The objectives of this program are to characterize the immunosuppressive properties of a retroviral envelope protein (p15E) and to determine its role in retroviral disease. Earlier, we demonstrated that FeLV p15E suppressed lymphocyte blastogenesis and lymphocyte membrane mobility (receptor capping) of cat, human, and dog peripheral blood lymphocytes (PBL). Recently, the protein was found to suppress the one-way mixed lymphocyte reaction and to inhibit proliferation of erythroid colony-forming cells but not granulocyte/macrophage colony-forming cells in vitro. Attempts to determine which specific cell types are affected have indicated that both B lymphocytes and macrophages are resistant, whereas T-cell functions appear sensitive. FeLV p15E did not interfere with B-cell immunoglobulin capping or macrophage production of interleukin 1, whereas it significantly affected Con A capping and interleukin 2 simulation, both T cell-dependent functions. The mechanism of the action of FeLV p15E is unknown; however, research with the prostaglandin and cyclic nucleotide systems has led to a possible answer. Using sensitive radioimmune precipitation assays to measure prostaglandin and cyclic nucleotide levels, we found that prostaglandin synthesis (PGE2, PGI2, PGF2, and TXB2) was not affected by FeLV p15E, whereas cyclic nucleotide (cAMP) levels were altered. Specific inhibitors of prostaglandin synthesis, indomethacin and nordihydroguaiaretic acid, reversed the FeLV p15E-induced suppression of lymphocyte blastogenesis and capping. Neither inhibitor had any effect on normal lymphocyte capping or blastogenesis. Indomethacin also increased capping and blastogenesis of lymphocytes from FeLV-infected (imunosuppressed) cats. Using other specific inhibitors of prostaglandin synthesis, we found that inhibitors of thromboxane synthesis and prostacyclin synthesis had no augmenting capabilities. Research to date indicates that modulation of AMP levels by FeLV p15E may mediate its immunosuppressive effect. This effect may be of secondary importance, in that altered cAMP levels may reflect changes caused by FeLV p15E at the level of the cell membrane. (IS)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA031547-05
Application #
3169664
Study Section
Experimental Immunology Study Section (EI)
Project Start
1982-02-01
Project End
1988-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Ohio State University
Department
Type
Schools of Veterinary Medicine
DUNS #
098987217
City
Columbus
State
OH
Country
United States
Zip Code
43210
Dezzutti, C S; Lafrado, L J; Lewis, M G et al. (1990) Inhibition of phorbol ester-induced neutrophil chemiluminescence by FeLV. Arch Virol 111:75-85
Lafrado, L J; Mathes, L E; Zack, P M et al. (1990) Biological effects of staphylococcal protein A immunotherapy in cats with induced feline leukemia virus infection. Am J Vet Res 51:482-6
Copelan, E A; Waddell, K S; Johnson, S C et al. (1990) Purine metabolism in feline lymphomas. Vet Pathol 27:117-21
Hayes, K A; Rojko, J L; Tarr, M J et al. (1989) Atypical localised viral expression in a cat with feline leukaemia. Vet Rec 124:344-6
Dezzutti, C S; Wright, K A; Lewis, M G et al. (1989) FeLV-induced immunosuppression through alterations in signal transduction: down regulation of protein kinase C. Vet Immunol Immunopathol 21:55-67
Lafrado, L J; Dezzutti, C S; Lewis, M G et al. (1989) Immunodeficiency in latent feline leukemia virus infections. Vet Immunol Immunopathol 21:39-46
Lewis, M G; Lafrado, L J; Haffer, K et al. (1988) Feline leukemia virus vaccine: new developments. Vet Microbiol 17:297-308
Wellman, M L; Kociba, G J; Mathes, L E et al. (1988) Suppression of feline bone marrow fibroblast colony-forming units by feline leukemia virus. Am J Vet Res 49:227-30
Bauer, R M; Olsen, R G (1988) Parameters of production and partial characterization of feline interleukin 2. Vet Immunol Immunopathol 19:173-83
Lewis, M G; Wright, K A; Lafrado, L J et al. (1987) Saliva as a source of feline leukemia virus antigen for diagnosis of disease. J Clin Microbiol 25:1320-2

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