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| ==Introduction== | | ==Introduction== |
| [[Image:Kinetics of FeLV 2.jpg|thumb|right|200px|Kinetics of FeLV - Copyright Dr Brian Catchpole BVetMed PhD MRCVS]] | | [[Image:Kinetics of FeLV 2.jpg|thumb|right|200px|Kinetics of FeLV - Copyright Dr Brian Catchpole BVetMed PhD MRCVS]] |
− | FeLV is an ncogenic retrovirus which causes neoplasia ([[Lymphoma|lymphoma]]), myelosuppression ([[Regenerative and Non-Regenerative Anaemias|anaemia]]) and immunosuppression (of [[Lymphocytes#T cells|T cells]]). Three different strains are currently recognised: | + | FeLV is an oncogenic retrovirus which causes neoplasia ([[Lymphoma|lymphoma]]), myelosuppression ([[Regenerative and Non-Regenerative Anaemias|anaemia]]) and immunosuppression (of [[Lymphocytes#T cells|T cells]]). Three different strains are currently recognised: |
| *FeLV-A -natural strain | | *FeLV-A -natural strain |
| *FeLV-B which formed through FeLV-A recombining with endogenous retroviral sequences in the feline genome. | | *FeLV-B which formed through FeLV-A recombining with endogenous retroviral sequences in the feline genome. |
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| *Reproductive tract | | *Reproductive tract |
| Most kittens but only 30% of adults become '''viraemic''' for life without producing antibody. The condition progresses in various forms: | | Most kittens but only 30% of adults become '''viraemic''' for life without producing antibody. The condition progresses in various forms: |
− | *20% of viremic cats die of tumors | + | *20% of viraemic cats die of tumors |
− | *30% of viremic cats die of FeLV-associated disease | + | *30% of viraemic cats die of FeLV-associated disease |
| *80% die within three years of exposure | | *80% die within three years of exposure |
− | 30% of adults exposed become '''latently infected''' and can become viremic when immunosuppressed. | + | 30% of adults exposed become '''latently infected''' and can become viraemic when immunosuppressed. |
| 40% of exposed adults remain healthy and develop Ab and CD8+ T cells after clearing the virus, without becoming reinfected or silent carriers. | | 40% of exposed adults remain healthy and develop Ab and CD8+ T cells after clearing the virus, without becoming reinfected or silent carriers. |
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| FeLV-associated disease: | | FeLV-associated disease: |
| *'''Immunodepression''' causing secondary disease | | *'''Immunodepression''' causing secondary disease |
− | *'''Reproductive failure''': FeLV crosses the placenta, causing fetal resorption or viremic kittens with thymic aplasia | + | *'''Reproductive failure''': FeLV crosses the placenta, causing fetal resorption or viraemic kittens with thymic aplasia |
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| ==Epidemiology== | | ==Epidemiology== |
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| *Group A is transmitted between cats and is monotypic: one vaccine covers all isolates. Infection with this viral subgroup leads to '''[[Lymphoma|lymphosarcoma]]'''. | | *Group A is transmitted between cats and is monotypic: one vaccine covers all isolates. Infection with this viral subgroup leads to '''[[Lymphoma|lymphosarcoma]]'''. |
| *Group B is recombinant with transmissible FeLV-A; infection with viruses of this subgroup increases the chance of developing '''[[Thymus - Pathology|thymic tumours]]'''. | | *Group B is recombinant with transmissible FeLV-A; infection with viruses of this subgroup increases the chance of developing '''[[Thymus - Pathology|thymic tumours]]'''. |
− | *Group C is a mutant of subgroup A. Isolates are rare, and occur as A+C mixtures, leading to an increased chance of developing '''[[Regenerative and Non-Regenerative Anaemias|anaemia]]'''. | + | *Group C is a mutant of subgroup A. Isolates are rare, and occur as A+C mixes, leading to an increased chance of developing '''[[Regenerative and Non-Regenerative Anaemias|anaemia]]'''. |
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| ==Diagnosis== | | ==Diagnosis== |
− | *FeLV should be suspect in any cat with '''recurrent bacterial infections''', '''anemia''' or '''weight loss'''. Diagnostic tests available for cinfirmation of disease sttus includes: | + | *FeLV should be suspect in any cat with '''recurrent bacterial infections''', '''anemia''' or '''weight loss'''. Diagnostic tests available for confirmation of disease status include: |
| *'''[[ELISA testing|ELISA]]''' for FeLV antigens (capsid protein p27 or envelope protein gp70) | | *'''[[ELISA testing|ELISA]]''' for FeLV antigens (capsid protein p27 or envelope protein gp70) |
| *'''Immunochromatography''' is now preferred as ELISA testing can give false positives | | *'''Immunochromatography''' is now preferred as ELISA testing can give false positives |