Abstract |
Pig-tailed macaques were vaccinated with a human T-cell lymphotropic virus type I (HTLV-I) subunit vaccine. Vaccinates and controls were challenged with simian T-cell lymphotropic virus type I (STLV-I)-infected cells. Vaccination yielded antibody responses to HTLV-I and STLV-I gag and env precursors. Controls developed HTLV-I and STLV-I antibody to gag and tax protein. Immunization produced syncytium inhibiting antibody and cellular cytotoxicity to virus-infected cells. Reverse transcriptase activity was present in control macaques only, implying that the subunit vaccine was protective against STLV-I infection.
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Authors | C S Dezzutti, D E Frazier, L J Lafrado, R G Olsen |
Journal | Journal of medical primatology
(J Med Primatol)
Vol. 19
Issue 3-4
Pg. 305-16
( 1990)
ISSN: 0047-2565 [Print] Denmark |
PMID | 2172541
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antibodies, Viral
- Antigens, Viral
- Gene Products, env
- Gene Products, gag
- HTLV-I Antibodies
- Viral Vaccines
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Topics |
- Animals
- Antibodies, Viral
(biosynthesis)
- Antibody-Dependent Cell Cytotoxicity
- Antigens, Viral
(immunology)
- Blotting, Western
- Cell Line
- Gene Products, env
(immunology)
- Gene Products, gag
(immunology)
- Giant Cells
- HTLV-I Antibodies
(biosynthesis)
- Human T-lymphotropic virus 1
(immunology)
- Macaca nemestrina
- Retroviridae Infections
(prevention & control)
- Simian T-lymphotropic virus 1
(immunology)
- Vaccination
- Viral Vaccines
(immunology)
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