against certain stimuli remains functional.